Literature DB >> 34330821

Current Understanding of Membrane Transporters as Regulators or Targets for Cisplatin-Induced Hearing Loss.

Kyle Z Pasquariello1, Jason M Dey1, Jason A Sprowl2.   

Abstract

Cisplatin is a platinum-based drug, which remains among the most efficacious anticancer treatment options. Unfortunately, use of cisplatin is hindered by dose-limiting toxicities, including irreversible hearing loss, which can grossly affect patient quality of life. Cisplatin-induced ototoxicity is the result of cochlear hair cell damage through a mechanism that is poorly understood. However, cisplatin cytotoxicity is reliant on intracellular accumulation, a process that is largely dependent on the presence of particular membrane transporters. This review will provide an update on our current understanding of the various transporters known to be involved in the disposition and cytotoxicity of platinum drugs or their metabolites, as well as their role in mediating cisplatin-induced hearing loss. We also provide a summary of the successes and opportunities in therapeutically targeting membrane transporters to alleviate platinum-induced hearing loss. Moreover, we describe how this approach could be used to reduce the severity or onset of other adverse events associated with exposure to various forms of platinum drugs, without diminishing antitumor efficacy. SIGNIFICANCE STATEMENT: Cisplatin-induced hearing loss is a dose-limiting and irreversible adverse event with no current preventative or curative treatment measures. Pharmacological targeting of membrane transporters that regulate platinum uptake into cochlear hair cells, if conducted appropriately, may alleviate this devastating side effect and could be applied to alleviate other platinum-induced toxicities.
Copyright © 2021 by The American Society for Pharmacology and Experimental Therapeutics.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 34330821      PMCID: PMC8626641          DOI: 10.1124/molpharm.121.000274

Source DB:  PubMed          Journal:  Mol Pharmacol        ISSN: 0026-895X            Impact factor:   4.054


  85 in total

1.  Drug resistance and ATP-dependent conjugate transport mediated by the apical multidrug resistance protein, MRP2, permanently expressed in human and canine cells.

Authors:  Y Cui; J König; J K Buchholz; H Spring; I Leier; D Keppler
Journal:  Mol Pharmacol       Date:  1999-05       Impact factor: 4.436

2.  Enhanced transport of anticancer agents and leukotriene C4 by the human canalicular multispecific organic anion transporter (cMOAT/MRP2).

Authors:  T Kawabe; Z S Chen; M Wada; T Uchiumi; M Ono; S Akiyama; M Kuwano
Journal:  FEBS Lett       Date:  1999-08-06       Impact factor: 4.124

3.  Disruption of multidrug and toxin extrusion MATE1 potentiates cisplatin-induced nephrotoxicity.

Authors:  Takanori Nakamura; Atsushi Yonezawa; Shinya Hashimoto; Toshiya Katsura; Ken-Ichi Inui
Journal:  Biochem Pharmacol       Date:  2010-09-09       Impact factor: 5.858

4.  Inhibition of OCT2, MATE1 and MATE2-K as a possible mechanism of drug interaction between pazopanib and cisplatin.

Authors:  C Sauzay; M White-Koning; I Hennebelle; T Deluche; C Delmas; D C Imbs; E Chatelut; F Thomas
Journal:  Pharmacol Res       Date:  2016-05-10       Impact factor: 7.658

5.  The use of probenecid as a chemoprotector against cisplatin nephrotoxicity.

Authors:  C Jacobs; S Kaubisch; J Halsey; B L Lum; M Gosland; C N Coleman; B I Sikic
Journal:  Cancer       Date:  1991-03-15       Impact factor: 6.860

6.  Neuronal uptake transporters contribute to oxaliplatin neurotoxicity in mice.

Authors:  Kevin M Huang; Alix F Leblanc; Muhammad Erfan Uddin; Ji Young Kim; Mingqing Chen; Eric D Eisenmann; Alice A Gibson; Yang Li; Kristen W Hong; Duncan DiGiacomo; Sherry H Xia; Paola Alberti; Alessia Chiorazzi; Stephen N Housley; Timothy C Cope; Jason A Sprowl; Jing Wang; Charles L Loprinzi; Anne Noonan; Maryam B Lustberg; Guido Cavaletti; Navjot Pabla; Shuiying Hu; Alex Sparreboom
Journal:  J Clin Invest       Date:  2020-09-01       Impact factor: 14.808

Review 7.  Prevention of cisplatin-induced ototoxicity in children and adolescents with cancer: a clinical practice guideline.

Authors:  David R Freyer; Penelope R Brock; Kay W Chang; L Lee Dupuis; Sidnei Epelman; Kristin Knight; Denise Mills; Robert Phillips; Emma Potter; Demie Risby; Philippa Simpkin; Michael Sullivan; Sandra Cabral; Paula D Robinson; Lillian Sung
Journal:  Lancet Child Adolesc Health       Date:  2019-12-19

8.  Transgenic expression of the human MRP2 transporter reduces cisplatin accumulation and nephrotoxicity in Mrp2-null mice.

Authors:  Xia Wen; Brian Buckley; Elizabeth McCandlish; Michael J Goedken; Samira Syed; Ryan Pelis; José E Manautou; Lauren M Aleksunes
Journal:  Am J Pathol       Date:  2014-03-15       Impact factor: 4.307

9.  Replication of TPMT and ABCC3 genetic variants highly associated with cisplatin-induced hearing loss in children.

Authors:  K Pussegoda; C J Ross; H Visscher; M Yazdanpanah; B Brooks; S R Rassekh; Y F Zada; M-P Dubé; B C Carleton; M R Hayden
Journal:  Clin Pharmacol Ther       Date:  2013-04-10       Impact factor: 6.875

10.  Monocarboxylate Transporter 6-Mediated Interactions with Prostaglandin F: In Vitro and In Vivo Evidence Utilizing a Knockout Mouse Model.

Authors:  Robert S Jones; Mark D Parker; Marilyn E Morris
Journal:  Pharmaceutics       Date:  2020-02-26       Impact factor: 6.321

View more
  1 in total

1.  Repositioning of Lansoprazole as a Protective Agent Against Cisplatin-Induced Ototoxicity.

Authors:  Eri Wakai; Kenji Ikemura; Toshiro Mizuno; Kazuhiko Takeuchi; Satoshi Tamaru; Masahiro Okuda; Yuhei Nishimura
Journal:  Front Pharmacol       Date:  2022-07-15       Impact factor: 5.988

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.