Pivalopril improves anti-cancer efficiency of cDDP in breast cancer through inhibiting proliferation, angiogenesis and metastasis

被引:8
|
作者
Li Fei [1 ,2 ]
Huang Huimei [3 ]
Chang Dongmin [1 ]
机构
[1] Xi An Jiao Tong Univ, Dept Surg Oncol, Affiliated Hosp 1, 277 Yanta West Rd, Xian 710061, Peoples R China
[2] Shaanxi Prov Tumor Hosp, Dept Galactophore, Xian 710061, Peoples R China
[3] Xian Childrens Hosp, Dept Nephrol, Xian 710002, Peoples R China
关键词
Breast cancer; Pivalopril (PP); cDDP; Proliferation; Angiogenesis; Metastasis; CONVERTING ENZYME-INHIBITORS; TUMOR-GROWTH; VEGF; CONTRIBUTES; RECURRENCE; RESISTANCE; CAPTOPRIL; DELIVERY; MODELS; DRUG;
D O I
10.1016/j.bbrc.2020.07.059
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Breast cancer is the most common cancer type among female worldwide. Cisplatin (cDDP) is one of the most effective chemotherapies for the treatment of breast cancer. Nevertheless, there is an urgent requirement to reduce its systemic side effects and chemoresistance. In this present study, pivalopril (PP), a clinically used antihypertensive drug, has been verified as a chemosensitizer that extremely improves the sensitivity of breast cancer cells to cDDP. PP treatment markedly promoted the capacity of cDDP to reduce the proliferation of breast cancer cells. The combination of PP and cDDP significantly induced apoptosis and inhibited vascular endothelial growth factor (VEGF) expression in breast cancer cells, accompanied with reduced angiogenesis. Furthermore, PP plus cDDP effectively reduced the cell migration and invasion in breast cancer cells. The in vivo studies confirmed that the anti-metastatic effect of cDDP was further improved by PP, as evidenced by the markedly decreased number of metastatic nodules in lungs. Moreover, we confirmed that PP combined with cDDP cooperatively suppressed tumor growth in breast cancer xenograft mouse models without extra toxicity. Together, the present study provided the first evidence that PP greatly sensitized breast cancer cells to cDDP without additional toxicity, and the synergistic effect may be mainly through cooperatively inhibiting proliferation, angiogenesis, metastasis, and inducing apoptotic cell death. (C) 2020 Published by Elsevier Inc.
引用
收藏
页码:853 / 860
页数:8
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