前列腺癌
基因亚型
分子医学
癌症研究
癌症
肽
生物
遗传学
基因
细胞周期
生物化学
作者
Athanasios Armakolas,Maria Kaparelou,Andreas Dimakakos,Efstathia Papageorgiou,Nikolaos Armakolas,Athanasios Antonopoulos,Constantina Petraki,Maria Lekarakou,Pavlos Lelovas,Martha Stathaki,Constantinos Psarros,Ismene Donta,Panagiotis Galanos,Paul Msaouel,Vassilis G. Gorgoulis,Michael Koutsilieris
标识
DOI:10.2119/molmed.2014.00222
摘要
IGF-1 is one of the key molecules in cancer biology; however, little is known about the role of the preferential expression of the premature IGF-1 isoforms in prostate cancer. We have examined the role of the cleaved COO- terminal peptide (PEc) of the third IGF-1 isoform, IGF-1Ec, in prostate cancer. Our evidence suggests that endogenously produced PEc induces cellular proliferation in the human prostate cancer cells (PC-3) in vitro and in vivo, by activating the ERK1/2 pathway in an autocrine/paracrine manner. PEc overexpressing cells and tumors presented evidence of epithelial to mesenchymal transition, whereas the orthotopic injection of PEc-overexpressing, normal prostate epithelium cells (HPrEC) in SCID mice was associated with increased metastatic rate. In humans, the IGF-1Ec expression was detected in prostate cancer biopsies, where its expression correlates with tumor stage. Our data describes the action of PEc in prostate cancer biology and defines its potential role in tumor growth, progression and metastasis.
科研通智能强力驱动
Strongly Powered by AbleSci AI