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核仁素的细胞定位决定癌症的预后:一项荟萃分析。

Cellular localization of nucleolin determines the prognosis in cancers: a meta-analysis.

机构信息

Department of Immunology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand.

Biomedical Sciences Graduate Program, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand.

出版信息

J Mol Med (Berl). 2022 Aug;100(8):1145-1157. doi: 10.1007/s00109-022-02228-w. Epub 2022 Jul 21.

Abstract

Nucleolin (NCL) is a multifunctional protein expressed in the nucleus, cytoplasm, and cell membrane. Overexpression of NCL has a controversial role as a poor prognostic marker in cancers. In this study, a meta-analysis was performed to evaluate the prognostic value of NCL in different subcellular localizations (cytoplasmic (CyNCL) and nuclear (NuNCL)) across a range of cancers. PubMed was searched for relevant publications. Data were extracted and analyzed from 12 studies involving 1221 patients with eight cancer types. The results revealed high total NCL was significantly associated with poor overall survival (OS) (HR = 2.85 (1.94, 4.91), p < 0.00001, I = 59%) and short disease-free survival (DFS) (HR = 3.57 (2.76, 4.62), p < 0.00001, I = 2%). High CyNCL was significantly associated with poor OS (HR = 4.32 (3.01, 6.19), p < 0.00001, I = 0%) and short DFS (HR = 3.00 (2.17, 4.15), p < 0.00001, I = 0%). In contrast, high NuNCL correlated with increased patient OS (HR = 0.42 (0.20, 0.86), p = 0.02, I = 66%), with no significant correlation to DFS observed (HR = 0.46 (0.19, 1.14), p = 0.09, I = 57%). This study supports the role of subcellular NCL as a poor prognostic cancer biomarker.

摘要

核仁素(NCL)是一种多功能蛋白,在细胞核、细胞质和细胞膜中表达。NCL 的过表达作为癌症不良预后标志物的作用存在争议。本研究通过荟萃分析评估了细胞质(CyNCL)和核(NuNCL)不同亚细胞定位的 NCL 在多种癌症中的预后价值。在 PubMed 中搜索相关文献。从涉及 8 种癌症类型的 12 项研究中提取和分析数据,共纳入 1221 例患者。结果表明,高总 NCL 与较差的总生存期(OS)(HR=2.85(1.94,4.91),p<0.00001,I=59%)和较短的无病生存期(DFS)(HR=3.57(2.76,4.62),p<0.00001,I=2%)显著相关。高 CyNCL 与较差的 OS(HR=4.32(3.01,6.19),p<0.00001,I=0%)和较短的 DFS(HR=3.00(2.17,4.15),p<0.00001,I=0%)显著相关。相反,高 NuNCL 与增加的患者 OS 相关(HR=0.42(0.20,0.86),p=0.02,I=66%),DFS 无显著相关性(HR=0.46(0.19,1.14),p=0.09,I=57%)。本研究支持亚细胞 NCL 作为癌症不良预后生物标志物的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98ad/9329415/4a8dada0714b/109_2022_2228_Fig1_HTML.jpg

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