Targeting PSG1 to enhance chemotherapeutic efficacy: new application for anti-coagulant the dicumarol

Author:

He Dong-xu1,Gu Feng2,Wu Jian3,Gu Xiao-Ting4,Lu Chun-Xiao4,Mao Ai-qin4,Zhang Guang-yuan1,Ding Zhong-yang1,Wang Jin-ke3,Hao Jun-jun5,Fu Li2,Ma Xin4

Affiliation:

1. National Engineering Laboratory for Cereal Fermentation Technology, Jiangnan University, Wuxi 214122, China

2. Department of Breast Cancer Pathology and Research Laboratory, State Key Laboratory of Breast Cancer Research, Cancer Institute and Hospital, Tianjin Medical University, Tianjin 300060, China

3. State Key Laboratory of Bioelectronics, Southeast University Sipailou 2#, Nanjing 210096, China

4. Department of Cellular and Molecular Pharmacology, School of Pharmaceutical Sciences, Jiangnan University, Wuxi 214122, China

5. State Key Lab of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan 650223, China

Abstract

Chemotherapeutic response is critical for the successful treatment and good prognosis in cancer patients. In this study, we analysed the gene expression profiles of preoperative samples from oestrogen receptor (ER)-negative breast cancer patients with different responses to taxane-anthracycline-based (TA-based) chemotherapy, and identified a group of genes that was predictive. Pregnancy specific beta-1-glycoprotein 1 (PSG1) played a central role within signalling pathways of these genes. Inhibiting PSG1 can effectively reduce chemoresistance via a transforming growth factor-β (TGF-β)-related pathway in ER-negative breast cancer cells. Drug screening then identified dicumarol (DCM) to target the PSG1 and inhibit chemoresistance to TA-based chemotherapy in vitro, in vivo, and in clinical samples. Taken together, this study highlights PSG1 as an important mediator of chemoresistance, whose effect could be diminished by DCM.

Publisher

Portland Press Ltd.

Subject

General Medicine

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