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益生菌多粘类芽孢杆菌通过抑制 ErbB2 和 ErbB3 发挥其抗结肠癌作用。

The anticancer effect of probiotic Bacillus polyfermenticus on human colon cancer cells is mediated through ErbB2 and ErbB3 inhibition.

机构信息

Inflammatory Bowel Disease Center, Division of Digestive Diseases, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA.

出版信息

Int J Cancer. 2010 Aug 15;127(4):780-90. doi: 10.1002/ijc.25011.

Abstract

A wealth of data implicates that ErbB receptors have essential roles in tumor development. Probiotic bacteria are known to exert an anticancer activity in animal studies. Bacillus polyfermenticus (B.P.), a probiotic bacterium, has been clinically used for a variety of gastrointestinal disorders in East Asia. Here, we investigated the effect of B.P. on the growth of tumors and its putative mechanism of actions. Conditioned medium of B.P. cultures (B.P. CM) inhibited the growth of human colon cancer cells including HT-29, DLD-1 and Caco-2 cells. Moreover, B.P. CM suppressed colony formation of HT-29 cells cultured on soft agar and reduced carcinogen-induced colony formation of normal colonocytes. Furthermore, data from the mouse xenograft model of human colon cancer cells showed reduced tumor size in B.P. CM-injected mice when compared to E. coli conditioned medium-injected mice. Exposure of B.P. CM to HT-29 cells for 24 hr, 48 hr and 2 weeks reduced ErbB2 and ErbB3 protein expression as well as mRNA levels. Moreover, cyclin D1 expression that is required for ErbB-dependent cell transformation was decreased by B.P. CM. Furthermore, transcription factor E2F-1 that regulates cyclin D1 expression was also decreased by B.P. CM. These results show that B.P. inhibits tumor growth and its anticancer activity occurs, at least in part, through suppressing ErbB2 and ErbB3. Taken together, our study suggests that this probiotic may be clinically used as a prophylactic treatment to prevent colon cancer development.

摘要

大量数据表明,ErbB 受体在肿瘤发展中具有重要作用。益生菌在动物研究中已被证实具有抗癌活性。多粘类芽孢杆菌(B.P.)是一种益生菌,已在东亚被临床用于治疗各种胃肠道疾病。在这里,我们研究了 B.P. 对肿瘤生长的影响及其可能的作用机制。B.P. 培养物的条件培养基(B.P. CM)抑制了包括 HT-29、DLD-1 和 Caco-2 细胞在内的人结肠癌细胞的生长。此外,B.P. CM 抑制了软琼脂上 HT-29 细胞集落的形成,并减少了致癌物诱导的正常结肠细胞集落的形成。此外,人结肠癌细胞的小鼠异种移植模型数据显示,与大肠杆菌条件培养基注射小鼠相比,B.P. CM 注射小鼠的肿瘤体积减小。将 B.P. CM 暴露于 HT-29 细胞 24 小时、48 小时和 2 周后,ErbB2 和 ErbB3 蛋白表达以及 mRNA 水平降低。此外,B.P. CM 还降低了 ErbB 依赖性细胞转化所需的细胞周期蛋白 D1 表达。此外,调节 cyclin D1 表达的转录因子 E2F-1 也被 B.P. CM 下调。这些结果表明,B.P. 抑制肿瘤生长,其抗癌活性至少部分通过抑制 ErbB2 和 ErbB3 来实现。综上所述,我们的研究表明,这种益生菌可能在临床上被用作预防结肠癌发展的预防性治疗。

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