Department of Pharmacology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Department of Pharmaceutical Botany, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand.
Molecules. 2022 May 31;27(11):3544. doi: 10.3390/molecules27113544.
Breast cancer is the most common cancer among women worldwide. Chemotherapy followed by endocrine therapy is the standard treatment strategy after surgery or radiotherapy. However, breast cancer is highly resistant to the treatments leading to the recurrence of breast cancer. As a result, the development of alternative medicines derived from natural plants with fewer side effects is being emphasized. Andrographolide isolated from is one of the potential substances with anti-cancer properties in a variety of cell types, including breast cancer cells. This study aims to investigate the anti-cancer effects of andrographolide in breast cancer cells by evaluating cell viability and apoptosis as well as its underlying mechanisms through estrogen receptor (ER)-dependent and PI3K/AKT/mTOR signaling pathways. Cell viability, cell apoptosis, mRNA or miRNA, and protein expression were examined by MTT assay, Annexin V-FITC, qRT-PCR, and Western blot analysis, respectively. MCF-7 and MDA-MB-231 cell viability was reduced in a concentration- and time-dependent manner after andrographolide treatment. Moreover, andrographolide induced cell apoptosis in both MCF-7 and MDA-MB-231 cells by inhibiting Bcl-2 and enhancing Bax expression at both mRNA and protein levels. In MCF-7 cells, the ER-positive breast cancer, andrographolide showed an inhibitory effect on cell proliferation through downregulation of ERα, PI3K, and mTOR expression levels. Andrographolide also inhibited MDA-MB-231 breast cancer cell proliferation via induction of cell apoptosis. However, the inhibition of MCF-7 and MDA-MB-231 cell proliferation of andrographolide treatment did not disrupt miR-21. Our findings showed that andrographolide possesses an anti-estrogenic effect by suppressing cell proliferation in MCF-7 cells. The effects were comparable to those of the anticancer drug fulvestrant in MCF-7 cells. This study provides new insights into the anti-cancer effect of andrographolide on breast cancer and suggests andrographolide as a potential alternative from the natural plant for treating breast cancer types that are resistant to tamoxifen and fulvestrant.
乳腺癌是全球女性中最常见的癌症。手术后或放疗后,化疗加内分泌治疗是标准的治疗策略。然而,乳腺癌对治疗具有高度抗性,导致乳腺癌的复发。因此,人们越来越强调开发副作用较少的天然植物衍生的替代药物。从穿心莲中分离出的穿心莲内酯是多种细胞类型(包括乳腺癌细胞)具有抗癌特性的潜在物质之一。本研究旨在通过评估细胞活力和细胞凋亡以及通过雌激素受体(ER)依赖性和 PI3K/AKT/mTOR 信号通路,研究穿心莲内酯在乳腺癌细胞中的抗癌作用。通过 MTT 测定、Annexin V-FITC、qRT-PCR 和 Western blot 分析分别检测细胞活力、细胞凋亡、mRNA 或 miRNA 和蛋白质表达。穿心莲内酯处理后,MCF-7 和 MDA-MB-231 细胞的活力呈浓度和时间依赖性降低。此外,穿心莲内酯通过抑制 Bcl-2 并增强 Bax 的 mRNA 和蛋白表达,在 MCF-7 和 MDA-MB-231 细胞中诱导细胞凋亡。在 MCF-7 细胞中,ER 阳性乳腺癌,穿心莲内酯通过下调 ERα、PI3K 和 mTOR 表达水平对细胞增殖表现出抑制作用。穿心莲内酯还通过诱导细胞凋亡抑制 MDA-MB-231 乳腺癌细胞的增殖。然而,穿心莲内酯对 MCF-7 和 MDA-MB-231 细胞增殖的抑制并未破坏 miR-21。我们的研究结果表明,穿心莲内酯通过抑制 MCF-7 细胞的增殖而具有抗雌激素作用。其作用与 MCF-7 细胞中的抗癌药物氟维司群相当。这项研究为穿心莲内酯对乳腺癌的抗癌作用提供了新的见解,并表明穿心莲内酯可能是一种潜在的替代天然植物药物,用于治疗对他莫昔芬和氟维司群耐药的乳腺癌类型。