Evidence map›Paper›PMID 32256143›Full record

ArticleTurkish journal of biology = Turk biyoloji dergisi2020

Transcriptional splice variants of CD40 and its prognostic value in breast cancer.

Neşe Ünver, Diğdem Yöyen Ermiş, Bahar Zehra Weber, Güneş Esendağli

Open access · diamondAbstract read
In one paragraph

Article in Turkish journal of biology = Turk biyoloji dergisi, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. CD40/CD40L expression and its prognostic value in cervical cancer.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2023
    Article
  6. 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

4 authors at 4 institutions in 2 countries.

Neşe ÜnverDepartment of Stem Cell Sciences, Graduate School of Health Sciences, Center for Stem Cell Research and Development,Hacettepe University, Ankara Turkey.ORCID https://orcid.org/0000-0002-4925-7179
Diğdem Yöyen ErmişDepartment of Medical Biology, Faculty of Medicine, Lokman Hekim University, Ankara Turkey.ORCID https://orcid.org/0000-0001-5871-8769
Bahar Zehra WeberInstitute of Cancer Research, Medical University of Vienna, Vienna Austria.ORCID https://orcid.org/0000-0003-3719-4673
Güneş EsendağliDepartment of Basic Oncology, Cancer Institute, Hacettepe University, Ankara Turkey.ORCID https://orcid.org/0000-0003-4865-2377
Comprehensive Cancer Center Vienna · ATHacettepe University · TRHacettepe University Hospital · TRLokman Hekim Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD40 is an important tumor necrosis factor receptor (TNFR) family protein for the development of antitumor response against cancer cells, apart from its role in the regulation of the immune system as a costimulatory molecule. It is broadly expressed on the surface of immune cells and in diverse cancer types, including breast cancer. Here, we analyzed both CD40/CD40 ligand expression in breast cancer cells and tissues using public data sets and overall survival analysis in ungrouped breast cancer patients, as well as in the triple-negative breast cancer subtype. We detected CD40 gene expression along with its 3 different splice variants (variants 1-3), predominantly in the triple-negative subgroup of breast cancer cell lines. The results of the overall survival analysis showed that high CD40 gene expression, particularly in the triple-negative subgroup of breast cancer patients, is associated with better survival. In addition to the transcriptional levels of CD40 splice variants, investigation of protein levels of these variants will allow the categorization of breast cancer cells and reveal their potential as an immunotherapeutic target.

Indexed as

alternative splicingantitumor responsebreast cancerCD4transcriptional variant

Identifiers

PMID32256143
PMCPMC7129065
OpenAlexW3015118245

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.