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. 2022 Apr 1;23(4):1359-1364.
doi: 10.31557/APJCP.2022.23.4.1359.

Sequencing of Chromosomal Locus 6q25.1 Revealed Two Significant SNPs rs2046210 and rs2046211 Associated with Breast Cancer: A Case-Control Study in Egyptian Women

Affiliations

Sequencing of Chromosomal Locus 6q25.1 Revealed Two Significant SNPs rs2046210 and rs2046211 Associated with Breast Cancer: A Case-Control Study in Egyptian Women

Marwa H Saied et al. Asian Pac J Cancer Prev. .

Abstract

Background: Breast cancer (BC) is one of the major health problems affecting females in Egypt. Certain chromosomal loci abnormalities were proved to be associated with BC in different populations. One of them is chromosomal locus 6q25.1, that affects estrogen receptor gene (ESR) which controls ER receptor expression. Therefore, the aim of this study was to investigate locus 6q25.1 among group of Egyptian female BC patients and compare the results to healthy matched age controls.

Methods: Formalin fixed paraffin embedded (FFPE) samples of sixty newly diagnosed BC patients were sequenced for locus 6q25.1 using genetic analyzer with capillary electrophoresis (3500 GA). The identified single nucleotide polymorphisms (SNPs) were compared to blood samples of forty controls. Realtime PCR using TaqMan probes was used for validation.

Results: Two SNPs rs2046210 and rs2046211 were significantly associated with BC. Frequency of rs2046210-A minor allele was 30% in controls, while the frequency of rs2046211-G minor allele was 15%. Rs2046210-A allele was associated with increased risk of BC (P=0.0001), while rs2046211-G allele was associated with reduced risk of BC (P=0.021). Combined analysis of both SNPs showed that haplotype A/C was associated with increased risk of BC (P = 0.042). No significant correlation was found between rs2046210-A allele and ER status, while positive association was observed between rs204621-C allele and ER status (p= 0.005).

Conclusion: Our data confirmed the important association between locus 6q25.1 and risk of BC in other populations. The frequencies of minor alleles of both significant SNPs will pave the way for a wider large-scale genome study and to be investigated with other BC risk factors.

Keywords: Single nucleotide polymorphism; breast cancer; chromosomal locus; risk.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Gel Electrophoresis of the Amplified Chromosomal 6q25.1 Locus. The lane on the left represents 1-KB ladder, lanes (1-8) contain amplified patients’ samples by PCR. The product size is 322bp
Figure 2
Figure 2
Sequencing Chromatogram of each rs2046210 Genotype and Realtime PCR Amplification Curves
Figure 3
Figure 3
Sequencing Chromatogram of rs2046211 Genotypes i.e. CC and CG

References

    1. Bilal E, Vassallo K, Toppmeyer D, et al. Amplified loci on chromosomes 8 and 17 predict early relapse in ER-positive breast cancers. PLoS One. 2012;7:e38575. - PMC - PubMed
    1. Cai Q, Wen W, Qu S, et al. Replication and functional genomic analyses of the breast cancer susceptibility locus at 6q25 1 generalize its importance in women of chinese, Japanese, and European ancestry. Cancer Res. 2011;71:1344–55. - PMC - PubMed
    1. Cain EH, Saha A, Harowicz MR, et al. Multivariate machine learning models for prediction of pathologic response to neoadjuvant therapy in breast cancer using MRI features: a study using an independent validation set. Breast Cancer Res Treat. 2019;173:455–63. - PMC - PubMed
    1. Chan M, Ji SM, Liaw CS, et al. Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population. Breast Cancer Res Treat. 2012;136:209–20. - PubMed
    1. Collins A, Politopoulos I. The genetics of breast cancer: risk factors for disease. Appl Clin Genet. 2011;4:11–9. - PMC - PubMed