Saindane Madhuri, Rallabandi Harikrishna Reddy, Park Kyoung Sik, Heil Alexander, Nam Sang Eun, Yoo Young Bum, Yang Jung-Hyun, Yun Ik Jin
Konkuk University, School of Medicine, Seoul, South Korea.
Research Institute of Medical Science, School of Medicine, Konkuk University, Seoul, South Korea.
Cancer Inform. 2020 Nov 6;19:1176935120969696. doi: 10.1177/1176935120969696. eCollection 2020.
Prostaglandin-endoperoxide synthase-2 () plays a pivotal role in inflammation and carcinogenesis in human breast cancer. Our aim of the study is to find the prognostic value of in breast cancer. We conducted a multiomic analysis to determine whether functions as a prognostic biomarker in human breast cancer. We explored mRNA expressions using different public bioinformatics portals. Oncomine, Serial Analysis of Gene Expression (SAGE), GEPIA, ULCAN, PrognoScan database, Kaplan-Meier Plotter, bc-GenExMiner, USC XENA, and Cytoscape/STRING DB were used to identify the prognostic roles of in breast cancer. Based on the clinicopathological analysis, decreased expressions correlated positively with older age, lymph node status, the human epidermal growth factor receptor 2 (HER2) status ( < .0001), estrogen receptor (ER+) expression ( < .0001) Luminal A ( < .0001), and Luminal B ( < .0001). Interestingly, progesterone receptor (PR) ( < .0001) negative showed a high expression of . Prostaglandin-endoperoxide synthase-2 was downregulated in breast cancer tissues than in normal tissues. In the PrognoScan database and, Kaplan-Meier Scanner, downregulated expressions of associated with poor overall survival (OS), relapse-free survival (RFS), and distant metastasis-free survival. The methylation levels were significantly higher in the Luminal B subtype. Through oncomine coexpressed gene analysis, we found a positive correlation between and interleukin-6 (6) expression in breast cancer tissues. These results indicate that downregulated expressions of can be used as a promising prognostic biomarker and Luminal B hyper methylation may play an important role in the development of breast cancers. However, to clarify our results, extensive study is required.
前列腺素内过氧化物合酶-2()在人类乳腺癌的炎症和致癌过程中起关键作用。我们这项研究的目的是找出在乳腺癌中的预后价值。我们进行了多组学分析,以确定在人类乳腺癌中是否作为一种预后生物标志物发挥作用。我们使用不同的公共生物信息学平台探索了的mRNA表达。Oncomine、基因表达序列分析(SAGE)、GEPIA、ULCAN、PrognoScan数据库、Kaplan-Meier Plotter、bc-GenExMiner、南加州大学XENA以及Cytoscape/STRING数据库被用于确定在乳腺癌中的预后作用。基于临床病理分析,表达降低与年龄较大、淋巴结状态、人表皮生长因子受体2(HER2)状态(<0.0001)、雌激素受体(ER+)表达(<0.0001)、Luminal A(<0.0001)和Luminal B(<0.0001)呈正相关。有趣的是,孕激素受体(PR)(<0.0001)阴性显示的高表达。与正常组织相比,前列腺素内过氧化物合酶-2在乳腺癌组织中表达下调。在PrognoScan数据库和Kaplan-Meier Scanner中,表达下调与总生存期(OS)、无复发生存期(RFS)和无远处转移生存期较差相关。Luminal B亚型中的甲基化水平显著更高。通过Oncomine共表达基因分析,我们发现乳腺癌组织中和白细胞介素-6(IL-6)表达之间呈正相关。这些结果表明,表达下调可作为一种有前景的预后生物标志物,且Luminal B高甲基化可能在乳腺癌的发展中起重要作用。然而,为了阐明我们的结果,还需要进行广泛的研究。