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Interaction between fortilin and transforming growth factor-beta stimulated clone-22 (TSC-22) prevents apoptosis via the destabilization of TSC-22

Authors
Lee, Jeong HeonRho, Seung BaePark, Sang-YoonChun, Taehoon
Issue Date
9-4월-2008
Publisher
ELSEVIER SCIENCE BV
Keywords
apoptosis; fortilin; ovarian carcinoma cell; TSC-22; yeast two hybrid
Citation
FEBS LETTERS, v.582, no.8, pp.1210 - 1218
Indexed
SCIE
SCOPUS
Journal Title
FEBS LETTERS
Volume
582
Number
8
Start Page
1210
End Page
1218
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/123737
DOI
10.1016/j.febslet.2008.01.066
ISSN
0014-5793
Abstract
Yeast two-hybrid screening was conducted using a human ovary cDNA library to search for a novel binding protein using transforming growth factor-beta stimulated clone-22 (TSC-22). The selected protein was fortilin, which has; been characterized as a nuclear anti-apoptotic protein. Overexpression of fortilin in ovarian carcinoma cells reversed TSC-22-mediated apoptosis, and the inhibition of fortilin expression via small interfering RNA (siRNA) resulted in an increase in the apoptosis of ovarian carcinoma cells. Moreover, fortilin overexpression promoted the degradation of TSC-22. Thus, an interaction between fortilin and TSC-22 prevents apoptosis via the destabilization of TSC-22 in ovarian carcinoma cells.
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