Evidence map›Paper›PMID 30791940›Full record

ReviewJournal of experimental & clinical cancer research : CR2019

New combinatorial strategies to improve the PARP inhibitors efficacy in the urothelial bladder Cancer treatment.

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

Open access · goldAbstract readReview
In one paragraph

Review in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
11.7field-weighted citation impact, top 1% 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

39 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Elucidating DNA Damage-Dependent Immune System Activation.International journal of molecular sciences · 2025
    Review
  6. Article
  7. Article
  8. The KLF16/MYC feedback loop is a therapeutic target in bladder cancer.Journal of experimental & clinical cancer research : CR · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. RelB upregulates PD-L1 and exacerbates prostate cancer immune evasion.Journal of experimental & clinical cancer research : CR · 2022
    Article
  17. Article
  18. Article
  19. Review
  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

6 authors at 2 institutions in 1 country.

Daniela CriscuoloInstitute for the Experimental Endocrinology and Oncology, Research National Council, CNR, Naples, Italy.
Francesco MorraInstitute for the Experimental Endocrinology and Oncology, Research National Council, CNR, Naples, Italy.
Riccardo GiannellaUrology Surgery Unit, A.Cardarelli Hospital, Naples, Italy.
Roberta ViscontiInstitute for the Experimental Endocrinology and Oncology, Research National Council, CNR, Naples, Italy.
Aniello CerratoInstitute for the Experimental Endocrinology and Oncology, Research National Council, CNR, Naples, Italy.
Angela CelettiInstitute for the Experimental Endocrinology and Oncology, Research National Council, CNR, Naples, Italy. celetti@unina.it.ORCID http://orcid.org/0000-0001-5166-3507
Institute for Experimental Endocrinology and Oncology · ITFatebenefratelli Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNovel therapeutic strategies are urgently needed for the treatment of metastatic Urothelial Bladder Cancer. DNA damaging repair (DDR) targeting has been introduced in cinical trials for bladder cancer patients that carry alterations in homologous DNA repair genes, letting to envisage susceptibility to the Poly (adenosine diphosphate [ADP]) ribose polymerase (PARP) inhibitors. MAIN BODY: PARP inhibition, by amplifying the DNA damage, augments the mutational burden and promotes the immune priming of the tumor by increasing the neoantigen exposure and determining upregulation of programmed death ligand 1 (PD-L1) expression. Thus, the combination of PARP-inhibition and the PD/PD-L1 targeting may represent a compelling strategy to treat bladder cancer and has been introduced in recent clinical trials. The targeting of DDR has been also used in combination with epigenetic drugs able to modulate the expression of genes involved in DDR, and also able to act as immunomodulator agents suggesting their use in combination with immune-checkpoint inhibitors.

conclusionIn conclusion, it may be envisaged the combination of three classes of drugs to treat bladder cancer, by targeting the DDR process in a tumor context of DDR defect, together with epigenetic agents and immune-checkpoint inhibitors, whose association may amplify the effects and reduce the doses and the toxicity of each single drug.

Indexed as

B7-H1 AntigenDNA DamageDNA RepairHumansPoly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) PolymerasesUp-RegulationUrinary Bladder NeoplasmsB7-H1 AntigenPoly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) PolymerasesBiomarkersBRCAnessCCDC6DNA damage responseEpigenetic agentsImmunotherapyPARP trappingRRx-001Synthetic lethalityViral mimicry

Identifiers

PMID30791940
PMCPMC6385418
OpenAlexW2939862456

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.