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Human drug efflux transporter ABCC5 confers acquired resistance to pemetrexed in breast cancer

AIM: Pemetrexed, a new generation antifolate drug, has been approved for the treatment of locally advanced or metastatic breast cancer. However, factors affecting its efficacy and resistance have not been fully elucidated yet. ATP-binding cassette (ABC) transporters are predictors of prognosis as we...

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Autores principales: Chen, Jihui, Wang, Zhipeng, Gao, Shouhong, Wu, Kejin, Bai, Fang, Zhang, Qiqiang, Wang, Hongyu, Ye, Qin, Xu, Fengjing, Sun, Hong, Lu, Yunshu, Liu, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908708/
https://www.ncbi.nlm.nih.gov/pubmed/33632224
http://dx.doi.org/10.1186/s12935-021-01842-x
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author Chen, Jihui
Wang, Zhipeng
Gao, Shouhong
Wu, Kejin
Bai, Fang
Zhang, Qiqiang
Wang, Hongyu
Ye, Qin
Xu, Fengjing
Sun, Hong
Lu, Yunshu
Liu, Yan
author_facet Chen, Jihui
Wang, Zhipeng
Gao, Shouhong
Wu, Kejin
Bai, Fang
Zhang, Qiqiang
Wang, Hongyu
Ye, Qin
Xu, Fengjing
Sun, Hong
Lu, Yunshu
Liu, Yan
author_sort Chen, Jihui
collection PubMed
description AIM: Pemetrexed, a new generation antifolate drug, has been approved for the treatment of locally advanced or metastatic breast cancer. However, factors affecting its efficacy and resistance have not been fully elucidated yet. ATP-binding cassette (ABC) transporters are predictors of prognosis as well as of adverse effects of several xenobiotics. This study was designed to explore whether ABC transporters affect pemetrexed resistance and can contribute to the optimization of breast cancer treatment regimen. METHODS: First, we measured the expression levels of ABC transporter family members in cell lines. Subsequently, we assessed the potential role of ABC transporters in conferring resistance to pemetrexed in primary breast cancer cells isolated from 34 breast cancer patients and the role of ABCC5 in mediating pemetrexed transport and apoptotic pathways in MCF-7 cells. Finally, the influence of ABCC5 expression on the therapeutic effect of pemetrexed was evaluated in an in vivo xenograft mouse model of breast cancer. RESULTS: The expression levels of ABCC2, ABCC4, ABCC5, and ABCG2 significantly increased in the pan-resistant cell line, and the ABCC5 level in the MCF-7-ADR cell line was 5.21 times higher than that in the control group. ABCC5 expression was inversely correlated with pemetrexed sensitivity (IC(50), r = 0.741; p < 0.001) in breast cancer cells derived from 34 patients. Furthermore, we found that the expression level of ABCC5 influenced the efflux and cytotoxicity of pemetrexed in MCF-7 cells, with IC(50) values of 0.06 and 0.20 μg/mL in ABCC5 knockout and over-expression cells, respectively. In the in vivo study, we observed that ABCC5 affected the sensitivity of pemetrexed in breast tumor-bearing mice, and the tumor volume was much larger in the ABCC5-overexpressing group than in the control group when compared with their own initial volumes (2.7-fold vs. 1.3-fold). CONCLUSIONS: Our results indicated that ABCC5 expression was associated with pemetrexed resistance in vitro and in vivo, and it may serve as a target or biomarker for the optimization of pemetrexed regimen in breast cancer treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-01842-x.
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spelling pubmed-79087082021-02-26 Human drug efflux transporter ABCC5 confers acquired resistance to pemetrexed in breast cancer Chen, Jihui Wang, Zhipeng Gao, Shouhong Wu, Kejin Bai, Fang Zhang, Qiqiang Wang, Hongyu Ye, Qin Xu, Fengjing Sun, Hong Lu, Yunshu Liu, Yan Cancer Cell Int Primary Research AIM: Pemetrexed, a new generation antifolate drug, has been approved for the treatment of locally advanced or metastatic breast cancer. However, factors affecting its efficacy and resistance have not been fully elucidated yet. ATP-binding cassette (ABC) transporters are predictors of prognosis as well as of adverse effects of several xenobiotics. This study was designed to explore whether ABC transporters affect pemetrexed resistance and can contribute to the optimization of breast cancer treatment regimen. METHODS: First, we measured the expression levels of ABC transporter family members in cell lines. Subsequently, we assessed the potential role of ABC transporters in conferring resistance to pemetrexed in primary breast cancer cells isolated from 34 breast cancer patients and the role of ABCC5 in mediating pemetrexed transport and apoptotic pathways in MCF-7 cells. Finally, the influence of ABCC5 expression on the therapeutic effect of pemetrexed was evaluated in an in vivo xenograft mouse model of breast cancer. RESULTS: The expression levels of ABCC2, ABCC4, ABCC5, and ABCG2 significantly increased in the pan-resistant cell line, and the ABCC5 level in the MCF-7-ADR cell line was 5.21 times higher than that in the control group. ABCC5 expression was inversely correlated with pemetrexed sensitivity (IC(50), r = 0.741; p < 0.001) in breast cancer cells derived from 34 patients. Furthermore, we found that the expression level of ABCC5 influenced the efflux and cytotoxicity of pemetrexed in MCF-7 cells, with IC(50) values of 0.06 and 0.20 μg/mL in ABCC5 knockout and over-expression cells, respectively. In the in vivo study, we observed that ABCC5 affected the sensitivity of pemetrexed in breast tumor-bearing mice, and the tumor volume was much larger in the ABCC5-overexpressing group than in the control group when compared with their own initial volumes (2.7-fold vs. 1.3-fold). CONCLUSIONS: Our results indicated that ABCC5 expression was associated with pemetrexed resistance in vitro and in vivo, and it may serve as a target or biomarker for the optimization of pemetrexed regimen in breast cancer treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-01842-x. BioMed Central 2021-02-25 /pmc/articles/PMC7908708/ /pubmed/33632224 http://dx.doi.org/10.1186/s12935-021-01842-x Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Primary Research
Chen, Jihui
Wang, Zhipeng
Gao, Shouhong
Wu, Kejin
Bai, Fang
Zhang, Qiqiang
Wang, Hongyu
Ye, Qin
Xu, Fengjing
Sun, Hong
Lu, Yunshu
Liu, Yan
Human drug efflux transporter ABCC5 confers acquired resistance to pemetrexed in breast cancer
title Human drug efflux transporter ABCC5 confers acquired resistance to pemetrexed in breast cancer
title_full Human drug efflux transporter ABCC5 confers acquired resistance to pemetrexed in breast cancer
title_fullStr Human drug efflux transporter ABCC5 confers acquired resistance to pemetrexed in breast cancer
title_full_unstemmed Human drug efflux transporter ABCC5 confers acquired resistance to pemetrexed in breast cancer
title_short Human drug efflux transporter ABCC5 confers acquired resistance to pemetrexed in breast cancer
title_sort human drug efflux transporter abcc5 confers acquired resistance to pemetrexed in breast cancer
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908708/
https://www.ncbi.nlm.nih.gov/pubmed/33632224
http://dx.doi.org/10.1186/s12935-021-01842-x
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