王晓芳, 陶仪声, 柴大敏. 细胞周期素G1和G2在人食管鳞状细胞癌中的表达及其临床意义[J]. 中国肿瘤临床, 2011, 38(15): 894-897. DOI: 10.3969/j.issn.1000-8179.2011.15.007
引用本文: 王晓芳, 陶仪声, 柴大敏. 细胞周期素G1和G2在人食管鳞状细胞癌中的表达及其临床意义[J]. 中国肿瘤临床, 2011, 38(15): 894-897. DOI: 10.3969/j.issn.1000-8179.2011.15.007
Xiaofang WANG, Yisheng TAO, Damin CHAI. Expression and Clinical Significance of Cyclin G1 and Cyclin G2 in Human Esophageal Squamous Cell Carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2011, 38(15): 894-897. DOI: 10.3969/j.issn.1000-8179.2011.15.007
Citation: Xiaofang WANG, Yisheng TAO, Damin CHAI. Expression and Clinical Significance of Cyclin G1 and Cyclin G2 in Human Esophageal Squamous Cell Carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2011, 38(15): 894-897. DOI: 10.3969/j.issn.1000-8179.2011.15.007

细胞周期素G1和G2在人食管鳞状细胞癌中的表达及其临床意义

Expression and Clinical Significance of Cyclin G1 and Cyclin G2 in Human Esophageal Squamous Cell Carcinoma

  • 摘要: 探讨细胞周期素G1和G2(Cyclin G1,G2)在人类食管鳞状细胞癌中的表达及其临床意义。方法:收集2007年2月至2008年5月间蚌埠医学院第一附属医院病理科食管鳞状细胞癌存档蜡块60例,正常食管黏膜组织20例,所收集病例均有完整临床和病理资料。采用免疫组织化学Elivision染色方法检测上述组织中细胞周期素G1和G2的表达情况。结果:细胞周期素G1在食管鳞状细胞癌组织中表达的阳性率(61.7%)显著高于正常食管黏膜的阳性率25.0%(P<0.05),细胞周期素G2在食管鳞状细胞癌组织中表达阳性率(66.7%)显著低于正常食管黏膜的阳性率(90.0%)(P<0.05),两者的表达情况均与肿瘤组织的分化程度及有无淋巴结转移有相关性(P<0.05);食管鳞状细胞癌组织中细胞周期素G1和G2的表达呈显著负相关(P<0.05)。结论:随着食管鳞癌中Cyclin G1表达的增高,Cyclin G2的表达却下降,提示Cyclin G1和Cyclin G2相互之间存在负相调节作用,两者在食管鳞状细胞癌的发生、发展中具有重要作用。

     

    Abstract: Abstract Objective: To investigate the expression and clinical significance of cyclin G1 and cyclin G2 in human esophageal squamous cell carcinoma ( ESCC ). Methods: A total of 60 paraffin-blocked ESCC specimens filed in the Department of Pathology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, China from 2007 to 2008 were enrolled in our study, in which 20 cases were normal esophageal mucosa. All the enrolled cases have complete clinical and pathologic data. Immunohistochemical Elivision staining was used to assay cyclin G1 and cyclin G2 expression in the aforementioned tissues. Results: The cyclin G1 was positive in 61.7% of the ESCC cases, which is apparently higher than that in normal esophageal mucosa ( 25.0%; P < 0.05 ). In addition, the positive rate of cyclin G2 was significantly lower in ESCC ( 66.7% ) than in the normal esophageal mucosa ( 90.0 % ) ( P < 0.05 ). In ESCC, cyclin G1 expression is negatively correlated with that of cyclin G2 ( P < 0.05 ). Conclusion: With the increase in cyclin G1 expression in esophageal squamous cells, the expression of cyclin G2 protein decreases, which suggests a mutual negative feedback mechanism between cyclin G1 and G2. Both proteins play an important role in the occurrence and progression of ESCC.

     

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