IMR Press / FBS / Volume 16 / Issue 4 / DOI: 10.31083/j.fbs1604025
Open Access Original Research
Interferon Gamma Gene Polymorphisms in Greek Primary Breast Cancer Patients
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Affiliation
1 Institute for Health and Sport, Victoria University, Melbourne, VIC 3030, Australia
2 Department of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Reno, NV 89557, USA
3 Prolipsis Diagnostic Centre - Clinic, 11528 Athens, Greece
4 Australian Institute for Musculoskeletal Science (AIMSS), Melbourne, VIC 3021, Australia
5 Department of Medicine Western Health, Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Melbourne, VIC 3021, Australia
6 School of Health and Biomedical Sciences, RMIT University, Bundoora, VIC 3083, Australia
*Correspondence: vasso.apostolopoulos@rmit.edu.au (Vasso Apostolopoulos)
These authors contributed equally.
Front. Biosci. (Schol Ed) 2024, 16(4), 25; https://doi.org/10.31083/j.fbs1604025
Submitted: 7 May 2024 | Revised: 19 August 2024 | Accepted: 28 August 2024 | Published: 24 December 2024
Copyright: © 2024 The Author(s). Published by IMR Press.
This is an open access article under the CC BY 4.0 license.
Abstract
Background:

Breast cancer is a heterogeneous disease with distinct clinical subtypes, categorized by hormone receptor status, which exhibits different prognoses and requires personalized treatment approaches. These subtypes included luminal A and luminal B, which have different prognoses. Breast cancer development and progression involve many factors, including interferon-gamma (IFNG). Moreover, single nucleotide polymorphisms (SNPs) in IFNG have been associated with cancer risk. However, the functional role of IFNG polymorphisms in primary breast cancer subtypes, luminal A and luminal B, is unclear.

Methods:

A total of 138 breast cancer tissues were acquired: 81 had luminal A, 42 had luminal B, 10 had triple-negative, and 3 had human epidermal growth factor receptor 2 (HER2) subtypes, while 2 had missing data. The tissues were evaluated in relation to luminal A and luminal B primary breast cancer subtypes. DNA was extracted from freshly frozen samples, and three SNPs (rs1861493 (chr12:68157416 (GRCh38.p13)), rs1861494 (chr12:68157629 (GRCh38.p13)) and rs2430561 (chr12:68158742 (GRCh38.p13))) in the IFNG gene were selected and evaluated based on previously published associations with cancer or other diseases.

Results:

The data showed that IFNG polymorphisms rs1861493 and rs1861494 were associated with breast cancer risk, with the A allele of rs1861493 and T allele of rs1861494 being noted as the risk alleles. Furthermore, the IFNG polymorphism rs2430561 was associated with breast cancer risk, with the A allele being the risk allele. In addition, the risk alleles were more prevalent in the more aggressive subtype, luminal B breast cancer, compared to luminal A. Similarly, the rs2430561 AA genotype was associated with the breast cancer severity.

Conclusion:

IFNG polymorphisms rs1861493, rs1861494, and rs2430561, with their respective risk alleles, are associated with increased breast cancer risk and severity. These risk alleles are more prevalent in the aggressive luminal B subtype compared to luminal A, indicating their role in both the prevalence and prognosis of breast cancer in a Greek population.

Keywords
breast cancer
subtypes
luminal A
luminal B
interferon-gamma
single nucleotide polymorphisms
SNPs
Highlights

•    The IFNG single nucleotide polymorphisms (SNPs) have been associated with risk of cancer. 
•    The functional SNPs of IFNG in 138 ex vivo human breast cancer tissues in relation to primary breast cancer subtypes, luminal A and luminal B were evaluated. 
•    IFNG polymorphisms rs1861493 and rs1861494 are associated with the risk of breast cancer, with the A allele of rs1861493 and T allele of rs1861494 being the risk alleles 
•    IFNG polymorphism rs2430561 was associated with the risk of breast cancer, with the A allele being the risk allele 
•    The risk alleles were more prevalent in the more aggressive subtype, luminal B breast cancer 
•    rs2430561 AA genotype was associated with the severity of breast cancer. 

Funding
The Thelma and Paul Constantinou Foundation
Graeme & Angelina Wise
AHEPA Victoria Unit Athena 2 Daughters of Penelope
Australian Postgraduate Research Award
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