Combination therapy of cisplatin with cilastatin enables an increased dose of cisplatin, enhancing its antitumor effect by suppression of nephrotoxicity
Abstract Cisplatin, one of the most active anticancer agents, is widely used in standard chemotherapy for various cancers. Cisplatin is more poorly tolerated than other chemotherapeutic drugs, and the main dose-limiting toxicity of cisplatin is its nephrotoxicity, which is dose-dependent. Although l...
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Nature Publishing Group
2021-01-01
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Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-020-80853-6 |
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doaj-71f2c5bdd1594bf081bb9c4162ab9c10 |
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Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Masashi Arita Satoshi Watanabe Nobumasa Aoki Shoji Kuwahara Ryo Suzuki Sawako Goto Yuko Abe Miho Takahashi Miyuki Sato Satoshi Hokari Aya Ohtsubo Satoshi Shoji Koichiro Nozaki Kosuke Ichikawa Rie Kondo Masachika Hayashi Yasuyoshi Ohshima Hideyuki Kabasawa Michihiro Hosojima Toshiyuki Koya Akihiko Saito Toshiaki Kikuchi |
spellingShingle |
Masashi Arita Satoshi Watanabe Nobumasa Aoki Shoji Kuwahara Ryo Suzuki Sawako Goto Yuko Abe Miho Takahashi Miyuki Sato Satoshi Hokari Aya Ohtsubo Satoshi Shoji Koichiro Nozaki Kosuke Ichikawa Rie Kondo Masachika Hayashi Yasuyoshi Ohshima Hideyuki Kabasawa Michihiro Hosojima Toshiyuki Koya Akihiko Saito Toshiaki Kikuchi Combination therapy of cisplatin with cilastatin enables an increased dose of cisplatin, enhancing its antitumor effect by suppression of nephrotoxicity Scientific Reports |
author_facet |
Masashi Arita Satoshi Watanabe Nobumasa Aoki Shoji Kuwahara Ryo Suzuki Sawako Goto Yuko Abe Miho Takahashi Miyuki Sato Satoshi Hokari Aya Ohtsubo Satoshi Shoji Koichiro Nozaki Kosuke Ichikawa Rie Kondo Masachika Hayashi Yasuyoshi Ohshima Hideyuki Kabasawa Michihiro Hosojima Toshiyuki Koya Akihiko Saito Toshiaki Kikuchi |
author_sort |
Masashi Arita |
title |
Combination therapy of cisplatin with cilastatin enables an increased dose of cisplatin, enhancing its antitumor effect by suppression of nephrotoxicity |
title_short |
Combination therapy of cisplatin with cilastatin enables an increased dose of cisplatin, enhancing its antitumor effect by suppression of nephrotoxicity |
title_full |
Combination therapy of cisplatin with cilastatin enables an increased dose of cisplatin, enhancing its antitumor effect by suppression of nephrotoxicity |
title_fullStr |
Combination therapy of cisplatin with cilastatin enables an increased dose of cisplatin, enhancing its antitumor effect by suppression of nephrotoxicity |
title_full_unstemmed |
Combination therapy of cisplatin with cilastatin enables an increased dose of cisplatin, enhancing its antitumor effect by suppression of nephrotoxicity |
title_sort |
combination therapy of cisplatin with cilastatin enables an increased dose of cisplatin, enhancing its antitumor effect by suppression of nephrotoxicity |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-01-01 |
description |
Abstract Cisplatin, one of the most active anticancer agents, is widely used in standard chemotherapy for various cancers. Cisplatin is more poorly tolerated than other chemotherapeutic drugs, and the main dose-limiting toxicity of cisplatin is its nephrotoxicity, which is dose-dependent. Although less toxic methods of cisplatin administration have been established, cisplatin-induced nephrotoxicity remains an unsolved problem. Megalin is an endocytic receptor expressed at the apical membrane of proximal tubules. We previously demonstrated that nephrotoxic drugs, including cisplatin, are reabsorbed through megalin and cause proximal tubular cell injury. We further found that cilastatin blocked the binding of cisplatin to megalin in vitro. In this study, we investigated whether cilastatin could reduce cisplatin-induced nephrotoxicity without influencing the antitumor effects of cisplatin. Nephrotoxicity was decreased or absent in mice treated with cisplatin and cilastatin, as determined by kidney injury molecule-1 staining and the blood urea nitrogen content. Combined with cilastatin, a twofold dose of cisplatin was used to successfully treat the mice, which enhanced the antitumor effects of cisplatin but reduced its nephrotoxicity. These findings suggest that we can increase the dose of cisplatin when combined with cilastatin and improve the outcome of cancer patients. |
url |
https://doi.org/10.1038/s41598-020-80853-6 |
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doaj-71f2c5bdd1594bf081bb9c4162ab9c102021-01-17T12:32:37ZengNature Publishing GroupScientific Reports2045-23222021-01-0111111010.1038/s41598-020-80853-6Combination therapy of cisplatin with cilastatin enables an increased dose of cisplatin, enhancing its antitumor effect by suppression of nephrotoxicityMasashi Arita0Satoshi Watanabe1Nobumasa Aoki2Shoji Kuwahara3Ryo Suzuki4Sawako Goto5Yuko Abe6Miho Takahashi7Miyuki Sato8Satoshi Hokari9Aya Ohtsubo10Satoshi Shoji11Koichiro Nozaki12Kosuke Ichikawa13Rie Kondo14Masachika Hayashi15Yasuyoshi Ohshima16Hideyuki Kabasawa17Michihiro Hosojima18Toshiyuki Koya19Akihiko Saito20Toshiaki Kikuchi21Department of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesLaboratory of Clinical Nutrition, Department of Nutrition, Graduate School of Human Cultures, The University of Shiga PrefectureDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Applied Molecular Medicine, Kidney Research Center, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Clinical Nutrition Science, Niigata University Graduate School of Medical and Dental SciencesDepartment of Clinical Nutrition Science, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesDepartment of Applied Molecular Medicine, Kidney Research Center, Niigata University Graduate School of Medical and Dental SciencesDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental SciencesAbstract Cisplatin, one of the most active anticancer agents, is widely used in standard chemotherapy for various cancers. Cisplatin is more poorly tolerated than other chemotherapeutic drugs, and the main dose-limiting toxicity of cisplatin is its nephrotoxicity, which is dose-dependent. Although less toxic methods of cisplatin administration have been established, cisplatin-induced nephrotoxicity remains an unsolved problem. Megalin is an endocytic receptor expressed at the apical membrane of proximal tubules. We previously demonstrated that nephrotoxic drugs, including cisplatin, are reabsorbed through megalin and cause proximal tubular cell injury. We further found that cilastatin blocked the binding of cisplatin to megalin in vitro. In this study, we investigated whether cilastatin could reduce cisplatin-induced nephrotoxicity without influencing the antitumor effects of cisplatin. Nephrotoxicity was decreased or absent in mice treated with cisplatin and cilastatin, as determined by kidney injury molecule-1 staining and the blood urea nitrogen content. Combined with cilastatin, a twofold dose of cisplatin was used to successfully treat the mice, which enhanced the antitumor effects of cisplatin but reduced its nephrotoxicity. These findings suggest that we can increase the dose of cisplatin when combined with cilastatin and improve the outcome of cancer patients.https://doi.org/10.1038/s41598-020-80853-6 |