Labile plasma iron in iron overload: redox activity and susceptibility to chelation
Open accessAbstract
Plasma non-transferrin-bound-iron (NTBI) is believed to be responsible for catalyzing the formation of reactive radicals in the circulation of iron overloaded subjects, resulting in accumulation of oxidation products. We assessed the redox active component of NTBI in the plasma of healthy and β-thalassemic patients. The labile plasma iron (LPI) was determined with the fluorogenic dihydrorhodamine 123 by monitoring the generation of reactive radicals prompted by ascorbate but blocked by iron chelators. The assay was LPI specific since it was generated by physiologic concentrations of ascorbate, involved no sample manipulation, and was blocked by iron chelators that bind iron selectively. LPI, essentially absent from sera of healthy individuals, was present in those of β-thalassemia patients at levels (1-16 μM) that correlated significantly with those of NTBI measured as mobilizer-dependent chelatable iron or desferrioxamine chelatable iron. Oral treatment of patients with deferiprone (L1) raised plasma NTBI due to iron mobilization but did not lead to LPI appearance, indicating that L1-chelated iron in plasma was not redox active. Moreover, oral L1 treatment eliminated LPI in patients. The approach enabled the assessment of LPI susceptibility to in vivo or in vitro chelation and the potential of LPI to cause tissue damage, as found in iron overload conditions. (Blood. 2003;102:2670-2677)
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
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.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Free radicals in biology and medicine
Gutteridge, J. M. C. (1991) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(91)90478-o · Cited by 17,178 · see citing works
[1] Role of free radicals and catalytic metal ions in human disease: An overview
Halliwell, B., & Gutteridge, J. M. C. (1990) · Methods in Enzymology · doi:10.1016/0076-6879(90)86093-b · Cited by 4,994 · see citing works
Royall, J. A., & Ischiropoulos, H. (1993) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1993.1222 · Cited by 1,123 · see citing works
Does vitamin C act as a pro‐oxidant under physiological conditions?
Carr, A. C., & Frei, B. B. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.9.1007 · Cited by 883 · see citing works
Molecular and cellular mechanisms of iron homeostasis and toxicity in mammalian cells
Crichton, R. R., Wilmet, S., Legssyer, R., & Ward, R. J. (2002) · Journal of Inorganic Biochemistry · doi:10.1016/s0162-0134(02)00461-0 · Cited by 494 · see citing works
Ascorbic Acid: Chemistry, Metabolism, and Uses
(1982) · Advances in Chemistry · doi:10.1021/ba-1982-0200 · Cited by 458 · see citing works
The importance of non-transferrin bound iron in disorders of iron metabolism
Breuer, W., Hershko, C., & Cabantchik, Z. I. (2000) · Transfusion Science · doi:10.1016/s0955-3886(00)00087-4 · Cited by 268 · see citing works
Self-citationPathophysiology of Iron Overloada
Hershko, C., Link, G., & Cabantchik, I. Z. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb10475.x · Cited by 246 · see citing works
Self-citationRedox Reactions of Hemoglobin and Myoglobin: Biological and Toxicological Implications
Alayash, A. I., Patel, R. P., & Cashon, R. E. (2001) · Antioxidants & Redox Signaling · doi:10.1089/152308601300185250 · Cited by 243 · see citing works
A Review of Fluorescence Methods for Assessing Labile Iron in Cells and Biological Fluids
Espósito, B. P., Epsztejn, S., Breuer, W. V., & Cabantchik, Z. I. (2002) · Analytical Biochemistry · doi:10.1006/abio.2002.5611 · Cited by 241 · see citing works
Self-citationQuantification of Non-Transferrin-Bound Iron in the Presence of Unsaturated Transferrin
Gosriwatana, I., Loréal, O., Lu, S., Brissot, P., Porter, J. B., & Hider, R. C. (1999) · Analytical Biochemistry · doi:10.1006/abio.1999.4216 · Cited by 167 · see citing works
Ischiropoulos, H., Gow, A. J., Thom, S. R., Kooy, N. W., Royall, J. A., & Crow, J. P. (1999) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(99)01100-3 · Cited by 156 · see citing works
Breuer, W. V., Ermers, M. J. J., Pootrakul, P., Abramov, A., Hershko, C., & Cabantchik, Z. I. (2001) · Blood · doi:10.1182/blood.v97.3.792 · Cited by 155 · see citing works
Self-citationOhashi, T., Mizutani, A., Murakami, A., Kojo, S., Ishii, T., & Taketani, S. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)03262-8 · Cited by 143 · see citing works
Oxidative status and malondialdehyde in β‐thalassaemia patients
Cighetti, G., Duca, L., Bortone, L., Sala, S., Nava, I., Fiorelli, G., & Cappellini, M. D. (2002) · European Journal of Clinical Investigation · doi:10.1046/j.1365-2362.2002.0320s1055.x · Cited by 136 · see citing works
Perinatal aspects of iron metabolism
Rao, R., & Georgieff, M. K. (2002) · Acta Paediatrica · doi:10.1111/j.1651-2227.2002.tb02917.x · Cited by 132 · see citing works
Iron primes hepatic macrophages for NF-κB activation in alcoholic liver injury
Tsukamoto, H., Lin, M., Ohata, M., Giulivi, C., French, S. W., & Brittenham, G. M. (1999) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.277.6.g1240 · Cited by 121 · see citing works
A Fluorescence-Based One-Step Assay for Serum Non-Transferrin-Bound Iron
Breuer, W. V., & Cabantchik, Z. I. (2001) · Analytical Biochemistry · doi:10.1006/abio.2001.5378 · Cited by 102 · see citing works
Self-citationShalev, O., Repka, T. L., Goldfarb, A. W., Grinberg, L. N., Abrahamov, A., Olivieri, N. F., Rachmilewitz, E. A., & Hebbel, R. (1995) · Blood · doi:10.1182/blood.v86.5.2008.bloodjournal8652008 · Cited by 94 · see citing works
Deferiprone protects against doxorubicin-induced myocyte cytotoxicity
Barnabé, N., Zastre, J. A., Venkataram, S., & Hasinoff, B. B. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)00873-0 · Cited by 87 · see citing works
Blood antioxidant status and urinary levels of catecholamine metabolites in β -thalassemia
Luca, C. D., Filosa, A., GRANDINETTI, M., Maggio, F. D., Lamba, M., & Passi, S. (1999) · Free Radical Research · doi:10.1080/10715769900300491 · Cited by 80 · see citing works
EFFECT OF DOSE, TIME, AND ASCORBATE ON IRON EXCRETION AFTER SUBCUTANEOUS DESFERRIOXAMINE
Hussain, M. A. M., Green, N., Flynn, D. M., & Hoffbrand, A. V. (1977) · The Lancet · doi:10.1016/s0140-6736(77)92279-6 · Cited by 77 · see citing works
Minetti, M., Forte, T. M., Soriani, M., Quaresima, V., Menditto, A., & Ferrari, M. (1992) · Biochemical Journal · doi:10.1042/bj2820459 · Cited by 75 · see citing works
Morel, I., Cillard, J., Lescoat, G., Sergent, O., Pasdeloup, N., Ocaktan, A., Abdallah, M. A., Brissot, P., & Cillard, P. (1992) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(92)90144-6 · Cited by 70 · see citing works
The Action of Nine Chelators on Iron-Dependent Radical Damage
Dean, R. T., & Nicholson, P. (1994) · Free Radical Research · doi:10.3109/10715769409147506 · Cited by 70 · see citing works
Iron and Atherosclerosis: Inhibition by the Iron Chelator Deferiprone (L1)
Matthews, A. J., Vercellotti, G. M., Menchaca, H. J., Bloch, P. H. S., Michalek, V. N., Marker, P. H., Murar, J., & Buchwald, H. (1997) · Journal of Surgical Research · doi:10.1006/jsre.1997.5180 · Cited by 68 · see citing works
Martell, A. E. (1982) · Advances in chemistry series · doi:10.1021/ba-1982-0200.ch007 · Cited by 68 · see citing works
The Iron Chelator L1 Potentiates Oxidative DNA Damage in Iron-Loaded Liver Cells
Cragg, L., Hebbel, R. P., Miller, W. J., Solovey, A., Selby, S. A., & Enright, H. (1998) · Blood · doi:10.1182/blood.v92.2.632 · Cited by 66 · see citing works
Intracellular and Extracellular Labile Iron Pools
Cabantchik, Z. I., Kakhlon, O., Epsztejn, S., Zanninelli, G., & Breuer, W. V. (2002) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-0593-8_4 · Cited by 39 · see citing works
Self-citationFree Radical and Cytotoxic Effects of Chelators and Their Iron Complexes in the Hepatocyte
Mostert, L. J., van Dorst, J. A. L. M., Koster, J. F., van Eijk, H. G., & Kontoghiorghes, G. J. (1987) · Free Radical Research Communications · doi:10.3109/10715768709088079 · Cited by 35 · see citing works
Reactivity of hypervalent iron with biological compounds
Bielski, B. H. J. (1992) · Annals of Neurology · doi:10.1002/ana.410320707 · Cited by 35 · see citing works
Moridani, M. Y., & O'Brien, P. J. (2001) · Biochemical Pharmacology · doi:10.1016/s0006-2952(01)00821-8 · Cited by 34 · see citing works
Chelates of ascorbic acid. Formation and catalytic properties.
Martell, A. E. (1982) · Advances in chemistry series · Cited by 33 · see citing works
Deferiprone, an Oral Iron Chelator, Ameliorates Experimental Colitis and Gastric Ulceration in Rats
Ablin, J. N., Shalev, O., Okon, E., Karmeli, F., & Rachmilewitz, D. (1999) · Inflammatory Bowel Diseases · doi:10.1097/00054725-199911000-00003 · Cited by 26 · see citing works
Morel, I., Sergent, O., Cogrel, P., et al. (1995) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(94)e0144-8 · Cited by 24 · see citing works
Bartfay, W. J., Lehotay, D. C., Sher, G. D., Bartfay, E., Tyler, B., Luo, X., & Liu, P. P. (1999) · Hematology · doi:10.1080/10245332.1999.11746432 · Cited by 21 · see citing works
Iron-hydroxypyridone redox chemistry: kinetic and thermodynamic limitations to Fenton activity
Jammal, A. E., & Templeton, D. M. (1996) · Inorganica Chimica Acta · doi:10.1016/0020-1693(95)04814-6 · Cited by 20 · see citing works
Mouithys-Mickalad, A. A., Deby, C. M. T., Deby-Dupont, G. P., et al. (1998) · BioMetals · doi:10.1023/a:1009265625781 · Cited by 12 · see citing works
Afanasʹev, I. B., Afanas’ev, I. I., Deeva, I. B., & Korkina, L. G. (2000) · Transfusion Science · doi:10.1016/s0955-3886(00)00091-6 · Cited by 8 · see citing works
Flagged first, then by citations
Research works printed but not linked: 3
- Hershko C, Link G, Cabantchik I. Pathophysiol- ogy of iron overload. Ann N Y Acad Sci. 1998; 850:191-201.
- Minetti M, Forte T, Soriani M, Quaresima V, Men- ditto A, Ferrari M. Iron-induced ascorbate oxida- tion in plasma as monitored by ascorbate free radical formation. Biochem J. 1992;282:459-465.
- Moridani MJ, O'Brien PJ. Iron complexes of de- feriprone and dietary plant cathecols as cytopro- tective superoxide radical scavengers. Biochem Pharmacol. 2001;62:1579-1585.
Cited by
Sorted by citations
Non-transferrin bound iron: a key role in iron overload and iron toxicity
Brissot, P., Ropert, M., Le Lan, C., & Loréal, O. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2011.07.014 · Cited by 654 · see citing works
Brissot, P., Pietrangelo, A., Adams, P. C., de Graaff, B., McLaren, C. E., & Loréal, O. (2018) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2018.16 · Cited by 430 · see citing works
Koskenkorva-Frank, T. S., Weiss, G., Koppenol, W. H., & Burckhardt, S. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.09.001 · Cited by 406 · see citing works
Iron in infection and immunity
Nairz, M., & Weiss, G. (2020) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2020.100864 · Cited by 359 · see citing works
Iron at the interface of immunity and infection
Nairz, M., Haschka, D., Demetz, E., & Weiss, G. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00152 · Cited by 325 · see citing works
“REVIEW ARTICLE published: 16 July 2014 doi: 10.3389/fphar.2014.00152 Iron at the interface of immunity and infection”
BackgroundInfluentialLabile iron in cells and body fluids: Physiology, pathology, and pharmacology
Cabantchik, Z. I. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00045 · Cited by 306 · see citing works
Self-citationOxidative Stress and the Homeodynamics of Iron Metabolism
Bresgen, N., & Eckl, P. (2015) · Biomolecules · doi:10.3390/biom5020808 · Cited by 247 · see citing works
Arezes, J., Jung, G., Gabayan, V., Valore, E., Ruchala, P., Gulig, P. A., Ganz, T., Nemeth, E., & Bulut, Y. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2014.12.001 · Cited by 227 · see citing works
“The hosts have evolved several countermeasures to restrict the bioavailability of iron and effectively starve the microbes (Ganz, 2009).”
BackgroundInfluentialRedistribution of accumulated cell iron: a modality of chelation with therapeutic implications
Sohn, Y.-S., Breuer, W., Munnich, A., & Cabantchik, Z. I. (2008) · Blood · doi:10.1182/blood-2007-07-102335 · Cited by 167 · see citing works
Self-citationIron in the Tumor Microenvironment-Connecting the Dots
Pfeifhofer-Obermair, C., Tymoszuk, P., Petzer, V., Weiss, G., & Nairz, M. (2018) · Frontiers in Oncology · doi:10.3389/fonc.2018.00549 · Cited by 151 · see citing works
Stefanova, D., Raychev, A., Arezes, J., Ruchala, P., Gabayan, V., Skurnik, M., Dillon, B. J., Horwitz, M. A., Ganz, T., Bulut, Y., et al. (2017) · Blood · doi:10.1182/blood-2017-03-772715 · Cited by 145 · see citing works
Jacobs, E. M. G., Hendriks, J. C. M., van Tits, B. L. J. H., Evans, P. J., Breuer, W., Liu, D. Y., Jansen, E. H. J. M., Jauhiainen, K., Sturm, B., Porter, J. B., et al. (2005) · Analytical Biochemistry · doi:10.1016/j.ab.2005.03.008 · Cited by 101 · see citing works
Self-citationHepcidin-mediated iron sequestration protects against bacterial dissemination during pneumonia
Michels, K. R., Zhang, Z., Bettina, A. M., Cagnina, R. E., Stefanova, D., Burdick, M. D., Vaulont, S., Nemeth, E., Ganz, T., & Mehrad, B. (2017) · JCI Insight · doi:10.1172/jci.insight.92002 · Cited by 93 · see citing works
Stefanova, D., Raychev, A., Deville, J., Humphries, R., Campeau, S., Ruchala, P., Nemeth, E., Ganz, T., & Bulut, Y. (2018) · Infection and Immunity · doi:10.1128/iai.00253-18 · Cited by 68 · see citing works
Zimmermann, M. B., Fucharoen, S., Winichagoon, P., Sirankapracha, P., Zeder, C., Gowachirapant, S., Judprasong, K., Tanno, T., Miller, J. L., & Hurrell, R. F. (2008) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/88.4.1026 · Cited by 69 · see citing works
Self-citationHepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait
Jones, E., Pasricha, S.-R., Allen, A., Evans, P., Fisher, C. A., Wray, K., Premawardhena, A., Bandara, D., Perera, A., Webster, C., et al. (2015) · Blood · doi:10.1182/blood-2014-10-606491 · Cited by 68 · see citing works
Labile plasma iron levels predict survival in patients with lower-risk myelodysplastic syndromes
de Swart, L., Reiniers, C., Bagguley, T., van Marrewijk, C., Bowen, D., Hellström-Lindberg, E., Tatic, A., Symeonidis, A., Huls, G., Cermak, J., et al. (2018) · Haematologica · doi:10.3324/haematol.2017.171884 · Cited by 48 · see citing works
Bellmann-Weiler, R., Schroll, A., Engl, S., Nairz, M., Talasz, H., Seifert, M., & Weiss, G. (2013) · Immunobiology · doi:10.1016/j.imbio.2012.11.004 · Cited by 43 · see citing works
Singh, N., & Sun, H.-Y. (2008) · Liver Transplantation · doi:10.1002/lt.21587 · Cited by 40 · see citing works
Doulias, P.-T., Vlachou, C., Boudouri, C., Kanavaros, P., Siamopoulos, K. C., & Galaris, D. (2008) · Free Radical Research · doi:10.1080/10715760801911649 · Cited by 21 · see citing works
Optimizing Therapy for Iron Overload in the Myelodysplastic Syndromes: Recent Developments
Leitch, H. A. (2011) · Drugs · doi:10.2165/11585280-000000000-00000 · Cited by 17 · see citing works
- Authors
- Esposito, B. P., Breuer, W., Sirankapracha, P., Pootrakul, P., Hershko, C., & Cabantchik, Z. I.
- Affiliations
- From the Department of Biological Chemistry, Institute of Life Sciences, Hebrew University of Jerusalem, Israel; Thalassemia Research Center, Institute of Science and Technology for Research and Development, Mahidol University, Salaya Campus, Nakornpathom, Thailand; and the Department of Hematology, Shaare Zedek Medical Center, Jerusalem, Israel.
- Hebrew University of Jerusalem (IL)
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2003-10-01
- Volume
- 102
- Issue
- 7
- Pages
- 2670-2677
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W2068337287
- Cited by
- 475
- References
- 40
- Citations by year
- 2026: 5 · 2025: 16 · 2024: 9 · 2023: 15 · 2022: 12 · 2021: 19 · 2020: 18 · 2019: 19 · 2018: 26 · 2017: 32 · 2016: 32 · 2015: 25 · 2014: 33 · 2013: 25 · 2012: 29
- FWCI
- 5.45
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Blood (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Hebrew University of Jerusalem
- National Research Council of Thailand
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Health Sciences › Medicine › Genetics › Hemoglobinopathies and Related Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Hemoglobin structure and function
- Keywords
- labile plasma iron, non-transferrin-bound iron, iron overload, beta-thalassemia, redox activity, reactive oxygen radicals, iron chelation, deferiprone, dihydrorhodamine 123, vitamin C, iron mobilization, tissue damage
- MeSH terms
- Ascorbic Acid, Humans, Iron, Iron Chelating Agents, Oxidation-Reduction, Rhodamines, Thalassemia, Transferrin, Cohort Studies, Iron Overload
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