화학공학소재연구정보센터
Biochemical and Biophysical Research Communications, Vol.436, No.3, 467-472, 2013
Autocrine TNF-alpha-mediated NF-kappa B activation is a determinant for evasion of CD40-induced cytotoxicity in cancer cells
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-kappa B activation in CD40-mediated cytotoxicity in cancer cells. The results show that activation of CD40 by recombinant soluble CD40 ligand (rsCD40L) readily induced NF-kappa B activation and blocking NF-kappa B significantly enhanced rsCD40L-induced apoptosis in cancer cells. Importantly, autocrine of TNF-alpha induced by rsCD40L was indispensable for both NF-kappa B activation and cytotoxicity induction, establishing a dual role of autocrine TNF-alpha that constitutes both pro-apoptotic and anti-apoptotic arms of CD40 signaling. Our results indicate that autocrine TNF-alpha-mediated NF-kappa B activation is a determinant for cancer cells' evasion of CD40L-induced cytotoxicity and blocking NF-kappa B may have potential for improve the value of CD40 as an anticancer agent. (C) 2013 Elsevier Inc. All rights reserved.