The DOI matches its Crossref record; 45 of the 45 references it cites were found in a registry or an index.
Analysis of the biologic functions of H- and L-ferritins in HeLa cells by transfection with siRNAs and cDNAs: evidence for a proliferative role of L-ferritin
Open accessAbstract
We describe the use of small interfering RNAs (siRNAs) to down-regulate H- and L-ferritin levels in HeLa cells. siRNAs repressed H- and L-ferritin expression to about 20% to 25% of the background level in both stable and transient transfections. HeLa cells transfected with H- and L-ferritin cDNAs were analyzed in parallel to compare the effects of ferritin up- and down-regulation. We found that large modifications of L-ferritin levels did not affect iron availability in HeLa cells but positively affected cell proliferation rate in an iron-independent manner. The transient down-regulation of H-ferritin modified cellular iron availability and resistance to oxidative damage, as expected. In contrast, the stable suppression of H-ferritin in HeLa cell clones transfected with siRNAs did not increase cellular iron availability but made cells less resistant to iron supplementation and chelation. The results indicate that L-ferritin has no direct effects on cellular iron homeostasis in HeLa cells, while it has new, iron-unrelated functions. In addition, they suggest that H-ferritin function is to act as an iron buffer.
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“In addition, HeLa cells that express mutant ferritin L chains exhibited a phenotype of iron loading (61).”
From Intracellular iron transport and storage: from molecular mechanisms to health implications (2008) · cites this paper as [61]
In the citing paper
“Studies with recombinant mutant ferritin L showed that, although it was able to assemble into 24-subunit ferritin shells, the efficiency of assembly and capacity to incorporate iron were both decreased in vitro (61).”
From Intracellular iron transport and storage: from molecular mechanisms to health implications (2008) · cites this paper as [61]
Citations
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Items 101–135 of 135
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“In HeLa cells and glioblastoma cells, the expression of FTL can promote the growth of cancer cells [43, 44].”
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Jiang, H., Sun, Z., He, P., Li, F., & Chen, Q.-X. (2024) · Inflammation · doi:10.1007/s10753-024-02110-6 · Cited by 10
“Additionally, ferritin affects cell death and proliferation rates in an iron-independent manner [12].”
de la Peña, T. C., Cárcamo, C. B., Díaz, M. I., Winkler, F. M., Lange, B. M., Mercado, L. A., & Brokordt, K. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2018.08.030 · Cited by 10
“Hrfer2 may play a role as mitogen for cell proliferation, as it was observed in animal models [59,60].”
BackgroundNuclear ferritin mediated regulation of JNK signaling in corneal epithelial cells
Kubilus, J. K., Beazley, K. E., Talbot, C. J., & Linsenmayer, T. F. (2016) · Experimental Eye Research · doi:10.1016/j.exer.2016.02.002 · Cited by 8
“In K562 and HeLA cells in vitro the downregulation of ferritin has been associated with increased reactive oxygen species (Cozzi et al., 2004; Kakhlon et al., 2001), which then in turn increase the activity JNK and lead to apoptosis (Pham et al., 2004).”
BackgroundUnexplained isolated hyperferritinemia without iron overload
Ravasi, G., Pelucchi, S., Mariani, R., Casati, M., Greni, F., Arosio, C., Pelloni, I., Majore, S., Santambrogio, P., Levi, S., et al. (2017) · American Journal of Hematology · doi:10.1002/ajh.24641 · Cited by 7
Self-citationNaz, N., Ahmad, S., Cameron, S., Moriconi, F., Rave‐Fränk, M., Christiansen, H., Hess, C. F., Ramadori, G. P., & Malik, I. A. (2013) · BioMed Research International · doi:10.1155/2013/353106 · Cited by 8
“It has, however, become increasingly evident that several clinical conditions can be associated with elevated serum ferritin levels in the absence of iron overload [28, 31], while the identity of serum ferritin is not clear and its source is still a matter of debate [32].”
BackgroundThe Role of Haptoglobin and Its Genetic Polymorphism in Cancer: A Review
Clara, M., da Silva, A. P., Medeiros, R., & Bicho, M. (2013) · InTech eBooks · doi:10.5772/56695 · Cited by 6
“In macrophages, after the endocytosis of the Hp-Hb complex and CD163, increased levels of cytoplasmic iron ocurr, inducing the synthesis of ferritin, a primary iron storage, which can subtract it from inflammation site (Cozzi et al 2004).”
BackgroundChekhun, V. F., Lukianova, N. Y., Demash, D. V., Borikun, T., Chekhun, S. V., & Shvets, Y. V. (2013) · CellBio · doi:10.4236/cellbio.2013.24025 · Cited by 5
“tion of ROS-generating substances (ATDR, iron-containing nanoparticles) by cells caused oxidation of these residues, formation of disulfide bonds and resulted in disturbances in protein conformation and interaction with mRNA causing increase of TFR1 expression [33].”
BackgroundConcentrating, Storing, and Detoxifying Iron: The Ferritins and Hemosiderin
Theil, E. C. (2011) · Humana Press eBooks · doi:10.1007/978-1-60327-485-2_4 · Cited by 4
Iron, Oxidative Stress and Diabetes
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“Thus, it is important to understand that higher values of serum inflammatory markers (including C-reactive protein, ferritin, and D-dimer), a difference in the neutrophil/lymphocyte ratio [39, 40], and increased amount of inflammatory cytokines and chemokines, are associated with the disease severity and a higher risk…”
BackgroundThe Prognostic value of Serum Ferritin in Breast cancer patients
Raya, A., Hussein, F., & Kamis, A. (2022) · Research Journal of Pharmacy and Technology · doi:10.52711/0974-360x.2022.00666 · Cited by 2
Ferritin and hiperferritinemic syndrome: Its impact on the seriously ill; current concepts
Esper, R. C., Pérez, C. P., Mendoza, A. D. Z., Márquez, J. M. M., Maldonado, R. N., Meza-Ayala, C. M., Córdova, D. M. C., & Córdova, C. A. C. (2015) · Medicina Crítica · Cited by 2
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Shi, Y., Zheng, W., Yang, G., Liu, H., & Xing, L. (2025) · Discover Oncology · doi:10.1007/s12672-025-02270-3 · Cited by 1
“High ferritin levels in TAM might guard them from iron-induced harm, thereby promoting survival, angiogenesis, and proliferation [41].”
Ahmad, S. (2014) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4633
Molecular coordination of iron homeostasis by microRNA
Davis, M. (2013) · SHAREOK (University of Oklahoma; Oklahoma State University; Central Oklahoma University) · Cited by 1
The Spectrum of Hyperferritinemic SyndromesPreprint
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Ironing out the role of Nrf2 in cardiac iron metabolism during myocardial infarctionPreprint
Jayakumar, D., Narasimhan, K. K. S., Rajkumar, A., Panchalingam, G., Chandrasekar, N., Ravikumar, V. C., & Kalaiselvi, P. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.25.615071 · Cited by 1
“Moreover, FTH might function as a modulator of iron levels, responding to immediate demands of iron homeostasis rather than chronic overload or chelation (Cozzi et al., 2004).”
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Hyperferritinemic Syndromes and Long COVID
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Metadata
- Authors
- Cozzi, A., Corsi, B., Levi, S., Santambrogio, P., Biasiotto, G., & Arosio, P.
- Affiliations
- IRCCS San Raffaele Roma (IT)
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2004-03-15
- Volume
- 103
- Issue
- 6
- Pages
- 2377-2383
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W1519013154
- Cited by
- 132
- References
- 43
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 3 · 2023: 7 · 2022: 3 · 2021: 2 · 2020: 6 · 2019: 5 · 2018: 1 · 2017: 3 · 2016: 4 · 2015: 7 · 2014: 9 · 2013: 21 · 2012: 4
- FWCI
- 3.07
- Type
- journal article
- Language
- en
- Open access
- Licence
- other-oa
- Locations
- Blood (publishedVersion)
- PubMed (publishedVersion)
- INFM-OAR (INFN Catania) (submittedVersion, other-oa)
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Ferroptosis and cancer prognosis
- Life Sciences › Neuroscience › Neurology › Neurological diseases and metabolism
- Keywords
- H-ferritin, L-ferritin, HeLa cells, cell proliferation, iron homeostasis, iron availability, iron supplementation, chelation, siRNA knockdown
- MeSH terms
- Quaternary Ammonium Compounds, Buffers, Cell Division, Ferric Compounds, Ferritins, HeLa Cells, Humans, Iron, Transfection, Down-Regulation, Up-Regulation, Gene Expression, DNA, Complementary, Oxidative Stress, RNA, Small Interfering
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