Journal of Otolaryngology and Ophthalmology of Shandong University ›› 2024, Vol. 38 ›› Issue (5): 145-152.doi: 10.6040/j.issn.1673-3770.0.2023.117
• Review • Previous Articles
YANG Yuyun1,2, HUANG Yanli1,3, LI Junzhen1,4
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[1] Kim BE, Nevitt T, Thiele DJ. Mechanisms for copper acquisition, distribution and regulation[J]. Nat Chem Biol, 2008, 4(3): 176-185. doi:10.1038/nchembio.72 [2] Turski ML, Brady DC, Kim HJ, et al. A novel role for copper in Ras/mitogen-activated protein kinase signaling[J]. Mol Cell Biol, 2012, 32(7): 1284-1295. doi:10.1128/MCB.05722-11 [3] Denoyer D, Clatworthy SAS, Cater MA. Copper complexes in cancer therapy[J]. Met Ions Life Sci, 2018, 18: /books/9783110470734/9783110470734-/books/9783110470734/9783110470022/9783110470734-022.xml. doi:10.1515/9783110470734-022 [4] Tsvetkov P, Detappe A, Cai K, et al. Mitochondrial metabolism promotes adaptation to proteotoxic stress[J]. Nat Chem Biol, 2019, 15(7): 681-689. doi:10.1038/s41589-019-0291-9 [5] Modica-Napolitano JS, Bharath LP, Hanlon AJ, et al. The anticancer agent elesclomol has direct effects on mitochondrial bioenergetic function in isolated mammalian mitochondria[J]. Biomolecules, 2019, 9(8): 298. doi: 10.3390/biom9080298 [6] Nagai M, Vo NH, Shin Ogawa L, et al. The oncology drug elesclomol selectively transports copper to the mitochondria to induce oxidative stress in cancer cells[J]. Free Radic Biol Med, 2012, 52(10): 2142-2150. doi:10.1016/j.freeradbiomed.2012.03.017 [7] Tsvetkov P, Coy S, Petrova B, et al. Copper induces cell death by targeting lipoylated TCA cycle proteins[J]. Science, 2022, 375(6586): 1254-1261. doi: 10.1126/science.abf0529 [8] Lee JH, Cho YS, Jung KH, et al. Genipin enhances the antitumor effect of elesclomol in A549 lung cancer cells by blocking uncoupling protein-2 and stimulating reactive oxygen species production[J]. Oncol Lett, 2020, 20(6): 374. doi: 10.3892/ol.2020.12237 [9] Soma S, Latimer AJ, Chun H, et al. Elesclomol restores mitochondrial function in genetic models of copper deficiency[J]. Proc Natl Acad Sci USA, 2018, 115(32): 8161-8166. doi:10.1073/pnas.1806296115 [10] Chen SJ, Sun LJ, Koya K, et al. Syntheses and antitumor activities of N'1, N'3-dialkyl-N'1, N'3-di-(alkylcarbonothioyl)malonohydrazide: the discovery of elesclomol[J]. Bioorg Med Chem Lett, 2013, 23(18): 5070-5076. doi:10.1016/j.bmcl.2013.07.032 [11] O'Day SJ, Eggermont AMM, Chiarion-Sileni V, et al. Final results of phase III SYMMETRY study: randomized, double-blind trial of elesclomol plus paclitaxel versus paclitaxel alone as treatment for chemotherapy-naive patients with advanced melanoma[J]. J Clin Oncol, 2013, 31(9): 1211-1218. doi:10.1200/JCO.2012.44.5585 [12] O'Day S, Gonzalez R, Lawson D, et al. Phase II, randomized, controlled, double-blinded trial of weekly elesclomol plus paclitaxel versus paclitaxel alone for stage IV metastatic melanoma[J]. J Clin Oncol, 2009, 27(32): 5452-5458. doi:10.1200/JCO.2008.17.1579 [13] Hedley D, Shamas-Din A, Chow S, et al. A phase I study of elesclomol sodium in patients with acute myeloid leukemia[J]. Leuk Lymphoma, 2016, 57(10): 2437-2440. doi:10.3109/10428194.2016.1138293 [14] Monk BJ, Kauderer JT, Moxley KM, et al. A phase II evaluation of elesclomol sodium and weekly paclitaxel in the treatment of recurrent or persistent platinum-resistant ovarian, fallopian tube or primary peritoneal cancer: an NRG oncology/gynecologic oncology group study[J]. Gynecol Oncol, 2018, 151(3): 422-427. doi:10.1016/j.ygyno.2018.10.001 [15] Li YY, Yang J, Zhang QQ, et al. Copper ionophore elesclomol selectively targets GNAQ/11-mutant uveal melanoma[J]. Oncogene, 2022, 41(27): 3539-3553. doi:10.1038/s41388-022-02364-0 [16] Buccarelli M, D'Alessandris QG, Matarrese P, et al. Elesclomol-induced increase of mitochondrial reactive oxygen species impairs glioblastoma stem-like cell survival and tumor growth[J]. J Exp Clin Cancer Res, 2021, 40(1): 228. doi:10.1186/s13046-021-02031-4 [17] Albayrak G, Korkmaz FD, Tozcu D, et al. The outcomes of an impaired powerhouse in KRAS mutant lung adenocarcinoma cells by Elesclomol[J]. J Cell Biochem, 2019, 120(6): 10564-10571. doi:10.1002/jcb.28342 [18] Li H, Wang J, Wu C, et al. The combination of disulfiram and copper for cancer treatment[J]. Drug Discov Today, 2020, 25(6): 1099-1108. doi: 10.1016/j.drudis.2020.04.003 [19] Wang NN, Wang LH, Li Y, et al. Targeting ALDH2 with disulfiram/copper reverses the resistance of cancer cells to microtubule inhibitors[J]. Exp Cell Res, 2018, 362(1): 72-82. doi:10.1016/j.yexcr.2017.11.004 [20] Yang Z, Guo F, Albers AE, et al. Disulfiram modulates ROS accumulation and overcomes synergistically cisplatin resistance in breast cancer cell lines[J]. Biomed Pharmacother, 2019, 113: 108727. doi:10.1016/j.biopha.2019.108727 [21] Li Y, Chen F, Chen J, et al. Disulfiram/Copper induces antitumor activity against both nasopharyngeal cancer cells and cancer-associated fibroblasts through ROS/MAPK and ferroptosis pathways[J]. Cancers(Basel), 2020, 12(1): 138. doi: 10.3390/cancers12010138 [22] Guo F, Yang Z, Kulbe H, et al. Inhibitory effect on ovarian cancer ALDH+ stem-like cells by Disulfiram and Copper treatment through ALDH and ROS modulation[J]. Biomed Pharmacother, 2019, 118: 109371. doi:10.1016/j.biopha.2019.109371 [23] Shukla S, Sauna ZE, Prasad R, et al. Disulfiram is a potent modulator of multidrug transporter Cdr1p of Candida albicans[J]. Biochem Biophys Res Commun, 2004, 322(2): 520-525. doi:10.1016/j.bbrc.2004.07.151 [24] Cong J, Wang YY, Zhang X, et al. A novel chemoradiation targeting stem and nonstem pancreatic cancer cells by repurposing disulfiram[J]. Cancer Lett, 2017, 409: 9-19. doi:10.1016/j.canlet.2017.08.028 [25] Li Y, Wang LH, Zhang HT, et al. Disulfiram combined with copper inhibits metastasis and epithelial-mesenchymal transition in hepatocellular carcinoma through the NF-κB and TGF-β pathways[J]. J Cell Mol Med, 2018, 22(1): 439-451. doi:10.1111/jcmm.13334 [26] Zhou BH, Guo L, Zhang B, et al. Disulfiram combined with copper induces immunosuppression via PD-L1 stabilization in hepatocellular carcinoma[J]. Am J Cancer Res, 2019, 9(11): 2442-2455 [27] Brewer GJ. The promise of copper lowering therapy with tetrathiomolybdate in the cure of cancer and in the treatment of inflammatory disease[J]. J Trace Elem Med Biol, 2014, 28(4): 372-378. doi:10.1016/j.jtemb.2014.07.015 [28] Tian Y, Fang TT, Yuan SM, et al. Tetrathiomolybdate inhibits the reaction of cisplatin with human copper chaperone Atox1[J]. Metallomics, 2018, 10(5): 745-750. doi:10.1039/c8mt00084k [29] McAuslan BR, Reilly W. Endothelial cell phagokinesis in response to specific metal ions[J]. Exp Cell Res, 1980, 130(1): 147-157. doi: 10.1016/0014-4827(80)90051-8 [30] Jiang YC, Huo ZY, Qi XL, et al. Copper-induced tumor cell death mechanisms and antitumor theragnostic applications of copper complexes[J]. Nanomedicine(Lond), 2022, 17(5): 303-324. doi:10.2217/nnm-2021-0374 [31] Kim KK, Lange TS, Singh RK, et al. Tetrathiomolybdate sensitizes ovarian cancer cells to anticancer drugs doxorubicin, fenretinide, 5-fluorouracil and mitomycin C[J]. BMC Cancer, 2012, 12: 147. doi:10.1186/1471-2407-12-147 [32] Rieber M. Cancer pro-oxidant therapy through copper redox cycling: Repurposing disulfiram and tetrathiomolybdate[J]. Curr Pharm Des, 2020, 26(35): 4461-4466. doi:10.2174/1381612826666200628022113 [33] Zhang ML, Qiu HM, Mao LJ, et al. Ammonium tetrathiomolybdate triggers autophagy-dependent?NRF2?activation in vascular endothelial cells[J]. Cell Death Dis, 2022, 13(8): 733. doi:10.1038/s41419-022-05183-z [34] Yang T, Zhang F. Targeting transcription factor Nrf2(nuclear factor erythroid 2-related factor 2)for the intervention of vascular cognitive impairment and dementia[J]. Arterioscler Thromb Vasc Biol, 2021, 41(1): 97-116. doi: 10.1161/ATVBAHA.120.314804 [35] Glasauer A, Sena LA, Diebold LP, et al. Targeting SOD1 reduces experimental non-small-cell lung cancer[J]. J Clin Invest, 2014, 124(1): 117-128. doi:10.1172/JCI71714 [36] Ramchandani D, Berisa M, Tavarez DA, et al. Copper depletion modulates mitochondrial oxidative phosphorylation to impair triple negative breast cancer metastasis[J]. Nat Commun, 2021, 12(1): 7311. doi:10.1038/s41467-021-27559-z [37] Liu YL, Bager CL, Willumsen N, et al. Tetrathiomolybdate(TM)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancer[J]. NPJ Breast Cancer, 2021, 7(1): 108. doi:10.1038/s41523-021-00313-w [38] Morisawa A, Okui T, Shimo T, et al. Ammonium tetrathiomolybdate enhances the antitumor effects of cetuximab via the suppression of osteoclastogenesis in head and neck squamous carcinoma[J]. Int J Oncol, 2018, 52(3): 989-999. doi:10.3892/ijo.2018.4242 [39] Ryumon S, Okui T, Kunisada Y, et al. Ammonium tetrathiomolybdate enhances the antitumor effect of cisplatin via the suppression of ATPase copper transporting beta in head and neck squamous cell carcinoma[J]. Oncol Rep, 2019, 42(6): 2611-2621. doi:10.3892/or.2019.7367 [40] Hsiao K, Chapman P, Nilsen S, et al. Correlative memory deficits, aβ elevation, and amyloid plaques in transgenic mice[J]. Science, 1996, 274(5284): 99-103. doi:10.1126/science.274.5284.99 [41] Cherny RA, Atwood CS, Xilinas ME, et al. Treatment with a copper-zinc Chelatoz markedly and rapidly inhibits β-amyloid accumulation in Alzheimer's disease transgenic mice[J]. Neuron, 2001, 30(3): 665-676. doi:10.1016/S0896-6273(01)00317-8 [42] Du T, Filiz G, Caragounis A, et al. Clioquinol promotes cancer cell toxicity through tumor necrosis factor alpha release from macrophages[J]. J Pharmacol Exp Ther, 2008, 324(1): 360-367. doi:10.1124/jpet.107.130377 [43] Perez D, Simons PC, Smagley Y, et al. A High-Throughput Flow Cytometry Assay for Identification of Inhibitors of 3', 5'-Cyclic Adenosine Monophosphate Efflux[M] // High Throughput Screening. New York: Humana Press, 2016: 227-244.10.1007/978-1-4939-3673-1_15 [44] Levy JMM, Towers CG, Thorburn A. Targeting autophagy in cancer[J]. Nat Rev Cancer, 2017, 17(9): 528-542. doi:10.1038/nrc.2017.53 [45] Chen D, Cui QC, Yang HJ, et al. Clioquinol, a therapeutic agent for Alzheimer's disease, has proteasome-inhibitory, androgen receptor-suppressing, apoptosis-inducing, and antitumor activities in human prostate cancer cells and xenografts[J]. Cancer Res, 2007, 67(4): 1636-1644. doi:10.1158/0008-5472.CAN-06-3546 [46] Mao X, Li X, Sprangers R, et al. Clioquinol inhibits the proteasome and displays preclinical activity in leukemia and myeloma[J]. Leukemia, 2009, 23(3): 585-590. doi: 10.1038/leu.2008.232 [47] Arnesano F, Scintilla S, Calò V, et al. Copper-triggered aggregation of ubiquitin[J]. PLoS One, 2009, 4(9): e7052. doi:10.1371/journal.pone.0007052 [48] Ding WQ, Liu BL, Vaught JL, et al. Anticancer activity of the antibiotic clioquinol[J]. Cancer Res, 2005, 65(8): 3389-3395. doi:10.1158/0008-5472.CAN-04-3577 [49] Schimmer AD, Jitkova Y, Gronda M, et al. A phase I study of the metal ionophore clioquinol in patients with advanced hematologic malignancies[J]. Clin Lymphoma Myeloma Leuk, 2012, 12(5): 330-336. doi: 10.1016/j.clml.2012.05.005 |
[1] | HUANG Yanli, LI Junzheng. The mechanism of copper-induced tumor cell death and its research progress in cancer therapy [J]. Journal of Otolaryngology and Ophthalmology of Shandong University, 2023, 37(5): 198-205. |
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