The DOI matches its Crossref record; 193 of the 196 references it cites were found in a registry or an index.
Molecular mechanisms of cisplatin resistance
Abstract
Platinum-based drugs, and in particular cis-diamminedichloroplatinum(II) (best known as cisplatin), are employed for the treatment of a wide array of solid malignancies, including testicular, ovarian, head and neck, colorectal, bladder and lung cancers. Cisplatin exerts anticancer effects via multiple mechanisms, yet its most prominent (and best understood) mode of action involves the generation of DNA lesions followed by the activation of the DNA damage response and the induction of mitochondrial apoptosis. Despite a consistent rate of initial responses, cisplatin treatment often results in the development of chemoresistance, leading to therapeutic failure. An intense research has been conducted during the past 30 years and several mechanisms that account for the cisplatin-resistant phenotype of tumor cells have been described. Here, we provide a systematic discussion of these mechanism by classifying them in alterations (1) that involve steps preceding the binding of cisplatin to DNA (pre-target resistance), (2) that directly relate to DNA-cisplatin adducts (on-target resistance), (3) concerning the lethal signaling pathway(s) elicited by cisplatin-mediated DNA damage (post-target resistance) and (4) affecting molecular circuitries that do not present obvious links with cisplatin-elicited signals (off-target resistance). As in some clinical settings cisplatin constitutes the major therapeutic option, the development of chemosensitization strategies constitute a goal with important clinical implications.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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
“Also, constant or prolonged cisplatin treatment often results in the acquisition of resistance through the selection bias of alternative cell survival pathways, leading to therapeutic failure and poor prognosis [9, 10].”
From Advances in platinum-based cancer therapy: overcoming platinum resistance through rational combinatorial strategies (2025) · cites this paper as [9]
In the citing paper
“Mechanistically, cells can prevent cisplatin from reaching and harming DNA by reducing drug uptake, increasing drug efflux, and inactivating the drug through covalent binding to glutathione or metalloproteins [9, 10].”
From Advances in platinum-based cancer therapy: overcoming platinum resistance through rational combinatorial strategies (2025) · cites this paper as [9]
In the citing paper
“However, mitotic catastrophe appears to constitute a major mechanism of action of anticancer chemotherapeutics, mostly reflecting the increased resistance of neoplastic cells to the induction of intrinsic apoptosis [1004–1009].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [1007]
Citations
Cites
Studies of the HER-2/ neu Proto-Oncogene in Human Breast and Ovarian Cancer
Slamon, D. J., Godolphin, W. J., Jones, L. A., Holt, J. A., Wong, S., Keith, D. E., Levin, W. J., Stuart, S. G., Udove, J. A., Ullrich, A., et al. (1989) · Science · doi:10.1126/science.2470152 · Cited by 6,817
Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy
Farmer, H., McCabe, N., Lord, C. J., Tutt, A. N. J., Johnson, D. A., Richardson, T. B., Santarosa, M., Dillon, K. J., Hickson, I., Knights, C., et al. (2005) · Nature · doi:10.1038/nature03445 · Cited by 6,683
Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase
Bryant, H. E., Schultz, N., Thomas, H. D., Parker, K. M., Flower, D., Lopez, E., Kyle, S., Meuth, M., Curtin, N. J., & Helleday, T. (2005) · Nature · doi:10.1038/nature03443 · Cited by 5,198
The resurgence of platinum-based cancer chemotherapy
Kèlland, L. R. (2007) · Nature reviews. Cancer · doi:10.1038/nrc2167 · Cited by 4,733
de Gramont, A., Figer, A., Seymour, M., Homerin, M., Hmissi, A., Cassidy, J., Boni, C., Cortes-Funes, H., Cervantes, A., Freyer, G., et al. (2000) · Journal of Clinical Oncology · doi:10.1200/jco.2000.18.16.2938 · Cited by 3,815
Mitochondrial membrane permeabilization in cell death
Kroemer, G., Galluzzi, L., & Brenner, C. (2007) · Physiological Reviews · doi:10.1152/physrev.00013.2006 · Cited by 3,598
Self-citationAutophagy and the Integrated Stress Response
Kroemer, G., Mariño, G., & Levine, B. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.023 · Cited by 3,506
Self-citationCisplatin: mode of cytotoxic action and molecular basis of resistance
Siddik, Z. H. (2003) · Oncogene · doi:10.1038/sj.onc.1206933 · Cited by 3,335
Molecular Mechanisms of Mammalian DNA Repair and the DNA Damage Checkpoints
Sancar, A., Lindsey-Boltz, L. A., Ünsal-Kaçmaz, K., & Linn, S. (2004) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.73.011303.073723 · Cited by 3,317
Calreticulin exposure dictates the immunogenicity of cancer cell death
Obeid, M., Tesniere, A., Ghiringhelli, F., Fimia, G. M., Apetoh, L., Perfettini, J.-L., Castedo, M., Mignot, G., Panaretakis, T., Casares, N., et al. (2007) · Nature Medicine · doi:10.1038/nm1523 · Cited by 3,216
Self-citation
Flagged first, then by citations
3 of the 196 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Kato J, Kuwabara Y, Mitani M, Shinoda N, Sato A, Toyama T et al. (2001). Expression of survivin in esophageal cancer: correlation with the prognosis and response to chemotherapy. Int J Cancer 95: 92–95. · DOI
Cited by
Sorted by citations
Items 601–700 of 1,001
Scheller, J. S., Irvine, G. W., Wong, D. L., Hartwig, A., & Stillman, M. J. (2017) · Metallomics · doi:10.1039/c7mt00041c · Cited by 51
Raji, G. R., Sruthi, T. V., Edatt, L., Haritha, K., Shankar, S. S., & Kumar, V. B. S. (2017) · Cellular Signalling · doi:10.1016/j.cellsig.2017.07.005 · Cited by 48
Brown Seaweed Fucoidan in Cancer: Implications in Metastasis and Drug Resistance
Reyes, M. E., Riquelme, I., Salvo, T., Zanella, L., Letelier, P. J., & Brebi, P. (2020) · Marine Drugs · doi:10.3390/md18050232 · Cited by 49
The functional role of long noncoding RNA in resistance to anticancer treatment
Qu, Y., Tan, H., Chan, Y.-T., Jiang, H.-B., Wang, N., & Wang, D. (2020) · Therapeutic Advances in Medical Oncology · doi:10.1177/1758835920927850 · Cited by 47
New insights into long non-coding RNAs in non-small cell lung cancer
Ye, R., Tang, R., Gan, S., Li, R., Cheng, Y., Guo, L., Zeng, C., & Sun, Y. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110775 · Cited by 48
Moro, M., Bertolini, G., Pastorino, U., Roz, L., & Sozzi, G. (2015) · Journal of Thoracic Oncology · doi:10.1097/jto.0000000000000563 · Cited by 50
Tyler, A., Johansson, A., Karlsson, T., Gudey, S. K., Brännström, T., Grankvist, K., & Behnam‐Motlagh, P. (2015) · Experimental Cell Research · doi:10.1016/j.yexcr.2015.05.012 · Cited by 48
Gallium (III) Complexes in Cancer Chemotherapy
Peng, X., Gao, S. W., & Zhang, J. (2021) · European Journal of Inorganic Chemistry · doi:10.1002/ejic.202100953 · Cited by 48
The effect of caffeine on cisplatin-induced apoptosis of lung cancer cells
Wang, G., Bhoopalan, V., Wang, D., Wang, L., & Xu, X. (2015) · Experimental Hematology and Oncology · doi:10.1186/2162-3619-4-5 · Cited by 47
Ko, J., Shin, N., Jung, T.-Y., Shin, I., Moon, C., Kim, S., Lee, I.-C., Kim, S., Yun, W.-K., Kim, H.-C., et al. (2019) · Food and Chemical Toxicology · doi:10.1016/j.fct.2019.04.049 · Cited by 47
Potential synergistic effect of phosphodiesterase inhibitors with chemotherapy in lung cancer
Domvri, K., Zarogoulidis, P., Ziogas, N. K., Zarogoulidis, P., Petanidis, S., Porpodis, Κ., Kioseoglou, E., & Hohenforst‐Schmidt, W. (2017) · Journal of Cancer · doi:10.7150/jca.21783 · Cited by 47
Vinay, S. P., Udayabhanu, Nagaraju, G., Chandrappa, C. P., & Chandrasekhar, N. (2019) · Journal of Cluster Science · doi:10.1007/s10876-019-01598-5 · Cited by 48
pH- and photothermal-driven multistage delivery nanoplatform for overcoming cancer drug resistance
Huang, W., Zhao, H., Wan, J., Zhou, Y., Xu, Q., Zhao, Y., Yang, X., & Gan, L. (2019) · Theranostics · doi:10.7150/thno.33958 · Cited by 47
Lernoux, M., Schnekenburger, M., Losson, H., Vermeulen, K., Hahn, H., Gérard, D., Lee, J., Mazumder, A., Ahamed, M., Christov, C., et al. (2020) · Clinical Epigenetics · doi:10.1186/s13148-020-00839-z · Cited by 49
Rasouli, M., Mehdian, H., Hajisharifi, K., Amini, E., Ostrikov, K., & Robert, É. (2021) · Plasma Processes and Polymers · doi:10.1002/ppap.202100074 · Cited by 47
SIRT1/PGC-1α/PPAR-γ Correlate With Hypoxia-Induced Chemoresistance in Non-Small Cell Lung Cancer
Xu, R., Luo, X., Ye, X., Li, H., Liu, H., Du, Q., & Zhai, Q. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.682762 · Cited by 44
Šimoničová, K., Janotka, Ľ., Kavcová, H., Sulová, Z., Breier, A., & Messingerová, L. (2022) · Drug Resistance Updates · doi:10.1016/j.drup.2022.100805 · Cited by 47
Ghobashi, A. H., & Kamel, M. A. E.-N. (2018) · Journal of Applied Genetics · doi:10.1007/s13353-018-0432-y · Cited by 47
Exploiting the potential of autophagy in cisplatin therapy: A new strategy to overcome resistance
García‐Cano, J., Ambroise, G., Pascual‐Serra, R., Carrión, M. C., Serrano‐Oviedo, L., Ortega‐Muelas, M., Cimas, F. J., Sabater, S., Ruiz‐Hidalgo, M. J., Sánchez‐Pérez, I., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.3902 · Cited by 46
Sun, Y., Bao, X., Ren, Y., Jia, L., Zou, S., Han, J., Zhao, M., Han, M., Li, H., Hua, Q., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1597-y · Cited by 46
Shi, F., Huang, X., Hong, Z., Lü, N., Huang, X., Liu, L., Liang, T., & Bai, X. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216167 · Cited by 46
Zhang, Y., Zheng, S., Zheng, J.-S., Wong, K., Huang, Z., Ngai, S. M., Zheng, W., Wong, Y.-S., & Chen, T. (2014) · Molecular Pharmaceutics · doi:10.1021/mp400749f · Cited by 46
Vittorio, O., Brandl, M., Cirillo, G., Kimpton, K., Hinde, E., Gaus, K., Yee, E. M. H., Kumar, N., Duong, H. T. T., Fleming, C., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.10201 · Cited by 46
ACE2 overexpression inhibits acquired platinum resistance-induced tumor angiogenesis in NSCLC
Cheng, Q., Zhou, L., Zhou, J., Wan, H., Li, Q. Y., & Feng, Y. (2016) · Oncology Reports · doi:10.3892/or.2016.4967 · Cited by 46
Purushothaman, B., Arumugam, P., Ju, H., Kulsi, G., Samson, A. A. S., & Song, J. M. (2018) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2018.07.048 · Cited by 46
Disulfiram Overcomes Cisplatin Resistance in Human Embryonal Carcinoma Cells
Schmidtova, S., Kaľavská, K., Gercakova, K., Čierna, Z., Miklikova, S., Smolková, B., Buociková, V., Miskovska, V., Durinikova, E., Buríková, M., et al. (2019) · Cancers · doi:10.3390/cancers11091224 · Cited by 45
Apigenin Enhanced Antitumor Effect of Cisplatin in Lung Cancer via Inhibition of Cancer Stem Cells
Li, Y., Chen, X., He, W., Xia, S., Jiang, X., Li, X., Bai, J., Li, N., Chen, L., & Yang, B. (2020) · Nutrition and Cancer · doi:10.1080/01635581.2020.1802494 · Cited by 47
Okamura, S., Yoshino, H., Kuroshima, K., Tsuruda, M., Osako, Y., Sakaguchi, T., Yonemori, M., Yamada, Y., Tatarano, S., Nakagawa, M., et al. (2021) · BMC Cancer · doi:10.1186/s12885-020-07717-0 · Cited by 46
Novel strategies to improve tumour therapy by targeting the proteins MCT1, MCT4 and LAT1
Wang, Y., Qin, L., Chen, W., Chen, Q., Sun, J., & Wang, G. (2021) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2021.113806 · Cited by 45
Sui, Q., Chen, Z., Hu, Z., Huang, Y., Liang, J., Bi, G., Bian, Y., Zhao, M., Zhan, C., Lin, Z., et al. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03372-0 · Cited by 45
Targeting of the intracellular redox balance by metal complexes towards anticancer therapy
Murillo, M. I., Gaiddon, C., & Lagadec, R. L. (2022) · Frontiers in Chemistry · doi:10.3389/fchem.2022.967337 · Cited by 45
CHD4 promotes acquired chemoresistance and tumor progression by activating the MEK/ERK axis
Wu, J., Zhou, Z., Li, J., Liu, H., Zhang, H., Zhang, J., Huang, W., He, Y., Zhu, S., Huo, M., et al. (2022) · Drug Resistance Updates · doi:10.1016/j.drup.2022.100913 · Cited by 45
Vacchelli, E., Galluzzi, L., Rousseau, V., Rigoni, A., Tesnière, A., Delahaye, N., Schlemmer, F., Menger, L., Sukkurwala, A. Q., Adjemian, S., et al. (2012) · OncoImmunology · doi:10.4161/onci.18684 · Cited by 53
Self-citationCCN2 Enhances Resistance to Cisplatin-Mediating Cell Apoptosis in Human Osteosarcoma
Tsai, H., Huang, C., Su, H., & Tang, C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0090159 · Cited by 45
Bello, E., Taraboletti, G., Colella, G., Zucchetti, M., Forestieri, D., Licandro, S. A., Berndt, A., Richter, P., D’Incalci, M., Cavalletti, E., et al. (2012) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-12-0275-t · Cited by 45
Jia, Y., Sun, H., Hongqiao, W., Zhang, H., Zhang, X., Xiao, D., Ma, X., & Wang, Y. (2016) · PLoS ONE · doi:10.1371/journal.pone.0149120 · Cited by 45
Histone Deacetylase Inhibitor SAHA as Potential Targeted Therapy Agent for Larynx Cancer Cells
Grabarska, A., Łuszczki, J. J., Nowosadzka, E., Gumbarewicz, E., Jeleniewicz, W., Dmoszyńska‐Graniczka, M., Kowalczuk, K., Kupisz, K., Polberg, K., & Stepulak, A. (2016) · Journal of Cancer · doi:10.7150/jca.16655 · Cited by 46
Krieger, V., Hamacher, A., Gertzen, C. G. W., Senger, J., Zwinderman, M. R. H., Marek, M., Romier, C., Dekker, F. J., Kurz, T., Jung, M., et al. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b00197 · Cited by 46
Rodríguez‐Fanjul, V., López‐Torres, E., Mendiola, M. A., & Pizarro, A. M. (2018) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2018.02.009 · Cited by 45
Catanzaro, D., Nicolosi, S., Cocetta, V., Salvalaio, M., Pagetta, A., Ragazzi, E., Montopoli, M., & Pasut, G. (2018) · Oncotarget · doi:10.18632/oncotarget.24708 · Cited by 45
Huang, W., Liu, Y., Wang, J., Yuan, X., Jin, H.-W., Zhang, L.-R., Zhang, J., Liu, Z.-M., & Cui, J.-R. (2018) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2018.08.037 · Cited by 45
Søgaard, C. K., Blindheim, A., Røst, L. M., Petrović, V., Nepal, A., Bachke, S., Liabakk, N., Gederaas, O. A., Viset, T., Arum, C., et al. (2018) · Oncotarget · doi:10.18632/oncotarget.25963 · Cited by 45
Epigenetic drugs and their molecular targets in testicular germ cell tumours
Jostes, S., Nettersheim, D., & Schorle, H. (2019) · Nature Reviews Urology · doi:10.1038/s41585-019-0154-x · Cited by 45
Immune-Checkpoint Inhibitors in Platinum-Resistant Ovarian Cancer
Indini, A., Nigro, O., Lengyel, C. G., Ghidini, M., Petrillo, A., Lopez, S., Raspagliesi, F., Trapani, D., Khakoo, S. S., & Bogani, G. (2021) · Cancers · doi:10.3390/cancers13071663 · Cited by 46
Shen, W., Jia, C., Mo, A., Liang, H., & Chen, Z. (2021) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2021.113636 · Cited by 46
Ge, H., Du, J., Zheng, J., Xu, N., Yao, Q., Long, S., Fan, J., & Peng, X. (2022) · Chemical Engineering Journal · doi:10.1016/j.cej.2022.137040 · Cited by 45
The developmental origin of cancers defines basic principles of cisplatin resistance
Skowron, M. A., Oing, C., Bremmer, F., Ströbel, P., Murray, M. J., Coleman, N., Amatruda, J. F., Honecker, F. U., Bokemeyer, C., Albers, P., et al. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.07.037 · Cited by 44
Tyagi, A., Kaushal, K., Chandrasekaran, A. P., Sarodaya, N., Das, S., Park, C., Hong, S., Kim, K.-S., & Ramakrishna, S. (2022) · Theranostics · doi:10.7150/thno.72826 · Cited by 44
Huang, Y., Kou, Q., Su, Y., Lu, L., Li, X., Jiang, H., Gui, R., Huang, R., Nie, X., & Li, J. (2023) · Journal of Nanobiotechnology · doi:10.1186/s12951-023-01840-3 · Cited by 44
Research Progress of Metal Anticancer Drugs
Bai, Y., Aodeng, G., Ga, L., Hai, W., & Ai, J. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15122750 · Cited by 46
APC selectively mediates response to chemotherapeutic agents in breast cancer
VanKlompenberg, M. K., Bedalov, C. O., Soto, K. F., & Prosperi, J. R. (2015) · BMC Cancer · doi:10.1186/s12885-015-1456-x · Cited by 44
miRNAs and ovarian cancer: a miRiad of mechanisms to induce cisplatin drug resistance
Samuel, P., Pink, R. C., Brooks, S. A., & Carter, D. R. F. (2015) · Expert Review of Anticancer Therapy · doi:10.1586/14737140.2016.1121107 · Cited by 44
Multifaceted Mechanisms of Cisplatin Resistance in Long-Term Treated Urothelial Carcinoma Cell Lines
Skowron, M. A., Melnikova, M., van Roermund, J. G. H., Romano, A., Albers, P., Thomale, J., Schulz, W. A., Niegisch, G., & Hoffmann, M. J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19020590 · Cited by 44
Phase I trial of selenium plus chemotherapy in gynecologic cancers
Song, M., Kumaran, M. N., Gounder, M. K., Gibbon, D. G., Nieves‐Neira, W., Vaidya, A. P., Hellmann, M., Kane, M. P., Buckley, B., Shih, W. J., et al. (2018) · Gynecologic Oncology · doi:10.1016/j.ygyno.2018.07.001 · Cited by 44
Liu, S., Zou, B., Tian, T., Luo, X., Mao, B., Zhang, X., & Lei, H. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.28032 · Cited by 44
Shi, X., Xiao, L., Mao, X., He, J., Ding, Y., Huang, J., Peng, C., & Xu, Z. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00555 · Cited by 45
Nano-Based Systems and Biomacromolecules as Carriers for Metallodrugs in Anticancer Therapy
Poursharifi, M., Wlodarczyk, M. T., & Mieszawska, A. J. (2018) · Inorganics · doi:10.3390/inorganics7010002 · Cited by 44
Selectivity of Terpyridine Platinum Anticancer Drugs for G-quadruplex DNA
Morel, E., Beauvineau, C., Naud‐Martin, D., Guetta, C., Verga, D., Ghosh, D., Achelle, S., Mahuteau‐Betzer, F., Bombard, S., & Teulade‐Fichou, M. (2019) · Molecules · doi:10.3390/molecules24030404 · Cited by 44
Chang, P., Tsai, F., BAU, D.-T., Hsu, Y., Yang, J., Tu, M., & Chiang, S. (2020) · Journal of the Formosan Medical Association · doi:10.1016/j.jfma.2020.06.025 · Cited by 44
Shi, H., Li, K., Feng, J., Liu, G., Feng, Y., & Zhang, X. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.01034 · Cited by 44
Murray, D. L., & Mirzayans, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21165766 · Cited by 43
miR-194-5p inhibits SLC40A1 expression to induce cisplatin resistance in ovarian cancer
Wu, J., Zhang, L., Wu, S., Yi, X., & Liu, Z. (2020) · Pathology - Research and Practice · doi:10.1016/j.prp.2020.152979 · Cited by 42
Wang, Y., Wang, X., Xu, G., & Gou, S. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.1c00079 · Cited by 43
Improved Clearance during Treatment of HPV-Positive Head and Neck Cancer through mTOR Inhibition
Coppock, J. D., Wieking, B. G., Molinolo, A., Gutkind, J. S., Miskimins, W. K., & Lee, J. H. (2013) · Neoplasia · doi:10.1593/neo.13432 · Cited by 43
Identification of Cisplatin-Regulated Metabolic Pathways in Pluripotent Stem Cells
von Stechow, L., Ruiz‐Aracama, A., van de Water, B., Peijnenburg, A., Danen, E. H. J., & Lommen, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076476 · Cited by 44
Inhibition of Glucosylceramide Synthase Sensitizes Head and Neck Cancer to Cisplatin
Roh, J., Kim, E. H., Park, J. Y., & Kim, J. W. (2015) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-15-0171 · Cited by 42
p53 overexpression increases chemosensitivity in multidrug-resistant osteosarcoma cell lines
Ye, S., Shen, J. K., Choy, E., Cao, Y., Mankin, H. J., Hornicek, F. J., & Duan, Z. (2015) · Cancer Chemotherapy and Pharmacology · doi:10.1007/s00280-015-2944-z · Cited by 43
Wlodarczyk, M. T., Dragulska, S. A., Camacho‐Vanegas, O., Dottino, P., Jarzęcki, A. A., Martignetti, J. A., & Mieszawska, A. J. (2018) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.7b00921 · Cited by 43
Zhou, D. R., Eid, R., Miller, K. A., Boucher, É. L., Mandato, C. A., & Greenwood, M. T. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2019.01.016 · Cited by 43
Hsp90B enhances MAST1-mediated cisplatin resistance by protecting MAST1 from proteosomal degradation
Pan, C., Chun, J., Li, D., Boese, A. C., Li, J., Kang, J., Umano, A. D., Jiang, Y., Song, L., Magliocca, K. R., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci125963 · Cited by 42
Han, C. Y., Patten, D. A., Lee, S. G., Parks, R. J., Chan, D. W., Harper, M., & Tsang, B. K. (2019) · Molecular Carcinogenesis · doi:10.1002/mc.23106 · Cited by 44
Cisplatin induces chemoresistance through the PTGS2-mediated anti-apoptosis in gastric cancer
Lin, X.-M., Li, S., Zhou, C., Li, R.-Z., Wang, H., Luo, W., Huang, Y.-S., Chen, L.-K., Cai, J.-L., Wang, T.-X., et al. (2019) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2019.105610 · Cited by 43
Fanelli, M., Tavanti, E., Patrizio, M. P., Vella, S., Fernandez-Ramos, A., Magagnoli, F., Luppi, S., Hattinger, C. M., & Serra, M. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00331 · Cited by 43
Crosstalk of Exosomal Non-Coding RNAs in The Tumor Microenvironment: Novel Frontiers
Jia, Z., Jia, J., Yao, L., & Li, Z. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.900155 · Cited by 44
Das, S. K., Roy, S., Das, A., Chowdhury, A., Chatterjee, N., & Bhaumik, A. (2022) · Nanoscale Advances · doi:10.1039/d2na00103a · Cited by 43
Folk, W. P., Kumari, A., Iwasaki, T., Pyndiah, S., Johnson, J. C., Cassimere, E. K., Abdulovic-Cui, A. L., & Sakamuro, D. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.005699 · Cited by 42
Potential of natural products in osteosarcoma treatment: Focus on molecular mechanisms
Tobeiha, M., Rajabi, A., Raisi, A., Mohajeri, M., Yazdi, S. M., Davoodvandi, A., Aslanbeigi, F., Vaziri, M., Hamblin, M. R., & Mirzaei, H. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.112257 · Cited by 44
Overcoming Chemotherapy Resistance in Germ Cell Tumors
Országhová, Z., Kaľavská, K., Mego, M., & Chovanec, M. (2022) · Biomedicines · doi:10.3390/biomedicines10050972 · Cited by 42
Karaca, B., Atmaca, H., Bozkurt, E., Kısım, A., Uzunoğlu, S., Karabulut, B., Sezgin, C., Şanlı, U. A., & Uslu, R. (2012) · Molecular Biology Reports · doi:10.1007/s11033-012-2469-z · Cited by 42
Zhao, J., Ren, K., & Tang, J. (2014) · Tumor Biology · doi:10.1007/s13277-014-2543-3 · Cited by 42
Bradley, A. T., Zheng, H., Ziebarth, A., Sakati, W. R., Branham-O’Connor, M., Blumer, J., Liu, Y., Kistner‐Griffin, E., Rodriguez‐Aguayo, C., Lopez‐Berestein, G., et al. (2013) · Carcinogenesis · doi:10.1093/carcin/bgt489 · Cited by 42
Im, J., Lee, K.-W., Won, K., Kim, B., Ban, H. S., Yoon, S.-H., Lee, Y.-J., Kim, Y., Song, K., & Won, M. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2015.10.011 · Cited by 42
Asplatin enhances drug efficacy by altering the cellular response
Cheng, Q., Shi, H., Wang, H., Wang, J., & Liu, Y. (2016) · Metallomics · doi:10.1039/c6mt00066e · Cited by 42
Kim, J., Chen, C., Yang, J., & Mochly‐Rosen, D. (2017) · Journal of Biomedical Science · doi:10.1186/s12929-017-0338-8 · Cited by 42
Hong, W., Huang, F., Huan, T., Xu, X., Han, Q., Wang, G., Xu, H. Y., Duan, S., Duan, Y., Long, X., et al. (2017) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2017.11.024 · Cited by 42
Autocrine activation of JAK2 by IL-11 promotes platinum drug resistance
Zhou, W., Sun, W., Yung, M. M. H., Dai, S., Cai, Y., Chen, C., Meng, Y., Lee, J. B., Braisted, J. C., Xu, Y., et al. (2018) · Oncogene · doi:10.1038/s41388-018-0238-8 · Cited by 41
Rahman, F., Bhatti, M. Z., Ali, A., Duong, H., Zhang, Y., Ji, X., Lin, Y., Wang, H., Li, Z., & Zhang, D. (2018) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2018.08.054 · Cited by 42
Half-sandwich IridiumIII N-heterocyclic carbene antitumor complexes and biological applications
Han, Y., Tian, Z., Zhang, S., Liu, X., Li, J., Li, Y., Liu, Y., Gao, M., & Liu, Z. (2018) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2018.09.009 · Cited by 42
Wang, T., Hao, D., Yang, S., Ma, J., Yang, W., Zhu, Y., Weng, M., An, X., Wang, X. J., Li, Y., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1715-x · Cited by 42
Deo, K. M., Sakoff, J. A., Gilbert, J., Zhang, Y., & Aldrich-Wright, J. R. (2019) · Dalton Transactions · doi:10.1039/c9dt04049h · Cited by 42
Zhang, C., Guan, R., Liao, X., Ouyang, C., Liu, J., Ji, L., & Chao, H. (2020) · Inorganic Chemistry Frontiers · doi:10.1039/d0qi00224k · Cited by 42
Lipid, polymeric, inorganic-based drug delivery applications for platinum-based anticancer drugs
Boztepe, T., Castro, G. R., & León, I. E. (2021) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2021.120788 · Cited by 41
Niu, B., Zhou, Y., Liao, K., Wen, T., Lao, S., Quan, G., Pan, X., & Wu, C. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.10.013 · Cited by 42
Decreased Levels of GSH Are Associated with Platinum Resistance in High-Grade Serous Ovarian Cancer
Criscuolo, D., Avolio, R., Parri, M., Romano, S., Chiarugi, P., Matassa, D. S., & Esposito, F. (2022) · Antioxidants · doi:10.3390/antiox11081544 · Cited by 41
Cisplatin in the era of PARP inhibitors and immunotherapy
Duan, M., Leng, S., & Mao, P. (2024) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2024.108642 · Cited by 45
Wang, P., Cui, J., Wen, J., Guo, Y., Zhang, L., & Chen, X. (2016) · Oncology Letters · doi:10.3892/ol.2016.5288 · Cited by 41
Wei, L., Chintala, S., Ciamporcero, E. S., Ramakrishnan, S., Elbanna, M., Wang, J., Hu, Q., Glenn, S. T., Murakami, M., Liu, L., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.13062 · Cited by 41
Zhou, Y., Liu, F., Xu, Q., Yang, B., Li, X., Jiang, S., Hu, L.-P., Zhang, X., Zhu, L., Li, Q., et al. (2020) · Oncogene · doi:10.1038/s41388-020-1384-3 · Cited by 41
Wang, Y., Xie, Q., Tan, H., Liao, M., Zhu, S., Zheng, L., Huang, H., & Liu, B. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105702 · Cited by 41
Metadata
- Authors
- Galluzzi, L., Senovilla, L., Vitale, I., Michels, J., Martins, I., Kepp, O., Castedo, M., & Kroemer, G.
- Affiliations
- Inserm (FR)
- Université Paris-Sud (FR)
- Corresponding author
- Kroemer, G
- Venue
- Oncogene
- Published
- 2011-09-05
- Volume
- 31
- Issue
- 15
- Pages
- 1869-1883
- ISSN
- 0950-9232 (ISSN-L)
- 1476-5594
- OpenAlex
- W2141037581
- Cited by
- 2,760
- References
- 196
- Citations by year
- 2026: 154 · 2025: 187 · 2024: 244 · 2023: 220 · 2022: 247 · 2021: 308 · 2020: 252 · 2019: 213 · 2018: 169 · 2017: 167 · 2016: 159 · 2015: 160 · 2014: 145 · 2013: 89 · 2012: 44
- FWCI
- 7.83
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Oncogene (publishedVersion)
- PubMed (publishedVersion)
- Funders
- European Commission
- Ligue Contre le Cancer
- Fondation Bettencourt Schueller
- Labex Immuno-Oncology
- Topics
- Health Sciences › Medicine › Oncology › Metal complexes synthesis and properties
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cancer therapeutics and mechanisms
- Keywords
- cisplatin resistance, chemoresistance, platinum anticancer drugs, DNA damage response, mitochondrial apoptosis, chemosensitization, DNA lesions
- MeSH terms
- Cisplatin, DNA Damage, DNA Repair, Humans, Signal Transduction, DNA Adducts, Drug Resistance, Neoplasm
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