Evidence map›Paper›PMID 41790366›Full record

ArticleMolecular biology reports2026

Expression patterns of ANRIL and GAS-5 and genetic variants in breast cancer.

Ibrahim T Ibrahim, M A Kandeil, Olfat G Shaker, Dalia Refaat, Rasha M Hussein

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Ibrahim T IbrahimDepartment of Biochemistry, Faculty of Pharmacy, Beni-Suef University, 62514, Beni-Suef, Egypt.
M A KandeilDepartment of Biochemistry, Faculty of Veterinary Medicine, Beni- Suef University, Beni- Suef, Egypt.
Olfat G ShakerDepartment of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Cairo University, Cairo, Egypt. olfat.shaker@kasralainy.edu.eg.
Dalia RefaatDepartment of Biochemistry, Faculty of Pharmacy, Beni-Suef University, Clinical pharmacist at El-Fayoum Health Administration, Beni-Suef, El-Fayoum, Egypt.
Rasha M HusseinDepartment of Biochemistry, Faculty of Pharmacy, Beni-Suef University, 62514, Beni-Suef, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer (BC) is the most malignancy diagnosed cancer worldwide. Antisense non-coding RNA(ANRIL) and Growth arrest specific-5(GAS-5) are types of Long non-coding RNAs(lncRNAs) that are essential regulators for BC development. Several single nucleotide polymorphisms (SNPs) in ANRIL and GAS-5 genes are associated with BC pathophysiology. AIM OF WORK: To measure levels of ANRIL and GAS-5 in patients with BC compared to controls. Also, investigate the distribution of SNP (rs11515) and (rs145204276) genotypes with the clinic-pathological parameters of patients. PATIENTS AND

methodsThirty-five BC patients and 20 healthy-matched age individuals were enrolled in this study. Real-time PCR (RT-qPCR) for relative quantitation of gene expression levels of ANRIL and GAS-5 was used.

resultsANRIL level was upregulated in patients group with median and interquartile (IQR) of 6.0(12.65). Meanwhile, GAS-5 was downregulated 0.46(0.58) with p < 0.0001 and P = 0.006 respectively between BC patients and controls. For ANRIL (rs11515), the distribution of ‘CG’ genotype was the majority in both groups versus ‘CC’ and ‘GG’ genotypes. While for GAS-5(rs145204276), ‘ins/ins’ genotype was more frequent in BC group. For controls, ‘ins/ins’ and ‘ins/del’ genotypes were the most followed by ‘del/del’ genotype. A significant difference was detected between the two groups as regards to ‘ins/ins’ genotype (p < 0.0001). ANRIL levels tended to decrease with the severity of the stage across all genotypes. While GAS-5 tended to increase with the severity across polymorphisms. There was a positive correlation between levels of biomarkers (ANRIL and GAS-5) ( (r = 0.497,p = 0.0024).

conclusionThe association of ANRIL and GAS-5 with genotype polymorphism suggests a potential link between genotype variations, biomarkers expression and disease progression.

Indexed as

Breast NeoplasmsRNA, Long NoncodingAdultCase-Control StudiesFemaleGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseGenotypeHumansMiddle AgedPolymorphism, Single NucleotideCDKN2B antisense RNA, humanGAS5 long non-coding RNA, humanRNA, Long NoncodingAntisense non-coding RNACancerGrowth arrest specific 5TNM staging

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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.