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Use of the Naphthoquinone YM155 (Sepantronium Bromide) in the Treatment of Cancer: A Systematic Review and Meta-Synthesis

Dariimaa Ganbat1,2, Bat-Erdene Jugder3, Lkhamaa Ganbat4, Miki Tomoeda5, Erdenetsogt Dungubat2,6, Ambaga Miyegombo7, Gantsetseg Garmaa8, Yoshihisa Takahashi6, Ryuji Fukuzawa6, Ichiro Mori6, Takayuki Shiomi6, Akinori Nakata9, Yasuhiko Tomita6,*

1 Department of Public Health, Graduate School of Medicine, International University of Health and Welfare, Tokyo, 107-8402, Japan
2 Department of Pathology, School of Medicine, Mongolian National University of Medical Sciences, Ulan-Bator, 14210, Mongolia
3 Division of Immunology, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02115, USA
4 Department of Administration, MCS Property, Ulan-Bator, 14200, Mongolia
5 Department of Rehabilitation, Kobe International University, Kobe, 658-0032, Japan
6 Department of Pathology, School of Medicine, International University of Health and Welfare, Narita, 286-8686, Japan
7 New Medical University, Ulan-Bator, 18104, Mongolia
8 Institute of Translational Medicine, Semmelweis University, Budapest, 1085, Hungary
9 Department of Epidemiology and Social Medicine, Graduate School of Public Health, International University of Health and Welfare, Tokyo, 107-8402, Japan

* Corresponding Author: Yasuhiko Tomita. Email: email

Oncologie 2022, 24(2), 195-225. https://doi.org/10.32604/oncologie.2022.022299

Abstract

Most cancer cells overexpress the anti-apoptotic protein survivin and display redox dysregulation originating from genotypic and phenotypic alterations. These disturbances contribute to the uncontrolled proliferation, invasion, and chemoresistance of cancer cells, yet they also represent a specific vulnerability that could be exploited therapeutically in selected tumors. YM155 (sepantronium bromide) is a naphthoquinone-containing imidazolebased compound that selectively inhibits survivin expression at the transcriptional and post-transcriptional levels. Here, we performed a systematic review and meta-analysis of clinical studies in which YM155 was administered as monotherapy or combination therapy for patients with cancer. We assessed fully or partially reported clinical outcomes and pharmacological parameters, and further performed subgroup analysis based on tumor type and treatment regimen. Our comprehensive analysis, which included patients of many ethnicities, demonstrated that YM155 was effective as a monotherapy or combination therapy. Clinical benefits, including regression and/or stabilization of tumor progression and prolonged survival, were observed within a reasonable time after treatment initiation, and YM155 displayed good synergistic effects with combination drugs. YM155 appears to be effective against a wide range of tumor types and has an acceptable safety profile, with the main toxicities being decreased blood cell counts; fatigue/weakness; renal, hepatic, and/or cardiac issues; and electrolyte disturbance.

Keywords


Cite This Article

APA Style
Ganbat, D., Jugder, B., Ganbat, L., Tomoeda, M., Dungubat, E. et al. (2022). Use of the naphthoquinone YM155 (sepantronium bromide) in the treatment of cancer: A systematic review and meta-synthesis. Oncologie, 24(2), 195-225. https://doi.org/10.32604/oncologie.2022.022299
Vancouver Style
Ganbat D, Jugder B, Ganbat L, Tomoeda M, Dungubat E, Miyegombo A, et al. Use of the naphthoquinone YM155 (sepantronium bromide) in the treatment of cancer: A systematic review and meta-synthesis. Oncologie . 2022;24(2):195-225 https://doi.org/10.32604/oncologie.2022.022299
IEEE Style
D. Ganbat et al., "Use of the Naphthoquinone YM155 (Sepantronium Bromide) in the Treatment of Cancer: A Systematic Review and Meta-Synthesis," Oncologie , vol. 24, no. 2, pp. 195-225. 2022. https://doi.org/10.32604/oncologie.2022.022299



cc Copyright © 2022 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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