| First Author | Subramaniam PS | Year | 2012 |
| Journal | Cancer Cell | Volume | 21 |
| Issue | 4 | Pages | 459-72 |
| PubMed ID | 22516257 | Mgi Jnum | J:189332 |
| Mgi Id | MGI:5445059 | Doi | 10.1016/j.ccr.2012.02.029 |
| Citation | Subramaniam PS, et al. (2012) Targeting nonclassical oncogenes for therapy in T-ALL. Cancer Cell 21(4):459-72 |
| abstractText | Constitutive phosphoinositide 3-kinase (PI3K)/Akt activation is common in T cell acute lymphoblastic leukemia (T-ALL). Although four distinct class I PI3K isoforms (alpha, beta, gamma, delta) could participate in T-ALL pathogenesis, none has been implicated in this process. We report that in the absence of PTEN phosphatase tumor suppressor function, PI3Kgamma or PI3Kdelta alone can support leukemogenesis, whereas inactivation of both isoforms suppressed tumor formation. The reliance of PTEN null T-ALL on the combined activities of PI3Kgamma/delta was further demonstrated by the ability of a dual inhibitor to reduce disease burden and prolong survival in mice as well as prevent proliferation and promote activation of proapoptotic pathways in human tumors. These results support combined inhibition of PI3Kgamma/delta as therapy for T-ALL. |
