Evidence map›Paper›PMID 34258703›Full record

ArticleEnvironmental science and pollution research international2021

The correlation between single nucleotide polymorphisms of the thymic stromal lymphopoietin receptor and breast cancer in a cohort of female patients in Saudi Arabia.

Abdelhabib Semlali, Mikhlid H Almutairi, Sultan N Alharbi, Abdullah M Alamri, Abdulwahed F Alrefaei, Bader O Almutairi, Mahmoud Rouabhia

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In one paragraph

Article in Environmental science and pollution research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

7 authors at 3 institutions in 2 countries.

Abdelhabib Semlali *Groupe de Recherche en Écologie Buccale, Faculté de Médecine Dentaire- Université Laval, Québec, Québec, Canada. abdelhabib.semlali@greb.ulaval.ca.ORCID http://orcid.org/0000-0002-1643-0377
Mikhlid H Almutairi *Zoology DepartmentCollege of Science, King Saud University, P.O. Box: 2455, 11451, Riyadh, Kingdom of Saudi Arabia. malmutari@ksu.edu.sa.
Sultan N AlharbiNational Center for Stem Cell Technology, King Abdulaziz City for Science and Technology, Riyadh, 11461, Saudi Arabia.
Abdullah M AlamriGenome Research ChairDepartment of Biochemistry, College of Science King Saud University, Riyadh, Kingdom of Saudi Arabia.
Abdulwahed F AlrefaeiZoology DepartmentCollege of Science, King Saud University, P.O. Box: 2455, 11451, Riyadh, Kingdom of Saudi Arabia.
Bader O AlmutairiZoology DepartmentCollege of Science, King Saud University, P.O. Box: 2455, 11451, Riyadh, Kingdom of Saudi Arabia.
Mahmoud RouabhiaGroupe de Recherche en Écologie Buccale, Faculté de Médecine Dentaire- Université Laval, Québec, Québec, Canada.
King Saud University · SAUniversité Laval · CAKing Abdulaziz City for Science and Technology · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current study aimed to examine thymic stromal lymphopoietin receptor (TSLPR) genetic variation and breast cancer (BC) susceptibility in women in Saudi Arabia. Therefore, 127 blood samples from female patients diagnosed with BC and 116 blood samples from healthy female controls were studied using a genotyping assay to determine the association between three TSLPR single nucleotide polymorphisms (SNPs)-P196L, X201W, and A238V-and the risk of BC progression. In addition, gene expression was evaluated in 20 matching BC and normal tissues using immunohistochemistry. TSLPR protein levels were higher among BC patients than those with matching normal breast tissue. In addition, TSLPR SNP P196L was found to have a significant protective effect on BC progression (OR = 0.4427), although only the T allele for TSLPR P196L had this protective effect against BC progression in participants who were younger than 48 years old. In contrast, no association was found between the T allele and risk of BC in participants who were older than 48 years old, and the CT and TT genotypes were significantly associated with BC risk protection in the older group. The effects of the TT genotype and the T allele were closely associated with a decreased risk of BC in participants with estrogen receptors (ER+) and without them (ER-). Overall, the findings revealed a significant correlation between SNPs in the TSLPR genes and BC progression among women in Saudi Arabia.

Indexed as

Breast NeoplasmsPolymorphism, Single NucleotideCase-Control StudiesCytokinesFemaleGenotypeHumansMiddle AgedSaudi ArabiaThymic Stromal LymphopoietinCytokinesThymic Stromal LymphopoietinBreast cancer progressionPolymorphismsTSLPRTSLPR expression

Identifiers

PMID34258703
OpenAlexW3164011084

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.