Unique roles of Akt1 and Akt2 in IGF-IR mediated lung tumorigenesis
Metrics: HTML 1148 views | ?
S. Elizabeth Franks1, Ritesh Briah1, Robert A. Jones1, Roger A. Moorehead1
1Department of Biomedical Science, Ontario Veterinary College, University of Guelph, Guelph, Ontario, Canada
Roger A. Moorehead, e-mail: email@example.com
Keywords: Akt, lung cancer, IGF-IR, transgenic mice, tumor development
Received: July 27, 2015 Accepted: November 16, 2015 Published: December 07, 2015
AKT is a serine-threonine kinase that becomes hyperactivated in a number of cancers including lung cancer. Based on AKT's association with malignancy, molecules targeting AKT have entered clinical trials for solid tumors including lung cancer. However, the AKT inhibitors being evaluated in clinical trials indiscriminately inhibit all three AKT isoforms (AKT1–3) and it remains unclear whether AKT isoforms have overlapping or divergent functions. Using a transgenic mouse model where IGF-IR overexpression drives lung tumorigenesis, we found that loss of Akt1 inhibited while loss of Akt2 enhanced lung tumor development. Lung tumors that developed in the absence of Akt2 were less likely to appear as discrete nodules and more frequently displayed a dispersed growth pattern. RNA sequencing revealed a number of genes differentially expressed in lung tumors lacking Akt2 and five of these genes, Actc1, Bpifa1, Mmp2, Ntrk2, and Scgb3a2 have been implicated in human lung cancer. Using 2 human lung cancer cell lines, we observed that a selective AKT1 inhibitor, A-674563, was a more potent regulator of cell survival than the pan-AKT inhibitor, MK-2206. This study suggests that compounds selectively targeting AKT1 may prove more effective than compounds that inhibit all three AKT isoforms at least in the treatment of lung adenocarcinoma.
All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.