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长链非编码 RNA HMMR-AS1 在卵巢上皮性癌中的表达增加:一个独立的预后因素。

Increased expression of long noncoding RNA HMMR-AS1 in epithelial ovarian cancer: an independent prognostic factor.

机构信息

Department of Obstetrics and Gynecology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Dec;22(23):8145-8150. doi: 10.26355/eurrev_201812_16506.

Abstract

OBJECTIVE

Evidence has indicated that long noncoding RNA (lncRNAs) may have significant roles in cancer. In this study, we aimed to investigate the expression pattern and prognostic value of a noncoding RNA named as HMMR antisense RNA 1 (HMMR-AS1) in epithelial ovarian cancer (EOC).

PATIENTS AND METHODS

Differences in the expression of HMMR-AS1 between EOC and matched normal tissues were analyzed using RT-PCR. The correlation between HMMR-AS1 levels and the clinicopathological factors of the EOC patients was analyzed by x2-test. Kaplan-Meier analysis and Cox proportional hazards regression models were explored to reveal the correlations of HMMR-AS1 expression with survival of patients.

RESULTS

HMMR-AS1 was significantly upregulated in human EOC tissues compared with adjacent normal tissues (p < 0.01). Clinicopathologic analysis revealed that high expression of HMMR-AS1 was associated with advanced FIGO stage (p = 0.013) and positive lymphatic metastasis (p = 0.010). Moreover, patients with higher HMMR-AS1 expression displayed shorter overall survival time (p = 0.0075) and progression-free survival time (p = 0.0013) than those with lower HMMR-AS1 expression. More importantly, multivariate analysis suggested that high expression of HMMR-AS1 was an independent prognostic indicator for EOC patients.

CONCLUSIONS

Our data suggested that HMMR-AS1 may be considered a novel prognostic factor in EOC and a specific diagnostic indicator for patients with EOC.

摘要

目的

有证据表明,长链非编码 RNA(lncRNA)可能在癌症中发挥重要作用。本研究旨在探讨一种名为 HMMR 反义 RNA 1(HMMR-AS1)的非编码 RNA 在卵巢上皮性癌(EOC)中的表达模式和预后价值。

患者和方法

采用 RT-PCR 分析 EOC 与配对正常组织中 HMMR-AS1 的表达差异。x2 检验分析 HMMR-AS1 水平与 EOC 患者临床病理因素的相关性。Kaplan-Meier 分析和 Cox 比例风险回归模型探讨 HMMR-AS1 表达与患者生存的相关性。

结果

与相邻正常组织相比,HMMR-AS1 在人 EOC 组织中显著上调(p < 0.01)。临床病理分析显示,HMMR-AS1 高表达与 FIGO 分期较晚(p = 0.013)和阳性淋巴转移(p = 0.010)相关。此外,HMMR-AS1 高表达的患者总生存时间(p = 0.0075)和无进展生存时间(p = 0.0013)均短于 HMMR-AS1 低表达的患者。更重要的是,多因素分析表明,HMMR-AS1 高表达是 EOC 患者的独立预后指标。

结论

我们的数据表明,HMMR-AS1 可作为 EOC 的一种新的预后因素和 EOC 患者的特定诊断指标。

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