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The protein p17 signaling pathways in cancer

Authors
Heese, Klaus
Issue Date
Dec-2013
Publisher
SAGE PUBLICATIONS LTD
Keywords
Cancer; Oncology; FAM72A; Ugene; p53
Citation
TUMOR BIOLOGY, v.34, no.6, pp.4081 - 4087
Indexed
SCIE
SCOPUS
Journal Title
TUMOR BIOLOGY
Volume
34
Number
6
Start Page
4081
End Page
4087
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/161268
DOI
10.1007/s13277-013-0999-1
ISSN
1010-4283
Abstract
P17 is a novel neuronal protein expressed under physiological conditions only at very low levels in other tissues. Accumulating data indicate its crucial involvement in tumorigenic effects. Using molecular, cellular, and biocomputational methods, the current study unraveled p17 mode of action. Data indicate that mitochondria-associated p17 interacts with the proteins TMEM115, YPEL3, ERP44, CDK5RAP, and NNAT. Moreover, p17 drives the cell cycle into the G0/G1 phase and enhances survival of proliferating cells. Interference with p17 activities thus might become a novel option to influence also the tumor suppressor protein p53 signaling pathways for the treatment of tumors.
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Heese, Klaus
GRADUATE SCHOOL OF BIOMEDICAL SCIENCE AND ENGINEERING (DEPARTMENT OF BIOMEDICAL SCIENCE)
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