Title | Repurposing dasatinib for diffuse large B cell lymphoma. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Scuoppo C, Wang J, Persaud M, Mittan SK, Basso K, Pasqualucci L, Rabadan R, Inghirami G, Grandori C, Bosch F, Dalla-Favera R |
Journal | Proc Natl Acad Sci U S A |
Volume | 116 |
Issue | 34 |
Pagination | 16981-16986 |
Date Published | 2019 08 20 |
ISSN | 1091-6490 |
Keywords | Animals, Cell Line, Tumor, Dasatinib, Drug Resistance, Neoplasm, Humans, Lymphoma, Large B-Cell, Diffuse, Mechanistic Target of Rapamycin Complex 2, Mice, Phosphatidylinositol 3-Kinases, Proof of Concept Study, PTEN Phosphohydrolase, Pyrazoles, Pyrimidines, Xenograft Model Antitumor Assays |
Abstract | To repurpose compounds for diffuse large B cell lymphoma (DLBCL), we screened a library of drugs and other targeted compounds approved by the US Food and Drug Administration on 9 cell lines and validated the results on a panel of 32 genetically characterized DLBCL cell lines. Dasatinib, a multikinase inhibitor, was effective against 50% of DLBCL cell lines, as well as against in vivo xenografts. Dasatinib was more broadly active than the Bruton kinase inhibitor ibrutinib and overcame ibrutinib resistance. Tumors exhibiting dasatinib resistance were commonly characterized by activation of the PI3K pathway and loss of PTEN expression as a specific biomarker. PI3K suppression by mTORC2 inhibition synergized with dasatinib and abolished resistance in vitro and in vivo. These results provide a proof of concept for the repurposing approach in DLBCL, and point to dasatinib as an attractive strategy for further clinical development in lymphomas. |
DOI | 10.1073/pnas.1905239116 |
Alternate Journal | Proc Natl Acad Sci U S A |
PubMed ID | 31383760 |
PubMed Central ID | PMC6708382 |
Grant List | P50 CA192937 / CA / NCI NIH HHS / United States U54 CA193313 / CA / NCI NIH HHS / United States P30 CA013696 / CA / NCI NIH HHS / United States U01 CA217883 / CA / NCI NIH HHS / United States R35 CA210105 / CA / NCI NIH HHS / United States T34 GM007823 / GM / NIGMS NIH HHS / United States |
Related Faculty:
Giorgio Inghirami, M.D.