The DOI matches its Crossref record; 38 of the 39 references it cites were found in a registry or an index; 11 of the 45 sources its claims cite were checked for support.
Chemiexcitation of melanin derivatives induces DNA photoproducts long after UV exposure
Open accessAbstract
The dark side of melanin exposed: Sun worshippers may have more to worry about than the DNA damage that occurs while they're relaxing on the beach. It seems that the DNA photoproducts responsible for cancer-causing mutations in skin cells continue to be generated for hours after sunlight exposure. Premi et al. find that a key mediator of this delayed damage is melanin, a pigment thought to protect against cancer (see the Perspective by Taylor). They propose a “chemiexcitation” model in which reactive oxygen and nitrogen species induced by ultraviolet light excite an electron in melanin fragments. This energy is then transferred to DNA, inducing the same damage as ultraviolet light, but in the dark. Conceivably, this energy could be dissipated by adding quenchers to sunscreens. Science , this issue p. 842 ; see also p. 824
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Claims the paper makes
11 of 45 cited sources checked · 3 supported · 0 flagged · accuracy not yet measured
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“The melanin requirement suggests that the NO• requirement in melanocytes is distinct from that observed in cultured keratinocytes (18).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
What the sources say
- Could not verifycites [18] sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) describes UVA-induced reactive oxygen species in keratinocytes as arising primarily through Nox1-based NADPH oxidase. It does not address a nitric oxide requirement in keratinocytes or compare one with melanocytes; searches for nitric oxide, NO synthase, and nitration found no passage supporting that comparison. (LLM, conf=0.75)
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Could not verify
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Braf-mutant mice develop 10 times more spontaneous melanomas if they carry the pheomelanin-associated Mc1re/e allele (4).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Abstract
What the sources say
- Partly supportedcites [4] sourceExperimental — accuracy not yet measured
The paper’s results passage (labelled Abstract; page unavailable) reports that red Mc1re/e Braf-mutant mice developed melanomas without UV exposure at a higher rate than black Braf-mutant mice, with more than 50% of red mice having tumors after one year. Our copy does not give a tenfold comparison, so the precise magnitude attributed to the paper is not supported. (LLM, conf=0.88)
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The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“This double nature would explain the apparent cancer-facilitating effects of melanin seen in mice and in human epidemiology (2-4, 6).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Proposed Scheme for the Participation of Melanin in Melanoma Development
What the sources say
- Not checked — no full text of the sourcecites [2] source
- Supportedcites [3] source
The Discussion describes melanin’s protective role in darker skin alongside its melanoma-promoting role in the mouse model. It also presents the mouse findings as a potential explanation for human observations, including melanoma risks associated with UVA tanning and pigmented nevi. The claim’s tentative wording matches that interpretation. (LLM, conf=0.90)
- Supportedcites [4] source
The paper’s Abstract (page not provided) reports UV-independent melanoma and oxidative damage linked to the pheomelanin pathway in red mice, while also describing melanin’s UV-protective role. It connects that proposed carcinogenic pathway to the elevated melanoma risk observed in red-haired, fair-skinned humans. The citing sentence’s tentative “would explain” matches the paper’s qualified interpretation. (LLM, conf=0.87)
- Partly supportedcites [6] sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) describes a balance between melanin’s protection and photosensitizing damage, and suggests photosensitization may contribute to the elevated skin-cancer risk associated with red or blonde hair. It also proposes that melanin-related cell death could favor expansion of mutant cells. The paper does not report cancer-facilitating effects of melanin in mice; its mouse experiments measured UV-induced cell death, not cancer. (LLM, conf=0.82)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Yet melanin's ROS generating properties do not explain its role in melanoma development because most mutations in human melanomas display the UV signature of C →T substitutions at sites of adjacent pyrimidines (8, 9).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Abstract
What the sources say
- Partly supportedcites [8] sourceExperimental — accuracy not yet measured
The Introduction and “Canonical Mutations vs Signature Mutations” section report a preponderance of UV-signature mutations in melanomas from sun-exposed body sites. The claim omits that restriction and extends the finding to human melanomas generally. Page numbers are unavailable in our copy. (LLM, conf=0.88)
- Partly supportedcites [9] sourceExperimental — accuracy not yet measured
The Results (Landscape of nonsynonymous somatic mutations; page unavailable) report an excess of UV-linked C>T mutations at dipyrimidines in sun-exposed melanomas. The Discussion says the UV signature was not detected in acral, mucosal, or ocular melanomas. Thus the source supports the signature in sun-exposed melanomas, but not the claim as stated for human melanomas generally. (LLM, conf=0.85)
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“UVA-irradiated mice do not develop melanoma if they lack melanin (3)”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Abstract
What the sources say
- Supportedcites [3] source
The Results section (‘Ultraviolet B and Ultraviolet A dependence of melanoma’; page unavailable) reports that UVA did not initiate melanoma in albino mice, whereas it did in pigmented mice. This supports the claim for the mouse models and exposure conditions discussed in the paper. (LLM, conf=0.91)
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
In the paper
“A O2•–-initiated radical chain reaction in lipids was one possible conduit (26), but inducing lipid peroxidation in isolated nuclei using cumene hydroperoxide did not appear to induce CPD in nuclear DNA (fig. S3).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Electronically Excited Melanin as a Molecular Vector
What the sources say
- Not checked — no full text of the sourcecites [26] source
Load-bearingStrength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Unexpectedly, melanin-containing murine melanocytes instead continued to generate CPD for at least three hours after UVA exposure, at which point generation was offset by DNA repair (Fig. 1B,C).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Delayed Cyclobutane Pyrimidine Dimer Induction in Melanocytes
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The (TC + CT)/TT ratio in melanin-containing cells increased from the UVA-like 0.37 at 0 h (directly-induced CPD) to 1.33 in the CPD arising during the following 2 h (p = 0.027), a ratio more typical of cells irradiated with the higher-energy UVB.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Cytosine-containing Dark CPD
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“To determine if NO• is required for production of dark CPD, we inhibited iNOS by treating melanocytes with aminoguanidine. This resulted in complete suppression of dark CPD production (Fig. 3C).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In support of an additional UV role, we found that exposing melanin-containing melanocytes to UVA created as much nuclear and cytoplasmic nitrotyrosine in 30 min as had accumulated from basal induction over ~8 days (Fig. 3D,E) (fig. S2D) (see Methods).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes
- It may state two separate claims as one. 33
- Probably not a substantial claim. 11
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“The UVB process was also dependent on melanin and thus it differs from the delayed production of CPD that has been reported occasionally in other cell types after UVC or UVB exposure (16-18).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Delayed Cyclobutane Pyrimidine Dimer Induction in Melanocytes
What the sources say
- Not matchedcites [16]
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not checked — no full text of the sourcecites [17] source
- Could not verifycites [18] sourceExperimental — accuracy not yet measured
The UVA irradiation and NADPH oxidase sections describe reactive oxygen species in UVA-exposed keratinocytes, not UVB-induced dark CPDs. Searches for melanin, CPDs, and delayed CPD production after UVB or UVC found no passage addressing the claim in our copy. (LLM, conf=0.75)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Not matched
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“The lower-energy UVA (315-400 nm), which constitutes ~95% of the ultraviolet energy that penetrates the atmosphere, also induces melanoma in mice and in humans who use tanning beds, but it is inefficient at making the cytosine-containing CPD that cause C→T mutations (12, 13).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Abstract
What the sources say
- Partly supportedcites [12] sourceExperimental — accuracy not yet measured
The Abstract Results report elevated melanoma odds among indoor tanners, including users of primarily UVA-emitting devices. The Discussion cautions that the study cannot determine whether UVA or UVB caused those associations. The paper does not report melanoma induction in mice or address cytosine-containing CPDs and C→T mutations. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [13] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: UVA accounts for about 95% of the ultraviolet energy that reaches the Earth's surface.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“UV-irradiated melanin, especially pheomelanin, triggers apoptosis and production of reactive oxygen species (ROS) and DNA strand breaks (5, 6).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Abstract
What the sources say
- Not checked — no full text of the sourcecites [5] source
- Partly supportedcites [6] sourceExperimental — accuracy not yet measured
The Abstract concludes that UV-irradiated melanin, particularly pheomelanin, photosensitizes nearby cells to apoptosis. It also says irradiated melanin generates reactive oxygen species in vitro or in cultured cells, which can indirectly cause DNA strand breaks. The claim overstates the strand-break finding: the Results report no detectable signal above background for single-strand breaks immediately after UV irradiation of mouse skin. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“UVA-irradiated melanocytes generated ultra-weak chemiluminescence for several hours post-irradiation and only in cells containing melanin (Fig. 3F,G).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Assays for 3-nitrotyrosine revealed that basal nitration activity was present even without UV, that it was located primarily in the nucleus, and that its appearance required melanin (Fig. 3D,E) (fig. S2D).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Human melanocytes also generated dark CPD after UVA or UVB exposure (Fig. 1E, fig. S1I) although there was inter-individual variation in the response, particularly for UVA.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Delayed Cyclobutane Pyrimidine Dimer Induction in Melanocytes
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Because DBAS diverts triplet energy to luminescence, this compound also blocked dark CPD (fig. S2E).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The former suppressed production of dark CPD by 64% and the latter abolished it (figs. S2A,B).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Unirradiated normal melanocytes but not albino melanocytes showed dark granules in the cytoplasm, especially in the perinuclear area (fig. S5).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Electronically Excited Melanin as a Molecular Vector
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The eumelanin monomer 5,6-dihydroxyindole-2-carboxylic acid (DHICA) and the pheomelanin monomer 5-S-cysteinyldopa (5SCD) also generated chemiluminescence when oxidized (Fig. 4A).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Electronically Excited Melanin as a Molecular Vector
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Scanning this fraction of the HPLC eluate across the small-molecule region of the mass spectrometer revealed four principal m/z peaks, of which the second largest was 224 daltons (Fig. 4F).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Electronically Excited Melanin as a Molecular Vector
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“We found that chemiluminescence began immediately and proceeded for >10 min.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Electronically Excited Melanin as a Molecular Vector
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“CPD were inhibited to a level below that at 0 h, indicating that dark CPD were also induced during the irradiation itself.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The negative result with albino melanocytes implicated melanin in the process and ruled out the involvement of photosensitizing compounds in the growth medium.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Delayed Cyclobutane Pyrimidine Dimer Induction in Melanocytes
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“This suggests that pheomelanin is both a poorer shield against normal CPD formation and a more potent dark CPD generator.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Delayed Cyclobutane Pyrimidine Dimer Induction in Melanocytes
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Mass spectrometry ruled out the possibilities that (i) the ELISA and comet assays cross-reacted with melanin-DNA adducts and (ii) the delayed CPD appearance reflected greater access of the antibody or endonuclease due to a change in DNA conformation after UV exposure.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Cytosine-containing Dark CPD
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“This likely reflects genetic differences between the donors.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Delayed Cyclobutane Pyrimidine Dimer Induction in Melanocytes
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds.
In the paper
“The lifetime of triplet carbonyls is ~10 μs (24), so a signal persistent over the course of hours indicates ongoing creation.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
What the sources say
- Not checked — no full text of the sourcecites [24] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Blondes and redheads, who have a higher ratio of yellow pheomelanin to brown eumelanin in their skin and hair, have a 2-4 times greater risk for melanoma than dark-haired individuals and the pheomelanin/eumelanin ratio accounts for some of this risk (2).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Abstract
What the sources say
- Not checked — no full text of the sourcecites [2] source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Such mutations arise from cyclobutane pyrimidine dimers (CPD), which join adjacent pyrimidines to distort the DNA helix (10, 11);”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Abstract
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“An effect of antioxidants on CPD detectable immediately after UV has been reported, but was linked to changes in chromatin structure (20).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
What the sources say
- Not checked — no full text of the sourcecites [20] source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“A diagnostic for excited triplet states is that their energy can also discharge via ultra-weak blue or green luminescence (23).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
What the sources say
- Not checked — no full text of the sourcecites [23] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
In the paper
“The DHICA analog of the predicted eumelanin degradation product (29) (Fig. 4E, structure 1) has a molecular weight of 225 daltons and would be highly polar.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Electronically Excited Melanin as a Molecular Vector
What the sources say
- Not checked — no full text of the sourcecites [29] source
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The sustained time course of dark CPD generation can be accounted for by the prolonged steps of UV-induction of NOX and iNOS, peroxynitrite-induced solubilization of melanin to fragments or release of pre-melanin monomers from UV-damaged melanosomes and vesicles, and migration to the nucleus.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Proposed Scheme for the Participation of Melanin in Melanoma Development
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“A consequence of these events is that melanin may be carcinogenic as well as protective against cancer.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Proposed Scheme for the Participation of Melanin in Melanoma Development
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“An alternative reaction is formation of a dioxetane moiety at the pyrrole ring (32), also leading to a polar structure of 225 daltons (structure 2).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Electronically Excited Melanin as a Molecular Vector
What the sources say
- Not checked — no full text of the sourcecites [32] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Melanin is an unusual polymer whose properties set the stage for the events we have described (33).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Proposed Scheme for the Participation of Melanin in Melanoma Development
What the sources say
- Not checked — no full text of the sourcecites [33] source
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✗ Checkable: fails✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may be too vague to check against evidence.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“It was proposed long ago that chemiexcitation – the creation of chemical reaction products containing excited electrons that underlie bioluminescence in lower organisms – has broad importance in biology (22, 23).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Proposed Scheme for the Participation of Melanin in Melanoma Development
What the sources say
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“UV exposure additionally excites the rings to an energy that, especially for pheomelanin, ejects an electron that is captured by oxygen to yield more O2•- (5, 34).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Proposed Scheme for the Participation of Melanin in Melanoma Development
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Peroxynitrite's presence in the nucleus without UV exposure is plausible because synthesis of melanin monomers is a redox reaction that releases O2•– (7) and melanosomes are assembled in the perinuclear space.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
What the sources say
- Not checked — no full text of the sourcecites [7] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
In the paper
“These monomers are lipophilic and are therefore potentially able to enter the nucleus, and are concentrated in perinuclear coated vesicles before transfer to melanosomes (27).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Electronically Excited Melanin as a Molecular Vector
What the sources say
- Not checked — no full text of the sourcecites [27]
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These evanescent electronically excited products transfer their triplet energy to DNA hours after the original UV exposure, creating mutagenic cyclobutane pyrimidine dimers in the dark.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Proposed Scheme for the Participation of Melanin in Melanoma Development
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In summary, we have shown that exposing melanin-containing cells to UV radiation induces superoxide and nitric oxide, causing an orders-of-magnitude peroxynitrite spike that degrades melanin, allows melanin-like granules to appear in the nucleus, and excites melanin derivatives to a triplet state that has the high energy of a UV photon (Fig. 5).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Proposed Scheme for the Participation of Melanin in Melanoma Development
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“A longer-lasting source of O2•– in cells is NADPH oxidase (NOX), which is rapidly induced by UVA (19).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
What the sources say
- Not checked — no full text of the sourcecites [19] source
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In the paper
“One of the few biologically-synthesized molecules that can initiate such “photochemistry in the dark” (22, 23) is peroxynitrite (ONOO–) (24), which is generated by the reaction of O2•– with nitric oxide (NO•).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
What the sources say
- Not checked — no full text of the sourcecites [24] source
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A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“One benefit of dark photochemistry's slow course is that it allows intervention.”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Proposed Scheme for the Participation of Melanin in Melanoma Development
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In the paper
“The pigment melanin protects against sunlight-induced burns, DNA damage, and skin cancer due to an unusually broad absorption spectrum and perhaps radical scavenging activity (1).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Abstract
What the sources say
- Not checked — no full text of the sourcecites [1] source
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“NOX and the NO• generator iNOS are UV-inducible within minutes and are expressed in melanocytes, including nuclear NOX4 (25).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Photochemical Pathway
What the sources say
- Not checked — no full text of the sourcecites [25] source
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In the paper
“A blocker of dark CPD, α-tocopherol (vitamin E), is not only an antioxidant but also inactivates dioxetanes by converting them to a pair of diols (35).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Proposed Scheme for the Participation of Melanin in Melanoma Development
What the sources say
- Not checked — no full text of the sourcecites [35] source
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None of the sources cited for this claim have been checked yet.
In the paper
“Melanin polymer rapidly solubilizes when exposed to hydrogen peroxide (H2O2) (28) and its degradation by peroxidation or UV-photoionization has been proposed to involve dioxetane and triplet carbonyls (29, 30).”
§ Chemiexcitation of Melanin Derivatives Induces DNA Photoproducts Long after UV Exposure > Electronically Excited Melanin as a Molecular Vector
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
The paper relies on this without support.
UVA accounts for about 95% of the ultraviolet energy that reaches the Earth's surface.
“The lower-energy UVA (315-400 nm), which constitutes ~95% of the ultraviolet energy that penetrates the atmosphere, also induces melanoma in mice and in humans who use tanning beds, but it is inefficient at making the cytosine-containing CPD that cause C→T mutations (12, 13).”
The paper relies on this without support.
Disorders of CPD repair, such as xeroderma pigmentosum, increase childhood melanoma risk by 10,000-fold.
“genetic disorders of CPD repair such as xeroderma pigmentosum elevate the risk for childhood melanoma by 10,000-fold.”
The paper relies on this without support.
Peroxynitrite and nitric oxide can diffuse far enough from where they are made to reach their target molecules.
“Peroxynitrite and NO• are stable enough to diffuse significant distances from the site of generation to the target molecule.”
The authors state this as an assumption.
The dark cytoplasmic granules seen in unirradiated normal melanocytes are melanin aggregates located in melanosomes, coated vesicles, and endoplasmic reticulum.
“We presume these are melanin aggregates in melanosomes, coated vesicles, and endoplasmic reticulum because they have the same size and cellular locations as granules seen in melanocytes immunostained for tyrosinase (31).”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source doesn’t support the claim as written.
In the citing paper
“This result suggests that melanin-like reactants might be creating dCPDs by a reaction other than the indole ring dioxetane proposed in reference (32).”
From Chemiexcitation: Mammalian Photochemistry in the Dark† (2023) · cites this paper as [32]
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“This means that UV-filtering melanin can be found in all keratinocytes of the epidermis whereas it is absent in corneal epidermal cells [ 70 ].”
From Faster DNA Repair of Ultraviolet-Induced Cyclobutane Pyrimidine Dimers and Lower Sensitivity to Apoptosis in Human Corneal Epithelial Cells than in Epidermal Keratinocytes (2016) · cites this paper as [70]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The generation of ROS and peroxynitrites, mainly in mouse melanocytes that only synthesize pheomelanin, contributes to the delayed induction of cyclobutane pyrimidine dimers, the major form of DNA photoproducts, post-UV exposure, which increases the risk for UV signature mutations that are prevalent in melanoma [ 20 ].”
From Differential Induction of Reactive Oxygen Species and Expression of Antioxidant Enzymes in Human Melanocytes Correlate with Melanin Content: Implications on the Response to Solar UV and Melanoma Susceptibility (2022) · cites this paper as [20]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“a brief UV exposure activates the enzymes nitric oxide synthase (NOS) and NADPH oxidase (NOX) to generate the radicals nitric oxide (•NO) and superoxide (O2•−) for hours afterward; the mechanism of induction is still not known.”
From Chemiexcitation: Mammalian Photochemistry in the Dark† (2023) · cites this paper as [32]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“That process was initiated by nitric oxide and superoxide, radicals triggered by ultraviolet light or inflammation.”
From Chemiexcitation: Mammalian Photochemistry in the Dark† (2023) · cites this paper as [32]
Experimental — accuracy not yet measured
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Based on analogous reactions in the literature, it is proposed that ambient O2 adds to create a peroxyl radical, which then cyclizes to create a strained 4-atom ring containing C–O–O–C, termed a dioxetane”
From Chemiexcitation: Mammalian Photochemistry in the Dark† (2023) · cites this paper as [32]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In mammals, chemiexcitation was discovered as energy transferred directly from excited melanin to DNA, creating the lethal and carcinogenic cyclobutane pyrimidine dimer.”
From Chemiexcitation: Mammalian Photochemistry in the Dark† (2023) · cites this paper as [32]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The chemiexcitation events were discovered in melanocyte cell cultures and in murine skin, using a fluorescent triplet-state reporter to detect the transient triplet state, blocking these events with the radical scavenger vitamin E or the triplet-specific quencher sorbate, and identifying dCPDs using mass spectrometry and immunohistochemistry.”
From Chemiexcitation: Mammalian Photochemistry in the Dark† (2023) · cites this paper as [32]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Recently our laboratory discovered that chemiexciting the skin pigment melanin sends melanocytes down the path to melanoma even in the dark”
From Chemiexcitation: Mammalian Photochemistry in the Dark† (2023) · cites this paper as [32]
The cited source says what the claim attributes to it.
In the citing paper
“The pyrrole ring was implicated as the site of a dioxetane (Fig. 4c) (32); the catechol ring of eumelanin has also been proposed as a site for dioxetane formation (43).”
From Chemiexcitation: Mammalian Photochemistry in the Dark† (2023) · cites this paper as [32]
In the citing paper
“Pheomelanins have also been implicated in UV-radiation-independent carcinogenic contributions to melanomagenesis by inducing oxidative DNA damage [65,66,67].”
From “Fifty Shades” of Black and Red or How Carboxyl Groups Fine Tune Eumelanin and Pheomelanin Properties (2016) · cites this paper as [67]
In the citing paper
“This shows that MAA may have even greater potential for photoprotection over current filters”
From Mycosporine-Like Amino Acids for Skin Photoprotection (2019) · cites this paper as [5]
In the citing paper
“the recent discovery of delayed (also know as ‘dark’) CPD formation, which suggests that CPD can form for hours after exposure through a triplet photoexcitation mechanism [5]”
From Mycosporine-Like Amino Acids for Skin Photoprotection (2019) · cites this paper as [5]
In the citing paper
“Therefore, this work is a strong indication that the consequences of UVA exposure for the development of melanoma have been underestimated.”
From Sunlight damage to cellular DNA: focus on oxidatively generated lesions (2017) · cites this paper as [99]
In the citing paper
“Recently, it was demonstrated that CPDs could also continue to be generated in the skin for more than 3 h after exposure to UVA [99].”
From Sunlight damage to cellular DNA: focus on oxidatively generated lesions (2017) · cites this paper as [99]
In the citing paper
“UVB irradiation can cause the loss of cellular integrity, direct damage to DNA and trigger various cellular responses including apoptosis [3] and inflammation [4] in skin cells including melanocytes (MC).”
From Nrf2 in keratinocytes modulates UVB-induced DNA damage and apoptosis in melanocytes through MAPK signaling (2017) · cites this paper as [3]
In the citing paper
“ROS and reactive nitrogen species (RNS) generated in melanocytes in response to UVA radiation lead to the production of “dark CPDs” hours after UVA exposure74.”
From Mechanisms and prevention of UV‐induced melanoma (2018) · cites this paper as [74]
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“Noticeably, the CPDs generated through this indirect process have been shown to occur after rather than during UV exposure and are thus referred to as “dark CPDs” [49].”
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““Dark” CPDs are formed in melanin-containing keratinocytes and melanocytes > 3 h after UVA or B exposure due to the resulting ROS, and were most prominent in pheomelanin containing cells (Premi et al., 2015).”
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“The experimental results demonstrated that pheomelanin not only was poorly effective in protecting from CPD formation but it also induced dark CPD generation [53].”
BackgroundNahhas, A. F., ABDEL‐MALEK, Z. A., Kohli, I., Braunberger, T. L., Lim, H. W., & Hamzavi, I. H. (2018) · Photodermatology Photoimmunology & Photomedicine · doi:10.1111/phpp.12423 · Cited by 101
Delinasios, G. J., Karbaschi, M., Cooke, M. S., & Young, A. R. (2018) · Scientific Reports · doi:10.1038/s41598-017-18924-4 · Cited by 95
“13 for “dark” CPD. Whilst it is not possible to distinguish between ‘dark” CPD and the formation of those from direct UVR absorption (“light” CPD), we speculate that CPD burden at time 0 h primarily represents the latter and that the peak at 0.5–1 h represents the addition of “dark” to “light” CPD.”
BackgroundResultInfluentialCurrent challenges in photoprotection
Lim, H. W., Arellano‐Mendoza, M. I., & Stengel, F. M. (2016) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2016.09.040 · Cited by 97
UV and ionizing radiations induced DNA damage, differences and similarities
Ravanat, J.-L., & Douki, T. (2016) · Radiation Physics and Chemistry · doi:10.1016/j.radphyschem.2016.07.007 · Cited by 94
Self-citationYeager, D. G., & Lim, H. W. (2019) · Dermatologic Clinics · doi:10.1016/j.det.2018.11.003 · Cited by 91
Targeting MC1R depalmitoylation to prevent melanomagenesis in redheads
Chen, S., Han, C., Miao, X., Li, X., Yin, C., Zou, J., Liu, M., Li, S., Stawski, L., Zhu, B., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08691-3 · Cited by 87
Autophagy in UV Damage Response
Sample, A., & He, Y. (2016) · Photochemistry and Photobiology · doi:10.1111/php.12691 · Cited by 90
“The abundance of UVA-induced CPDs, and ineffective repair of these lesions, may therefore form a significant source of UVA-induced skin damage (56).”
BackgroundUV Radiation in DNA Damage and Repair Involving DNA-Photolyases and Cryptochromes
Vechtomova, Y. L., Telegina, T. A., Buglak, A. A., & Kritsky, M. (2021) · Biomedicines · doi:10.3390/biomedicines9111564 · Cited by 98
“However, as previously described, melanin can also be carcinogenic, contributing to the formation of CPD even after irradiation termination [8,26].”
BackgroundZheng, X., Jia, Y., & Chen, A. (2021) · Nature Communications · doi:10.1038/s41467-021-25178-2 · Cited by 90
Belozerskaya, T. A., Гесслер, Н. Н., & Aver‘yanov, A. A. (2015) · Springer eBooks · doi:10.1007/978-3-319-19456-1_29-1 · Cited by 92
Melanin Transfer and Fate within Keratinocytes in Human Skin Pigmentation
Benito-Martínez, S., Salavessa, L., Raposo, G., Marks, M. S., & Delevoye, C. (2021) · Integrative and Comparative Biology · doi:10.1093/icb/icab094 · Cited by 78
Adaptive redox homeostasis in cutaneous melanoma
Arslanbaeva, L. R., & Santoro, M. M. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101753 · Cited by 87
Ultraviolet radiation-mediated development of cutaneous melanoma: An update
Emri, G., Paragh, G., Tósaki, Á., Janka, E. A., Kollár, S., Hegedűs, C., Gellén, E., Horkay, I., Koncz, G., & Remenyik, É. (2018) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2018.06.005 · Cited by 87
Endogenous Photosensitizers in Human Skin
Bastos, E. L., Quina, F. H., & Baptista, M. S. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.2c00787 · Cited by 86
Allegra, A., Pioggia, G., Tonacci, A., Musolino, C., & Gangemi, S. (2020) · Antioxidants · doi:10.3390/antiox9050448 · Cited by 84
“Thus, areas of the genome with a high frequency of adjacent pyrimidines are considered “UV hotspots” and show high rates of C > T and CC > TT “UV signature” mutations [14].”
BackgroundBrouwer, N. J., Verdijk, R. M., Heegaard, S., Marinkovic, M., Esmaeli, B., & Jager, M. J. (2021) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2021.100971 · Cited by 81
“Eumelanin has protective effects on melanoma formation, by shielding against UV radiation (De Leeuw et al., 2001) and scavenging reactive oxygen species (ROS) and free radicals (Brenner and Hearing, 2008); pheomelanin can be involved in DNA damage via UVA (Premi et al., 2015) and by itself via independent ROS formatio…”
BackgroundInfluentialAll You Need Is Light. Photorepair of UV-Induced Pyrimidine Dimers
Banaś, A. K., Zgłobicki, P., Kowalska, E., Bażant, A., Dziga, D., & Strzałka, W. (2020) · Genes · doi:10.3390/genes11111304 · Cited by 80
“It has been demonstrated that melanin may act in vivo as a photosensitizer [35].”
BackgroundJeayeng, S., Wongkajornsilp, A., Slominski, A. T., Jirawatnotai, S., Sampattavanich, S., & Panich, U. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.05.009 · Cited by 78
“UVB irradiation can cause the loss of cellular integrity, direct damage to DNA and trigger various cellular responses including apoptosis [3] and inflammation [4] in skin cells including melanocytes (MC).”
BackgroundUVA Radiation, DNA Damage, and Melanoma
Jin, S., Padron, F., & Pfeifer, G. P. (2022) · ACS Omega · doi:10.1021/acsomega.2c04424 · Cited by 87
Photoprotection versus photodamage: updating an old but still unsolved controversy about melanin
Solano, F. (2016) · Polymer International · doi:10.1002/pi.5117 · Cited by 76
NNT mediates redox-dependent pigmentation via a UVB- and MITF-independent mechanism
Allouche, J., Rachmin, I., Adhikari, K., Pardo, L. M., Lee, J. H., McConnell, A. M., Kato, S., Fan, S., Kawakami, A., Suita, Y., et al. (2021) · Cell · doi:10.1016/j.cell.2021.06.022 · Cited by 72
“UV radiation can interact photochemically with DNA to form cyclobutane pyrimidine dimers (CPD) and 6,4-photoproducts 10 and can cause the production of reactive oxygen species (ROS) through multiple mechanisms, thereby increasing the risk of developing skin cancer (Premi et al., 2015).”
BackgroundSelf-citationNguyen, T. M. H., Kim, S., & Bark, C. W. (2020) · Journal of Materials Chemistry A · doi:10.1039/d0ta08738f · Cited by 74
Frequent DPH3 promoter mutations in skin cancers
Denisova, E., Heidenreich, B., Nagore, E., Rachakonda, P. S., Hosen, M. I., Akrap, I., Traves, V., García‐Casado, Z., López‐Guerrero, J. A., Requena, C., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.5771 · Cited by 68
Edge, R., & Truscott, T. (2021) · Oxygen · doi:10.3390/oxygen1020009 · Cited by 64
“It has been recognised for many years that even though melanins are photoprotective they can also be photosenstisers and, therefore, lead to skin damage [34,35].”
BackgroundKim, E., Kang, M., Tschirhart, T., Malo, M. E., Dadachova, E., Cao, G., Yin, J., Bentley, W. E., Wang, Z., & Payne, G. F. (2017) · Biomacromolecules · doi:10.1021/acs.biomac.7b01166 · Cited by 70
Four‐membered cyclic peroxides: Carriers of chemical energy
Bastos, E. L., Farahani, P., Bechara, E. J. H., & Baader, W. J. (2017) · Journal of Physical Organic Chemistry · doi:10.1002/poc.3725 · Cited by 68
Self-citationMalignant Melanoma: An Overview, New Perspectives, and Vitamin D Signaling
Slominski, R. M., Kim, T., Janjetović, Z., Brożyna, A. A., Podgórska, E., Dixon, K. M., Mason, R. S., Tuckey, R. C., Sharma, R., Crossman, D. K., et al. (2024) · Cancers · doi:10.3390/cancers16122262 · Cited by 79
Significance of melanin distribution in the epidermis for the protective effect against UV light
Zamudio Díaz, D. F., Busch, L., Kröger, M., Klein, A. L., Lohan, S. B., Mewes, K. R., Vierkotten, L., Witzel, C., Rohn, S., & Meinke, M. C. (2024) · Scientific Reports · doi:10.1038/s41598-024-53941-0 · Cited by 71
Boosting the Optical Absorption of Melanin-like Polymers
Bai, W., Yang, P., Liu, H., Zou, Y., Wang, X., Yang, Y., Gu, Z., & Li, Y. (2022) · Macromolecules · doi:10.1021/acs.macromol.2c00506 · Cited by 66
Netcharoensirisuk, P., Abrahamian, C., Tang, R., Chen, C., Rosato, A. S., Beyers, W. C., Chao, Y., Filippini, A., Pietro, S. M. D., Bartel, K., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-88196-6 · Cited by 69
“parviflora (upper panel), and endolysosomal patch-clamp measurement demonstrating effect of the extract (10 μg/ ml) to block TPC2 stimulated by PI(3,5)P2 (1 μM).”
BackgroundMethodInfluentialSelenomelanin: An Abiotic Selenium Analogue of Pheomelanin
Cao, W., McCallum, N. C., Ni, Q. Z., Li, W., Boyce, H., Mao, H., Zhou, X., Sun, H. R., Thompson, M. P., Battistella, C., et al. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c05573 · Cited by 67
Shi, Y., Manco, M. C., Moyal, D. D., Huppert, G., Araki, H., Banks, A. R., Joshi, H., McKenzie, R., Seewald, A., Griffin, G., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0190233 · Cited by 67
Effect of ultraviolet radiation on the Nrf2 signaling pathway in skin cells
Ryšavá, A., Vostálová, J., & Svobodová, A. R. (2021) · International Journal of Radiation Biology · doi:10.1080/09553002.2021.1962566 · Cited by 69
de Assis, L. V. M., Moraes, M. N., Cruz‐Machado, S. D. S., & Castrucci, A. M. D. L. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.03.001 · Cited by 62
Kim, J., Hong, A., Kim, Y.-H., et al. (2020) · Theranostics · doi:10.7150/thno.41502 · Cited by 64
“For instance, skin tissue is directly exposed to ultraviolet radiation (UVR), which renders skin tissue highly susceptible to carcinogenesis via somatic mutations through the generation of reactive oxygen and nitrogen species [1].”
Backgroundde Assis, L. V. M., Moraes, M. N., Magalhães-Marques, K. K., & Castrucci, A. M. D. L. (2018) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2018.01.004 · Cited by 65
Shedding a New Light on Skin Aging, Iron- and Redox-Homeostasis and Emerging Natural Antioxidants
Pourzand, C., Albieri, A., & Raczek, N. N. (2022) · Antioxidants · doi:10.3390/antiox11030471 · Cited by 68
“The formation of ‘dark’ CPDs in melanocytes and pigmented skin appear to occur long after UVA irradiation via the chemo-excitation of melanin [94].”
BackgroundHerráiz, C., Martínez‐Vicente, I., & Maresca, V. (2021) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.12980 · Cited by 65
“In human melanocytes, exposure to UVR causes chemical excitation of fragments of the pigment melanin, resulting in the formation of additional CPDs (Premi et al., 2015). α- MSH has been shown to protect against the UVR- induced oxidative stress by several pigment- independent mechanisms, including…”
BackgroundInfluentialImpact of Age and Insulin-Like Growth Factor-1 on DNA Damage Responses in UV-Irradiated Human Skin
Kemp, M. G., Spandau, D. F., & Travers, J. B. (2017) · Molecules · doi:10.3390/molecules22030356 · Cited by 65
“UVA is also capable of inducing CPD formation by direct photon absorption [12,13] and via a recently characterized process termed chemiexcitation, in which reactive oxygen and nitrogen species induced by UVA combine to excite electrons in fragments of melanin that ultimately induce CPD production in genomic DNA [14,15…”
BackgroundThe dark side of the light: mechanisms of photocarcinogenesis
Coelho, M. M. V., Matos, T. R., & Apetato, M. (2016) · Clinics in Dermatology · doi:10.1016/j.clindermatol.2016.05.022 · Cited by 61
Lee, V., Bashir, H. M., & Seykora, J. (2017) · Journal of Ophthalmic and Vision Research · doi:10.4103/jovr.jovr_114_17 · Cited by 60
“[32,33] The corneal epithelium lacks features skin possesses to resist UV damage, such as a thicker epithelial layer, stratum corneum, and melanocytes, which all help to mitigate the effects of UV radiation.[34,35] Mallet et al show instead that corneal epithelium appears to repair signature UV‐induced mutations more…”
BackgroundMolecular Frontiers in Melanoma: Pathogenesis, Diagnosis, and Therapeutic Advances
Kim, H. J., & Kim, Y. H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052984 · Cited by 69
Goswami, L., Pandey, R., & Gupta, G. (2020) · Optical Materials · doi:10.1016/j.optmat.2020.109820 · Cited by 58
Hierarchical Micro‐/Nanostructures from Human Hair for Biomedical Applications
Zheng, D., Hong, S., Xu, L., Li, C., Li, K., Cheng, S., & Zhang, X. (2018) · Advanced Materials · doi:10.1002/adma.201800836 · Cited by 57
Stark, M. S., Tan, J. M., Tom, L. N., Jagirdar, K., Lambie, D., Schaider, H., Soyer, H. P., & Sturm, R. A. (2018) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2018.02.012 · Cited by 56
“This notion is supported by the study by Premi et al. (2015), which described that the many of cyclobutane pyrimidine dimers arise via the breakdown of melanin pigment.”
ResultUltraviolet light and melanoma
Craig, S., Earnshaw, C. H., & Virós, A. (2018) · The Journal of Pathology · doi:10.1002/path.5039 · Cited by 56
“A novel mechanism by which UVA can induce any type of CPD formation has been recently suggested, and, paradoxically, this depends on melanin [52].”
BackgroundRajkumar, S., & Watson, I. R. (2016) · British Journal of Cancer · doi:10.1038/bjc.2016.195 · Cited by 61
“However, recent studies have shown that UVA can induce C4T signature mutations through a reactive oxygen species (ROS)-dependent mechanism involving both the the photoprotective black eumelanin and the phototoxic red pheomelanin (Noonan et al, 2012; Premi et al, 2015).”
BackgroundThe Dark Side of Melanin Secretion in Cutaneous Melanoma Aggressiveness
Cabaço, L. C., Tomás, A., Pojo, M., & Barral, D. C. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.887366 · Cited by 60
“melanin and contribute to mutations triggering CM cell immortalization and carcinogenesis (33).”
BackgroundInfluentialGrigalavicius, M., Moan, J. E., Dahlback, A., & Juzeniene, A. (2015) · International Journal of Dermatology · doi:10.1111/ijd.13065 · Cited by 57
Dong, M., Zheng, X., Li, Q., et al. (2024) · Materials Today · doi:10.1016/j.mattod.2024.03.004 · Cited by 55
Prevention of DNA damage in human skin by topical sunscreens
Olsen, C. M., Wilson, L. F., Green, A. C., Biswas, N., Loyalka, J., & Whiteman, D. C. (2017) · Photodermatology Photoimmunology & Photomedicine · doi:10.1111/phpp.12298 · Cited by 54
“For that study, biopsies were taken 24 h and 14 days following UVR exposure, which covers the time period during which ‘dark CPDs’ can form, putatively as a result of UVA-induced reactive oxygen and nitrogen species (28).”
Background
Metadata
- Authors
- Premi, S., Wallisch, S., Mano, C. M., Weiner, A. B., Bacchiocchi, A., Wakamatsu, K., Bechara, E. J. H., Halaban, R., Douki, T., & Brash, D. E.
- Affiliations
- Yale University (US)
- Universidade de São Paulo (BR)
- Fujita Health University (JP)
- Yale Cancer Center (US)
- Université Joseph Fourier (FR)
- Corresponding author
- Bechara, Etelvino J. H.
- Douki, Thierry
- Brash, Douglas E.
- ORCID
- Venue
- Science
- Published
- 2015-02-20
- Volume
- 347
- Issue
- 6224
- Pages
- 842-847
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC4432913
- OpenAlex
- W2093971029
- Semantic Scholar
- 26c414be169fcb7ec90f18696beb5729a3815347
- Cited by
- 550
- References
- 39
- Citations by year
- 2026: 34 · 2025: 47 · 2024: 43 · 2023: 43 · 2022: 54 · 2021: 66 · 2020: 46 · 2019: 45 · 2018: 45 · 2017: 46 · 2016: 53 · 2015: 24
- FWCI
- 38.23
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- Funders
- Department of Defense CDMRP (CA093473P1, CA093473)
- University of Veterinary Medicine, Vienna
- Fundacao de Amparo a Pesquisa do Estado de Sao Paulo
- FAPESP (06/56530-4)
- NIH (P50 CA121974, P30 DK34989)
- Topics
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Photochemistry and Electron Transfer Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
- Health Sciences › Medicine › Dermatology › Skin Protection and Aging
- Keywords
- melanin, chemiexcitation, cyclobutane pyrimidine dimers, DNA photoproducts, melanoma, UVA, melanocytes, triplet state, reactive oxygen species, reactive nitrogen species, tanning beds
- MeSH terms
- Animals, Cells, Cultured, Cytosine, DNA, DNA Damage, Energy Transfer, Humans, Melanins, Melanocytes, Melanoma, Mice, Inbred C57BL, Mutation, Neoplasms, Radiation-Induced, Pyrimidine Dimers, Skin Neoplasms, Sunlight, Thymine, Ultraviolet Rays, Mutagenesis, Photons, Receptor, Melanocortin, Type 1, Mice
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