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细胞周期蛋白 H 和细胞周期依赖性激酶 7 表达水平降低可抑制人食管鳞癌细胞的增殖。

Low expression of cyclinH and cyclin-dependent kinase 7 can decrease the proliferation of human esophageal squamous cell carcinoma.

机构信息

Department of Immunology, Medical College, Nantong University, 19 Qi-Xiu Road, Nantong 226001, Jiangsu, People's Republic of China.

出版信息

Dig Dis Sci. 2013 Jul;58(7):2028-37. doi: 10.1007/s10620-013-2597-x. Epub 2013 Mar 2.

Abstract

BACKGROUND

Increased expression of cyclinH (CCNH) and cyclin-dependent kinase 7 (CDK7) has a relationship with poor prognosis in most human cancers.

AIM

Investigate the expression of CCNH and CDK7 in human esophageal squamous cell carcinoma (ESCC) and the effect of chemotherapy on their expression.

METHODS

Western blotting and immunohistochemistry were used to measure the expression of CCNH and CDK7 proteins in ESCC and adjacent normal tissue in 98 patients. We use Cell Counting Kit-8 and cell flow to analyze the effects of cisplatin and interference of CCNH and CDK7 in cell cycle process.

RESULTS

Immunohistochemical analysis showed that CCNH and CDK7 expression were significantly associated with unfavorable clinicopathologic variables. CCNH and CDK7 protein levels were elevated in ESCC tissues in comparison with adjacent normal tissues. Survival analysis revealed that CCNH and CDK7 overexpression were significantly associated with overall survival (P < 0.001). Cisplatin or interference of CCNH or CDK7 led cells to grow slowly. Overexpression of CCNH and CDK7 in TE1 cells can lead to resistance to cisplatin.

CONCLUSIONS

We can conclude that CCNH and CDK7 may play an important role in the tumorigenesis and development of ESCC. CCNH and CDK7 expression affected the chemotherapy of tumor.

摘要

背景

细胞周期蛋白 H(CCNH)和细胞周期依赖性激酶 7(CDK7)的表达增加与大多数人类癌症的预后不良有关。

目的

研究 CCNH 和 CDK7 在人食管鳞状细胞癌(ESCC)中的表达及化疗对其表达的影响。

方法

采用 Western blot 和免疫组织化学法检测 98 例 ESCC 及癌旁正常组织中 CCNH 和 CDK7 蛋白的表达,用细胞计数试剂盒-8 和细胞流式检测顺铂及 CCNH、CDK7 干扰对细胞周期进程的影响。

结果

免疫组化分析显示,CCNH 和 CDK7 的表达与不良临床病理变量显著相关。与癌旁正常组织相比,ESCC 组织中 CCNH 和 CDK7 蛋白水平升高。生存分析显示,CCNH 和 CDK7 过表达与总生存期显著相关(P<0.001)。顺铂或 CCNH 或 CDK7 的干扰可导致细胞生长缓慢。CCNH 和 CDK7 的过表达可导致 TE1 细胞对顺铂产生耐药性。

结论

CCNH 和 CDK7 可能在 ESCC 的发生发展中起重要作用。CCNH 和 CDK7 的表达影响肿瘤的化疗效果。

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