Jin Qin, Liu Gang, Bao Luri, Ma Yuzhen, Qi Huidong, Yun Zhizhong, Dai Yanfeng, Zhang Shu
Department of Pathology, Affiliated Hospital of Nantong University, Nantong, People's Republic of China,
State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, College of Life Science, Inner Mongolia University, Hohhot, People's Republic of China,
Cancer Manag Res. 2018 Aug 16;10:2757-2765. doi: 10.2147/CMAR.S169329. eCollection 2018.
Spy1 (SPDYA) is a new discovered cell cycle protein capable of promoting cell proliferation dependent on cyclin-dependent kinase-2 activation. However, to the best of our knowledge, the expression of Spy1 in colorectal cancer (CRC) tissues remains virtually unknown.
In this retrospective study, we investigated the mRNA and protein expression levels of Spy1 in CRC tissues and corresponding non-cancerous tissues with the analyses of quantitative real-time polymerase chain reaction, western blotting, and immunohistochemistry. In our research, the prognostic significances of Spy1 expression were further explored by univariate and multivariate survival analyses of 203 patients who were followed up.
The results demonstrated that the levels of mRNA were significantly higher in CRC tissues compared with corresponding non-cancerous tissues (=0.0002). The results of immunohistochemistry demonstrated that the expressions of Spy1 were significantly associated with clinicopathological parameters, including T stage (=7.126, =0.028) and TNM stage (=9.461, =0.009). Kaplan-Meier analysis results indicated that high Spy1 expression (HR=2.573, <0.001) and TNM stage (HR=1.494, =0.011) were independent factors to predict poor prognosis for patients with CRC.
We concluded that high Spy1 expression is significantly associated with unfavorable prognosis in CRC and could serve as a potential prognostic marker in clinical diagnosis of CRC.
Spy1(SPDYA)是一种新发现的细胞周期蛋白,能够依赖细胞周期蛋白依赖性激酶2的激活来促进细胞增殖。然而,据我们所知,Spy1在结直肠癌(CRC)组织中的表达情况几乎未知。
在这项回顾性研究中,我们通过定量实时聚合酶链反应、蛋白质免疫印迹法和免疫组织化学分析,研究了Spy1在CRC组织及相应癌旁组织中的mRNA和蛋白质表达水平。在我们的研究中,通过对203例接受随访患者的单因素和多因素生存分析,进一步探讨了Spy1表达的预后意义。
结果表明,CRC组织中的mRNA水平显著高于相应的癌旁组织(P = 0.0002)。免疫组织化学结果表明,Spy1的表达与临床病理参数显著相关,包括T分期(P = 7.126,P = 0.028)和TNM分期(P = 9.461,P = 0.009)。Kaplan-Meier分析结果表明,Spy1高表达(HR = 2.573,P < 0.001)和TNM分期(HR = 1.494,P = 0.011)是预测CRC患者预后不良的独立因素。
我们得出结论,Spy1高表达与CRC患者的不良预后显著相关,可作为CRC临床诊断中潜在的预后标志物。