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Association of and Polymorphisms with Pain and Opioid Adverse Reactions in Colorectal Cancer

Overview
Publisher MDPI
Specialty Chemistry
Date 2025 Feb 26
PMID 40006034
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Abstract

: Pain management in colorectal cancer is influenced by genetic variability in opioid receptor genes ( and ), potentially affecting opioid efficacy and adverse drug reactions (ADRs). This study evaluated the association of (rs1799971 and rs510769) and (rs2236861) polymorphisms with pain severity, opioid efficacy, and ADRs in Chilean colorectal cancer patients. : The genotypes of and polymorphisms and clinical data from 69 colorectal cancer patients were analyzed. Associations between genotypes, ADRs, and pain severity (maximum Visual Analog Scale, VAS) were evaluated under inheritance models. : The rs1799971 G allele was significantly associated with pain presence ( = 0.008), while rs2236861 was linked to ADR risk ( = 0.042). Allelic distribution analysis revealed higher frequencies of the G allele and rs510769 T allele in patients with ADRs and pain, respectively. For rs510769, the dominant model showed a significant association with pain severity ( = 0.033), while the overdominant model revealed a trend toward significance ( = 0.0504). Logistic regression model tests showed no significant predictive associations for the maximum VAS or ADRs under inheritance models. : Genetic variations in and may play a role in pain perception and ADRs in colorectal cancer patients. These findings contribute to the understanding of pharmacogenomic factors in opioid therapy, emphasizing the need for further research to validate the clinical utility of these genetic markers.

References
1.
Young E, Lariviere W, Belfer I . Genetic basis of pain variability: recent advances. J Med Genet. 2011; 49(1):1-9. PMC: 3821734. DOI: 10.1136/jmedgenet-2011-100386. View

2.
Yu Z, Wen L, Shen X, Zhang H . Effects of the OPRM1 A118G Polymorphism (rs1799971) on Opioid Analgesia in Cancer Pain: A Systematic Review and Meta-Analysis. Clin J Pain. 2018; 35(1):77-86. DOI: 10.1097/AJP.0000000000000636. View

3.
Dang V, Christie M . Mechanisms of rapid opioid receptor desensitization, resensitization and tolerance in brain neurons. Br J Pharmacol. 2011; 165(6):1704-1716. PMC: 3372824. DOI: 10.1111/j.1476-5381.2011.01482.x. View

4.
Zhang Y, Wang D, Johnson A, Papp A, Sadee W . Allelic expression imbalance of human mu opioid receptor (OPRM1) caused by variant A118G. J Biol Chem. 2005; 280(38):32618-24. DOI: 10.1074/jbc.M504942200. View

5.
Caraceni A, Davies A, Poulain P, Cortes-Funes H, Panchal S, Fanelli G . Guidelines for the management of breakthrough pain in patients with cancer. J Natl Compr Canc Netw. 2013; 11 Suppl 1:S29-36. DOI: 10.6004/jnccn.2013.0211. View