Abstract

Association between leptin and leptin receptor gene polymorphisms and breast cancer risk in premenopausal and postmenopausal Mexican women

Highlights

  • Breast cancer (BC) is a heterogeneous and complex disease due to an interaction between environmental factors and genetic susceptibility

  • Purpose: This study aims to evaluate the association between leptin (-2548 G>A) and leptin receptor (p.K109R, p.Q223R, p.K656N) polymorphisms with breast cancer (BC) risk in premenopausal and postmenopausal Mexican women

  • Four polymorphisms were genotyped by polymerase chain reaction (PCR), High Resolution Melting, and DNA direct sequencing. χ2, logistic regression analysis was performed with SPSS and XLSTAT software

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Summary

Introduction

Breast cancer (BC) is a heterogeneous and complex disease due to an interaction between environmental factors and genetic susceptibility. A cytokine of the adipocytes encoded by the leptin (LEP) gene, interacts with the leptin receptor (LEPR), which is present in breast and other tissues [4]. LEP 2548G>A polymorphism seems to influence leptin mRNA expression in breast cancer cell lines affecting signaling capacity and receptor functionality, increasing the LEPR-LEP binding capacity [7,8]. This induces a cascade of events in the tumor microenvironment, causing the proliferation, angiogenesis, and invasion of the cell [9, 10]. QR and RR genotypes of the LEPR p.Q223R polymorphism have been associated with modest risk for BC in nonobese premenopausal women [11], whereas QR and QR+QQ genotypes of the LEPR p.Q223R polymorphism with BC in overweight postmenopausal women [12]

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