Baker P R, Wilton J C, Jones C E, Stenzel D J, Watson N, Smith G J
Department of Surgery, University of Birmingham, UK.
Br J Cancer. 1992 Apr;65(4):566-72. doi: 10.1038/bjc.1992.115.
The effects of the major human serum bile acid, glycochenodeoxycholic acid (GCDC), as well as unconjugated chenodeoxycholic acid (CDC), on the MCF-7 human breast cancer cell line have been studied in vitro under oestrogen and bile acid deprived culture conditions. GCDC increased the growth of the breast cancer cells over the range 10-300 microM. At concentrations in excess of the bile acid binding capacity of the medium cell growth was prevented. In contrast 10 microM CDC tended to reduce cell growth. Oestrogen (ER) and progesterone (PgR) receptors, pS2 and total cathepsin D were quantified by monoclonal antibody based immunoassays. Ten to 100 microM GCDC and 10 microM CDC down-regulated ER protein and this was accompanied by induction of the oestrogen-regulated proteins PgR, pS2 and possibly cathepsin D, including increased secretion of the latter two proteins into the culture medium. All these changes were quantitatively similar to those observed with 10 nM oestradiol. The bile acid effects on ER and PgR were not due to interference with the assay procedures. Cells incubated with 50 microM GCDC or 10 microM CDC had higher pmolar concentrations of the bile acids than controls. This study suggests that naturally occurring bile acids influence the growth and steroid receptor function of human breast cancer cells.
在雌激素和胆汁酸缺乏的培养条件下,已在体外研究了主要的人血清胆汁酸甘氨鹅去氧胆酸(GCDC)以及未结合的鹅去氧胆酸(CDC)对MCF-7人乳腺癌细胞系的影响。GCDC在10 - 300微摩尔范围内可促进乳腺癌细胞的生长。当浓度超过培养基的胆汁酸结合能力时,细胞生长受到抑制。相比之下,10微摩尔的CDC倾向于抑制细胞生长。通过基于单克隆抗体的免疫测定法定量雌激素(ER)和孕激素(PgR)受体、pS2和组织蛋白酶D的总量。10至100微摩尔的GCDC和10微摩尔的CDC可下调ER蛋白,同时伴随着雌激素调节蛋白PgR、pS2以及可能的组织蛋白酶D的诱导,包括后两种蛋白向培养基中的分泌增加。所有这些变化在数量上与用10纳摩尔雌二醇观察到的变化相似。胆汁酸对ER和PgR的影响并非由于干扰检测程序所致。用50微摩尔GCDC或10微摩尔CDC孵育的细胞比对照细胞具有更高的皮摩尔浓度的胆汁酸。这项研究表明,天然存在的胆汁酸会影响人乳腺癌细胞的生长和类固醇受体功能。