BRAF和KRAS基因在鼻息肉病中的表达评价。

IF 0.7 Q4 OTORHINOLARYNGOLOGY
Gül Özbilen Acar, Filiz Özen, Halil İbrahim Yıldırım, Osman İlkay Özdamar, Tolga Çiçek
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引用次数: 0

摘要

目的:探讨Kirsten大鼠肉瘤病毒癌基因同源物(KRAS)和B-raf原癌基因(BRAF)基因在鼻息肉病(NP)中的表达模式及其潜在关系。方法:29例患者纳入研究。在每次手术中从鼻息肉中收集小穿孔活检,并立即在液氮中冷冻。术中还从患者的下鼻甲或鼻中隔粘膜作为对照组进行了穿刺活检,这些样本也被冷冻。用TRIzol试剂分离总核糖核酸(RNA)。采用实时聚合酶链反应法对KRAS和BRAF基因进行基因表达分析。结果:与对照组相比,29例患者中有21例KRAS鼻息肉基因表达升高,8例表达降低。经统计学分析,鼻息肉组与对照组的差异有统计学意义(p=0.023)。与KRAS一样,6例患者BRAF基因表达减少,23例患者BRAF基因表达增加(p=0.011)。结论:我们的研究结果提示BRAF和KRAS基因表达与NP之间存在潜在的关联,但需要进一步的研究来证实这种关系。这一发现表明NP的遗传背景可能是一个促成因素,其中BRAF和KRAS突变发挥了作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of BRAF and KRAS Gene Expression in Nasal Polyposis.

Objective: The goal of this study was to investigate the expression patterns and potential relationship of the Kirsten rat sarcoma viral oncogene homolog (KRAS) and B-raf proto-oncogene (BRAF) genes in nasal polyposis (NP).

Methods: Twenty-nine patients were included in the study. Small punch biopsies were collected from nasal polyps during each operation and immediately frozen in liquid nitrogen. Punch biopsies were also taken during surgery from the inferior turbinate or the septum mucosa of the patients as a control group, and these samples were also frozen. Total ribonucleic acid (RNA) was isolated using TRIzol reagent. The gene expression analyses of the KRAS and BRAF genes were performed by the real-time polymerase chain reaction method.

Results: When compared to control subjects, KRAS nasal polyp gene expression increased in 21, but decreased in eight of the 29 patients. This statistical analysis revealed a statistically significant difference between the nasal polyp group and the controls (p=0.023). Like KRAS, a decrease was observed in BRAF gene expression in six, and an increase in 23 patients (p=0.011).

Conclusion: Our findings suggest a potential association between BRAF and KRAS genes expression and NP, but further studies are needed to confirm this relationship. This finding suggests that the genetic background of NP could be a contributing factor, with the BRAF and KRAS mutations playing a role.

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