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头颈部鳞状细胞癌癌症干细胞特征的鉴定

Identification of a Cancer Stem Cells Signature of Head and Neck Squamous Cell Carcinoma.

作者信息

Wu Zeng-Hong, Li Cheng, Zhang You-Jing, Zhou Wen

机构信息

Department of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Department of Otolaryngology Head and Neck Surgery, The Central Hospital of Wuhan, Tongji Medical College Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Genet. 2022 May 11;13:814777. doi: 10.3389/fgene.2022.814777. eCollection 2022.

Abstract

Head and neck squamous cell carcinoma (HNSCC) ranks as the sixth most widespread and deadly cancer. In recent times, it has been determined that undifferentiated cell populations with stem cell-like properties in HNSCC are major factors influencing recurrence and progression. In this study, we determine key genes related to stemness by merging WGCNA with HNSCC mRNAsi based on the online database. We first download the mRNA expression-based stemness index (mRNAsi) data and contrast the expression levels of mRNAsi in cancers and control samples; we found significantly elevated mRNAsi expressions in HNSCC tissues ( = 0.002). Moreover, the brown module showed a relatively high negative correlation with mRNAsi (cor = -0.8). Thus, we selected the brown module as the interesting module and used it for following analysis. We screened 20 key genes (PDGFRB, PLPP4, CALU, ADAMTS14, COL5A3, KCNE4, LOXL1, CLEC11A, PODN,BGN, AEBP1, COL1A2, LAMA4, LOXL2, LRRC15, THY1, SPON2, COL1A1, NID2, and AC134312.5) including and as to decide the neighbor genes biological interaction network of these 20 stemness-related genes in HNSCC. The top 10 frequent alterations were PIK3CA, FGF3, FGF19, FGF4, DVL3, P3H2, GNB4, COL22A1, COL14A1, and PLOD2. This study showed the critical role of stemness-related genes in HNSCC. However, more related studies are needed to confirm these results.

摘要

头颈部鳞状细胞癌(HNSCC)是第六大常见且致命的癌症。近年来,已确定HNSCC中具有干细胞样特性的未分化细胞群是影响复发和进展的主要因素。在本研究中,我们基于在线数据库将加权基因共表达网络分析(WGCNA)与HNSCC的mRNA干性指数(mRNAsi)相结合,以确定与干性相关的关键基因。我们首先下载基于mRNA表达的干性指数(mRNAsi)数据,并对比癌症样本和对照样本中mRNAsi的表达水平;我们发现HNSCC组织中mRNAsi表达显著升高(P = 0.002)。此外,棕色模块与mRNAsi呈现出相对较高的负相关性(相关系数 = -0.8)。因此,我们选择棕色模块作为感兴趣的模块并用于后续分析。我们筛选出20个关键基因(血小板衍生生长因子受体β(PDGFRB)、磷脂磷酸酶4(PLPP4)、钙结合蛋白(CALU)、凝血酶敏感素14(ADAMTS14)、Ⅴ型胶原α3链(COL5A3)、钾通道蛋白家族成员4(KCNE4)、赖氨氧化酶1(LOXL1)、C型凝集素结构域家族11成员A(CLEC11A)、骨桥蛋白(PODN)、基底膜蛋白聚糖(BGN)、脂肪细胞增强结合蛋白1(AEBP1)、Ⅰ型胶原α2链(COL1A2)、层粘连蛋白α4(LAMA4)、赖氨氧化酶2(LOXL2)、富含亮氨酸重复序列蛋白15(LRRC15)、甲状腺抗原1(THY1)、血小板反应蛋白2(SPON2)、Ⅰ型胶原α1链(COL1A1)、巢蛋白2(NID2)和AC134312.5),并确定这些HNSCC中20个与干性相关基因的邻近基因生物相互作用网络。前10个常见的改变基因是磷脂酰肌醇-4,5-二磷酸3-激酶催化亚基α(PIK3CA)、成纤维细胞生长因子3(FGF3)、成纤维细胞生长因子19(FGF19)、成纤维细胞生长因子4(FGF4)、无翅型MMTV整合位点家族成员3(DVL3)、脯氨酰3-羟化酶2(P3H2)、鸟嘌呤核苷酸结合蛋白β亚基4(GNB4)、ⅩⅩⅡ型胶原α1链(COL22A1)、ⅩⅣ型胶原α1链(COL14A1)和赖氨酰羟化酶2(PLOD2)。本研究显示了干性相关基因在HNSCC中的关键作用。然而,需要更多相关研究来证实这些结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b8/9132479/19965e9d3ebf/fgene-13-814777-g001.jpg

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