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贯叶金丝桃水提取物通过影响 MAP 激酶和 PI3K/Akt 通路抑制人结直肠癌细胞的增殖。

Hypericum androsaemum water extract inhibits proliferation in human colorectal cancer cells through effects on MAP kinases and PI3K/Akt pathway.

机构信息

CBMA - Centre of Molecular and Environmental Biology/Department of Biology, University of Minho, 4710-057 Braga, Portugal.

出版信息

Food Funct. 2012 Aug;3(8):844-52. doi: 10.1039/c2fo10226a. Epub 2012 May 18.

Abstract

MAP kinase and PI3K/Akt signalling pathways are commonly altered in colorectal carcinoma (CRC) leading to tumor growth due to increased cell proliferation and inhibition of apoptosis. Several species of the genus Hypericum are used in Portugal to prepare herbal teas to which digestive tract effects are attributed. In the present study, the antiproliferative and proapoptotic effects of the water extracts of H. androsaemum (HA) and H. perforatum (HP) were investigated in two human colon carcinoma-derived cell lines, HCT15 and CO115, which harbour activating mutations of KRAS and BRAF, respectively. Contrarily to HP, HA significantly inhibited cell proliferation and induced apoptosis in both cell lines. HA decreased BRAF and phospho-ERK expressions in CO115, but not in HCT15. HA also decreased Akt phosphorylation in CO115 and induced p38 and JNK in both cell lines. HA induced cell cycle arrest at S and G2/M phases as well as caspase-dependent apoptosis in both cell lines. Chlorogenic acid (CA), the main phenolic compound present in the HA extract and less represented in the HP water extract, did, however, not show any of those effects when used individually. In conclusion, water extract of HA, but not of HP, controlled CRC proliferation and specifically acted on mutant and not wild-type BRAF. The effect of HA was, however, not due to CA alone.

摘要

MAP 激酶和 PI3K/Akt 信号通路在结直肠癌(CRC)中通常发生改变,导致肿瘤生长,这是由于细胞增殖增加和细胞凋亡抑制所致。葡萄牙有几种贯叶金丝桃属植物被用来制备草药茶,这些草药茶被认为具有消化道作用。在本研究中,研究了水提贯叶金丝桃(HA)和贯叶连翘(HP)对两种人结肠癌细胞系 HCT15 和 CO115 的增殖抑制和促凋亡作用,这两种细胞系分别携带 KRAS 和 BRAF 的激活突变。与 HP 相反,HA 显著抑制了这两种细胞系的细胞增殖并诱导了细胞凋亡。HA 降低了 CO115 中 BRAF 和磷酸化 ERK 的表达,但对 HCT15 没有影响。HA 还降低了 CO115 中的 Akt 磷酸化,并在两种细胞系中诱导了 p38 和 JNK。HA 诱导两种细胞系的细胞周期停滞在 S 和 G2/M 期,并诱导 caspase 依赖性细胞凋亡。然而,当单独使用时,HA 提取物中主要的酚类化合物绿原酸(CA)并没有表现出这些作用,而 HP 水提取物中 CA 的含量较少。总之,HA 的水提取物而非 HP 控制了 CRC 的增殖,并且对突变型而非野生型 BRAF 有特异性作用。然而,HA 的作用并非仅仅是由于 CA 所致。

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