首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Medicine >Increased expressions of integrin subunit β1 β2 and β3 in patients with cancer ------correlation analysis between risk factors of VTE and expression of core proteins
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Increased expressions of integrin subunit β1 β2 and β3 in patients with cancer ------correlation analysis between risk factors of VTE and expression of core proteins

机译:肿瘤患者整合素β1β2和β3亚基的表达增加------ VTE危险因素与核心蛋白表达的相关性分析

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摘要

Objective: Cancer is one of the most common risk factor of venous thromboembolism (VTE). Our previous studies have shown that integrin subunits β1, β2 and β3 were the core proteins of venous thrombi and potential useful biomarker of VTE. This study aimed to explore the expression status of core proteins (integrin subunits β1, β2 and β3) in cancer patients. Methods: This is a case-control study. A total of 144 inpatients (54 females) with clinically proven cancers were recruited into this study, meanwhile 200 inpatients without cancer matched in sex and age were recruited as control group. Flow cytometry was done to measure the expressions of blood integrin β1, β2, β3 and cellular immunity related variables (CD3, CD4, CD8, CD4/CD8, CD16CD56 and CD19). The association degree between increased core proteins and cancers was analyzed by calculating the relative risk (RR). Results: The expression of integrin β1 and β3 were markedly increased in patients with cancer (P=0.001 and 0.008). Integrin β2 was also mildly increased in patients with cancer (P=0.274). The relative risk ratio (RR) of increased integrin β1, β2 and β3 in cancer patients was 1.655 (95% CI: 1.321-2.074, P=0.000), 1.314 (95% CI: 1.052-1.642, P=0.021) and 1.852, (95% CI: 1.097-3.126, P=0.028), respectively. Combined analysis with integrin β1, β2 and β3 showed that the relative risk ratio (RR) of increased in cancer patients was 4.895 (95% CI: 1.645-14.563, P=0.002). CD3, CD4, CD4/CD8 and CD19 were significantly decreased (P=0.004, P=0.000, P=0.000, P=0.000, respectively) in patients with cancer, while CD8 and CD16CD56 were markedly increased in cancer patients (P=0.005, P=0.035). Conclusions: As the core proteins of venous thrombi, integrin β1 and β3 were markedly increased expression in patients with cancer, which maybe explain the increased risk of VTE in cancer patients. A weakened or disordered immune system might be the basis of VTE in condition.
机译:目的:癌症是静脉血栓栓塞(VTE)的最常见危险因素之一。我们以前的研究表明,整联蛋白亚基β1,β2和β3是静脉血栓的核心蛋白,并且是VTE的潜在有用生物标志物。本研究旨在探讨癌症患者中核心蛋白(整合素亚基β1,β2和β3)的表达状况。方法:这是一个病例对照研究。本研究共招募了144位住院患者(54位女性),这些患者已被临床证实为癌症,同时又招募了200位性别和年龄均无癌症的住院患者作为对照组。进行流式细胞术以测量血液整联蛋白β1,β2,β3的表达和细胞免疫相关变量(CD3,CD4,CD8,CD4 / CD8,CD16CD56和CD19)。通过计算相对风险(RR)分析增加的核心蛋白与癌症之间的关联度。结果:癌症患者中整联蛋白β1和β3的表达明显增加(P = 0.001和0.008)。在癌症患者中,整合素β2也轻度升高(P = 0.274)。癌症患者中整联蛋白β1,β2和β3增加的相对风险比(RR)为1.655(95%CI:1.321-2.074,P = 0.000),1.314(95%CI:1.052-1.642,P = 0.021)和1.852 ,(95%CI:1.097-3.126,P = 0.028)。整联蛋白β1,β2和β3的联合分析显示,癌症患者中升高的相对风险比(RR)为4.895(95%CI:1.645-14.563,P = 0.002)。癌症患者的CD3,CD4,CD4 / CD8和CD19显着降低(分别为P = 0.004,P = 0.000,P = 0.000,P = 0.000),而癌症患者中CD8和CD16CD56显着增加(P = 0.005 ,P = 0.035)。结论:整合素β1和β3作为静脉血栓的核心蛋白,在癌症患者中的表达明显增加,这可能解释了癌症患者VTE风险的增加。免疫系统减弱或紊乱可能是病情中VTE的基础。

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