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鼻咽癌中TGF-β/Smad信号通路分子的表达及意义

Expression of TGF-β/Smad Signal Transduction Pathway Members and Their Significance in Nasopharyngeal Carcinoma

  • 摘要: 目的 探讨TGF-β/Smad信号通路关键分子TGF-β1、TGF-β2、Smad7及其下游的转录因子RUNX3在鼻咽癌(Nasopharyngeal Carcinoma,NPC)中的表达,并分析它们的相关性及与NPC临床病理特征的关系。 方法 采用免疫组织化学SP法检测50例NPC和20例鼻咽慢性炎组织中TGF-β/Smad信号通路各关键分子的蛋白表达情况。 结果 TGF-β1、TGF-β2、Smad7及RUNX3在NPC中的阳性率分别为42%、70%、40%、56%,在黏膜慢性炎中的阳性率分别为0、100%、0、100%,四者的表达差异均有统计学意义(P<0.05);TGF-β1、Smad7的表达与NPC的临床分期和局部浸润转移有关(P<0.05),而TGF-β2、RUNX3与分期和局部浸润转移则无明显关系(P>0.05),TGF-β1与Smad7的表达呈正相关(rs=0.6286, P<0.05),TGF-β2则与RUNX3的表达呈正相关 (rs=0.4748, P<0.05);四者在性别、年龄和组织学分级的表达差异无统计学意义(P>0.05)。 结论 TGF-β1和Smad7在NPC中的表达上调,两者呈正相关,可能共同参与了NPC的发生、发展;TGF-β2和RUNX3的表达下调,呈正相关关系,则可能协同作用,是影响NPC进展的保护性因子,而它们相互的作用机制则有待进一步研究。

     

    Abstract: Objective To observe the expression of TGF-β1,TGF-β2, Smad7,key members of TGF-β/Smad signal transduction pathway, and it's downstream transcription factor RUNX3 in Nasopharyngeal Carcinoma(NPC), and analyze their internal relationship and their relationship with the clinicopathologic parameters of NPC patients. Methods The protein levels of the key members of TGF-β/Smad signal transduction pathway in 50 nasopharyngeal carcinoma and 20 chronic nasopharyngitis tissues were investigated with immunohistochemical SP method. Results The positive expression rate of TGF-β1、TGF-β2、Smad7 and RUNX3 in 50 nasopharyngeal carcinoma was 42%、70%、40% and 56% respectively, and 0、100%、0、100% in 20 chronic nasopharyngitis tissues. Each of these four factors has statistical difference between the two groups(P<0.05). The expression of TGF-β1 and Smad7 was correlated with tumor's clinical stage and local infiltration or metastasis (P<0.05), however,TGF-β2 and RUNX3 were not(P>0.05). TGF-β1 and Smad7 were positively related(rs=0.6286, P<0.05),and TGF-β2 and RUNX3 too (rs=0.4748, P<0.05). None of these four factors has any correlation the gender, age and histological grades(P>0.05). Conclusion In NPC, TGF-β1 and Smad7 were up-regulated expressed and positively related, and they may take part in the progression and metastasis of the cancer together; oppositely, TGF-β2 and RUNX3 were down-regulated and also positively related, which may be beneficial factors against NPC and had some cooperativeness. The mechanism of their interactions deserves further study.

     

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