摘要
目的:研究细胞间隙连接蛋白connexin43基因(Cx43)在膀胱移行细胞癌(transitional cell carcinoma of the bladder,BTCC)组织中的表达,及其与凋亡相关基因bcl-2、bax表达的相关性。方法:分别采用逆转录聚合酶链反应(RT-PCR)和免疫组织化学法检测60例BTCC中Cx43 mRNA和bcl-2、bax蛋白的表达,并与癌旁组织、正常膀胱组织各15例进行对照。结果:60例BTCC组织中Cx43 mRNA的表达率为43.33%,显著低于癌旁组织和正常膀胱组织的表达率73.33%及100%(χ2=17.58,P<0.01)。Cx43的表达与肿瘤的病理分级和淋巴转移均呈显著负相关(χ2=9.33和9.74,P均<0.01),而与患者性别、年龄、临床分期、肿瘤直径和肿瘤生长方式等均无相关性(P均>0.05)。相关性检验表明Cx43与bcl-2蛋白表达呈显著负相关(r=-0.63,P<0.01),而与bax蛋白表达则呈正相关(r=0.52,P<0.01)。结论:Cx43在BTCC组织中的表达下调提示其与膀胱癌的发生发展和侵袭转移密切相关,可作为判断其预后的重要参考指标。Cx43基因可能与凋亡相关基因bcl-2、bax在膀胱移行细胞癌的发生发展中分别起拮抗和协同作用。
Objective :To study the expression of connexin43 (Cx43) gene and its correlation with the expression of apoptosis related genes bcl-2 and bax in transitional cell carcinoma of the bladder ( BTCC ), and to investigate the role of Cx43 in the BTCC. Methods: Reverse transcription polymerase chain reaction was used to detect the expression of Cx43 mRNA and immunocytochemistry technique was used to detect the expression of bcl-2 and bax proteins in 60 cases of BTcc tissue, and compared with that of 15 cases of pericancerous tissue and 15 cases of normal bladder tissue. Results: The positive rate of Cx43 mRNA expression in 60 cases of BTCC tissues was 43.33% which was significantly lower than that in pericancerous tissues (73.33%) and normal tissues (100%) (x^2 = 17.58, P 〈 0.01 ). The expression of Cx43 had significant negative correlation with the pathological degree and lymph node metastasis of BTCC (x^2 = 9.33 and 9.74, respectively, P 〈 0.01 ). However, no correlation was found between the expression of Cx43 and the sex, age, clinical staging, and the diameter and the growth pattern of BTCC ( P 〉 0.05 ). Expression of Cx43 negatively correlated with bcl-2 protein ( r = 0.63, P 〈 0.01 ) and positively correlated with bax protein ( r = 0.52, P 〈 0.01 ). Conclusion: The down-regulated expression of Cx43 gene was closely associated with the development, invasion and metastasis of BTCC. It could be used a prognostic indicator for BTCC. Cx43 gene may have antagonistic effects with bcl-2 gene and synergistic effects with bax gene in the initiation and progression of BTCC.
出处
《肿瘤》
CAS
CSCD
北大核心
2007年第5期398-401,共4页
Tumor