Integrative Analysis of HMMR as a Potential Target of Prognosis and Therapy in Hepatocellular Carcinoma

Bin Yu, Qin Liu, Xuping Yang, Xin Liu, Wanlong Zhu, Xiaoyan Zhong, Heng Luo, Qimin Wei, Qingze Fan, Yilan Huang
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Abstract

Background: Previous work has indicated Hyaluronic acid-mediated motor receptor (HMMR) plays an important role in regulating tumor metastasis. However, few researchers address the clinical significance of HMMR and its underlying mechanisms for regulating hepatocellular carcinoma (HCC). This study focuses on the underlying effect of HMMR in the development and prognosis of HCC. Materials and Methods: In the present study, data of RNA and miRNA sequencing array were obtained from Oncomine dataset or The Cancer Genome Atlas (TCGA) dataset, the distinctive genomic patterns associated with HMMR expression and its correlation with prognosis were analysed by using R package. Gene set enrichment analysis (GSEA) were performed on genes expressed aberrantly. We also performed Reverse Transcription-polymerase Chain Reaction (RT-PCR), Immunohistochemical (IHC) staining and Western blotting analysis to evaluate the expression of HMMR in liver cancer cell lines or 12 HCC samples from The Affiliated Hospital of Southwest Medical University. Results: A total of 407 tumor tissue samples in TCGA dataset were evaluated, combined with analysis in Oncomine dataset, we found HMMR expression was increased in HCC compared to normal tissues. Higher expression of HMMR was correlated with poorer overall survival and disease-free survival outcomes. Moreover, multivariate Cox regression analysis revealed that HMMR expression was an independent risk factor for overall survival (HMMR: hazard ratio [HR] = 1.154, 95% confidence interval [CI] = 1.080-1.233, p<0.001). Consistently, RT-PCR, IHC staining and Western blotting analysis further confirmed that HMMR expression was increased in HCC compared with patient-matched adjacent normal liver tissues. Notably, GSEA analysis revealed that differential gene expression in HMMR-high patients (compared with HMMRlow patients) were enriched in cell proliferation and p53 signaling pathway. Moreover, comprehensive analysis showed a strong correlation between HMMR upregulation and miRNA changes. Conclusion: The high expression of HMMR is a poor prognostic factor in HCC and might serve as a potential target of therapy in patients with HCC.
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HMMR作为肝细胞癌预后和治疗潜在靶点的综合分析
背景:以往的研究表明,透明质酸介导的运动受体(HMMR)在调节肿瘤转移中起重要作用。然而,很少有研究涉及hmmr的临床意义及其调节肝细胞癌(HCC)的潜在机制。本研究的重点是HMMR在HCC的发展和预后中的潜在作用。材料与方法:本研究从Oncomine数据集或the Cancer Genome Atlas (TCGA)数据集获取RNA和miRNA测序阵列数据,利用R软件包分析与HMMR表达相关的独特基因组模式及其与预后的相关性。对异常表达基因进行基因集富集分析(GSEA)。我们采用逆转录聚合酶链反应(RT-PCR)、免疫组化(IHC)染色和western blotting分析了HMMR在西南医科大学附属医院肝癌细胞株和12例肝癌样本中的表达。结果:对TCGA数据集中407例肿瘤组织样本进行评估,结合对oncomine数据集的分析,我们发现HCC中HMMR表达较正常组织增加。HMMR的高表达与较差的总生存期和无病生存期相关。此外,多因素Cox回归分析显示,HMMR表达是影响总生存的独立危险因素(HMMR:风险比[HR] = 1.154, 95%可信区间[CI] = 1.080-1.233,p<0.001)。与此一致的是,RT-PCR、免疫组化染色和Western blotting分析进一步证实,与患者匹配的邻近正常肝组织相比,HCC中hmmre表达升高。值得注意的是,GSEA分析显示hmmr高患者(与hmmr低患者相比)的差异基因表达在细胞增殖和p53信号通路中富集。此外,综合分析显示HMMR上调与miRNA变化之间存在很强的相关性。结论:HMMR高表达是影响HCC预后的不良因素,可能是HCC患者治疗的潜在靶点。
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