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原儿茶醛通过靶向C末端结合蛋白1抑制乳腺癌细胞的增殖和迁移。

Protocatechuic Aldehyde Represses Proliferation and Migration of Breast Cancer Cells through Targeting C-terminal Binding Protein 1.

作者信息

Deng Yu, Guo Wanjun, Li Guancheng, Li Shuang, Li Hong, Li Xinyan, Niu Bei, Song Mingzhu, Zhang Yamei, Xu Zhijian, Li Fulun

机构信息

School of Medicine, Chengdu University, Chengdu, China.

Institute of Cancer Biology and Drug Discovery, Chengdu University, Chengdu, China.

出版信息

J Breast Cancer. 2020 Feb;23(1):20-35. doi: 10.4048/jbc.2020.23.e7.

Abstract

PURPOSE

C-terminal binding protein 1 (CtBP1) is a transcriptional co-repressor that is overexpressed in many cancers. CtBP1 transcriptionally represses a broad array of tumor suppressors, which promotes cancer cell proliferation, migration, invasion, and resistance to apoptosis. Recent studies have demonstrated that CtBP1 is a potential target for cancer therapy. This study was designed to screen for compounds that potentially target CtBP1.

METHODS

Using a structure-based virtual screening for CtBP1 inhibitors, we found protocatechuic aldehyde (PA), a natural compound found in the root of a traditional Chinese herb, , that directly binds to CtBP1. Microscale thermophoresis assay was performed to determine whether PA and CtBP1 directly bind to each other. Further, clustered regularly interspaced short palindromic repeats associated Cas9 nuclease-mediated CtBP1 knockout in breast cancer cells was used to validate the CtBP1 targeting specificity of PA.

RESULTS

Functional studies showed that PA repressed the proliferation and migration of breast cancer cells. Furthermore, PA elevated the expression of the downstream targets of CtBP1, p21 and E-cadherin, and decreased CtBP1 binding affinity for the promoter regions of p21 and E-cadherin in breast cancer cells. However, PA did not affect the expression of p21 and E-cadherin in the CtBP1 knockout breast cancer cells. In addition, the CtBP1 knockout breast cancer cells showed resistance to PA-induced repression of proliferation and migration.

CONCLUSION

Our findings demonstrated that PA directly bound to CtBP1 and inhibited the growth and migration of breast cancer cells through CtBP1 inhibition. Structural modifications of PA are further required to enhance its binding affinity and selectivity for CtBP1.

摘要

目的

C末端结合蛋白1(CtBP1)是一种转录共抑制因子,在许多癌症中过表达。CtBP1通过转录抑制多种肿瘤抑制因子,促进癌细胞增殖、迁移、侵袭及抗凋亡能力。近期研究表明,CtBP1是癌症治疗的潜在靶点。本研究旨在筛选潜在靶向CtBP1的化合物。

方法

通过基于结构的虚拟筛选寻找CtBP1抑制剂,我们发现了原儿茶醛(PA),一种存在于传统中草药根部的天然化合物,它能直接与CtBP1结合。采用微量热泳测定法确定PA与CtBP1是否直接相互结合。此外,利用成簇规律间隔短回文重复序列相关Cas9核酸酶介导的乳腺癌细胞CtBP1基因敲除来验证PA对CtBP1的靶向特异性。

结果

功能研究表明,PA可抑制乳腺癌细胞的增殖和迁移。此外,PA可提高CtBP1下游靶点p21和E-钙黏蛋白的表达,并降低乳腺癌细胞中CtBP1对p21和E-钙黏蛋白启动子区域的结合亲和力。然而,PA对CtBP1基因敲除的乳腺癌细胞中p21和E-钙黏蛋白的表达没有影响。此外,CtBP1基因敲除的乳腺癌细胞对PA诱导的增殖抑制和迁移抑制具有抗性。

结论

我们的研究结果表明,PA直接与CtBP1结合,并通过抑制CtBP1来抑制乳腺癌细胞的生长和迁移。进一步对PA进行结构修饰以增强其对CtBP1的结合亲和力和选择性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed95/7043946/4caaf70aa6a3/jbc-23-20-g001.jpg

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