Repurposing dasatinib for diffuse large B cell lymphoma.

TitleRepurposing dasatinib for diffuse large B cell lymphoma.
Publication TypeJournal Article
Year of Publication2019
AuthorsScuoppo C, Wang J, Persaud M, Mittan SK, Basso K, Pasqualucci L, Rabadan R, Inghirami G, Grandori C, Bosch F, Dalla-Favera R
JournalProc Natl Acad Sci U S A
Volume116
Issue34
Pagination16981-16986
Date Published2019 08 20
ISSN1091-6490
KeywordsAnimals, 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.

DOI10.1073/pnas.1905239116
Alternate JournalProc Natl Acad Sci U S A
PubMed ID31383760
PubMed Central IDPMC6708382
Grant ListP50 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.

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