Ru Yi, Chen Xiao-Jie, Zhao Zhi-Wei, Zhang Peng-Fei, Feng Shuai-Hao, Gao Qiang, Gao She-Gan, Feng Xiao-Shan
The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology , Luoyang, Henan 471003, China.
Medical College, Henan University of Science and Technology , Luoyang, Henan 471003, China.
Oncotarget. 2017 May 19;8(43):73860-73870. doi: 10.18632/oncotarget.18008. eCollection 2017 Sep 26.
This study aims to investigate the expression and significance of p57 and cyclinD1 in gastric cardia adenocarcinoma (GCA). p57 is a negative regulator in the cell cycle. On the contrary, cyclinD1 is a positive regulator of cell cycle progression.
Thirty-two cases of GCA tissues and adjacent non-cancerous tissues were collected for this study. Immunohistochemistry and fluorescence qualitative PCR was used to determine the level of p57 and cyclinD1 in GCA and its adjacent non-cancerous tissues. Furthermore, the correlation between the mRNA/protein and GCA clinical pathologic parameters were analyzed, and the relationship of p57 and cyclinD1 in GCA were also evaluated.
The expression of p57 significantly lower in GCA ( = 0.036), and there was a significant correlation in the different degrees of differentiation ( < 0.05). Furthermore, median survival time was 41 months for patients with high mRNA expression of p57. This was longer compared to patients with low mRNA expression of P57 (37 months, X = 4.788, = 0.029).The expression of cyclinD1 was significantly higher in GCA( = 0.002), and was significant correlated to clinical stage(P<0.05). Median survival time was 34 months in patients with high mRNA expression of cyclinD1, which was shorter than in patients with low expression of cyclinD1 mRNA (41 months, X = 4.071, = 0.044). The protein expression of p57 was not correlated to the protein expression of cyclinD1 ( = 0.55).
The expression of p57 and cyclinD1 are likely to suppress or promote the tumorigenesis and progression of GCA.
本研究旨在探讨p57和细胞周期蛋白D1(cyclinD1)在贲门腺癌(GCA)中的表达及其意义。p57是细胞周期中的负调节因子。相反,cyclinD1是细胞周期进程的正调节因子。
本研究收集了32例GCA组织及其癌旁非癌组织。采用免疫组织化学和荧光定量PCR检测GCA及其癌旁非癌组织中p57和cyclinD1的水平。此外,分析mRNA/蛋白与GCA临床病理参数之间的相关性,并评估GCA中p57和cyclinD1的关系。
p57在GCA中的表达显著降低(P = 0.036),且在不同分化程度中存在显著相关性(P<0.05)。此外,p57 mRNA高表达患者的中位生存时间为41个月。与p57 mRNA低表达患者(37个月,X = 4.788,P = 0.029)相比,该时间更长。cyclinD1在GCA中的表达显著升高(P = 0.002),且与临床分期显著相关(P<0.05)。cyclinD1 mRNA高表达患者的中位生存时间为34个月,短于cyclinD1 mRNA低表达患者(41个月,X = 4.071,P = 0.044)。p57的蛋白表达与cyclinD1的蛋白表达无相关性(P = 0.55)。
p57和cyclinD1的表达可能分别抑制或促进GCA的肿瘤发生和进展。