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Titolo:
Overexpression of p97(Eps8) leads to cellular transformation: implication of pleckstrin homology domain in p97(Eps8)-mediated ERK activation
Autore:
Maa, MC; Hsieh, CY; Leu, TH;
Indirizzi:
Natl Cheng Kung Univ, Coll Med, Dept Pharmacol, Tainan 70101, Taiwan Natl Cheng Kung Univ Tainan Taiwan 70101 Pharmacol, Tainan 70101, Taiwan Chung shan Med & Dent Coll, Inst Biochem, Taichung 402, Taiwan Chung shan Med & Dent Coll Taichung Taiwan 402 hem, Taichung 402, Taiwan
Titolo Testata:
ONCOGENE
fascicolo: 1, volume: 20, anno: 2001,
pagine: 106 - 112
SICI:
0950-9232(20010104)20:1<106:OOPLTC>2.0.ZU;2-6
Fonte:
ISI
Lingua:
ENG
Soggetto:
TYROSINE KINASE SUBSTRATE; BETA-GAMMA-SUBUNITS; PROTEIN-KINASE; HIGH-AFFINITY; PH DOMAIN; SH3 DOMAIN; V-SRC; EPS8; BINDING; GROWTH;
Keywords:
p97(Eps8); pleckstrin homology domain; transformation; ERK;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Citazioni:
31
Recensione:
Indirizzi per estratti:
Indirizzo: Leu, TH Natl Cheng Kung Univ, Coll Med, Dept Pharmacol, Tainan 70101, Taiwan Natl Cheng Kung Univ Tainan Taiwan 70101 l, Tainan 70101, Taiwan
Citazione:
M.C. Maa et al., "Overexpression of p97(Eps8) leads to cellular transformation: implication of pleckstrin homology domain in p97(Eps8)-mediated ERK activation", ONCOGENE, 20(1), 2001, pp. 106-112

Abstract

Two isoforms of Eps8, p(97Eps8) and p68(Eps8), have been identified as thesubstrates for receptor tyrosine kinases, Our previous studies indicated that both tyrosyl phosphorylation and protein expression of Eps8 were elevated in v-Src transformed cells, In an attempt to examine the role played by p97(Eps8) in tumorigenesis, we have first obtained cells overexpressing p97(Eps8) and its pleckstrin homology (PH)-truncated variant. We then demonstrated that cells overexpressing p97(Eps8) not only exhibited the ability of focus formation in cell culture but also promoted the tumor formation in mice as compared to controls, Furthermore, elevated serum-induced extracellular responsive kinase (ERK) activation was observed in p97(Eps8) overexpressors, This enhanced ERK activation was sensitive to a MEK1 specific inhibitor PD98059 and was important for p97(Eps8)-mediated transformation, since transfection of vectors expressing dominant negative MEK1 and p97(Eps8) abrogated focus formation by p97(Eps8) In contrast, PH-truncated p97(Eps8) failed to localize at the plasma membrane and that the truncated variant also did not elevate ERK activation and cellular transformation in response to serum stimulation, Our results thus indicated that: (1) the gene encoding p97(Eps8) was an oncogene; (ii) p97(Eps8)-induced oncogenesis was partly mediated by ERK activation; and (iii) the PH domain of p97(Eps8) was critical forits cellular localization, ERK activation and its ability to transform cells.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 22/01/20 alle ore 13:02:22