Notch 2和Notch 3的表达升高与结直肠癌的疾病进展有关

A. K. Sharma, Nimisha, Apurva, Arun R K Kumar, Asgar Ali, Sundeep Singh Saluja, B. Prasad
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引用次数: 1

摘要

背景:Notch信号通路在结直肠癌(CRC)实体瘤中可能参与细胞命运决定、肿瘤异质性和血管生成。这可能进一步有助于改善结直肠癌的预后。本文分析了Notch受体基因(Notch2和Notch3)启动子甲基化及其与下游转录因子Hes1的共表达。方法:选取72例结直肠癌患者,研究Notch2、Notch3和Hes1基因在结直肠癌中的作用。分别采用甲基化特异性PCR和实时荧光定量PCR检测肿瘤和邻近正常组织启动子甲基化和mRNA表达。采用SPSS进行统计学相关分析。结果:Notch2和Notch3分别在52/72例(72.22%)和54/72例(75%)中低甲基化。Notch 2和Notch 3的低甲基化分别与晚期(p= 0.001)和(p=0.003)以及淋巴结转移(p= 0.036)和(p= 0.012)有显著相关性。49例(68.05%)和51例(70.84%)患者的Notch 2和Notch 3 mRNA表达均升高,分别为3.37倍和5.43倍。两个基因的低甲基化与表达呈正相关。Hes1高表达53例(73.61%),与notch受体基因过表达高度相关。Notch 2、Notch 3和Hes1的上调与肿瘤的高分级、肿瘤的晚期和淋巴结转移有显著相关性,另外Notch 3和Hes1与远处转移有显著相关性。结论:Notch 2和3受体的低甲基化在CRC中调控这些基因的表达中起重要作用。Notch 2、Notch 3和Hes1的过表达与结直肠癌的疾病进展有关。
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Elevated Expression of Notch 2 & Notch 3 is associated with Disease Progression in Colorectal Cancer
Background: The potential involvement of Notch signaling pathway in cell fate decision, tumor heterogeneity and angiogenesis in solid tumors can be explored in colorectal cancer (CRC). This might further help to improve outcomes in CRC. Here, the promoter methylation of Notch receptor gene ( Notch2 and Notch3 ) and their co-expression with its downstream transcription factor Hes1 has been analyzed. Methods: Seventy-two CRC patients were enrolled to study the role of Notch2 , Notch3 and Hes1 genes in colorectal cancer. Promoter methylation and mRNA expression in tumor and adjoining normal tissue were assessed by Methylation Specific PCR and quantitative Real time PCR respectively. Statistical correlation was done by using SPSS. Results: We found that Notch2 and Notch3 were hypomethylated in 52/72 (72.22%) and 54/72 (75%) cases respectively. Hypomethylation of Notch 2 and Notch 3 showed significant association with advanced stage ( p =0.001) and (p=0.003) and nodal metastasis ( p =0.036) and ( p =0.012) respectively. Both Notch 2 and Notch 3 showed increased mRNA expression in 49 (68.05%) and 51(70.84%) patients with a fold change of 3.37 and 5.43 respectively. Positive correlation between hypomethylation and expression was observed for both genes. High expression of Hes1 was found in 53(73.61%) of cases which was highly relatable with over expression of notch receptor genes. Upregulation of Notch 2, Notch 3 and Hes1 showed significant association with high grade tumors, advance stage and presence of LN metastasis, additionally Notch 3 and Hes1 showed significant association with distant metastasis. Conclusion: Hypomethylation of Notch 2 and 3 receptors is playing crucial in regulating the expression of these genes in CRC. Overexpression of Notch 2, Notch 3 and Hes1 are associated with disease progression in CRC.
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