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formin-like 2 是鼻咽癌预后不良的潜在生物标志物。

Formin-Like 2 Is a Potential Biomarker of Poor Prognosis in Nasopharyngeal Carcinoma.

机构信息

Department of Radiation Oncology, Chi Mei Medical Center, Liouying, Taiwan.

Department of Radiation Oncology, Chi Mei Medical Center, Tainan, Taiwan.

出版信息

Oncology. 2022;100(9):475-484. doi: 10.1159/000525682. Epub 2022 Jun 30.

Abstract

Nasopharyngeal carcinoma (NPC) is the most common malignant tumor in southern China and Southeast Asia. Although substantial research on NPC has been conducted, the resulting improvement in clinical outcomes remains very disappointing. NPC treatment typically involves radiation therapy and chemotherapy, but the high incidence of metastasis and recurrence in NPC patients result in poor survival. Therefore, identifying potential biomarkers and discovering therapeutic targets are necessary to design tailored treatments based on the genetic profiles of NPC patients. Correlations of protein immunostaining with clinicopathological features were analyzed by Pearson's χ test. The Kaplan-Meier method with a log-rank test was used to generate survival curves. Multivariate analysis was performed using the Cox proportional hazards model. In this study, we comparatively analyzed cytoskeletal organization and biogenesis (GO:0007010) and tumorigenesis in the NPC transcriptome (GSE12452) and found that formin-like 2 () expression was significantly upregulated in NPC tumor tissues. Moreover, high FMNL2 expression was significantly correlated with primary tumor stage ( = 0.001), lymph node status ( = 0.004), cancer stage ( = 0.006), and histological grade ( = 0.040). More importantly, high FMNL2 expression was significantly correlated with poor survival in NPC patients according to univariate analysis and multivariate analysis. This study reveals that FMNL2 may be an important potential biomarker for evaluating the prognosis of NPC patients.

摘要

鼻咽癌(NPC)是中国南方和东南亚地区最常见的恶性肿瘤。尽管对 NPC 进行了大量研究,但临床结果的改善仍然非常令人失望。NPC 的治疗通常涉及放射治疗和化学疗法,但 NPC 患者的高转移和复发率导致生存状况不佳。因此,确定潜在的生物标志物和发现治疗靶点对于根据 NPC 患者的基因谱设计针对性治疗是必要的。通过 Pearson χ检验分析蛋白免疫染色与临床病理特征的相关性。采用对数秩检验的 Kaplan-Meier 方法生成生存曲线。使用 Cox 比例风险模型进行多变量分析。在这项研究中,我们比较分析了 NPC 转录组中的细胞骨架组织和生物发生(GO:0007010)和肿瘤发生(GSE12452),发现肌动蛋白样 2()在 NPC 肿瘤组织中表达显著上调。此外,高表达与原发性肿瘤分期(=0.001)、淋巴结状态(=0.004)、癌症分期(=0.006)和组织学分级(=0.040)显著相关。更重要的是,根据单因素分析和多因素分析,高表达与 NPC 患者的不良预后显著相关。这项研究表明,FMNL2 可能是评估 NPC 患者预后的一个重要潜在生物标志物。

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