Evidence map›Paper›PMID 36428581›Full record

ReviewCancers2022

Regulatory T Cells in Ovarian Carcinogenesis and Future Therapeutic Opportunities.

Emily Cassar, Apriliana E R Kartikasari, Magdalena Plebanski

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
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  17. TIGITJournal of ovarian research · 2024
    Article
  18. Review
  19. Immune pathway through endometriosis to ovarian cancer.World journal of clinical oncology · 2024
    Review
  20. 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

3 authors at 1 institution in 1 country.

Emily CassarSchool of Health and Biomedical Science, Royal Melbourne Institute of Technology, Bundoora, VIC 3083, Australia.
Apriliana E R KartikasariSchool of Health and Biomedical Science, Royal Melbourne Institute of Technology, Bundoora, VIC 3083, Australia.
Magdalena PlebanskiSchool of Health and Biomedical Science, Royal Melbourne Institute of Technology, Bundoora, VIC 3083, Australia.ORCID 0000-0001-6889-3667
RMIT University · AU

Funding

National Health and Medical Research Council 2011747RMIT University PhD Scholarship
6 · The paper itself

Abstract

Regulatory T cells (Tregs) have been shown to play a role in the development of solid tumors. A better understanding of the biology of Tregs, immune suppression by Tregs, and how cancer developed with the activity of Tregs has facilitated the development of strategies used to improve immune-based therapy. In ovarian cancer, Tregs have been shown to promote cancer development and resistance at different cancer stages. Understanding the various Treg-mediated immune escape mechanisms provides opportunities to establish specific, efficient, long-lasting anti-tumor immunity. Here, we review the evidence of Treg involvement in various stages of ovarian cancer. We further provide an overview of the current and prospective therapeutic approaches that arise from the modulation of Treg-related tumor immunity at those specific stages. Finally, we propose combination strategies of Treg-related therapies with other anti-tumor therapies to improve clinical efficacy and overcome tumor resistance in ovarian cancer.

Indexed as

cancerchemotherapycombination therapyepigeneticsimmunotherapyovarian cancerregulatory T cells

Identifiers

PMID36428581
PMCPMC9688690
OpenAlexW4308721502

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.