Evidence map›Paper›PMID 40887867›Full record

ArticleInternational journal of immunogenetics2025

The Association of IL-17RC Polymorphisms rs708567 and rs76999397 With Acute Lymphoblastic Leukaemia.

Ali Aljuaimlani, Lamjed Mansour, Jameel Al-Tamimi, Jamilah Alshammari, Safa A Alqarzae, Fadwa M Alkhulaifi, Suliman Alomar

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Article in International journal of immunogenetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Ali AljuaimlaniDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Lamjed MansourDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Jameel Al-TamimiDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Jamilah AlshammariDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Safa A AlqarzaeDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Fadwa M AlkhulaifiDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Suliman AlomarDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute lymphoblastic leukaemia (ALL) is characterized by the clonal proliferation of immature lymphoid precursors in the bone marrow or peripheral blood. This study investigates whether genetic polymorphisms in IL-17RC are associated with an increased risk of ALL in the Saudi population.

methodsThis case-control study included 95 patients with ALL and 95 matched controls. Genetic polymorphisms and their associations with ALL risk were identified using logistic regression analysis. Additionally, quantitative real-time polymerase chain reaction (qRT-PCR) was used to assess the level of IL-17RC mRNA.

resultsThe results revealed that carriers of the GA and AA genotypes of rs76999397 had a significantly increased risk of ALL (GA: odds ratios [OR] = 63.78, 95% confidence interval [CI] = 25.51-159.43, p < 0.0001; AA: OR = 18.22, 95% CI = 1.50-221.37, p < 0.0001). Additionally, we identified that an increased risk of ALL was associated with two haplotypes in IL-17RC, C-A and T-A (in the order of rs708567 and rs76999397) (OR = 46.73, 95% CI = 17.30-126.28; OR = 49.42, 95% CI = 6.95-351.45, respectively).

conclusionsThe results suggested that the GA and AA genotypes of rs76999397 were significantly associated with an increased risk of ALL, whereas rs708567 did not show a significant association. Furthermore, the CA and TA haplotypes (rs708567/rs76999397) were found to be associated with increased susceptibility to ALL.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotidePrecursor Cell Lymphoblastic Leukemia-LymphomaReceptors, Interleukin-17AdolescentAdultAllelesCase-Control StudiesChildChild, PreschoolFemaleGene FrequencyGenetic Association StudiesGenotypeHaplotypesHumansReceptors, Interleukin-17genetic | interleukin receptor C | polymorphism | T lymphocytes

Identifiers

PMID40887867
PMCPMC12595585

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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.