Evidence map›Paper›PMID 31383760›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Repurposing dasatinib for diffuse large B cell lymphoma.

Claudio Scuoppo, Jiguang Wang, Mirjana Persaud, Sandeep K Mittan, Katia Basso, Laura Pasqualucci, Raul Rabadan, Giorgio Inghirami, Carla Grandori, Francesc Bosch and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 35 citations in OpenAlex.

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  5. mHereditas · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Claudio ScuoppoInstitute for Cancer Genetics, Columbia University, New York, NY 10032; cs3064@cumc.columbia.edu rd10@cumc.columbia.edu.
Jiguang WangDepartment of Systems Biology, Columbia University, New York, NY 10032.
Mirjana PersaudInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Sandeep K MittanInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Katia BassoInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Laura PasqualucciInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Raul RabadanDepartment of Systems Biology, Columbia University, New York, NY 10032.
Giorgio InghiramiDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY 10065.
Carla GrandoriCure First and SEngine Precision Medicine, Seattle, WA 98109.
Francesc BoschInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Riccardo Dalla-FaveraInstitute for Cancer Genetics, Columbia University, New York, NY 10032; cs3064@cumc.columbia.edu rd10@cumc.columbia.edu.
Columbia University · USCancer Genetics (United States) · USCornell University · US

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
Translating Stress Response Targeted Therapy for B-Cell LymphomasP50CA192937 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI DALLA-FAVERA, RICCARDO, ZELENETZ, ANDREW D. · 2016 to 2020
$10.9M
Topology of Cancer Evolution and HeterogeneityU54CA193313 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IAVARONE, ANTONIO, RABADAN, RAUL · 2015 to 2020
$10.4M
From pathogenesis to new therapeutic targets in Diffuse Large B cell LymphomaR35CA210105 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Riccardo Dalla-Favera · 2016 to 2026
$10.0M
Undergraduate Biomedical Research Training at HunterT34GM007823 · NIGMS · HUNTER COLLEGE · PI FORD, JENNIFER S · 1985 to 2020
$8.2M
Personalized cancer models to discover and develop new therapeutic targets.U01CA217883 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KEMP, CHRISTOPHER J · 2017 to 2021
$4.3M
NCI NIH HHS P30 CA013696NCI NIH HHS P50 CA192937NCI NIH HHS R35 CA210105NCI NIH HHS U01 CA217883NCI NIH HHS U54 CA193313NIGMS NIH HHS T34 GM007823
6 · The paper itself

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.

Indexed as

Lymphoma, Large B-Cell, DiffuseAdenineAnimalsCell Line, TumorDasatinibDrug Resistance, NeoplasmHumansMechanistic Target of Rapamycin Complex 2MicePhosphatidylinositol 3-KinasesPiperidinesProof of Concept StudyPTEN PhosphohydrolasePyrazolesPyrimidinesXenograft Model Antitumor AssaysAdenineDasatinibibrutinibMechanistic Target of Rapamycin Complex 2Phosphatidylinositol 3-KinasesPiperidinesPTEN PhosphohydrolasePTEN protein, humanPyrazolesPyrimidinesdasatinibDLBCLPTEN

Identifiers

PMID31383760
PMCPMC6708382
OpenAlexW2966170143

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.