Cheng J Q, Godwin A K, Bellacosa A, Taguchi T, Franke T F, Hamilton T C, Tsichlis P N, Testa J R
Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111.
Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9267-71. doi: 10.1073/pnas.89.19.9267.
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.
我们分离出了包含推定癌基因AKT2完整编码区的cDNA克隆。序列分析和体外翻译表明,AKT2编码一种与丝氨酸/苏氨酸激酶具有同源性的56 kDa蛋白;此外,该蛋白含有一个类Src同源2结构域。在8个卵巢癌细胞系中的2个以及15个原发性卵巢肿瘤中的2个中,AKT2被证明存在扩增和过表达。通过荧光原位杂交,AKT2被定位到染色体区域19q13.1-q13.2。在两个显示出AKT2扩增的卵巢癌细胞系中,扩增序列定位于均匀染色区。我们得出结论,AKT2属于一个独特的含类Src同源2结构域的蛋白丝氨酸/苏氨酸激酶亚家族,并且AKT2的改变可能有助于卵巢癌的发病机制。