Evidence map›Paper›PMID 33632224›Full record

ArticleCancer cell international2021

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

Jihui Chen, Zhipeng Wang, Shouhong Gao, Kejin Wu, Fang Bai, Qiqiang Zhang, Hongyu Wang, Qin Ye, Fengjing Xu, Hong Sun and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 35 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Jihui Chen *Department of Pharmacy, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.
Zhipeng Wang *Department of Pharmacy, Changzheng Hospital, Second Military Medical University, Shanghai, 200003, China.
Shouhong GaoDepartment of Pharmacy, Changzheng Hospital, Second Military Medical University, Shanghai, 200003, China.
Kejin WuDepartment of Breast Surgery, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200011, China.
Fang BaiDepartment of Breast Surgery, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200011, China.
Qiqiang ZhangDepartment of Pharmacy, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.
Hongyu WangDepartment of Pharmacy, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.
Qin YeDepartment of Pharmacy, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.
Fengjing XuDepartment of Pharmacy, Changzheng Hospital, Second Military Medical University, Shanghai, 200003, China.
Hong SunDepartment of Pharmacy, Provincial Clinical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, 350001, China.
Yunshu LuDepartment of Breast Surgery, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200011, China. Luyunshu@xinhuamed.com.cn.
Yan LiuDepartment of Pharmacy, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China. liuyan03@xinhuamed.com.cn.ORCID http://orcid.org/0000-0002-5955-3326
Shanghai Jiao Tong University · CNObstetrics and Gynecology Hospital of Fudan University · CNSecond Military Medical University · CNFujian Medical University · CN

Funding

National Institutes of Chinese Natural Science Foundation 12JC1406800National Institutes of Chinese Natural Science Foundation 14411950206National Institutes of Chinese Natural Science Foundation 81202598National Institutes of Chinese Natural Science Foundation 81702588National Institutes of Chinese Natural Science Foundation grants 81403021Shanghai Collaborative Innovation Center for Translational Medicine TM201710Shanghai Municipal Bureau of Health 20ZR1435400
6 · The paper itself

Abstract

aimPemetrexed, 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.

methodsFirst, 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.

resultsThe 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

conclusionsOur 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.

Indexed as

ABC transporterBreast cancerDrug resistancePemetrexedSensitivity

Identifiers

PMID33632224
PMCPMC7908708
OpenAlexW3124841628

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.