Suppr超能文献

鞣酸可抑制低传代结直肠癌细胞的癌变作用,而牛链球菌可消除鞣酸的这种作用。

Streptococcus gallolyticus abrogates anti-carcinogenic properties of tannic acid on low-passage colorectal carcinomas.

机构信息

Institute of Medical Microbiology, Virology and Hygiene, Rostock University Medical Center, Rostock, Germany.

Department of Internal Medicine, Medical Clinic III - Hematology, Oncology, Palliative Care, Rostock University Medical Center, Rostock, Germany.

出版信息

Sci Rep. 2020 Mar 13;10(1):4714. doi: 10.1038/s41598-020-61458-5.

Abstract

The tannase-producing Gram-positive bacterial species Streptococcus gallolyticus subsp. gallolyticus (Sgg) is an opportunistic pathogen of the human gut and strongly associated with colorectal cancer (CRC). A unique feature of Sgg is its ability to degrade tannic acids (TA). TA constitute an important part of the human diet with known anti-tumorigenic properties. Here, we examined whether Sgg is able to protect tumor cells from the toxic effect of TA and thus drive tumorigenesis indirectly. Human CRC cell lines (n = 8) were treated with increasing concentrations of TA. We confirmed the cytotoxic activity of TA in a dose-dependent manner. In virtually all cell lines, viability decreased significantly (>60% inhibition). Moreover, pyrogallol, the degradation product of TA, had no effect on the tested cell lines. This suggests a specific effect of TA. Cytotoxicity was due to necrosis and induction of senescence in residual cells. Finally, when TA was degraded by Sgg, the cytotoxic effect could be abolished. Tumor cells even responded with boosted cell proliferation, highlighting the impact of Sgg on CRC progression. We here provide another piece of evidence for the active interplay between Sgg and cancer preventive components. These data will help to move forward in designing concepts for therapeutic and eventually also prophylactic approaches to combat gastrointestinal malignancies.

摘要

产单宁酶的革兰氏阳性细菌物种缓症链球菌亚种。 (Sgg)是人类肠道的机会性病原体,与结直肠癌(CRC)密切相关。Sgg 的一个独特特征是其降解单宁酸(TA)的能力。TA 构成了人类饮食的重要组成部分,具有已知的抗肿瘤特性。在这里,我们研究了 Sgg 是否能够保护肿瘤细胞免受 TA 的毒性作用,从而间接促进肿瘤发生。用递增浓度的 TA 处理人 CRC 细胞系(n = 8)。我们证实了 TA 的细胞毒性活性呈剂量依赖性。在几乎所有的细胞系中,细胞活力显著下降(> 60%抑制)。此外,焦倍酚,TA 的降解产物,对测试的细胞系没有影响。这表明 TA 具有特异性作用。细胞毒性是由于坏死和残留细胞衰老诱导所致。最后,当 Sgg 降解 TA 时,细胞毒性作用可以被消除。肿瘤细胞甚至表现出增强的细胞增殖,突出了 Sgg 对 CRC 进展的影响。我们在这里提供了另一个证据,证明 Sgg 与癌症预防成分之间存在积极的相互作用。这些数据将有助于设计治疗和最终预防胃肠道恶性肿瘤的方法的概念。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cf9/7070001/ae3310e76d76/41598_2020_61458_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验