Evidence map›Paper›PMID 35439318›Full record

ArticleMolecular cancer therapeutics2022

A Whole-Genome CRISPR Screen Identifies AHR Loss as a Mechanism of Resistance to a PARP7 Inhibitor.

Huadong Chen, Morgan E Diolaiti, Patrick C O'Leary, Ajda Rojc, Nevan J Krogan, Minkyu Kim, Alan Ashworth

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

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  13. Loss ofFrontiers in immunology · 2024
    Article
  14. PARP7-mediated ADP-ribosylation of FRA1 promotes cancer cell growth by repressing IRF1- and IRF3-dependent apoptosis.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

7 authors at 3 institutions in 1 country.

Huadong ChenHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California.ORCID 0000-0003-4681-0853
Morgan E DiolaitiHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California.ORCID 0000-0001-5900-3060
Patrick C O'LearyHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California.ORCID 0000-0002-2919-5943
Ajda RojcThe Cancer Cell Map Initiative, San Francisco and La Jolla, California.ORCID 0000-0002-6183-7109
Nevan J KroganThe Cancer Cell Map Initiative, San Francisco and La Jolla, California.ORCID 0000-0003-4902-337X
Minkyu KimThe Cancer Cell Map Initiative, San Francisco and La Jolla, California.ORCID 0000-0001-9317-1658
Alan AshworthHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California.ORCID 0000-0003-1446-7878
National Foundation for Cancer Research · USQB3 · USUCSF Helen Diller Family Comprehensive Cancer Center · US

Funding

Translational InformaticsP30CA082103 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jennifer Leigh Clarke · 1999 to 2026
$209.7M
Using Networks to Seed Hierarchical Whole-cell Models of CancerU54CA209891 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ASHWORTH, ALAN · 2017 to 2021
$10.9M
DNA repair alterations in metastatic prostate cancer: functional and therapeutic implicationsR01CA230516 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ASHWORTH, ALAN, FENG, FELIX YI-CHUNG · 2018 to 2022
$2.7M
NCI NIH HHS P30 CA082103NCI NIH HHS R01 CA230516NCI NIH HHS U54 CA209891
6 · The paper itself

Abstract

Inhibitors directed toward PARP1 and PARP2 are approved agents for the treatment of BRCA1 and BRCA2-related cancers. Other members of the PARP family have also been implicated in cancer and are being assessed as therapeutic targets in cancer and other diseases. Recently, an inhibitor of PARP7 (RBN-2397) has reached early-stage human clinical trials. Here, we performed a genome-wide CRISPR screen for genes that modify the response of cells to RBN-2397. We identify the polycyclic aromatic hydrocarbon receptor AHR and multiple components of the cohesin complex as determinants of resistance to this agent. Activators and inhibitors of AHR modulate the cellular response to PARP7 inhibition, suggesting potential combination therapy approaches.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsNeoplasmsGenomeHumansPoly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) Polymerase Inhibitors

Identifiers

PMID35439318
PMCPMC9769698
OpenAlexW4224222237

What OpenQuestion holds

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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 OpenQuestion graph.