P13K-MTORC1-S6K1 signaling pathway biomarkers predictive of anti-cancer responses
The present invention is based, in part, on the identification of novel FI.3K-mTORCI-S6K 1 signaling pathway biomarkers predictive of responsiveness to anti-cancer therapies.
1. A method of treating a human subject afflicted with T cell acute lymphoblastic leukemia characterized by reduced Pten function and amplification or overexpression of a c-Myc transcript comprising a 5′-untranslated region (5′-UTR) relative to a normal control, comprising administering to the subject an inhibitor of eukaryotic initiation factor-4A (eIF4A) and/or an inhibitor of eukaryotic initiation factor-4B (eIF4B), wherein the inhibitor is selected from the group consisting of RNA interference-mediating nucleic acids that bind eIF4A or eIF4B, hippuristanol, pateamine A, silvestrol, and rocaglamides, thereby treating the subject.
2. The method of claim 1 , wherein
i) the efficacy of the treatment is measured by at least one criteria selected from the group consisting of clinical benefit rate, survival until mortality, pathological complete response, semi-quantitative measures of pathologic response, clinical complete remission, clinical partial remission, clinical stable disease, recurrence-free survival, metastasis free survival, disease free survival, circulating tumor cell decrease, circulating marker response, and RECIST criteria; and/or
ii) the inhibitor of eIF4A and/or eIF4B is administered in a pharmaceutically acceptable formulation.
3. The method of claim 1 , wherein the eIF4A and/or eIF4B is selected from the group consisting of human eukaryotic initiation factor-4A (eIF4A) or an ortholog thereof, and human eukaryotic initiation factor-4B (eIF4B) or an ortholog thereof.
4. The method of claim 1 , further comprising administering one or more additional anti-cancer agents.