Evidence map›Paper›PMID 40736027›Full record

ArticleJournal of clinical laboratory analysis2025

Evaluating the Role of PD1 and MTNR1B Gene Variants in Breast Cancer Susceptibility: A Case-Control Study in Bangladesh.

Farhan Jamil, Mohammad Mahfuz Enam Elahi, Al-Shahriar Evan, Sakif Ahamed Khan, Israt Jahan Annee, Furhatun-Noor, Ankita Islam, Rana Tabassum, Md Aminul Haque

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Exploring the Role ofHealth science reports · 2026
    Article
  2. Human mutation · 2026
    Article
  3. 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

9 authors.

Farhan JamilResearch Lab, Rufaida BioMeds, Dhaka, Bangladesh.
Mohammad Mahfuz Enam ElahiResearch Lab, Rufaida BioMeds, Dhaka, Bangladesh.ORCID https://orcid.org/0000-0001-8148-3347
Al-Shahriar EvanResearch Lab, Rufaida BioMeds, Dhaka, Bangladesh.
Sakif Ahamed KhanResearch Lab, Rufaida BioMeds, Dhaka, Bangladesh.ORCID https://orcid.org/0009-0008-9397-4299
Israt Jahan AnneeResearch Lab, Rufaida BioMeds, Dhaka, Bangladesh.
Furhatun-NoorResearch Lab, Rufaida BioMeds, Dhaka, Bangladesh.
Ankita IslamResearch Lab, Rufaida BioMeds, Dhaka, Bangladesh.
Rana TabassumResearch Lab, Rufaida BioMeds, Dhaka, Bangladesh.
Md Aminul HaqueSchool of Pharmacy, BRAC University, Dhaka, Bangladesh.ORCID https://orcid.org/0000-0002-1680-3006

Funding

Rufaida BioMeds RBM20230310
6 · The paper itself

Abstract

objectivesBreast cancer is one of the most common malignancies in women. The PD1 and MTNR1B gene polymorphisms have been extensively studied for their potential role in cancer susceptibility. This study aimed to investigate associations between breast cancer risk and PD1 (rs36084323) and MTNR1B (rs10830963) polymorphisms.

methodsA case-control study was conducted with 112 breast cancer patients from Dhaka Cancer and General Hospital, Bangladesh, and 124 age- and sex-matched healthy controls. Genotyping of PD1 (rs36084323) and MTNR1B (rs10830963) polymorphisms was performed using the Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) method.

resultsThe genotype distributions for both SNPs adhered to Hardy-Weinberg equilibrium (HWE). The PD1 GG genotype was more prevalent in controls, indicating a protective effect, whereas the GG genotype of MTNR1B showed no statistically significant association with breast cancer risk. The recessive model of PD1 (GG vs. AG + AA) demonstrated a lower odds ratio (0.2873), while the recessive model of MTNR1B (2.307) suggested a potential risk. Dominant models for both genes (AG + GG vs. AA for PD1 and CG + GG vs. CC for MTNR1B) showed statistically significant associations with breast cancer susceptibility.

conclusionThe PD1 GG genotype exhibited a significant protective effect against breast cancer, while the MTNR1B CG genotype was associated with reduced risk, but GG showed no correlation. Larger studies across diverse populations are recommended to validate these findings.

Indexed as

Breast NeoplasmsGenetic Predisposition to DiseasePolymorphism, Single NucleotideProgrammed Cell Death 1 ReceptorAdultBangladeshCase-Control StudiesFemaleHumansMiddle AgedPDCD1 protein, humanProgrammed Cell Death 1 Receptorbreast cancercancer riskMTNR1B geneoncologyPD1 geneSNP

Identifiers

PMID40736027
PMCPMC12459217

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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.