Evidence map›Paper›PMID 38011562›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

PARP7-mediated ADP-ribosylation of FRA1 promotes cancer cell growth by repressing IRF1- and IRF3-dependent apoptosis.

Patrick Manetsch, Flurina Böhi, Kathrin Nowak, Deena M Leslie Pedrioli, Michael O Hottiger

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 38 citations in OpenAlex.

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  5. Unraveling CD4Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

5 authors at 1 institution in 1 country.

Patrick ManetschDepartment of Molecular Mechanisms of Disease, University of Zurich, 8057 Zurich, Switzerland.
Flurina BöhiDepartment of Molecular Mechanisms of Disease, University of Zurich, 8057 Zurich, Switzerland.ORCID 0009-0002-1752-8437
Kathrin NowakDepartment of Molecular Mechanisms of Disease, University of Zurich, 8057 Zurich, Switzerland.
Deena M Leslie PedrioliDepartment of Molecular Mechanisms of Disease, University of Zurich, 8057 Zurich, Switzerland.
Michael O HottigerDepartment of Molecular Mechanisms of Disease, University of Zurich, 8057 Zurich, Switzerland.ORCID 0000-0002-7323-2270
University of Zurich · CH

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) 310030_205202Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) IZLIZ3_200237
6 · The paper itself

Abstract

PARP7 was reported to promote tumor growth in a cell-autonomous manner and by repressing the antitumor immune response. Nevertheless, the molecular mechanism of how PARP7-mediated ADP-ribosylation exerts these effects in cancer cells remains elusive. Here, we identified PARP7 as a nuclear and cysteine-specific mono-ADP-ribosyltransferase that modifies targets critical for regulating transcription, including the AP-1 transcription factor FRA1. Loss of FRA1 ADP-ribosylation via PARP7 inhibition by RBN-2397 or mutation of the ADP-ribosylation site C97 increased FRA1 degradation by the proteasome via PSMC3. The reduction in FRA1 protein levels promoted IRF1- and IRF3-dependent cytokine as well as proapoptotic gene expression, culminating in CASP8-mediated apoptosis. Furthermore, high PARP7 expression was indicative of the PARP7 inhibitor response in FRA1-positive lung and breast cancer cells. Collectively, our findings highlight the connected roles of PARP7 and FRA1 and emphasize the clinical potential of PARP7 inhibitors for FRA1-driven cancers.

Indexed as

ADP-RibosylationNeoplasmsNucleoside Transport ProteinsProto-Oncogene Proteins c-fosADP Ribose TransferasesApoptosisCell Transformation, NeoplasticFos-Related Antigen 1Gene Expression RegulationHumansInterferon Regulatory Factor-1Interferon Regulatory Factor-3ADP Ribose TransferasesFos-Related Antigen 1Interferon Regulatory Factor-1Interferon Regulatory Factor-3IRF1 protein, humanIRF3 protein, humanNucleoside Transport ProteinsProto-Oncogene Proteins c-fosTiPARP protein, humanADP-ribosylationcancerFRA1PARP7proteasomal protein degradation

Identifiers

PMID38011562
PMCPMC10710093
OpenAlexW4389042136

What OpenQuestion holds

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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.