Abstract
Cisplatin is an effective chemotherapeutic drug widely used for the treatment of various solid tumors; however, its clinical use and efficacy are limited by its inherent nephrotoxicity. The pathogenesis of cisplatin-induced nephrotoxicity is complex and has not been fully elucidated. Cellular uptake and transport, DNA damage, apoptosis, oxidative stress, inflammatory response, and autophagy are involved in the development of cisplatin-induced nephrotoxicity. Currently, despite some deficiencies, hydration regimens remain the major protective measures against cisplatin-induced nephrotoxicity. Therefore, effective drugs must be explored and developed to prevent and treat cisplatin-induced kidney injury. In recent years, many natural compounds with high efficiency and low toxicity have been identified for the treatment of cisplatin-induced nephrotoxicity, including quercetin, saikosaponin D, berberine, resveratrol, and curcumin. These natural agents have multiple targets, multiple effects, and low drug resistance; therefore, they can be safely used as a supplementary regimen or combination therapy for cisplatin-induced nephrotoxicity. This review aimed to comprehensively describe the molecular mechanisms underlying cisplatin-induced nephrotoxicity and summarize natural kidney-protecting compounds to provide new ideas for the development of better therapeutic agents.
Similar content being viewed by others
Data availability
Not applicable.
References
Ansari MA (2017) Sinapic acid modulates Nrf2/HO-1 signaling pathway in cisplatin-induced nephrotoxicity in rats. Biomed Pharmacother 93:646–653. https://doi.org/10.1016/j.biopha.2017.06.085
Arab HH, Mohamed WR, Barakat BM et al (2016) Tangeretin attenuates cisplatin-induced renal injury in rats: impact on the inflammatory cascade and oxidative perturbations. Chem Biol Interact 258:205–213. https://doi.org/10.1016/j.cbi.2016.09.008
Arjumand W, Seth A, Sultana S (2011) Rutin attenuates cisplatin induced renal inflammation and apoptosis by reducing NFkappaB, TNF-alpha and caspase-3 expression in wistar rats. Food Chem Toxicol 49:2013–2021. https://doi.org/10.1016/j.fct.2011.05.012
Arnesano F, Natile G (2021) Interference between copper transport systems and platinum drugs. Semin Cancer Biol 76:173–188. https://doi.org/10.1016/j.semcancer.2021.05.023
Atessahin A, Ceribasi AO, Yuce A et al (2007) Role of ellagic acid against cisplatin-induced nephrotoxicity and oxidative stress in rats. Basic Clin Pharmacol Toxicol 100:121–126. https://doi.org/10.1111/j.1742-7843.2006.00015.x
Bunel V, Antoine MH, Nortier J et al (2015) Nephroprotective effects of ferulic acid, Z-ligustilide and E-ligustilide isolated from Angelica sinensis against cisplatin toxicity in vitro. Toxicol In Vitro 29:458–467. https://doi.org/10.1016/j.tiv.2014.12.017
Campbell R, Shim H, Choi J et al (2021) Implantable cisplatin synthesis microdevice for regional chemotherapy. Adv Healthc Mater 10:e2001582. https://doi.org/10.1002/adhm.202001582
Chao CS, Tsai CS, Chang YP et al (2016) Hyperin inhibits nuclear factor kappa B and activates nuclear factor E2-related factor-2 signaling pathways in cisplatin-induced acute kidney injury in mice. Int Immunopharmacol 40:517–523. https://doi.org/10.1016/j.intimp.2016.09.020
Chen B, Liu G, Zou P et al (2015) Epigallocatechin-3-gallate protects against cisplatin-induced nephrotoxicity by inhibiting endoplasmic reticulum stress-induced apoptosis. Exp Biol Med (Maywood) 240:1513–1519. https://doi.org/10.1177/1535370215573394
Chen Q, Peng H, Dong L et al (2016) Activation of the NRF2-ARE signalling pathway by the Lentinula edodes polysaccharose LNT alleviates ROS-mediated cisplatin nephrotoxicity. Int Immunopharmacol 36:1–8. https://doi.org/10.1016/j.intimp.2016.04.007
Chen X, Wei W, Li Y et al (2019) Hesperetin relieves cisplatin-induced acute kidney injury by mitigating oxidative stress, inflammation and apoptosis. Chem Biol Interact 308:269–278. https://doi.org/10.1016/j.cbi.2019.05.040
Chirino YI, Pedraza-Chaverri J (2009) Role of oxidative and nitrosative stress in cisplatin-induced nephrotoxicity. Exp Toxicol Pathol 61:223–242. https://doi.org/10.1016/j.etp.2008.09.003
Chirino YI, Trujillo J, Sanchez-Gonzalez DJ et al (2008) Selective iNOS inhibition reduces renal damage induced by cisplatin. Toxicol Lett 176:48–57. https://doi.org/10.1016/j.toxlet.2007.10.006
Chtourou Y, Aouey B, Aroui S et al (2016) Anti-apoptotic and anti-inflammatory effects of naringin on cisplatin-induced renal injury in the rat. Chem Biol Interact 243:1–9. https://doi.org/10.1016/j.cbi.2015.11.019
Cullen KJ, Yang Z, Schumaker L et al (2007) Mitochondria as a critical target of the chemotheraputic agent cisplatin in head and neck cancer. J Bioenerg Biomembr 39:43–50. https://doi.org/10.1007/s10863-006-9059-5
Do AC, Francescato HD, Coimbra TM et al (2008) Resveratrol attenuates cisplatin-induced nephrotoxicity in rats. Arch Toxicol 82:363–370. https://doi.org/10.1007/s00204-007-0262-x
Domitrovic R, Cvijanovic O, Pernjak-Pugel E et al (2013) Berberine exerts nephroprotective effect against cisplatin-induced kidney damage through inhibition of oxidative/nitrosative stress, inflammation, autophagy and apoptosis. Food Chem Toxicol 62:397–406. https://doi.org/10.1016/j.fct.2013.09.003
Domitrovic R, Cvijanovic O, Susnic V et al (2014) Renoprotective mechanisms of chlorogenic acid in cisplatin-induced kidney injury. Toxicology 324:98–107. https://doi.org/10.1016/j.tox.2014.07.004
Dos SN, Carvalho RM, Martins NM et al (2012) Cisplatin-induced nephrotoxicity and targets of nephroprotection: an update. Arch Toxicol 86:1233–1250. https://doi.org/10.1007/s00204-012-0821-7
Elseweidy MM, Askar ME, Elswefy SE et al (2017) Vanillin as a new modulator candidate for renal injury induced by cisplatin in experimental rats. Cytokine 99:260–265. https://doi.org/10.1016/j.cyto.2017.07.025
Erman F, Tuzcu M, Orhan C et al (2014) Effect of lycopene against cisplatin-induced acute renal injury in rats: organic anion and cation transporters evaluation. Biol Trace Elem Res 158:90–95. https://doi.org/10.1007/s12011-014-9914-x
Filipski KK, Mathijssen RH, Mikkelsen TS et al (2009) Contribution of organic cation transporter 2 (OCT2) to cisplatin-induced nephrotoxicity. Clin Pharmacol Ther 86:396–402. https://doi.org/10.1038/clpt.2009.139
Freitas-Lima LC, Budu A, Arruda AC et al (2020) PPAR-alpha deletion attenuates cisplatin nephrotoxicity by modulating renal organic transporters MATE-1 and OCT-2. Int J Mol Sci 21:7416. https://doi.org/10.3390/ijms21197416
Gao Z, Liu G, Hu Z et al (2014) Grape seed proanthocyanidin extract protects from cisplatin-induced nephrotoxicity by inhibiting endoplasmic reticulum stress-induced apoptosis. Mol Med Rep 9:801–807. https://doi.org/10.3892/mmr.2014.1883
Geyikoglu F, Emir M, Colak S et al (2017) Effect of oleuropein against chemotherapy drug-induced histological changes, oxidative stress, and DNA damages in rat kidney injury. J Food Drug Anal 25:447–459. https://doi.org/10.1016/j.jfda.2016.07.002
Giacomini I, Ragazzi E, Pasut G et al (2020) The pentose phosphate pathway and its involvement in cisplatin resistance. Int J Mol Sci 21:937. https://doi.org/10.3390/ijms21030937
Gomez-Virgilio L, Silva-Lucero MD, Flores-Morelos DS et al (2022) Autophagy: a key regulator of homeostasis and disease: an overview of molecular mechanisms and modulators. Cells-Basel 11:2262. https://doi.org/10.3390/cells11152262
Guerrero-Beltran CE, Calderon-Oliver M, Martinez-Abundis E et al (2010) Protective effect of sulforaphane against cisplatin-induced mitochondrial alterations and impairment in the activity of NAD(P)H: quinone oxidoreductase 1 and gamma glutamyl cysteine ligase: studies in mitochondria isolated from rat kidney and in LLC-PK1 cells. Toxicol Lett 199:80–92. https://doi.org/10.1016/j.toxlet.2010.08.009
Hajian S, Rafieian-Kopaei M, Nasri H (2014) Renoprotective effects of antioxidants against cisplatin nephrotoxicity. J Nephropharmacol 3:39–42
Han MS, Han IH, Lee D et al (2016) Beneficial effects of fermented black ginseng and its ginsenoside 20(S)-Rg3 against cisplatin-induced nephrotoxicity in LLC-PK1 cells. J Ginseng Res 40:135–140. https://doi.org/10.1016/j.jgr.2015.06.006
Hausheer FH, Parker AR, Petluru PN et al (2011) Mechanistic study of BNP7787-mediated cisplatin nephroprotection: modulation of human aminopeptidase N. Cancer Chemother Pharmacol 67:381–391. https://doi.org/10.1007/s00280-010-1333-x
Hirama M, Isonishi S, Yasuda M et al (2006) Characterization of mitochondria in cisplatin-resistant human ovarian carcinoma cells. Oncol Rep 16:997–1002
Hong SJ, Dawson TM, Dawson VL (2004) Nuclear and mitochondrial conversations in cell death: PARP-1 and AIF signaling. Trends Pharmacol Sci 25:259–264. https://doi.org/10.1016/j.tips.2004.03.005
Horvath B, Mukhopadhyay P, Kechrid M et al (2012) beta-Caryophyllene ameliorates cisplatin-induced nephrotoxicity in a cannabinoid 2 receptor-dependent manner. Free Radic Biol Med 52:1325–1333. https://doi.org/10.1016/j.freeradbiomed.2012.01.014
Huang D, Wang C, Duan Y et al (2017) Targeting Oct2 and P53: formononetin prevents cisplatin-induced acute kidney injury. Toxicol Appl Pharmacol 326:15–24. https://doi.org/10.1016/j.taap.2017.04.013
Hussein RM, Al-Dalain SM (2021) Betaine downregulates microRNA 34a expression via a p53-dependent manner in cisplatin-induced nephrotoxicity in rats. J Biochem Mol Toxicol 35:e22856. https://doi.org/10.1002/jbt.22856
Inoue K, Kuwana H, Shimamura Y et al (2010) Cisplatin-induced macroautophagy occurs prior to apoptosis in proximal tubules in vivo. Clin Exp Nephrol 14:112–122. https://doi.org/10.1007/s10157-009-0254-7
Jiang L, Liu Y, He P et al (2016) Geraniin ameliorates cisplatin-induced nephrotoxicity in mice. Free Radic Res 50:813–819. https://doi.org/10.3109/10715762.2016.1173206
Jiang M, Dong Z (2008) Regulation and pathological role of p53 in cisplatin nephrotoxicity. J Pharmacol Exp Ther 327:300–307. https://doi.org/10.1124/jpet.108.139162
Kandemir FM, Yildirim S, Caglayan C et al (2019) Protective effects of zingerone on cisplatin-induced nephrotoxicity in female rats. Environ Sci Pollut Res Int 26:22562–22574. https://doi.org/10.1007/s11356-019-05505-3
Katsuda H, Yamashita M, Katsura H et al (2010) Protecting cisplatin-induced nephrotoxicity with cimetidine does not affect antitumor activity. Biol Pharm Bull 33:1867–1871. https://doi.org/10.1248/bpb.33.1867
Kaushal GP (2012) Autophagy protects proximal tubular cells from injury and apoptosis. Kidney Int 82:1250–1253. https://doi.org/10.1038/ki.2012.337
Kaushal GP, Kaushal V, Hong X et al (2001) Role and regulation of activation of caspases in cisplatin-induced injury to renal tubular epithelial cells. Kidney Int 60:1726–1736. https://doi.org/10.1046/j.1523-1755.2001.00026.x
Kemp G, Rose P, Lurain J et al (1996) Amifostine pretreatment for protection against cyclophosphamide-induced and cisplatin-induced toxicities: results of a randomized control trial in patients with advanced ovarian cancer. J Clin Oncol 14:2101–2112. https://doi.org/10.1200/JCO.1996.14.7.2101
Kim J, Long KE, Tang K et al (2012a) Poly(ADP-ribose) polymerase 1 activation is required for cisplatin nephrotoxicity. Kidney Int 82:193–203. https://doi.org/10.1038/ki.2012.64
Kim TW, Song IB, Lee HK et al (2012b) Platycodin D, a triterpenoid sapoinin from Platycodon grandiflorum, ameliorates cisplatin-induced nephrotoxicity in mice. Food Chem Toxicol 50:4254–4259. https://doi.org/10.1016/j.fct.2012.05.022
Kim TW, Kim YJ, Kim HT et al (2016) NQO1 deficiency leads enhanced autophagy in cisplatin-induced acute kidney injury through the AMPK/TSC2/mTOR signaling pathway. Antioxid Redox Signal 24:867–883. https://doi.org/10.1089/ars.2015.6386
Kiss RC, Xia F, Acklin S (2021) Targeting DNA damage response and repair to enhance therapeutic index in cisplatin-based cancer treatment. Int J Mol Sci 22:8199. https://doi.org/10.3390/ijms22158199
Kumar P, Barua CC, Sulakhiya K et al (2017) Curcumin ameliorates cisplatin-induced nephrotoxicity and potentiates its anticancer activity in SD rats: potential role of curcumin in breast cancer chemotherapy. Front Pharmacol 8:132. https://doi.org/10.3389/fphar.2017.00132
Li C, Li L, Yi Y et al (2020) L-tetrahydropalmatine attenuates cisplatin-induced nephrotoxicity via selective inhibition of organic cation transporter 2 without impairing its antitumor efficacy. Biochem Pharmacol 177:114021. https://doi.org/10.1016/j.bcp.2020.114021
Li F, Yao Y, Huang H et al (2018) Xanthohumol attenuates cisplatin-induced nephrotoxicity through inhibiting NF-kappaB and activating Nrf2 signaling pathways. Int Immunopharmacol 61:277–282. https://doi.org/10.1016/j.intimp.2018.05.017
Li W, Yan MH, Liu Y et al (2016) Ginsenoside Rg5 ameliorates cisplatin-induced nephrotoxicity in mice through inhibition of inflammation, oxidative stress, and apoptosis. Nutrients 8:566. https://doi.org/10.3390/nu8090566
Lin JC, Tsao MF, Lin YJ (2016) Differential impacts of alternative splicing networks on apoptosis. Int J Mol Sci 17:2097. https://doi.org/10.3390/ijms17122097
Liu H, Baliga R (2005) Endoplasmic reticulum stress-associated caspase 12 mediates cisplatin-induced LLC-PK1 cell apoptosis. J Am Soc Nephrol 16:1985–1992. https://doi.org/10.1681/ASN.2004090768
Liu H, Gu LB, Tu Y et al (2016) Emodin ameliorates cisplatin-induced apoptosis of rat renal tubular cells in vitro by activating autophagy. Acta Pharmacol Sin 37:235–245. https://doi.org/10.1038/aps.2015.114
Liu YH, Li K, Tian HQ (2020) Renoprotective effects of a new free radical scavenger, XH-003, against cisplatin-induced nephrotoxicity. Oxid Med Cell Longev 2020:9820168. https://doi.org/10.1155/2020/9820168
Ma X, Dang C, Kang H et al (2015) Saikosaponin-D reduces cisplatin-induced nephrotoxicity by repressing ROS-mediated activation of MAPK and NF-kappaB signalling pathways. Int Immunopharmacol 28:399–408. https://doi.org/10.1016/j.intimp.2015.06.020
Mahgoub E, Kumaraswamy SM, Kader KH et al (2017) Genipin attenuates cisplatin-induced nephrotoxicity by counteracting oxidative stress, inflammation, and apoptosis. Biomed Pharmacother 93:1083–1097. https://doi.org/10.1016/j.biopha.2017.07.018
Mapuskar KA, Flippo KH, Schoenfeld JD et al (2017) Mitochondrial superoxide increases age-associated susceptibility of human dermal fibroblasts to radiation and chemotherapy. Cancer Res 77:5054–5067. https://doi.org/10.1158/0008-5472.CAN-17-0106
Mapuskar KA, Steinbach EJ, Zaher A et al (2021) Mitochondrial superoxide dismutase in cisplatin-induced kidney injury. Antioxidants (Basel) 10:1329. https://doi.org/10.3390/antiox10091329
Mapuskar KA, Wen H, Holanda DG et al (2019) Persistent increase in mitochondrial superoxide mediates cisplatin-induced chronic kidney disease. Redox Biol 20:98–106. https://doi.org/10.1016/j.redox.2018.09.020
Mata-Miranda MM, Bernal-Barquero CE, Martinez-Cuazitl A et al (2019) Nephroprotective effect of embryonic stem cells reducing lipid peroxidation in kidney injury induced by cisplatin. Oxid Med Cell Longev 2019:5420624. https://doi.org/10.1155/2019/5420624
Meng XM, Li HD, Wu WF et al (2018) Wogonin protects against cisplatin-induced acute kidney injury by targeting RIPK1-mediated necroptosis. Lab Invest 98:79–94. https://doi.org/10.1038/labinvest.2017.115
Michel HE, Menze ET (2019) Tetramethylpyrazine guards against cisplatin-induced nephrotoxicity in rats through inhibiting HMGB1/TLR4/NF-kappaB and activating Nrf2 and PPAR-gamma signaling pathways. Eur J Pharmacol 857:172422. https://doi.org/10.1016/j.ejphar.2019.172422
Miller RP, Tadagavadi RK, Ramesh G et al (2010) Mechanisms of Cisplatin nephrotoxicity. Toxins (Basel) 2:2490-2518. https://doi.org/10.3390/toxins2112490
Mitazaki S, Hashimoto M, Matsuhashi Y et al (2013) Interleukin-6 modulates oxidative stress produced during the development of cisplatin nephrotoxicity. Life Sci 92:694–700. https://doi.org/10.1016/j.lfs.2013.01.026
Monastyrska I, Klionsky DJ (2006) Autophagy in organelle homeostasis: peroxisome turnover. Mol Aspects Med 27:483–494. https://doi.org/10.1016/j.mam.2006.08.004
Mundhe NA, Kumar P, Ahmed S et al (2015) Nordihydroguaiaretic acid ameliorates cisplatin induced nephrotoxicity and potentiates its anti-tumor activity in DMBA induced breast cancer in female Sprague-Dawley rats. Int Immunopharmacol 28:634–642. https://doi.org/10.1016/j.intimp.2015.07.016
Nakamura T, Yonezawa A, Hashimoto S et al (2010) Disruption of multidrug and toxin extrusion MATE1 potentiates cisplatin-induced nephrotoxicity. Biochem Pharmacol 80:1762–1767. https://doi.org/10.1016/j.bcp.2010.08.019
Oh GS, Kim HJ, Shen A et al (2014) Cisplatin-induced kidney dysfunction and perspectives on improving treatment strategies. Electrolyte Blood Press 12:55–65. https://doi.org/10.5049/EBP.2014.12.2.55
Pabla N, Murphy RF, Liu K et al (2009) The copper transporter Ctr1 contributes to cisplatin uptake by renal tubular cells during cisplatin nephrotoxicity. Am J Physiol Renal Physiol 296:F505–F511. https://doi.org/10.1152/ajprenal.90545.2008
Park CR, Kim HY, Song MG et al (2020) Efficacy and safety of human serum albumin-cisplatin complex in U87MG xenograft mouse models. Int J Mol Sci 21:7932. https://doi.org/10.3390/ijms21217932
Periyasamy-Thandavan S, Jiang M, Wei Q et al (2008) Autophagy is cytoprotective during cisplatin injury of renal proximal tubular cells. Kidney Int 74:631–640. https://doi.org/10.1038/ki.2008.214
Peyrou M, Hanna PE, Cribb AE (2007) Cisplatin, gentamicin, and p-aminophenol induce markers of endoplasmic reticulum stress in the rat kidneys. Toxicol Sci 99:346–353. https://doi.org/10.1093/toxsci/kfm152
Potocnjak I, Domitrovic R (2016) Carvacrol attenuates acute kidney injury induced by cisplatin through suppression of ERK and PI3K/Akt activation. Food Chem Toxicol 98:251–261. https://doi.org/10.1016/j.fct.2016.11.004
Potocnjak I, Simic L, Vukelic I et al (2019) Oleanolic acid attenuates cisplatin-induced nephrotoxicity in mice and chemosensitizes human cervical cancer cells to cisplatin cytotoxicity. Food Chem Toxicol 132:110676. https://doi.org/10.1016/j.fct.2019.110676
Qi L, Luo Q, Zhang Y et al (2019a) Advances in toxicological research of the anticancer drug cisplatin. Chem Res Toxicol 32:1469–1486. https://doi.org/10.1021/acs.chemrestox.9b00204
Qi Z, Li W, Tan J et al (2019b) Effect of ginsenoside Rh2 on renal apoptosis in cisplatin-induced nephrotoxicity in vivo. Phytomedicine 61:152862. https://doi.org/10.1016/j.phymed.2019.152862
Qi ZL, Wang Z, Li W et al (2017) Nephroprotective effects of anthocyanin from the fruits of Panax ginseng (GFA) on cisplatin-induced acute kidney injury in mice. Phytother Res 31:1400–1409. https://doi.org/10.1002/ptr.5867
Qu X, Gao H, Tao L et al (2019) Astragaloside IV protects against cisplatin-induced liver and kidney injury via autophagy-mediated inhibition of NLRP3 in rats. J Toxicol Sci 44:167–175. https://doi.org/10.2131/jts.44.167
Ramesh G, Reeves WB (2002) TNF-alpha mediates chemokine and cytokine expression and renal injury in cisplatin nephrotoxicity. J Clin Invest 110:835–842. https://doi.org/10.1172/JCI15606
Ramesh G, Reeves WB (2005) p38 MAP kinase inhibition ameliorates cisplatin nephrotoxicity in mice. Am J Physiol Renal Physiol 289:F166–F174. https://doi.org/10.1152/ajprenal.00401.2004
Rawat DS, Thakur BK, Semalty M et al (2013) Baicalein-phospholipid complex: a novel drug delivery technology for phytotherapeutics. Curr Drug Discov Technol 10:224–232. https://doi.org/10.2174/1570163811310030005
Rjeibi I, Feriani A, Ben SA et al (2018) Lycium europaeum extract: a new potential antioxidant source against cisplatin-induced liver and kidney injuries in mice. Oxid Med Cell Longev 2018:1630751. https://doi.org/10.1155/2018/1630751
Rodrigues MA, Rodrigues JL, Martins NM et al (2011) Carvedilol protects against cisplatin-induced oxidative stress, redox state unbalance and apoptosis in rat kidney mitochondria. Chem Biol Interact 189:45–51. https://doi.org/10.1016/j.cbi.2010.10.014
Sahu BD, Rentam KK, Putcha UK et al (2011) Carnosic acid attenuates renal injury in an experimental model of rat cisplatin-induced nephrotoxicity. Food Chem Toxicol 49:3090–3097. https://doi.org/10.1016/j.fct.2011.08.018
Sanchez-Gonzalez PD, Lopez-Hernandez FJ, Lopez-Novoa JM et al (2011a) An integrative view of the pathophysiological events leading to cisplatin nephrotoxicity. Crit Rev Toxicol 41:803–821. https://doi.org/10.3109/10408444.2011.602662
Sanchez-Gonzalez PD, Lopez-Hernandez FJ, Perez-Barriocanal F et al (2011b) Quercetin reduces cisplatin nephrotoxicity in rats without compromising its anti-tumour activity. Nephrol Dial Transplant 26:3484–3495. https://doi.org/10.1093/ndt/gfr195
Sears S, Siskind L (2021) Potential therapeutic targets for cisplatin-induced kidney injury: lessons from other models of AKI and fibrosis. J Am Soc Nephrol 32:1559–1567. https://doi.org/10.1681/ASN.2020101455
Servais H, Ortiz A, Devuyst O et al (2008) Renal cell apoptosis induced by nephrotoxic drugs: cellular and molecular mechanisms and potential approaches to modulation. Apoptosis 13:11–32. https://doi.org/10.1007/s10495-007-0151-z
Sherif IO (2015) Amelioration of cisplatin-induced nephrotoxicity in rats by triterpenoid saponin of Terminalia arjuna. Clin Exp Nephrol 19:591–597. https://doi.org/10.1007/s10157-014-1056-0
Singh MP, Chauhan AK, Kang SC (2018) Morin hydrate ameliorates cisplatin-induced ER stress, inflammation and autophagy in HEK-293 cells and mice kidney via PARP-1 regulation. Int Immunopharmacol 56:156–167. https://doi.org/10.1016/j.intimp.2018.01.031
Suliman FA, Khodeer DM, Ibrahiem A et al (2018) Renoprotective effect of the isoflavonoid biochanin A against cisplatin induced acute kidney injury in mice: effect on inflammatory burden and p53 apoptosis. Int Immunopharmacol 61:8–19. https://doi.org/10.1016/j.intimp.2018.05.010
Sun CY, Nie J, Zheng ZL et al (2019) Renoprotective effect of scutellarin on cisplatin-induced renal injury in mice: impact on inflammation, apoptosis, and autophagy. Biomed Pharmacother 112:108647. https://doi.org/10.1016/j.biopha.2019.108647
Sung MJ, Kim DH, Jung YJ et al (2008) Genistein protects the kidney from cisplatin-induced injury. Kidney Int 74:1538–1547. https://doi.org/10.1038/ki.2008.409
Takahashi A, Kimura T, Takabatake Y et al (2012) Autophagy guards against cisplatin-induced acute kidney injury. Am J Pathol 180:517–525. https://doi.org/10.1016/j.ajpath.2011.11.001
Tan RZ, Wang C, Deng C et al (2020) Quercetin protects against cisplatin-induced acute kidney injury by inhibiting Mincle/Syk/NF-kappaB signaling maintained macrophage inflammation. Phytother Res 34:139–152. https://doi.org/10.1002/ptr.6507
Tsuruya K, Ninomiya T, Tokumoto M et al (2003) Direct involvement of the receptor-mediated apoptotic pathways in cisplatin-induced renal tubular cell death. Kidney Int 63:72–82. https://doi.org/10.1046/j.1523-1755.2003.00709.x
Ulu R, Dogukan A, Tuzcu M et al (2012) Regulation of renal organic anion and cation transporters by thymoquinone in cisplatin induced kidney injury. Food Chem Toxicol 50:1675–1679. https://doi.org/10.1016/j.fct.2012.02.082
Vasaikar N, Mahajan U, Patil KR et al (2018) D-pinitol attenuates cisplatin-induced nephrotoxicity in rats: impact on pro-inflammatory cytokines. Chem Biol Interact 290:6–11. https://doi.org/10.1016/j.cbi.2018.05.003
Volarevic V, Djokovic B, Jankovic MG et al (2019) Molecular mechanisms of cisplatin-induced nephrotoxicity: a balance on the knife edge between renoprotection and tumor toxicity. J Biomed Sci 26:25. https://doi.org/10.1186/s12929-019-0518-9
Wang D, Lippard SJ (2005) Cellular processing of platinum anticancer drugs. Nat Rev Drug Discov 4:307–320. https://doi.org/10.1038/nrd1691
Wang G, Bi Y, Xiong H et al (2021) Wedelolactone protects against cisplatin-induced nephrotoxicity in mice via inhibition of organic cation transporter 2. Hum Exp Toxicol 40:S447–S459. https://doi.org/10.1177/09603271211047915
Wang L, Cao Z, Wang Z et al (2022) Reactive oxygen species associated immunoregulation post influenza virus infection. Front Immunol 13:927593. https://doi.org/10.3389/fimmu.2022.927593
Wang X, Parrish AR (2015) Loss of alpha(E)-catenin promotes Fas mediated apoptosis in tubular epithelial cells. Apoptosis 20:921–929. https://doi.org/10.1007/s10495-015-1129-x
Wen X, Buckley B, McCandlish E et al (2014) Transgenic expression of the human MRP2 transporter reduces cisplatin accumulation and nephrotoxicity in Mrp2-null mice. Am J Pathol 184:1299–1308. https://doi.org/10.1016/j.ajpath.2014.01.025
Williams RM, Shah J, Mercer E et al (2021) Kidney-targeted redox scavenger therapy prevents cisplatin-induced acute kidney injury. Front Pharmacol 12:790913. https://doi.org/10.3389/fphar.2021.790913
Wu CH, Chen AZ, Yen GC (2015) Protective effects of glycyrrhizic acid and 18beta-glycyrrhetinic acid against cisplatin-induced nephrotoxicity in BALB/c mice. J Agric Food Chem 63:1200–1209. https://doi.org/10.1021/jf505471a
Wu CT, Sheu ML, Tsai KS et al (2011) Salubrinal, an eIF2alpha dephosphorylation inhibitor, enhances cisplatin-induced oxidative stress and nephrotoxicity in a mouse model. Free Radic Biol Med 51:671–680. https://doi.org/10.1016/j.freeradbiomed.2011.04.038
Xing JJ, Hou JG, Ma ZN et al (2019) Ginsenoside Rb3 provides protective effects against cisplatin-induced nephrotoxicity via regulation of AMPK-/mTOR-mediated autophagy and inhibition of apoptosis in vitro and in vivo. Cell Prolif 52:e12627. https://doi.org/10.1111/cpr.12627
Yang C, Guo Y, Huang TS et al (2018) Asiatic acid protects against cisplatin-induced acute kidney injury via anti-apoptosis and anti-inflammation. Biomed Pharmacother 107:1354–1362. https://doi.org/10.1016/j.biopha.2018.08.126
Yu X, Meng X, Xu M et al (2018) Celastrol ameliorates cisplatin nephrotoxicity by inhibiting NF-kappaB and improving mitochondrial function. EBioMedicine 36:266–280. https://doi.org/10.1016/j.ebiom.2018.09.031
Zang H, Yang Q, Li J (2019) Eleutheroside B protects against acute kidney injury by activating IGF pathway. Molecules 24:3876. https://doi.org/10.3390/molecules24213876
Zhai J, Gao H, Wang S et al (2021) Ginsenoside Rg3 attenuates cisplatin-induced kidney injury through inhibition of apoptosis and autophagy-inhibited NLRP3. J Biochem Mol Toxicol 35:e22896. https://doi.org/10.1002/jbt.22896
Zhang B, Ramesh G, Norbury CC et al (2007) Cisplatin-induced nephrotoxicity is mediated by tumor necrosis factor-alpha produced by renal parenchymal cells. Kidney Int 72:37–44. https://doi.org/10.1038/sj.ki.5002242
Zhang C, Xu C, Gao X et al (2022) Platinum-based drugs for cancer therapy and anti-tumor strategies. Theranostics 12:2115–2132. https://doi.org/10.7150/thno.69424
Zhang L, Gu Y, Li H et al (2018) Daphnetin protects against cisplatin-induced nephrotoxicity by inhibiting inflammatory and oxidative response. Int Immunopharmacol 65:402–407. https://doi.org/10.1016/j.intimp.2018.10.018
Zhang Y, Tao X, Yin L et al (2017) Protective effects of dioscin against cisplatin-induced nephrotoxicity via the microRNA-34a/sirtuin 1 signalling pathway. Br J Pharmacol 174:2512–2527. https://doi.org/10.1111/bph.13862
Zhang Y, Yuan F, Cao X et al (2014) P2X7 receptor blockade protects against cisplatin-induced nephrotoxicity in mice by decreasing the activities of inflammasome components, oxidative stress and caspase-3. Toxicol Appl Pharmacol 281:1–10. https://doi.org/10.1016/j.taap.2014.09.016
Zhou L, Zhang L, Zhang Y et al (2019) PINK1 deficiency ameliorates cisplatin-induced acute kidney injury in rats. Front Physiol 10:1225. https://doi.org/10.3389/fphys.2019.01225
Acknowledgements
We thank Zhaowei Zhang for editorial assistance in the preparation of the manuscript.
Funding
This study was financially supported by the National Natural Science Foundation of China (No. 82003755) and the Initial Scientific Research Foundation for Jinhua Municipal Central Hospital (No. JY2019-2-01).
Author information
Authors and Affiliations
Contributions
X.B. and L.H. provided the ideas for this review; D.Z., K.J., G.L., and J.K. wrote the manuscript; G.L. designed and supervised the manuscript writing. All authors have read and approved to the published version of the manuscript. The authors confirm that no paper mill and artificial intelligence was used.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Ethics approval
Not applicable.
Consent to participate
Not applicable.
Consent for publication
Not applicable.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Zhang, D., Luo, G., Jin, K. et al. The underlying mechanisms of cisplatin-induced nephrotoxicity and its therapeutic intervention using natural compounds. Naunyn-Schmiedeberg's Arch Pharmacol 396, 2925–2941 (2023). https://doi.org/10.1007/s00210-023-02559-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00210-023-02559-6