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Research article summary (published 29 Nov 2009):

RhoB induces apoptosis via direct interaction with TNFAIP1 in HeLa cells.

Full Abstract

RhoB, a tumor suppressor, has emerged as an interesting cancer target, and extensive studies aimed at understanding its role in apoptosis have been performed. In our study, we investigated the involvement of RhoB-interacting molecules in apoptosis. To identify RhoB-interacting proteins, we performed yeast-two hybrid screening assays using RhoB as a bait and isolated TNFAIP1, a TNFalpha-induced protein containing the BTB/POZ domain. The interaction between RhoB and TNFAIP1 was demonstrated in vivo through coimmunoprecipitation studies and in vitro binding assays. RFP-TNFAIP1 was found to be partially colocalized with EGFP-RhoB. The partial colocalization of RhoB and TNFAIP1 in endosomes suggests that RhoB-TNFAIP1 interactions may have a functional role in apoptosis. TNFAIP1 elicited proapoptotic activity, while simultaneous expression of RhoB and TNFAIP1 resulted in a dramatic increase in apoptosis in HeLa cells. Furthermore, knockdown of RhoB using siRNA clearly rescued cells from apoptosis induced by TNFAIP1. This finding suggests that interactions between RhoB and TNFAIP1 are crucial for induction of apoptosis in HeLa cells. The observation of increased SAPK/JNK phosphorylation in apoptotic cells and the finding that a JNK inhibitor suppressed apoptosis indicates that SAPK/JNK signaling may be involved in apoptosis induced by RhoB-TNFAIP1 interactions. In conclusion, we found that RhoB interacts with TNFAIP1 to regulate apoptosis via a SAPK/JNK-mediated signal transduction mechanism.

 

Author information

Author/s: Kim, Dong-Myung (DM); Chung, Kyung-Sook (KS); Choi, Shin-Jung (SJ); Jung, Yu-Jin (YJ); Park, Song-Kyu (SK); Han, Gyoon-Hee (GH); Ha, Jae-Seok (JS); Song, Kyung-Bin (KB); Choi, Nam-Song (NS); Kim, Hwan-Mook (HM); Won, Misun (M); Seo, Yeon-Soo (YS);

Affiliation: Department of Biological Science, KAIST, Daejeon 305-701, Korea.

Journal and publication information

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal: International journal of cancer. Journal international du cancer (Int J Cancer), published in United States. (Language: eng)

Reference: 2009-Dec; vol 125 (issue 11) : pp 2520-7

Dates: Created 2009/10/05; Completed 2009/11/06;

PMID: 19637314, status: MEDLINE (last retrieval date: 11/6/2009, IMS Date: )

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Associated Chemicals: Proteins (0) ; TNFAIP1 protein, human (0) ; JNK Mitogen-Activated Protein Kinases (EC 2.7.1.37) ; rhoB GTP-Binding Protein (EC 3.6.5.2)

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