首页> 外文期刊>Nutrition and Cancer: An International Journal >Deoxycholate, an Endogenous Tumor Promoter and DNA Damaging Agent, Modulates BRCA-1 Expression in Apoptosis-Sensitive Epithelial Cells: Loss of BRCA-1 Expression in Colonic Adenocarcinomas.
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Deoxycholate, an Endogenous Tumor Promoter and DNA Damaging Agent, Modulates BRCA-1 Expression in Apoptosis-Sensitive Epithelial Cells: Loss of BRCA-1 Expression in Colonic Adenocarcinomas.

机译:脱氧胆酸盐,一种内源性肿瘤促进剂和DNA损伤剂,调节凋亡敏感上皮细胞中BRCA-1的表达:结肠腺癌中BRCA-1的表达丧失。

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摘要

Deoxycholate, a bile salt present at high levels in the colonic lumen of individuals on a high-fat diet, is a promoter of colon cancer. Deoxycholate also causes DNA damage. BRCA-1 functions in repair of DNA and in induction of apoptosis. We show that, when cultured cells of colonic origin are exposed to deoxycholate at different concentrations, BRCA-1 expression is induced at a low noncytotoxic concentration (10 mM) but is strongly inhibited at higher cytotoxic concentrations ( superset 3100 mM). Indication of phosphorylation of BRCA-1 by deoxycholate (100 mM) at a lower dose was seen by Western blot analysis, whereas, at a higher dose, deoxycholate (200 and 300 mM) caused a complete loss of BRCA-1 expression. We show that BRCA-1 is substantially lower in colon adenocarcinomas from five patients compared with associated non-neoplastic colon tissue from the same patients, suggesting that the loss of BRCA-1 expression contributes to the malignant phenotype. In the non-neoplastic colon tissue, BRCA-1 was localized to the nongoblet cells. Our results imply that reduced expression of BRCA-1 may be associated with carcinoma of the colon.
机译:脱氧胆酸盐(一种以高脂饮食高浓度存在于个体的结肠腔中的胆汁盐)是结肠癌的促进剂。脱氧胆酸盐也会引起DNA损伤。 BRCA-1在修复DNA和诱导凋亡中起作用。我们表明,当结肠起源的培养细胞暴露于不同浓度的脱氧胆酸盐时,BRCA-1表达在低非细胞毒性浓度(10 mM)下被诱导,但在较高细胞毒性浓度(超集3100 mM)下被强烈抑制。 Western blot分析显示,较低剂量的脱氧胆酸盐(100 mM)指示BRCA-1磷酸化,而较高剂量的脱氧胆酸盐(200和300 mM)导致BRCA-1表达完全丧失。我们显示,与来自相同患者的相关非肿瘤结肠组织相比,来自五名患者的结肠腺癌中的BRCA-1显着较低,这表明BRCA-1表达的丧失有助于恶性表型。在非肿瘤结肠组织中,BRCA-1定位于非杯状细胞。我们的结果表明,BRCA-1表达降低可能与结肠癌有关。

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