The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.
New functions of XPC in the protection of human skin cells from oxidative damage
Open accessAbstract
Xeroderma pigmentosum (XP) C is involved in the recognition of a variety of bulky DNA-distorting lesions in nucleotide excision repair. Here, we show that XPC plays an unexpected and multifaceted role in cell protection from oxidative DNA damage. XP-C primary keratinocytes and fibroblasts are hypersensitive to the killing effects of DNA-oxidizing agents and this effect is reverted by expression of wild-type XPC. Upon oxidant exposure, XP-C primary keratinocytes and fibroblasts accumulate 8,5'-cyclopurine 2'-deoxynucleosides in their DNA, indicating that XPC is involved in their removal. In the absence of XPC, a decrease in the repair rate of 8-hydroxyguanine (8-OH-Gua) is also observed. We demonstrate that XPC-HR23B complex acts as cofactor in base excision repair of 8-OH-Gua, by stimulating the activity of its specific DNA glycosylase OGG1. In vitro experiments suggest that the mechanism involved is a combination of increased loading and turnover of OGG1 by XPC-HR23B complex. The accumulation of endogenous oxidative DNA damage might contribute to increased skin cancer risk and account for internal cancers reported for XP-C patients.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
In the citing paper
“Additionally, studies using human keratinocytes and fibroblasts from XPC patients showed that this protein is important to prevent the accumulation of oxidatively generated DNA damage and its killing effects after exposure to oxidants, such as potassium bromate, X-rays, and methylene blue plus visible light [244,245,253].”
From Sunlight damage to cellular DNA: focus on oxidatively generated lesions (2017) · cites this paper as [244]
In the citing paper
“In addition to the main role of the XPC complex in the recognition of DNA-distorting lesions, it has been demonstrated that it can functionally interact with several BER proteins, including 3-methyladenine DNA glycosylase, thymine DNA glycosylase (TDG), uracil-DNA glycosylases (UDG), apurinic/apyrimidinic endonuclease 1 (APE1), and 8-oxoguanine DNA glycosylase (OGG1) [244][245][246][247][248][249]”
From Sunlight damage to cellular DNA: focus on oxidatively generated lesions (2017) · cites this paper as [244]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Genome maintenance mechanisms for preventing cancer
Hoeijmakers, J. H. J. (2001) · Nature · doi:10.1038/35077232 · Cited by 3,939
Oxidative DNA damage and disease: induction, repair and significance
Evans, M. D., Dizdaroglu, M., & Cooke, M. S. (2004) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2003.11.001 · Cited by 1,372
Agar, N., Halliday, G. M., Barnetson, R. S., Ananthaswamy, H. N., Wheeler, M., & Jones, A. M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401141101 · Cited by 536
DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy
Lehmann, A. (2003) · Biochimie · doi:10.1016/j.biochi.2003.09.010 · Cited by 518
Subpathways of nucleotide excision repair and their regulation
Hanawalt, P. C. (2002) · Oncogene · doi:10.1038/sj.onc.1206096 · Cited by 447
A multistep damage recognition mechanism for global genomic nucleotide excision repair
Sugasawa, K., Okamoto, T., Shimizu, Y., Masutani, C., Iwai, S., & Hanaoka, F. (2001) · Genes & Development · doi:10.1101/gad.866301 · Cited by 435
Hill, J. W. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.2.430 · Cited by 416
Bjørås, M., Luna, L., Johnsen, B., Hoff, E., Haug, T., Rognes, T., & Seeberg, E. C. (1997) · The EMBO Journal · doi:10.1093/emboj/16.20.6314 · Cited by 353
Self-citationKuraoka, I., Bender, C., Romieu, A., Cadet, J., Wood, R. D., & Lindahl, T. L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.070471597 · Cited by 349
Araki, M., Masutani, C., Takemura, M., Uchida, A., Sugasawa, K., Kondoh, J., Ohkuma, Y., & Hanaoka, F. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100855200 · Cited by 335
Are we sure we know how to measure 8-oxo-7,8-dihydroguanine in DNA from human cells?
Collins, A. R., Cadet, J., Möller, L., Poulsen, H. E., & Viña, J. (2004) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2003.12.022 · Cited by 312
In situ analysis of repair processes for oxidative DNA damage in mammalian cells
Lan, L., Nakajima, S., Oohata, Y., Takao, M., Okano, S., Masutani, M., Wilson, S. H., & Yasui, A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406048101 · Cited by 299
Brooks, P. J., Wise, D. S., Berry, D. A., Kosmoski, J. V., Smerdon, M. J., Somers, R. L., Mackie, H., Spoonde, A. Y., Ackerman, E. J., Coleman, K. G., et al. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002259200 · Cited by 298
Measurement of DNA oxidation in human cells by chromatographic and enzymic methods
European Standards Committee on Oxidative DNA Damage (ESCODD) (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(03)00041-8 · Cited by 286
Vidal, A. E. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.6.1285 · Cited by 278
The Type of DNA Glycosylase Determines the Base Excision Repair Pathway in Mammalian Cells
Fortini, P., Parlanti, E., Sidorkina, O. M., Laval, J., & Dogliotti, E. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.21.15230 · Cited by 257
Self-citationThe base excision repair: mechanisms and its relevance for cancer susceptibility
Fortini, P. (2003) · Biochimie · doi:10.1016/j.biochi.2003.11.003 · Cited by 232
Characterization of a Mammalian Homolog of the Escherichia coli MutY Mismatch Repair Protein
McGoldrick, J. P., Yeh, Y.-C., Solomon, M. S., Essigmann, J. M., & Lu, A.-L. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.2.989 · Cited by 197
Sugasawa, K., Shimizu, Y., Iwai, S., & Hanaoka, F. (2002) · DNA repair · doi:10.1016/s1568-7864(01)00008-8 · Cited by 186
8-Oxoguanine DNA damage: at the crossroad of alternative repair pathways
Fortini, P., Pascucci, B., Parlanti, E., D’Errico, M., Simonelli, V., & Eugenia Dogliotti, Y. (2003) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2003.07.004 · Cited by 180
Self-citationHHR23B, a Human Rad23 Homolog, Stimulates XPC Protein in Nucleotide Excision Repair In Vitro
Sugasawa, K., Masutani, C., Uchida, A., Maekawa, T., Spek, P. J. V. D., Bootsma, D., Hoeijmakers, J. H. J., & Hanaoka, F. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.9.4852 · Cited by 164
Ordered Conformational Changes in Damaged DNA Induced by Nucleotide Excision Repair Factors
Tapias, A., Auriol, J., Forget, D., Enzlin, J. H., Schärer, O. D., Coin, F., Coulombe, B., & Egly, J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m312611200 · Cited by 156
Self-citationShimizu, Y., Iwai, S., Hanaoka, F., & Sugasawa, K. (2002) · The EMBO Journal · doi:10.1093/emboj/cdg016 · Cited by 142
Tuo, J., Jaruga, P., Rodriguez, H., Bohr, V. A., & Dizdaroğlu, M. (2003) · The FASEB Journal · doi:10.1096/fj.02-0851com · Cited by 141
Self-citationHollander, M. C., Philburn, R. T., Patterson, A. D., Velasco-Miguel, S., Friedberg, E. C., Linnoila, R. I., & Fornace, A. J. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503133102 · Cited by 135
Chavanne, F., Broughton, B. C., Pietra, D., Nardò, T., Browitt, A., Lehmann, A. R., & Stefanini, M. (2000) · PubMed · Cited by 133
Self-citationOxidative DNA damage induced by potassium bromate under cell-free conditions and in mammalian cells
Ballmaier, D., & Epe, B. (1995) · Carcinogenesis · doi:10.1093/carcin/16.2.335 · Cited by 133
Diversity of the damage recognition step in the global genomic nucleotide excision repair in vitro
Kusumoto, R., Masutani, C., Sugasawa, K., Iwai, S., Araki, M., Uchida, A., Mizukoshi, T., & Hanaoka, F. (2001) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(00)00082-3 · Cited by 133
Repair of 8-oxoguanine in DNA is deficient in Cockayne syndrome group B cells
Dianov, G. (1999) · Nucleic Acids Research · doi:10.1093/nar/27.5.1365 · Cited by 133
Shen, H., Sturgis, E. M., Khan, S. G., Qiao, Y., Shahlavi, T., Eicher, S. A., Xu, Y., Wang, X., Strom, S. S., Spitz, M. R., et al. (2001) · PubMed · Cited by 128
MutYH (MYH) and colorectal cancer
Sampson, J. R., Jones, S., Dolwani, S., & Cheadle, J. P. (2005) · Biochemical Society Transactions · doi:10.1042/bst0330679 · Cited by 121
3-Methyladenine-DNA Glycosylase (MPG Protein) Interacts with Human RAD23 Proteins
Miao, F., Bouziane, M., Dammann, R., Masutani, C., Hanaoka, F., Pfeifer, G. P., & O'Connor, T. R. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m001064200 · Cited by 120
Oxygen Free Radical Damage to DNA
Kuraoka, I., Robins, P., Masutani, C., Hanaoka, F., Gasparutto, D., Cadet, J., Wood, R. D., & Lindahl, T. L. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m107779200 · Cited by 116
Poor base stacking at DNA lesions may initiate recognition by many repair proteins
Yang, W. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.02.004 · Cited by 105
Khan, S. G., Oh, K., Shahlavi, T., Ueda, T., Busch, D. B., Inui, H., Emmert, S., Imoto, K., Muniz-Medina, V. M., Baker, C. C., et al. (2005) · Carcinogenesis · doi:10.1093/carcin/bgi204 · Cited by 100
DNA repair in neural cells: basic science and clinical implications
Brooks, P. J. (2002) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(02)00222-1 · Cited by 98
Cell type and DNA damage specific response of human skin cells to environmental agents
D’Errico, M., Lemma, T., Calcagnile, A., Santis, L. P. D., & Dogliotti, E. (2007) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2006.06.009 · Cited by 98
Self-citationDNA Base Damage by the Antitumor Agent 3-Amino-1,2,4-benzotriazine 1,4-Dioxide (Tirapazamine)
Birincioğlu, M., Jaruga, P., Chowdhury, G., Rodriguez, H., Dizdaroğlu, M., & Gates, K. S. (2003) · Journal of the American Chemical Society · doi:10.1021/ja0352146 · Cited by 96
Self-citationPoly (AT) Polymorphism in Intron 11 of the XPC DNA Repair Gene Enhances the Risk of Lung Cancer
Marín, M. S., López-Cima, M. F., García-Castro, L., Pascual, T., Marrón, M. G., & Tardón, A. (2004) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.1788.13.11 · Cited by 95
Giglia‐Mari, G., Dumaz, N., Drougard, C., Avril, M.-F., Daya–Grosjean, L., & Sarasin, A. R. (1998) · PubMed · Cited by 86
Mass Spectrometric Assays for the Tandem Lesion 8,5‘-Cyclo-2‘-deoxyguanosine in Mammalian DNA
Jaruga, P., Birincioğlu, M., Rodriguez, H., & Dizdaroğlu, M. (2002) · Biochemistry · doi:10.1021/bi016004d · Cited by 86
Self-citationPhosphorylation of XPB helicase regulates TFIIH nucleotide excision repair activity
Coin, F., Auriol, J., Tapias, A., Clivio, P., Vermeulen, W., & Egly, J. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600480 · Cited by 75 · cited 1×
“Purification of recombinant human XPAwas carried out as described by Tapias et al (2004).”
MethodSelf-citationMarietta, C. A., Gulam, H., & Brooks, P. J. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00148-9 · Cited by 74
Jaruga, P. (2004) · Nucleic Acids Research · doi:10.1093/nar/gnh087 · Cited by 68
Self-citationAge-dependent spontaneous mutagenesis in Xpc mice defective in nucleotide excision repair
Wijnhoven, S., Kool, H., Mullenders, L. H. F., van Zeeland, A. A., Friedberg, E. C., van der Horst, G. T. J., STEEG, H. V., & Vrieling, H. (2000) · Oncogene · doi:10.1038/sj.onc.1203844 · Cited by 65
D'Errico, M., Teson, M., Calcagnile, A., Nardo, T., De Luca, N., Lazzari, C., Soddu, S., Zambruno, G., Stefanini, M., & Dogliotti, E. (2005) · Cancer Research · doi:10.1158/0008-5472.432.65.2 · Cited by 64
Self-citationTranscriptional Activators Stimulate DNA Repair
Frit, P., Kwon, K.-R., Coin, F., Auriol, J., Dubaele, S., Salles, B., & Egly, J. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00732-3 · Cited by 62
Self-citationFriedberg, E. C., & Meira, L. B. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.06.016 · Cited by 27
Nahari, D., McDaniel, L. D., Task, L., Daniel, R. L., Velasco-Miguel, S., & Friedberg, E. C. (2004) · DNA repair · doi:10.1016/j.dnarep.2003.03.001 · Cited by 25
Different dynamics in nuclear entry of subunits of the repair/transcription factor TFIIH
Santagati, F. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.7.1574 · Cited by 22
Cappelli, E., Degan, P., Thompson, L. H., & Fròsina, G. (2000) · Biochemistry · doi:10.1021/bi992610l · Cited by 9
Self-citation
Cited by
Sorted by citations
DNA Base Damage by Reactive Oxygen Species, Oxidizing Agents, and UV Radiation
Cadet, J., & Wagner, J. R. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a012559 · Cited by 903
Mechanisms of free radical-induced damage to DNA
Dizdaroğlu, M., & Jaruga, P. (2012) · Free Radical Research · doi:10.3109/10715762.2011.653969 · Cited by 788
Self-citationThe impact of oxidative DNA damage and stress on telomere homeostasis
Barnes, R. P., Fouquerel, E., & Opresko, P. L. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2018.03.013 · Cited by 585
Oxidatively generated base damage to cellular DNA
Cadet, J., Douki, T., & Ravanat, J. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.03.025 · Cited by 566
Oxidative stress and oxidative damage in chemical carcinogenesis
Klaunig, J. E., Wang, Z., Pu, X., & Zhou, S. (2011) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2009.11.028 · Cited by 486
Metadata
- Authors
- D'Errico, M., Parlanti, E., Teson, M., de Jesus, B. M. B., Degan, P., Calcagnile, A., Jaruga, P., Bjørås, M., Crescenzi, M., Pedrini, A. M., Egly, J., Zambruno, G., Stefanini, M., Dizdaroglu, M., & Dogliotti, E.
- Affiliations
- Istituto Superiore di Sanità (IT)
- Istituto Dermopatico dell'Immacolata (IT)
- University of Oslo (NO)
- Istituto di Genetica Molecolare (IT)
- Centre National de la Recherche Scientifique (FR)
- ORCID
- Venue
- The EMBO Journal
- Published
- 2006-09-07
- Volume
- 25
- Issue
- 18
- Pages
- 4305-4315
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC1570445
- OpenAlex
- W2062150992
- Cited by
- 271
- References
- 51
- Citations by year
- 2026: 5 · 2025: 10 · 2024: 6 · 2023: 7 · 2022: 9 · 2021: 19 · 2020: 9 · 2019: 14 · 2018: 9 · 2017: 6 · 2016: 12 · 2015: 13 · 2014: 14 · 2013: 15 · 2012: 24
- FWCI
- 8.42
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- The EMBO Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Funders
- Fondazione Cariplo
- Ministero della Salute
- Ministero dell’Istruzione, dell’Università e della Ricerca
- Associazione Italiana per la Ricerca sul Cancro
- National Institute of Standards and Technology
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Carcinogens and Genotoxicity Assessment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Keywords
- XPC, xeroderma pigmentosum group C, oxidative DNA damage, base excision repair, 8-oxoguanine, OGG1, keratinocytes, fibroblasts, skin cancer risk, DNA glycosylase
- MeSH terms
- Bromates, Cells, Cultured, DNA Damage, DNA Repair, DNA-Binding Proteins, Guanine, Humans, Skin Neoplasms, X-Rays, Xeroderma Pigmentosum, Keratinocytes, Oxidants, DNA Repair Enzymes, DNA Glycosylases
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review