Evidence map›Paper›PMID 32020380›Full record

ReviewInternational journal of clinical oncology2020

Precision medicine for ovarian clear cell carcinoma based on gene alterations.

Takafumi Kuroda, Takashi Kohno

Abstract readReview
PubMed Publisher
In one paragraph

Review in International journal of clinical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Therapeutic Role of Synthetic Lethality inJournal of immunotherapy and precision oncology · 2024
    Review
  8. Article
  9. Article
  10. The Role ofFrontiers in oncology · 2021
    Review
  11. Review
  12. Article
  13. 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

2 authors.

Takafumi KurodaDepartment of Obstetrics and Gynecology, The Jikei University School of Medicine, Tokyo, Japan.
Takashi KohnoDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan. tkkohno@ncc.go.jp.ORCID http://orcid.org/0000-0002-5371-706X

Funding

National Cancer Center Research and Development Grant 30-A-6
6 · The paper itself

Abstract

Ovarian clear cell carcinoma (OCCC) is a histological subtype of epithelial ovarian carcinoma prevalent in Asians. No clear therapeutic selection based on molecular profile has been implemented for this disease. Oncogenic PIK3CA mutation, which activates the PIK3CA/AKT/mTOR signaling pathway, is a promising druggable alteration in OCCC. Recent studies by our group and others have identified the ARID1A mutation as another alteration linked to therapeutic selection based on synthetic lethality: deleterious ARID1A mutations, resulting in ARID1A deficiency, make OCCC cells sensitive to drugs targeting poly (ADP-ribose) polymerase and EZH2, as well as to glutathione inhibitors. In addition, we recently obtained evidence that ARID1A-deficient OCCC could benefit from gemcitabine treatment. Precision medicine based on gene alteration profiling might improve the prognosis of OCCC patients.

Indexed as

Adenocarcinoma, Clear CellAntimetabolites, AntineoplasticClass I Phosphatidylinositol 3-KinasesDeoxycytidineDNA-Binding ProteinsEnhancer of Zeste Homolog 2 ProteinFemaleGemcitabineGene DosageGlutathioneHumansMolecular Targeted TherapyMutationOvarian NeoplasmsPrecision MedicineTranscription FactorsAntimetabolites, AntineoplasticARID1A protein, humanClass I Phosphatidylinositol 3-KinasesDeoxycytidineDNA-Binding ProteinsEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanGemcitabineGlutathionePIK3CA protein, humanTranscription FactorsGemcitabineImmune checkpoint inhibitory therapyOvarian clear cell carcinomaPrecision medicineSynthetic lethality

Identifiers

What OpenQuestion holds

Textmetadata
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.