Chaudhry Gul-E-Saba, Jan Rehmat, Naveed Zafar Muhammad, Mohammad Habsah, Muhammad Tengku Sifzizul Tengku
Institute of Marine Biotechnology, Universiti Malaysia Terengganu, Kuala Terengganu, Malaysia.
Department of Chemistry, Quaid-i-Azam University, Islamabad, Pakistan.
Asian Pac J Cancer Prev. 2019 Dec 1;20(12):3555-3562. doi: 10.31557/APJCP.2019.20.12.3555.
Breast cancer is the most frequently diagnosed cancer worldwide. The main objective of the present study was to evaluate the cytotoxic effects and mechanism of cell death induced by the extract and fractions of Vitex rotundifolia (leaves) in breast cancer cell line, T-47D.
The cytotoxicity activity was measured using MTS assay. The mode of cell death was analysed by early (phosphatidylserine externalization) and late apoptosis (DNA fragmentation). The caspases 8, 9, 3/7 and apoptotic proteins bax, bcl-2 study were done by western blot and ELISA method.
The methanol extract was found to inhibit 50% growth of T-47D cells at the concentration of 79.43µg/ml respectively after 72hr. From seven fractions, fraction F1, F2 and F3 produced cytotoxicity effects in T-47D cell line with IC50 (72hr) < 30µg/ml. The results obtained by Annexin V/PI apoptosis detection assay and TUNEL assay suggest that active fractions of Vitex rotundifolia induced early and late apoptosis (DNA fragmentation) in T-47D cell line. Moreover, western blot analysis and Caspase GloTM luminescent assay demonstrated that fractions F2 and F3 triggered apoptotic cell death via activation of caspases -8, -9 and -3/7 and up-regulation of Bax and down-regulation of Bcl-2 protein. Furthermore, chemical profiling confirms the presence of potential metabolites (vitexicarpin) in fractions of Vitex rotundifolia.
Thus, the present study suggests the remarkable potential of active metabolites in fractions of Vitex rotundifolia as future cancer therapeutic agent for the treatment of breast cancer.
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乳腺癌是全球最常被诊断出的癌症。本研究的主要目的是评估蔓荆子(叶)提取物及其馏分对乳腺癌细胞系T-47D的细胞毒性作用及细胞死亡机制。
采用MTS法测定细胞毒性活性。通过早期(磷脂酰丝氨酸外化)和晚期凋亡(DNA片段化)分析细胞死亡模式。采用蛋白质免疫印迹法和酶联免疫吸附测定法对半胱天冬酶8、9、3/7以及凋亡蛋白bax、bcl-2进行研究。
发现甲醇提取物在浓度为79.43µg/ml时,72小时后可抑制T-47D细胞生长50%。在七个馏分中,馏分F1、F2和F3对T-47D细胞系产生细胞毒性作用,IC50(72小时)<30µg/ml。膜联蛋白V/碘化丙啶凋亡检测试验和末端脱氧核苷酸转移酶介导的缺口末端标记法获得的结果表明,蔓荆子的活性馏分在T-47D细胞系中诱导早期和晚期凋亡(DNA片段化)。此外,蛋白质免疫印迹分析和半胱天冬酶发光测定表明,馏分F2和F3通过激活半胱天冬酶-8、-9和-3/7以及上调Bax和下调Bcl-2蛋白引发凋亡性细胞死亡。此外,化学分析证实蔓荆子馏分中存在潜在代谢产物(紫铆素)。
因此,本研究表明蔓荆子馏分中的活性代谢产物作为未来治疗乳腺癌的癌症治疗剂具有显著潜力。