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自分泌 TNF-α 介导的 NF-κB 激活是癌细胞逃避 CD40 诱导的细胞毒性的决定因素。

Autocrine TNF-α-mediated NF-κB activation is a determinant for evasion of CD40-induced cytotoxicity in cancer cells.

机构信息

Department of Forensic Analytical Toxicology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu 610041, China.

出版信息

Biochem Biophys Res Commun. 2013 Jul 5;436(3):467-72. doi: 10.1016/j.bbrc.2013.05.128. Epub 2013 Jun 7.

Abstract

Activation of CD40 by CD40L results in diverse effects on different malignant cells, causing either promotion of survival, growth and resistance to chemotherapy, or induction of cytostasis and apoptosis. The molecular mechanisms underlying CD40-mediated growth regulation and apoptosis induction in cancer cell are not fully understood. In this study, we investigated the role of NF-κB activation in CD40-mediated cytotoxicity in cancer cells. The results show that activation of CD40 by recombinant soluble CD40 ligand (rsCD40L) readily induced NF-κB activation and blocking NF-κB significantly enhanced rsCD40L-induced apoptosis in cancer cells. Importantly, autocrine of TNF-α induced by rsCD40L was indispensable for both NF-κB activation and cytotoxicity induction, establishing a dual role of autocrine TNF-α that constitutes both pro-apoptotic and anti-apoptotic arms of CD40 signaling. Our results indicate that autocrine TNF-α-mediated NF-κB activation is a determinant for cancer cells' evasion of CD40L-induced cytotoxicity and blocking NF-κB may have potential for improve the value of CD40 as an anticancer agent.

摘要

CD40 与其配体(CD40L)的相互作用可导致不同的效应,在不同的恶性细胞中,既可促进生存、生长和对化疗的耐药性,也可诱导细胞停滞和凋亡。但是,CD40 介导的细胞生长调控和凋亡诱导的分子机制尚不完全清楚。在本研究中,我们探讨了 NF-κB 激活在 CD40 介导的癌细胞杀伤中的作用。结果表明,重组可溶性 CD40 配体(rsCD40L)激活 CD40 可迅速诱导 NF-κB 激活,阻断 NF-κB 可显著增强 rsCD40L 诱导的癌细胞凋亡。重要的是,rsCD40L 诱导的 TNF-α 自分泌对于 NF-κB 激活和细胞毒性诱导都是必需的,这确立了 TNF-α 自分泌在 CD40 信号传导中既具有促凋亡作用,又具有抗凋亡作用的双重作用。我们的研究结果表明,TNF-α 自分泌介导的 NF-κB 激活是癌细胞逃避 rsCD40L 诱导的细胞毒性的决定因素,阻断 NF-κB 可能会提高 CD40 作为抗癌药物的价值。

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