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Yippee Like 1 抑制神经胶质瘤进展并可作为一种新的预后因子。

Yippee Like 1 Suppresses Glioma Progression and Serves as a Novel Prognostic Factor.

机构信息

Department of Neurosurgery, Suining Central Hospital.

Department of Neurosurgery, Xichang People's Hospital.

出版信息

Tohoku J Exp Med. 2022 Feb;256(2):141-150. doi: 10.1620/tjem.256.141.

Abstract

Glioma is the most common tumor of central nervous system in adults with poor prognosis. Yippee Like 1 (YPEL1) is a newly discovered protein that plays contradictory roles in pancreatic cancer and colon cancer. Here we initially explored the expression, clinical significance, and function of YPEL1 in glioma. The transcription level of YPEL1 in glioma patients was extracted from TCGA datasets via GEPIA website. As a result, the mRNA level of YPEL1 was significantly lower in glioma tissues than that in normal brain tissues. Immunohistochemistry staining was next conducted to test protein expression of YPEL1 in glioma tissues (n = 130). Consistently, lower protein expression of YPEL1 was observed in cases with larger tumor size and advanced WHO grades. Univariate and multivariate analyses identified YPEL1 as a novel independent prognostic factor of gliomas. Finally, overexpression of YPEL1 was performed in U87 and U373 cell lines to further validate its tumor-related functions, followed by proliferation, invasion, and subcutaneous mice xenografts assays. In vitro and in vivo data demonstrated that overexpressing YPEL1 can remarkably prevent glioma cell proliferation and invasion. Taken together, our data revealed that low YPEL1 expression was significantly correlated with poor overall survival of glioma patients and may play anti-tumor effects.

摘要

神经胶质瘤是成年人中枢神经系统最常见的肿瘤,预后较差。Yippee Like 1(YPEL1)是一种新发现的蛋白质,在胰腺癌和结肠癌中发挥着矛盾的作用。在这里,我们初步探讨了 YPEL1 在神经胶质瘤中的表达、临床意义和功能。通过 GEPIA 网站从 TCGA 数据集中提取神经胶质瘤患者的 YPEL1 转录水平。结果表明,神经胶质瘤组织中 YPEL1 的 mRNA 水平明显低于正常脑组织。接下来通过免疫组织化学染色检测神经胶质瘤组织中 YPEL1 的蛋白表达(n = 130)。一致地,在肿瘤体积较大和 WHO 分级较高的病例中观察到 YPEL1 蛋白表达较低。单因素和多因素分析确定 YPEL1 是神经胶质瘤的一个新的独立预后因素。最后,在 U87 和 U373 细胞系中过表达 YPEL1 进一步验证其与肿瘤相关的功能,随后进行增殖、侵袭和皮下小鼠异种移植实验。体外和体内数据表明,过表达 YPEL1 可显著抑制神经胶质瘤细胞的增殖和侵袭。综上所述,我们的数据表明,YPEL1 表达水平低与神经胶质瘤患者的总体生存率显著相关,可能发挥抗肿瘤作用。

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