Afsar Tayyaba, Trembley Janeen H, Salomon Christine E, Razak Suhail, Khan Muhammad Rashid, Ahmed Khalil
Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Cellular and Molecular Biochemistry Research Laboratory (151), Minneapolis VA Health Care System, Minneapolis, MN USA.
Sci Rep. 2016 Mar 15;6:23077. doi: 10.1038/srep23077.
Acacia hydaspica R. Parker is known for its medicinal uses in multiple ailments. In this study, we performed bioassay-guided fractionation of cytotoxic compounds from A. hydaspica and investigated their effects on growth and signaling activity in prostate and breast cancer cell lines. Four active polyphenolic compounds were identified as 7-O-galloyl catechin (GC), catechin (C), methyl gallate (MG), and catechin-3-O-gallate (CG). The four compounds inhibited prostate cancer PC-3 cell growth in a dose-dependent manner, whereas CG and MG inhibited breast cancer MDA-MB-231 cell growth. All tested compounds inhibited cell survival and colony growth in both cell lines, and there was evidence of chromatin condensation, cell shrinkage and apoptotic bodies. Further, acridine orange, ethidium bromide, propidium iodide and DAPI staining demonstrated that cell death occurred partly via apoptosis in both PC-3 and MDA-MB-231 cells. In PC-3 cells treatment repressed the expression of anti-apoptotic molecules Bcl-2, Bcl-xL and survivin, coupled with down-regulation of signaling pathways AKT, NFκB, ERK1/2 and JAK/STAT. In MDA-MB-231 cells, treatment induced reduction of CK2α, Bcl-xL, survivin and xIAP protein expression along with suppression of NFκB, JAK/STAT and PI3K pathways. Our findings suggest that certain polyphenolic compounds derived from A. hydaspica may be promising chemopreventive/therapeutic candidates against cancer.
哈达斯金合欢(Acacia hydaspica R. Parker)因其在多种疾病中的药用价值而闻名。在本研究中,我们对哈达斯金合欢中的细胞毒性化合物进行了生物测定导向的分级分离,并研究了它们对前列腺癌细胞系和乳腺癌细胞系生长及信号传导活性的影响。鉴定出四种活性多酚化合物,分别为7-O-没食子酰儿茶素(GC)、儿茶素(C)、没食子酸甲酯(MG)和儿茶素-3-O-没食子酸酯(CG)。这四种化合物以剂量依赖性方式抑制前列腺癌PC-3细胞的生长,而CG和MG抑制乳腺癌MDA-MB-231细胞的生长。所有测试化合物均抑制两种细胞系中的细胞存活和集落生长,并且有染色质浓缩、细胞收缩和凋亡小体的证据。此外,吖啶橙、溴化乙锭、碘化丙啶和DAPI染色表明,PC-3和MDA-MB-231细胞中的细胞死亡部分是通过凋亡发生的。在PC-3细胞中,处理抑制了抗凋亡分子Bcl-2、Bcl-xL和survivin的表达,并伴随着信号通路AKT、NFκB、ERK1/2和JAK/STAT的下调。在MDA-MB-231细胞中,处理导致CK2α、Bcl-xL、survivin和XIAP蛋白表达降低,同时抑制NFκB、JAK/STAT和PI3K通路。我们的研究结果表明,从哈达斯金合欢中提取的某些多酚化合物可能是有前景的癌症化学预防/治疗候选物。