Evidence map›Paper›PMID 31242618›Full record

ReviewInternational journal of molecular sciences2019

Identification of Novel Biomarkers of Homologous Recombination Defect in DNA Repair to Predict Sensitivity of Prostate Cancer Cells to PARP-Inhibitors.

Daniela Criscuolo, Francesco Morra, Riccardo Giannella, Aniello Cerrato, Angela Celetti

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Response of the Urothelial Carcinoma Cell Lines to Cisplatin.International journal of molecular sciences · 2022
    Article
  11. Article
  12. Targeting mutations in cancer.The Journal of clinical investigation · 2022
    Review
  13. RelB upregulates PD-L1 and exacerbates prostate cancer immune evasion.Journal of experimental & clinical cancer research : CR · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Daniela CriscuoloInstitute for the Experimental Endocrinology and Oncology, Research National Council, CNR, 80131 Naples, Italy. daniela.cris@live.it.
Francesco MorraInstitute for the Experimental Endocrinology and Oncology, Research National Council, CNR, 80131 Naples, Italy. francesco.morra@unina.it.
Riccardo GiannellaUrology Surgery Unit, Antonio Cardarelli Hospital, 80131 Naples, Italy. riccardogiannella@libero.it.
Aniello CerratoInstitute for the Experimental Endocrinology and Oncology, Research National Council, CNR, 80131 Naples, Italy. aniellocerrato@gmail.com.
Angela CelettiInstitute for the Experimental Endocrinology and Oncology, Research National Council, CNR, 80131 Naples, Italy. celetti@unina.it.
Institute for Experimental Endocrinology and Oncology · ITOspedale Antonio Cardarelli · IT

Funding

POR FESR 2014-2020 TECHNOLOGY PLATFORM LOTTA ALLE PATOLOGIE ONCOLOGICHE Sviluppo di Approcci Terapeutici INnovativi per patologie neoplastiche resistenti ai trattamenti (SATIN) POR FESR 2014-2020
6 · The paper itself

Abstract

One of the most common malignancies in men is prostate cancer, for which androgen deprivation is the standard therapy. However, prostate cancer cells become insensitive to anti-androgen treatment and proceed to a castration-resistant state with limited therapeutic options. Therefore, besides the androgen deprivation approach, novel biomarkers are urgently required for specific targeting in this deadly disease. Recently, germline or somatic mutations in the homologous recombination (HR) DNA repair genes have been identified in at least 20-25% of metastatic castration-resistant prostate cancers (mCRPC). Defects in genes involved in HR DNA repair can sensitize cancer cells to poly(ADP-ribose) polymerase (PARP) inhibitors, a class of drugs already approved by the Food and Drug Administration (FDA) for breast and ovarian cancer carrying germline mutations in

Indexed as

Biomarkers, TumorRecombinational DNA RepairAntineoplastic Combined Chemotherapy ProtocolsClinical Trials as TopicDNA DamageDrug Resistance, NeoplasmGenomic InstabilityHumansMalePoly(ADP-ribose) Polymerase InhibitorsProstatic NeoplasmsReproducibility of ResultsSynthetic Lethal MutationsTreatment OutcomeBiomarkers, TumorPoly(ADP-ribose) Polymerase InhibitorsbiomarkersBRCAnessCCDC6DNA damage responsegenome instabilitysynthetic lethality

Identifiers

PMID31242618
PMCPMC6627216
OpenAlexW2954727256

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.