Ontology highlight
ABSTRACT: Background
The Phosphatidylinositol 3'-kinase is a key regulator in various cancer-associated signal transduction pathways. Genetic alterations of its catalytic subunit alpha, PIK3CA, have been identified in ovarian cancer. Our in vivo data suggests that PIK3CA activation is one of the early genetic events in ovarian cancer. However, its role in malignant transformation of ovarian surface epithelium (OSE) is largely unclear.Methodology/principal findings
Using the Müllerian inhibiting substance type II receptor (MISIIR) promoter, we generated transgenic mice that expressed activated PIK3CA in the Müllerian epithelium. Overexpression of PIK3CA in OSE induced remarkable hyperplasia, but was not able to malignantly transform OSE in vivo. The consistent result was also observed in primary cultured OSEs. Although enforced expression of PIK3CA could not induce OSE anchorage-independent growth, it significantly increased anchorage-independent growth of OSE transformed by mutant K-ras.Conclusions/significance
While PIK3CA activation may not be able to initiate OSE transformation, we conclude that activation of PIK3CA may be an important molecular event contributing to the maintenance of OSE transformation initiated by oncogenes such as K-ras.
SUBMITTER: Liang S
PROVIDER: S-EPMC2629728 | biostudies-literature | 2009
REPOSITORIES: biostudies-literature
Liang Shun S Yang Nuo N Pan Yue Y Deng Shan S Lin Xiaojuan X Yang Xiaojun X Katsaros Dionyssios D Roby Katherine F KF Hamilton Thomas C TC Connolly Denise C DC Coukos George G Zhang Lin L
PloS one 20090127 1
<h4>Background</h4>The Phosphatidylinositol 3'-kinase is a key regulator in various cancer-associated signal transduction pathways. Genetic alterations of its catalytic subunit alpha, PIK3CA, have been identified in ovarian cancer. Our in vivo data suggests that PIK3CA activation is one of the early genetic events in ovarian cancer. However, its role in malignant transformation of ovarian surface epithelium (OSE) is largely unclear.<h4>Methodology/principal findings</h4>Using the Müllerian inhib ...[more]