Evidence map›Paper›PMID 33334906›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

Attenuation of SRC Kinase Activity Augments PARP Inhibitor-mediated Synthetic Lethality in

Goutam Chakraborty, Nabeela Khan Patail, Rahim Hirani, Subhiksha Nandakumar, Ying Z Mazzu, Yuki Yoshikawa, Mohammad Atiq, Lina E Jehane, Konrad H Stopsack, Gwo-Shu Mary Lee and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Goutam Chakraborty *Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York. kantoff@mskcc.org chakrabg@mskcc.org.ORCID 0000-0002-4387-2621
Nabeela Khan Patail *Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Rahim HiraniDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-9304-9916
Subhiksha NandakumarCenter for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
Ying Z MazzuDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Yuki YoshikawaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Mohammad AtiqDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-4169-5983
Lina E JehaneDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Konrad H StopsackDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-0722-1311
Gwo-Shu Mary LeeDana-Farber Cancer Institute, Boston, Massachusetts.
Wassim AbidaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Michael J MorrisDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Lorelei A MucciDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Daniel DanilaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Philip W KantoffDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York. kantoff@mskcc.org chakrabg@mskcc.org.
Memorial Sloan Kettering Cancer Center · USDana-Farber Cancer Institute · USHarvard University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
The Impact of DNA Damage Repair Abnormalities in Prostate CancerP01CA228696 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI OFFIT, KENNETH, POMERANTZ, MARK M. · 2019 to 2024
$8.7M
NCI NIH HHS P01 CA228696NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeAlterations in DNA damage repair (DDR) pathway genes occur in 20%-25% of men with metastatic castration-resistant prostate cancer (mCRPC). Although PARP inhibitors (PARPis) have been shown to benefit men with mCRPC harboring DDR defects due to mutations in EXPERIMENTAL

designWe performed transcriptomic analysis of publicly available mCRPC cases, comparing

resultsWe observed significant enrichment of the SRC signaling pathway in

conclusionsThis work suggests that SRC activation may be a potential mechanism of PARPi resistance and that treatment with SRC inhibitors may overcome this resistance. Our preclinical study demonstrates that combining PARPis and SRC inhibitors may be a promising therapeutic strategy for patients with

Indexed as

Synthetic Lethal MutationsAnimalsAntineoplastic AgentsApoptosisBRCA2 ProteinCell ProliferationDrug SynergismDrug Therapy, CombinationGene Expression Regulation, NeoplasticHumansMaleMiceMice, NudePoly(ADP-ribose) Polymerase InhibitorsPrognosisProstatic Neoplasms, Castration-ResistantAntineoplastic AgentsBRCA2 ProteinBRCA2 protein, humanPoly(ADP-ribose) Polymerase Inhibitorssrc-Family Kinases

Identifiers

PMID33334906
PMCPMC7956224
OpenAlexW3113069527

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.