Pan Yue, Shao Dan, Zhao Yawei, Zhang Fan, Zheng Xiao, Tan Yongfei, He Kan, Li Jing, Chen Li
Department of Pharmacology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
School of Nursing, Jilin University, Changchun 130020, China.
Int J Biol Sci. 2017 Jun 1;13(6):794-803. doi: 10.7150/ijbs.18969. eCollection 2017.
Breast cancer is the most common type of cancer and the second leading cause of cancer death in American women. Chemoresistance is common and inevitable after a variable period of time. Therefore, chemosensitization is a necessary strategy on drug-resistant breast cancer. In this study, MCF-7 breast cancer cell was cultured under hypoxia for a week to induce the resistance to doxorubincin (DOX). The effect of different doses of berberine, a traditional Chinese medicine, on DOX sensitivity to MFC-7/hypoxia cells was observed. We found that hypoxia increased DOX resistance on breast cancer cells with the AMPK activation. Low-dose berberine could resensitize DOX chemosensitivity in MCF-7/hypoxia cell, however, high-dose berberine directly induced apoptosis. The intriguing fact was that the protein expressions of AMPK and HIF-1α were down-regulated by berberine, either low dose or high dose. But the downstream of HIF-1α occurred the bifurcation dependent on the dosage of berberine: AMPK-HIF-1α-P-gp inactivation played a crucial role on the DOX chemosensitivity of low-dose berberine, while AMPK-HIF-1α downregulaton inducing p53 activation led to apoptosis in high-dose berberine. These results were consistent to the transplanted mice model bearing MCF-7 drug-resistance tumor treated by berberine combined with DOX or high-dose berberine alone. This work shed light on a potentially therapeutic attempt to overcome drug-resistant breast cancer.
乳腺癌是美国女性中最常见的癌症类型,也是癌症死亡的第二大主要原因。化疗耐药在一段时间后很常见且不可避免。因此,化疗增敏是治疗耐药性乳腺癌的必要策略。在本研究中,将MCF-7乳腺癌细胞在缺氧条件下培养一周以诱导对多柔比星(DOX)的耐药性。观察了不同剂量的中药黄连素对MFC-7/缺氧细胞对DOX敏感性的影响。我们发现缺氧通过激活AMPK增加了乳腺癌细胞对DOX的耐药性。低剂量黄连素可使MCF-7/缺氧细胞对DOX的化疗敏感性恢复,然而,高剂量黄连素直接诱导细胞凋亡。有趣的是,低剂量和高剂量黄连素均可下调AMPK和HIF-1α的蛋白表达。但HIF-1α的下游因黄连素剂量不同而出现分歧:AMPK-HIF-1α-P-gp失活在低剂量黄连素对DOX的化疗敏感性中起关键作用,而AMPK-HIF-1α下调诱导p53激活导致高剂量黄连素诱导细胞凋亡。这些结果与用黄连素联合DOX或单独使用高剂量黄连素治疗的携带MCF-7耐药肿瘤的移植小鼠模型一致。这项工作为克服耐药性乳腺癌的潜在治疗尝试提供了线索。