AI Article Synopsis

  • Pesticide exposure is linked to an increased risk of diseases like breast cancer (BC), and the UGT2B7 gene variant rs7438135 (G > A) plays a role in detoxifying pesticides and potentially reducing oxidative stress.
  • A study examined 228 women with BC to see how their UGT2B7 variant affected oxidative stress caused by pesticide exposure, measuring specific markers in their plasma.
  • Results indicated that the rs7438135 variant did not provide protection against oxidative stress from pesticides, with significant lipid peroxidation and other stress markers observed in various aggressive tumor conditions.

Article Abstract

Pesticide exposure is a risk factor for the development of several diseases, including breast cancer (BC). The enzyme UGT2B7 participate in detoxification of pesticides and the presence rs7438135 (G > A) variant in your gene increases its glucuronidation potential, contributing to oxidative stress metabolites neutralization. Here we investigated the impact of occupational pesticide exposure on the systemic oxidative stress generation from 228 women with BC depending on their UGT2B7 rs7438135 (G > A) status. q-PCR investigated the presence of the rs7438135 variant, and oxidative stress markers (lipid peroxidation levels, total antioxidant capacity-TRAP, and nitric oxide metabolites-NOx) were measured in plasma. Pesticide exposure induced significant augment in the systemic lipid peroxidation in the presence of the variant for several clinicopathological conditions, including tumors with high proliferation index (ki67) and with high aggressiveness. NOx was augmented in high ki67, positive progesterone receptors, high-grade and triple-negative/Luminal B tumors, and low-risk stratified patients. TRAP was depleted in young patients at menopause and those with triple-negative/Luminal B tumors, as well as those stratified as at low risk for death and recurrence. These findings showed that the presence of the variant was not able to protect from pesticide-induced oxidative stress generation in BC patients.

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Source
http://dx.doi.org/10.1002/jbt.70013DOI Listing

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