TY - JOUR
T1 - Signaling from membrane receptors to tumor suppressor WW domain-containing oxidoreductase
AU - Chang, Jean Yun
AU - He, Ruei Yu
AU - Lin, Hsin Ping
AU - Hsu, Li Jin
AU - Lai, Feng Jie
AU - Hong, Qunying
AU - Chen, Shean Jen
AU - Chang, Nan Shan
N1 - Funding Information:
Research was supported in part by the Department of Defense, USA (W81XWH-08-1-0682), the National Science Council, Taiwan (NSC96-2320-B-006-014, 96-2628-B-006-041-MY3 and 96-2628-B-006-045-MY3), the National Health Research Institute, Taiwan (NHRI-EX97-9704BI) and the National Cheng Kung University Landmark Projects (C0167 and R026) to N-SC, and the Chi-Mei Hospital and National Cheng Kung University Collaborative Research (CMNCKU9801) to F-JL and N-SC.
PY - 2010/7
Y1 - 2010/7
N2 - The family of WW domain-containing proteins contains over 2000 members. The small WW domain module is responsible, in part, for protein/protein binding interactions and signaling. Many of these proteins are located at the membrane/cytoskeleton area, where they act as adaptors to receive signals from the cell surface. In this review, we provide molecular insights regarding recent novel findings on signaling from the cell surface toward WW domain-containing oxidoreductase, known as WWOX, FOR or WOX1. More specifically, transforming growth factor beta 1 utilizes cell surface hyaluronidase Hyal-2 (hyaluronoglucosaminidase 2) as a cognate receptor for signaling with WWOX and Smad4 to control gene transcription, growth and death. Complement C1q alone, bypassing the activation of classical pathway, signals a novel event of apoptosis by inducing microvillus formation and WWOX activation. Deficiency in these signaling events appears to favorably support cancer growth.
AB - The family of WW domain-containing proteins contains over 2000 members. The small WW domain module is responsible, in part, for protein/protein binding interactions and signaling. Many of these proteins are located at the membrane/cytoskeleton area, where they act as adaptors to receive signals from the cell surface. In this review, we provide molecular insights regarding recent novel findings on signaling from the cell surface toward WW domain-containing oxidoreductase, known as WWOX, FOR or WOX1. More specifically, transforming growth factor beta 1 utilizes cell surface hyaluronidase Hyal-2 (hyaluronoglucosaminidase 2) as a cognate receptor for signaling with WWOX and Smad4 to control gene transcription, growth and death. Complement C1q alone, bypassing the activation of classical pathway, signals a novel event of apoptosis by inducing microvillus formation and WWOX activation. Deficiency in these signaling events appears to favorably support cancer growth.
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U2 - 10.1258/ebm.2010.009351
DO - 10.1258/ebm.2010.009351
M3 - Short survey
C2 - 20542955
AN - SCOPUS:77953783825
SN - 1535-3702
VL - 235
SP - 796
EP - 804
JO - Experimental Biology and Medicine
JF - Experimental Biology and Medicine
IS - 7
ER -