» Articles » PMID: 34930150

ESR1 PvuII Polymorphism: from Risk Factor to Prognostic and Predictive Factor of the Success of Primary Systemic Therapy in Advanced Breast Cancer

Overview
Journal BMC Cancer
Publisher Biomed Central
Specialty Oncology
Date 2021 Dec 21
PMID 34930150
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The ESR1 gene encodes Estrogen Receptor alpha (ERα), which plays a role in the tumourigenesis of breast cancer. A single nucleotide polymorphism (SNP) in intron 1 of this gene called ESR1 PvuII (rs2234693) has been reported to increase the risk of breast cancer. This study aimed to investigate the ESR1 PvuII polymorphism as a prognostic and predictive factor guiding the choice of therapy for advanced breast cancer.

Methods: This retrospective study was conducted in 104 advanced breast cancer patients at Dharmais Cancer Hospital from 2011 to 2018. The ESR1 PvuII polymorphism was analysed by Sanger sequencing of DNA from primary breast tumour samples.

Results: The percentages of patients with ESR1 PvuII genotypes TT, TC, and CC were 42.3, 39.4, and 18.3%, respectively. Looking at prognosis, patients with ESR1 PvuII TC + CC had shorter overall survival than those with the TT genotype [HR = 1.79; 95% CI 1.05-3.04; p = 0.032]. As a predictive marker, TC + CC was associated with shorter survival (p = 0.041), but TC + CC patients on primary hormonal therapy had a median overall survival longer than TC + CC patients on primary chemotherapy (1072 vs 599 days).

Conclusion: The ESR1 PvuII TC + CC genotypes confer poor prognosis in advanced breast cancer, but these genotypes could be regarded as a good predictor of the therapeutic effect of hormonal treatment.

Citing Articles

Prediction of medication-related osteonecrosis of the jaws using machine learning methods from polymorphisms and clinical information.

Choi S, Kim J, Oh S, Cheon S, Yee J, Kim S Front Med (Lausanne). 2023; 10:1140620.

PMID: 37415765 PMC: 10321771. DOI: 10.3389/fmed.2023.1140620.


Identification of immune-related biomarkers for predicting neoadjuvant chemotherapy sensitivity in HER2 negative breast cancer via bioinformatics analysis.

Fang D, Li Y, Li Y, Chen Y, Huang Q, Luo Z Gland Surg. 2022; 11(6):1026-1036.

PMID: 35800743 PMC: 9253195. DOI: 10.21037/gs-22-234.

References
1.
Markiewicz A, Welnicka-Jaskiewicz M, Skokowski J, Jaskiewicz J, Szade J, Jassem J . Prognostic significance of ESR1 amplification and ESR1 PvuII, CYP2C19*2, UGT2B15*2 polymorphisms in breast cancer patients. PLoS One. 2013; 8(8):e72219. PMC: 3738574. DOI: 10.1371/journal.pone.0072219. View

2.
Kuo S, Yang S, You S, Lien H, Lin C, Lin P . Polymorphisms of ESR1, UGT1A1, HCN1, MAP3K1 and CYP2B6 are associated with the prognosis of hormone receptor-positive early breast cancer. Oncotarget. 2017; 8(13):20925-20938. PMC: 5400556. DOI: 10.18632/oncotarget.14995. View

3.
Billam M, Witt A, Davidson N . The silent estrogen receptor--can we make it speak?. Cancer Biol Ther. 2009; 8(6):485-96. PMC: 3901993. DOI: 10.4161/cbt.8.6.7582. View

4.
Wilcken N, Hornbuckle J, Ghersi D . Chemotherapy alone versus endocrine therapy alone for metastatic breast cancer. Cochrane Database Syst Rev. 2003; (2):CD002747. PMC: 8094405. DOI: 10.1002/14651858.CD002747. View

5.
Semiglazov V, Semiglazov V, Dashyan G, Ziltsova E, Ivanov V, Bozhok A . Phase 2 randomized trial of primary endocrine therapy versus chemotherapy in postmenopausal patients with estrogen receptor-positive breast cancer. Cancer. 2007; 110(2):244-54. DOI: 10.1002/cncr.22789. View