AKT1 rs1130233 SNP在日本胃肠道癌症姑息治疗患者中的临床影响

T. Morishita, A. Hishida, Y. Okugawa, Y. Morimoto, Y. Shirai, Kyoko Okamoto, Aki Ogawa, Koji Tanaka, R. Nishikawa, Y. Toiyama, Y. Inoue, H. Sakurai, H. Urata, Motoyoshi Tanaka, C. Miki
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引用次数: 1

摘要

目的:癌症患者常出现慢性炎症、厌食和由此导致的营养摄入减少,随之而来的是体重下降和肌肉萎缩,称为“肌肉减少症”。这种情况被称为“恶病质”。在这项研究中,我们检测了AKT1 rs1130233、ICAM1 rs281432、SELP rs6128和TNSRSF1A rs4149570的遗传多态性与日本姑息治疗的胃肠道癌症患者恶病质的相关性。据报道,AKT1 rs1130233、ICAM1 rs281432、SELP rs6128和TNSRSF1A rs4149570与LIF rs929271有关。方法:选取2011年12月至2015年8月在伊加综合医院门诊就诊的59例胃肠道肿瘤患者(男37例,女22例)作为研究对象。采用PCR-CTPP或Taqman SNP基因分型法对AKT1 rs1130233、ICAM1 rs281432、SELP rs6128、TNSRSF1A rs4149570和LIF rs929271进行基因分型。评估了这些snp与患者预后以及体重减轻(化疗开始后6个月内体重减轻超过5%)之间的关系。结果:A/G基因型AKT1 rs1130233多态性患者体重减轻5%的风险显著增加(AKT1 A/G vs. G/G,调整优势比[aOR]=7.11;95%CI: 1.41-35.7),或至少有一个AKT1 rs1130233等位基因A的患者(AKT1 A/G+A/A vs. G/G, aOR=4.57;95% CI: 1.14-18.3),经年龄、性别和UICC临床4期调整后。检查的多态性与患者的生存没有统计学意义的相关性。结论:本研究揭示AKT1 rs1130233a等位基因可能在癌症恶病质的发生发展中发挥关键作用。鉴于AKT1参与癌症的发生和细胞凋亡,在不久的将来,从临床、流行病学和生物学的角度进一步研究该分子在人类癌症中的作用是值得的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Impact of the AKT1 rs1130233 SNP in Japanese GastrointestinalCancer Patients with Palliative Care
Objective: Cancer patients often suffer from chronic inflammation, anorexia and the resultant decrease of nutrient intake, followed by weight loss and muscle wasting called “sarcopenia”. Such conditions are known as “cachexia”. In this study, we examined the associations between genetic polymorphisms of AKT1 rs1130233, ICAM1 rs281432, SELP rs6128 and TNSRSF1A rs4149570, which are reportedly associated with cachexia in Caucasians, together with LIF rs929271, in Japanese gastrointestinal cancer patients with palliative care. Methods: The study subjects were 59 patients (37 males and 22 females) with gastrointestinal cancers who visited the outpatient clinic at Iga General Hospital from December 2011 till August 2015. Genotypings for AKT1 rs1130233, ICAM1 rs281432, SELP rs6128, TNSRSF1A rs4149570 and LIF rs929271 were conducted with polymerase chain reaction with confronting two-pair primers (PCR-CTPP) or the Taqman SNP Genotyping assay. Associations of these SNPs with patients’ prognosis as well as weight loss defined as weight loss more than 5 percent during 6 months after the initiation of chemotherapy were evaluated. Results: A significant increase in the risk of 5% weight loss was observed in those with A/G genotype AKT1 rs1130233 polymorphism (AKT1 A/G vs. G/G, adjusted odds ratio [aOR]=7.11; 95%CI: 1.41-35.7), or in those with at least one A allele of AKT1 rs1130233 (AKT1 A/G+A/A vs. G/G, aOR=4.57; 95% CI: 1.14-18.3) when adjusted for age, sex and UICC clinical stage 4. There was no statistically significant correlation of the polymorphisms examined with patients’ survival. Conclusion: The present study revealed that AKT1 rs1130233 A allele may play a key role in the development of cancer cachexia. Given the involvement of AKT1 in the development of cancer as well as in apoptosis, it would be worth studying the roles of this molecule in human cancers further from clinical, epidemiological and biological viewpoints in the near future.
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