PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
October 1, 1992Proceedings of the National Academy of Sciences739 citationsOpen Access

AKT2, a putative oncogene encoding a member of a subfamily of protein-serine/threonine kinases, is amplified in human ovarian carcinomas.

View Full Paper
JCJ Q ChengAGAndrew K. GodwinABAlfonso Bellacosa

Key Points

Key points are not available for this paper at this time.

Abstract

We isolated cDNA clones containing the entire coding region of the putative oncogene AKT2. Sequence analysis and in vitro translation demonstrated that AKT2 encodes a 56-kDa protein with homology to serine/threonine kinases; moreover, this protein contains a Src homology 2-like domain. AKT2 was shown to be amplified and overexpressed in 2 of 8 ovarian carcinoma cell lines and 2 of 15 primary ovarian tumors. AKT2 was mapped to chromosome region 19q13.1-q13.2 by fluorescence in situ hybridization. In the two ovarian carcinoma cell lines exhibiting amplification of AKT2, the amplified sequences were localized within homogeneously staining regions. We conclude that AKT2 belongs to a distinct subfamily of protein-serine/threonine kinases containing Src homology 2-like domains and that alterations of AKT2 may contribute to the pathogenesis of ovarian carcinomas.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Cheng et al. (1992) studied this question.

synapsesocial.com/papers/6a0ccf6c243f79c7af34c70bhttps://doi.org/10.1073/pnas.89.19.9267
Ask AI
Helpful
Bookmark
Share
View Full Paper