评估 Survivin 的免疫组化表达及其与 qRT-PCR 结果的相关性,以此作为胃癌的有效诊断标记物

Khadijeh Fanaei, Fereshteh Ameli, Iman Salahshourifar, Shiva Irani, Mohsen Esfandbod
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摘要

背景:如今,存活素被认为是最具特异性的癌症蛋白之一;它提供了独特而实用的研究机会。存活素在胃癌(GC)中的临床价值尚未确定。为了确定存活素在伊朗 GC 患者中的表达水平及其诊断价值,我们评估了存活素表达与临床病理因素的关联。研究方法2008年至2018年期间,我们在伊朗德黑兰招募了60名匹配的正常对照者和60个GC样本,其中包括30个在我们研究时有转移证据的病例和30个没有转移证据的病例。通过定量实时聚合酶链反应(qRT-PCR)和免疫组化(IHC)研究评估了 Survivin 的表达。结果显示分别有 86.7% 和 71.6% 的病例发现存活素在 mRNA 和蛋白质水平的表达增加。有证据表明,肿瘤组织和非肿瘤组织(边缘组织)的存活素 mRNA 表达水平存在明显差异(P<0.001)。转移性和非转移性肿瘤组织中存活素 mRNA 的表达差异不显著(P=0.171)。存活素的阳性免疫反应主要出现在肿瘤细胞的细胞核中。在肿瘤组织和非肿瘤组织之间(P<0.001)以及转移性肿瘤组织和非转移性肿瘤组织之间(P<0.001),发现存活素蛋白表达存在明显差异。存活素 mRNA 表达与临床病理变量之间无明显关联。然而,survivin 蛋白表达与神经周围受累明显相关(P<0.018)。结论:这些数据支持将存活素作为 GC 的有用诊断标志物。尽管在这一领域还需要更多的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Immunohistochemical Expression of Survivin and its Correlation with qRT-PCR Results as a Useful Diagnostic Marker in Gastric Cancer
Background: Today, survivin is known as one of the most specific cancer proteins; provide unique and practical study opportunities. Clinical value of survivin in gastric cancer (GC) is not yet appointed. To establish the expression level of survivin and its diagnosis value in Iranian patients with GC, we evaluated the association of survivin expression with clinicopathologic factors. Methods: Overall, 60 matched-normal controls with 60 GC samples including 30 cases with evidence of metastasis at time of our study and 30 cases without evidence of metastasis were recruited, in Tehran, Iran during 2008 to 2018. Survivin expression was evaluated by quantitative Real-time polymerase chain reaction (qRT-PCR) and immunohistochemistry (IHC) study. Results: Increased expression of survivin at mRNA and protein levels was found in 86.7% and 71.6% of cases, respectively. Evidence indicated a significant difference in survivin mRNA expression level between tumor and non-tumoral (marginal) tissues (P<0.001). The difference in expression of survivin mRNA was not significant between metastatic and non-metastatic tumor tissues (P=0.171). Positive immunoreactivity of survivin was observed to be predominantly in the nucleus of tumor cells. A significant difference in survivin protein expression was detected between tumor and non-tumoral tissues (P<0.001) and between metastatic and non-metastatic tumor tissues (P<0.001). There was no significant association between survivin mRNA expression and clinicopathological variables. However, survivin protein expression was significantly correlated with perineural involvement (P<0.018). Conclusion: This data could be supportive of using survivin as a useful diagnostic marker in GC. Although, more research is needed in this area.
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