Evidence map›Paper›PMID 37445949›Full record

ReviewInternational journal of molecular sciences2023

Homologous Recombination Deficiency (HRD) in Cutaneous Oncology.

Favour A Akinjiyan, Renee Morecroft, Jordan Phillipps, Tolulope Adeyelu, Andrew Elliott, Soo J Park, Omar H Butt, Alice Y Zhou, George Ansstas

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Skin cancer risk in hereditary mixed cancer syndromes.Hereditary cancer in clinical practice · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
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 at 3 institutions in 1 country.

Favour A AkinjiyanDivision of Medical Oncology, Department of Medicine, Washington University in Saint Louis, St. Louis, MO 63130, USA.ORCID 0000-0003-0914-5567
Renee MorecroftDivision of Medical Oncology, Department of Medicine, Washington University in Saint Louis, St. Louis, MO 63130, USA.
Jordan PhillippsDivision of Medical Oncology, Department of Medicine, Washington University in Saint Louis, St. Louis, MO 63130, USA.
Tolulope AdeyeluCARIS Life Sciences, Irving, TX 75039, USA.
Andrew ElliottCARIS Life Sciences, Irving, TX 75039, USA.
Soo J ParkMoores Cancer Center, University of California San Diego, La Jolla, CA 92093, USA.
Omar H ButtDivision of Medical Oncology, Department of Medicine, Washington University in Saint Louis, St. Louis, MO 63130, USA.ORCID 0000-0003-2252-3673
Alice Y ZhouDivision of Medical Oncology, Department of Medicine, Washington University in Saint Louis, St. Louis, MO 63130, USA.
George AnsstasDivision of Medical Oncology, Department of Medicine, Washington University in Saint Louis, St. Louis, MO 63130, USA.
Washington University in St. Louis · USCaris Life Sciences (United States) · USUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skin cancers, including basal cell carcinoma (BCC), cutaneous squamous cell carcinoma (SCC), and melanoma, are the most common malignancies in the United States. Loss of DNA repair pathways in the skin plays a significant role in tumorigenesis. In recent years, targeting DNA repair pathways, particularly homologous recombination deficiency (HRD), has emerged as a potential therapeutic approach in cutaneous malignancies. This review provides an overview of DNA damage and repair pathways, with a focus on HRD, and discusses major advances in targeting these pathways in skin cancers. Poly(ADP-ribose) polymerase (PARP) inhibitors have been developed to exploit HRD in cancer cells. PARP inhibitors disrupt DNA repair mechanisms by inhibiting PARP enzymatic activity, leading to the accumulation of DNA damage and cell death. The concept of synthetic lethality has been demonstrated in HR-deficient cells, such as those with BRCA1/2 mutations, which exhibit increased sensitivity to PARP inhibitors. HRD assessment methods, including genomic scars, RAD51 foci formation, functional assays, and BRCA1/2 mutation analysis, are discussed as tools for identifying patients who may benefit from PARP inhibitor therapy. Furthermore, HRD has been implicated in the response to immunotherapy, and the combination of PARP inhibitors with immunotherapy has shown promising results. The frequency of HRD in melanoma ranges from 18% to 57%, and studies investigating the use of PARP inhibitors as monotherapy in melanoma are limited. Further research is warranted to explore the potential of PARP inhibition in melanoma treatment.

Indexed as

Carcinoma, Squamous CellMelanomaOvarian NeoplasmsSkin NeoplasmsBRCA1 ProteinBRCA2 ProteinFemaleHomologous RecombinationHumansPoly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) PolymerasesBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanPoly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) PolymerasesDNA repairgenomic scarshomologous recombination deficiencyimmunotherapymelanomaPARP inhibitorsskin cancersynthetic lethality

Identifiers

PMID37445949
PMCPMC10341889
OpenAlexW4382369689

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.