Fanaei Khadijeh, Ameli Fereshteh, Salahshourifar Iman, Irani Shiva, Esfandbod Mohsen
Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Department of Pathology, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
Iran J Public Health. 2024 Feb;53(2):462-471. doi: 10.18502/ijph.v53i2.14931.
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.
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.
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 nontumoral (marginal) tissues (<0.001). The difference in expression of survivin mRNA was not significant between metastatic and non-metastatic tumor tissues (=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 (<0.001) and between metastatic and non-metastatic tumor tissues (<0.001). There was no significant association between survivin mRNA expression and clinicopathological variables. However, survivin protein expression was significantly correlated with perineural involvement (<0.018).
This data could be supportive of using survivin as a useful diagnostic marker in GC. Although, more research is needed in this area.
如今,生存素被认为是最具特异性的癌症蛋白之一;它提供了独特且实用的研究机会。生存素在胃癌(GC)中的临床价值尚未明确。为了确定伊朗GC患者中生存素的表达水平及其诊断价值,我们评估了生存素表达与临床病理因素之间的关联。
2008年至2018年期间,在伊朗德黑兰招募了60例配对的正常对照和60例GC样本,其中30例在我们研究时已有转移证据,30例无转移证据。通过定量实时聚合酶链反应(qRT-PCR)和免疫组织化学(IHC)研究评估生存素表达。
分别在86.7%和71.6%的病例中发现生存素在mRNA和蛋白水平上表达增加。证据表明肿瘤组织与非肿瘤(边缘)组织之间生存素mRNA表达水平存在显著差异(<0.001)。转移瘤组织与非转移瘤组织之间生存素mRNA表达差异不显著(=0.171)。观察到生存素的阳性免疫反应主要在肿瘤细胞核中。在肿瘤组织与非肿瘤组织之间(<0.001)以及转移瘤组织与非转移瘤组织之间(<0.001)检测到生存素蛋白表达存在显著差异。生存素mRNA表达与临床病理变量之间无显著关联。然而,生存素蛋白表达与神经周围侵犯显著相关(<0.018)。
这些数据可能支持将生存素用作GC的有用诊断标志物。尽管如此,该领域仍需要更多研究。