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辣椒素通过下调 FBI-1 介导的 NF-κB 通路抑制乳腺癌增殖并诱导细胞凋亡。

Capsaicin Inhibits Proliferation and Induces Apoptosis in Breast Cancer by Down-Regulating FBI-1-Mediated NF-κB Pathway.

机构信息

Department of Breast Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi 530021, People's Republic of China.

Department of Microbiology and Immunology, School of Medicine and Public Health, Jinan University, Guangzhou, Guangdong, 510632, People's Republic of China.

出版信息

Drug Des Devel Ther. 2021 Jan 12;15:125-140. doi: 10.2147/DDDT.S269901. eCollection 2021.

Abstract

BACKGROUND

As a natural compound extracted from a variety of hot peppers, capsaicin has drawn increasing attention to its anti-cancer effects against multiple human cancers including breast cancer. FBI-1 is a major proto-oncogene negatively regulating the transcription of many tumor suppressor genes, and plays a vital role in tumorigenesis and progression. However, whether FBI-1 is involved in capsaicin-induced breast cancer suppression has yet to be ascertained. This study aimed to investigate the effects of capsaicin on proliferation and apoptosis and its association with FBI-1 expression in breast cancer.

METHODS

CCK-8 and morphological observation assay were employed to detect cell proliferation. Flow cytometry and TUNEL assay were conducted to detect cell apoptosis. RNA interference technique was used to overexpress or silence FBI-1 expression. qRT-PCR and/or Western blot analysis were applied to detect the protein expression of FBI-1, Ki-67, Bcl-2, Bax, cleaved-Caspase 3, Survivin and NF-κB p65. Xenograft model in nude mice was established to assess the in vivo effects.

RESULTS

Capsaicin significantly inhibited proliferation and induced apoptosis in breast cancer in vitro and in vivo, along with decreased FBI-1, Ki-67, Bcl-2 and Survivin protein expression, increased Bax protein expression and activated Caspase 3. Furthermore, FBI-1 overexpression obviously attenuated the capsaicin-induced anti-proliferation and pro-apoptosis effect, accompanied with the above-mentioned proteins reversed, whereas FBI-1 silencing generated exactly the opposite response. In addition, as a target gene of FBI-1, NF-κB was inactivated by p65 nuclear translocation suppressed with capsaicin treatment, which was perceptibly weakened with FBI-1 overexpression or enhanced with FBI-1 silencing.

CONCLUSION

This study reveals that FBI-1 is closely involved in capsaicin-induced anti-proliferation and pro-apoptosis of breast cancer. The underlying mechanism may be related to down-regulation of FBI-1-mediated NF-κB pathway. Targeting FBI-1 with capsaicin may be a promising therapeutic strategy in patients with breast cancer.

摘要

背景

辣椒素作为一种从多种辣椒中提取的天然化合物,其对多种人类癌症(包括乳腺癌)的抗癌作用引起了越来越多的关注。FBI-1 是一个主要的原癌基因,负调控许多肿瘤抑制基因的转录,在肿瘤发生和进展中起着至关重要的作用。然而,FBI-1 是否参与辣椒素诱导的乳腺癌抑制尚未确定。本研究旨在探讨辣椒素对乳腺癌增殖和凋亡的影响及其与 FBI-1 表达的关系。

方法

采用 CCK-8 和形态学观察法检测细胞增殖。流式细胞术和 TUNEL 检测细胞凋亡。采用 RNA 干扰技术过表达或沉默 FBI-1 表达。qRT-PCR 和/或 Western blot 分析检测 FBI-1、Ki-67、Bcl-2、Bax、cleaved-Caspase 3、Survivin 和 NF-κB p65 的蛋白表达。建立裸鼠异种移植模型评估体内效应。

结果

辣椒素显著抑制乳腺癌在体外和体内的增殖并诱导凋亡,同时降低 FBI-1、Ki-67、Bcl-2 和 Survivin 蛋白表达,增加 Bax 蛋白表达并激活 Caspase 3。此外,FBI-1 过表达明显减弱了辣椒素诱导的抗增殖和促凋亡作用,伴随着上述蛋白的逆转,而 FBI-1 沉默则产生了完全相反的反应。此外,作为 FBI-1 的靶基因,NF-κB 被辣椒素处理抑制 p65 核易位而失活,FBI-1 过表达或沉默可明显减弱或增强该作用。

结论

本研究揭示了 FBI-1 参与了辣椒素诱导的乳腺癌抗增殖和促凋亡。其潜在机制可能与 FBI-1 介导的 NF-κB 通路下调有关。用辣椒素靶向 FBI-1 可能是乳腺癌患者有前途的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9871/7811378/9e9b84c0ff5c/DDDT-15-125-g0002.jpg

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