Literature DB >> 11360191

UCS15A, a non-kinase inhibitor of Src signal transduction.

S V Sharma1, C Oneyama, Y Yamashita, H Nakano, K Sugawara, M Hamada, N Kosaka, T Tamaoki.   

Abstract

Src tyrosine kinase plays key roles in signal transduction following growth factor stimulation and integrin-mediated cell-substrate adhesion. Since src-signal transduction defects are implicated in a multitude of human diseases, we have sought to develop new ways to identify small molecule inhibitors using a yeast-based, activated-src over-expression system. In the present study, we describe the identification of a unique src-signal transduction inhibitor, UCS15A. UCS15A was found to inhibit the src specific tyrosine phosphorylation of numerous proteins in v-src-transformed cells. Two of these phosphoproteins were identified as bona-fide src substrates, cortactin and Sam68. UCS15A differed from conventional src-inhibitors in that it did not inhibit the tyrosine kinase activity of src. In addition, UCS15A appeared to differ from src-destabilizing agents such as herbimycin and radicicol that destabilize src by interfering with Hsp90. Our studies suggest that UCS15A exerted its src-inhibitory effects by a novel mechanism that involved disruption of protein-protein interactions mediated by src. One of the biological consequences of src-inhibition by UCS15A was its ability to inhibit the bone resorption activity of osteoclasts in vitro. These data suggest that UCS15A may inhibit the bone resorption activity of osteoclasts, not by inhibiting src tyrosine kinase activity, but by disrupting the interaction of proteins associated with src, thereby modulating downstream events in the src signal transduction pathway.

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Year:  2001        PMID: 11360191     DOI: 10.1038/sj.onc.1204296

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  5 in total

1.  Targeting AMAP1 and cortactin binding bearing an atypical src homology 3/proline interface for prevention of breast cancer invasion and metastasis.

Authors:  Shigeru Hashimoto; Mayumi Hirose; Ari Hashimoto; Masaki Morishige; Atsuko Yamada; Harumi Hosaka; Ken-ichi Akagi; Eiji Ogawa; Chitose Oneyama; Tsutomu Agatsuma; Masato Okada; Hidenori Kobayashi; Hiromi Wada; Hirofumi Nakano; Takahisa Ikegami; Atsushi Nakagawa; Hisataka Sabe
Journal:  Proc Natl Acad Sci U S A       Date:  2006-04-24       Impact factor: 11.205

2.  Total synthesis of luminacin D.

Authors:  J Brad Shotwell; Evan S Krygowski; John Hines; Brian Koh; Elliott W D Huntsman; Hui Won Choi; John S Schneekloth; John L Wood; Craig M Crews
Journal:  Org Lett       Date:  2002-09-05       Impact factor: 6.005

3.  Mammalian son of sevenless Guanine nucleotide exchange factors: old concepts and new perspectives.

Authors:  José M Rojas; José Luis Oliva; Eugenio Santos
Journal:  Genes Cancer       Date:  2011-03

4.  Potent and selective inhibition of SH3 domains with dirhodium metalloinhibitors.

Authors:  Farrukh Vohidov; Sarah E Knudsen; Paul G Leonard; Jun Ohata; Michael J Wheadon; Brian V Popp; John E Ladbury; Zachary T Ball
Journal:  Chem Sci       Date:  2015-06-03       Impact factor: 9.825

5.  Inhibition of IGF-1-Mediated Cellular Migration and Invasion by Migracin A in Ovarian Clear Cell Carcinoma Cells.

Authors:  Tamami Ukaji; Yinzhi Lin; Kouji Banno; Shoshiro Okada; Kazuo Umezawa
Journal:  PLoS One       Date:  2015-09-11       Impact factor: 3.240

  5 in total

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