The CD95/CD95L signaling pathway: A role in carcinogenesis

被引:52
作者
Fouque, Arnelie
Debure, Laure
Legembre, Patrick
机构
[1] Univ Rennes 1, F-35043 Rennes, France
[2] INSERM U1085, IRSET, F-35043 Rennes, France
[3] Equipe Labellisee Ligue Canc Death Receptors & Tu, F-35043 Rennes, France
[4] Ctr Eugene Marquis, Rennes, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2014年 / 1846卷 / 01期
关键词
Fas; Apoptosis; Cytokine; Inflammation; Carcinogenesis; TUMOR-NECROSIS-FACTOR; NF-KAPPA-B; FAS-INDUCED APOPTOSIS; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; VERSUS-HOST-DISEASE; COLON-CANCER CELLS; FACTOR RECEPTOR SUPERFAMILY; CONFER IMMUNE PRIVILEGE; X-LINKED INHIBITOR; DEATH RECEPTOR;
D O I
10.1016/j.bbcan.2014.04.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Apoptosis is a fundamental process that contributes to tissue homeostasis, immune responses, and development. The receptor CD95, also called Fas, is a member of the tumor necrosis factor receptor (TNF-R) superfamily. Its cognate ligand, CD95L, is implicated in immune homeostasis and immune surveillance, and various lineages of malignant cells exhibit loss-of-function mutations in this pathway; therefore, CD95 was initially classified as a tumor suppressor gene. However, more recent data indicate that in different pathophysiological contexts, this receptor can transmit non-apoptotic signals, promote inflammation, and contribute to carcinogenesis. A comparison with the initial molecular events of the TNF-R signaling pathway leading to non-apoptotic, apoptotic, and necrotic pathways reveals that CD95 is probably using different molecular mechanisms to transmit its non-apoptotic signals (NF-kappa B, MAPK, and PI3K). As discussed in this review, the molecular process by which the receptor switches from an apoptotic function to an inflammatory role is unknown. More importantly, the biological functions of these signals remain elusive. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:130 / 141
页数:12
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