Evidence map›Paper›PMID 39318358›Full record

ReviewOncoscience2024

Molecular mechanism of PARP inhibitor resistance.

Yi Huang, Simin Chen, Nan Yao, Shikai Lin, Junyi Zhang, Chengrui Xu, Chenxuan Wu, Guo Chen, Danyang Zhou

Abstract readReview
In one paragraph

Review in Oncoscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
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

9 authors.

Yi HuangSchool of Biopharmacy, China Pharmaceutical University, Nanjing 211198, P.R. China.
Simin ChenSchool of Biopharmacy, China Pharmaceutical University, Nanjing 211198, P.R. China.
Nan YaoSchool of Biopharmacy, China Pharmaceutical University, Nanjing 211198, P.R. China.
Shikai LinSchool of Biopharmacy, China Pharmaceutical University, Nanjing 211198, P.R. China.
Junyi ZhangSchool of Biopharmacy, China Pharmaceutical University, Nanjing 211198, P.R. China.
Chengrui XuSchool of Biopharmacy, China Pharmaceutical University, Nanjing 211198, P.R. China.
Chenxuan WuSchool of Public Health, Nanjing Medical University, Nanjing 210029, P.R. China.
Guo ChenSchool of Biopharmacy, China Pharmaceutical University, Nanjing 211198, P.R. China.
Danyang ZhouDepartment of Respiratory, Nanjing First Hospital, China Pharmaceutical University, Nanjing 210012, Jiangsu, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Poly (ADP-ribose) polymerases (PARP) inhibitors (PARPi) are the first-approved anticancer drug designed to exploit synthetic lethality. PARPi selectively kill cancer cells with homologous recombination repair deficiency (HRD), as a result, PARPi are widely employed to treated

Indexed as

BRCA1/2homologous recombination (HR) repairPARP inhibitorsynthetic lethality

Identifiers

PMID39318358
PMCPMC11420906

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.