Evidence map›Paper›PMID 36355490›Full record

ArticlePharmaceuticals (Basel, Switzerland)2022

The Expression Patterns of Human Cancer-Testis Genes Are Induced through Epigenetic Drugs in Colon Cancer Cells.

Mikhlid H Almutairi, Turki M Alrubie, Bader O Almutairi, Abdullah M Alamri, Abdulwahed F Alrefaei, Maha M Arafah, Mohammad Alanazi, Abdelhabib Semlali

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 30% 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, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. IncreasedPharmaceuticals (Basel, Switzerland) · 2024
    Article
  4. Heliyon · 2024
    Article
  5. Article
  6. Higher Expression Levels ofMedicina (Kaunas, Lithuania) · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Mikhlid H AlmutairiZoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-0337-6412
Turki M AlrubieZoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Bader O AlmutairiZoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-4697-5204
Abdullah M AlamriGenome Research Chair, Department of Biochemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-3045-1350
Abdulwahed F AlrefaeiZoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-3761-6656
Maha M ArafahPathology Department, College of Medicine, King Saud University, Riyadh 11451, Saudi Arabia.
Mohammad AlanaziGenome Research Chair, Department of Biochemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Abdelhabib SemlaliGroupe de Recherche en Écologie Buccale, Faculté de Médecine Dentaire, Université Laval, 2420 Rue de la Terrasse, Local 1758, Québec, QC G1V 0A6, Canada.
King Saud University · SAUniversité Laval · CA

Funding

King Abdulaziz City for Science and Technology 2-17-01-001-0069
6 · The paper itself

Abstract

backgroundThe expression of human germline genes is restricted to the germ cells of the gonads, which produce sperm and eggs. The germline genes involved in testis development and potentially activated in cancer cells are known as cancer-testis (CT) genes. These genes are potential therapeutic targets and biomarkers, as well as drivers of the oncogenic process. CT genes can be reactivated by treatment with drugs that demethylate DNA. The majority of the existing literature on CT gene activation focuses on X-chromosome-produced CT genes. We tested the hypothesis that epigenetic landscape changes, such as DNA methylation, can alter several CT gene expression profiles in cancer and germ cells.

methodsColon cancer (CC) cell lines were treated with the DNA methyltransferase inhibitor (DNMTi) 5-aza-2'-deoxycytidine, or with the histone deacetylase inhibitor (HDACi) trichostatin A (TSA). The effects of these epigenetic treatments on the transcriptional activation of previously published CT genes (

resultsWe found that treatment of CC cell lines with 5-aza-2'-deoxycytidine or TSA correlated with activation of X-encoded CT genes and non-X-encoded CT genes in somatic (non-germline) cells.

conclusionThese findings confirm that a subset of CT genes can be regulated by hypomethylating drugs and subsequently provide a potential therapeutic target for cancer.

Indexed as

cancer-testis (CT) genecolon cancerDNA methyl-transferase inhibitor (DNMTi)histone deacetylase inhibitor (HDACi)immunotherapy

Identifiers

PMID36355490
PMCPMC9692864
OpenAlexW4307291166

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.