Asiaticoside inhibits breast cancer progression and tumor angiogenesis via YAP1/VEGFA signal pathway

被引:0
|
作者
Guo, Mengmeng [1 ]
Ying, Yu [2 ]
Chen, Yun [3 ]
Miao, Xian [4 ]
Yu, Zhenghong [5 ]
机构
[1] Nanjing Univ Chinese Med, Nantong Hosp, Gen Surg Dept, 41,Jianshe Rd, Nantong 220000, Jiangsu, Peoples R China
[2] Jiangsu Prov Hosp Tradit Chinese Med, Breast Dis Dept, 155,Hanzhong Rd, Nanjing, Jiangsu, Peoples R China
[3] Jiangsu Canc Hosp, Dept Med Oncol, 42,Baizi Pavil,Kunlun Rd, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Univ Chinese Med, Nantong Hosp, Oncol Dept, 41,Jianshe Rd, Nantong 226000, Jiangsu, Peoples R China
[5] Nanjing Univ Chinese Med, Jinling Clin Med Coll, Rheumatol & Immunol Dept, 278, Cent Rd, Nanjing, Peoples R China
关键词
Asiaticoside; Breast cancer; YAP1/VEGFA; HIPPO PATHWAY; YAP1; PROLIFERATION; APOPTOSIS; MIGRATION; INVASION;
D O I
10.1016/j.heliyon.2024.e37169
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective: Breast cancer poses a major health risk to millions of females globally. Asiaticoside (AC) is a naturally occurring compound derived from Centella asiatica, a widely used medicinal plant in the oriental countries and has potential antitumor properties. The primary aim of this study was to investigate the anti-cancer effects of synthesized AC at the cellular level and assess its ability to inhibit tumor growth and angiogenesis in breast cancer. Methods: The proliferative capacities of MCF-7 and MDA-MB-231 cells were determined using CCK-8 assay. To analyze invasion and migration, Transwell assays were conducted on the same cell lines. Additionally, apoptosis was analyzed in vitro using flow cytometry. Real-time RT-PCR was used to examine mRNA expression, and Western-blotting assay was employed to examine protein expression. Subcutaneous injection of MDA-MB-231 cells into female BALB/c nude mice was followed by treatment with AC to study its anti-tumor effects in vivo. Results: AC treatment reduced cell proliferation and triggered apoptosis in MCF-7 and MDA-MB-231 cells. The invasive and pro-angiogenesis ability were also impaired upon AC treatment. AC administration also impeded the tumor growth and tumor-associated angiogenesis of MDA-MB-231 cells in nude mice, which was accompanied by the decreased levels of YAP1 and VEGFA. Conclusion: Taken together, our results demonstrated the anti-cancer activity of AC in breast cancer. AC is able to suppress the malignancy of breast cancercells via YAP1/VEGFA signal pathway.
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页数:10
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