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五种蛋白组合的免疫组化表达在亚洲口腔癌中显示为预后标志物

Immunohistochemical Expression of Five Protein Combinations Revealed as Prognostic Markers in Asian Oral Cancer.

作者信息

Wang Hui-Ching, Chiang Chien-Jung, Liu Ta-Chih, Wu Chun-Chieh, Chen Yi-Ting, Chang Jan-Gowth, Shieh Grace S

机构信息

Graduate Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.

Division of Hematology and Oncology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.

出版信息

Front Genet. 2021 Apr 15;12:643461. doi: 10.3389/fgene.2021.643461. eCollection 2021.

Abstract

Oral squamous cell carcinoma (OSCC) has a high mortality rate (∼50%), and the 5-year overall survival rate is not optimal. Cyto- and histopathological examination of cancer tissues is the main strategy for diagnosis and treatment. In the present study, we aimed to uncover (IHC) markers for prognosis in Asian OSCC. From the collected 742 synthetic lethal gene pairs (of various cancer types), we first filtered genes relevant to OSCC, performed 29 IHC stains at different cellular portions and combined these IHC stains into 398 distinct pairs. Next, we identified novel prognostic markers in OSCC among Taiwanese population, from the single and paired IHC staining by univariate Cox regression analysis. Increased nuclear expression of RB1 [RB1(N)↑], CDH3(C)↑-STK17A(N)↑ and FLNA(C)↑-KRAS(C)↑were associated with survival, but not independent of tumor stage, where C and N denote cytoplasm and nucleus, respectively. Furthermore, multivariate Cox regression analyses revealed that CSNK1E(C)↓-SHC1(N)↓ ( = 5.9 × 10; recommended for clinical use), BRCA1(N)↓-SHC1(N)↓ ( = 0.030), CSNK1E(C)↓-RB1(N)↑ ( = 0.045), [CSNK1E(C)-SHC1(N), FLNA(C)-KRAS(C)] ( = 0.000, rounded to three decimal places) and [BRCA1(N)-SHC1(N), FLNA(C)-KRAS(C)] ( = 0.020) were significant factors of poor prognosis, independent of lymph node metastasis, stage and alcohol consumption. An external dataset from The Cancer Genome Atlas HNSCC cohort confirmed that ↑-↑ was a significant predictor of poor survival. Our approach identified prognostic markers with components involved in different pathways and revealed IHC marker pairs while neither single IHC was a marker, thus it improved the current state-of-the-art for identification of IHC markers.

摘要

口腔鳞状细胞癌(OSCC)死亡率很高(约50%),5年总生存率并不理想。癌组织的细胞和组织病理学检查是诊断和治疗的主要策略。在本研究中,我们旨在发现亚洲OSCC预后的免疫组化(IHC)标志物。从收集的742对(各种癌症类型的)合成致死基因对中,我们首先筛选出与OSCC相关的基因,在不同细胞部位进行29次IHC染色,并将这些IHC染色组合成398个不同的对。接下来,我们通过单变量Cox回归分析,从台湾人群的单重和配对IHC染色中识别出OSCC新的预后标志物。RB1核表达增加[RB1(N)↑]、CDH3(C)↑-STK17A(N)↑和FLNA(C)↑-KRAS(C)↑与生存相关,但不独立于肿瘤分期,其中C和N分别表示细胞质和细胞核。此外,多变量Cox回归分析显示,CSNK1E(C)↓-SHC1(N)↓(=5.9×10;推荐临床使用)、BRCA1(N)↓-SHC1(N)↓(=0.030)、CSNK1E(C)↓-RB1(N)↑(=0.045)、[CSNK1E(C)-SHC1(N),FLNA(C)-KRAS(C)](=0.000,四舍五入到三位小数)和[BRCA1(N)-SHC1(N),FLNA(C)-KRAS(C)](=0.020)是预后不良的显著因素,独立于淋巴结转移、分期和饮酒情况。来自癌症基因组图谱头颈部鳞状细胞癌队列的一个外部数据集证实,↑-↑是生存不良的显著预测指标。我们的方法识别出了涉及不同途径成分的预后标志物,并揭示了IHC标志物对,而单个IHC均不是标志物,因此改进了当前识别IHC标志物的技术水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9e8/8083901/e85dd9c015a1/fgene-12-643461-g001.jpg

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