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本文引用的文献

1
The functions and regulation of the PTEN tumour suppressor: new modes and prospects.PTEN 肿瘤抑制因子的功能与调节:新模式与新前景。
Nat Rev Mol Cell Biol. 2018 Sep;19(9):547-562. doi: 10.1038/s41580-018-0015-0.
2
Intrahepatic cholangiocarcinoma patients without indications of lymph node metastasis not benefit from lymph node dissection.无淋巴结转移指征的肝内胆管癌患者无法从淋巴结清扫术中获益。
Oncotarget. 2017 Dec 1;8(69):113817-113827. doi: 10.18632/oncotarget.22852. eCollection 2017 Dec 26.
3
MiR-142-5p act as an oncogenic microRNA in colorectal cancer: Clinicopathological and functional insights.miR-142-5p 在结直肠癌中作为致癌 microRNA 的作用:临床病理和功能见解。
Exp Mol Pathol. 2018 Feb;104(1):98-107. doi: 10.1016/j.yexmp.2018.01.006. Epub 2018 Jan 11.
4
MiR-142-5p Suppresses Tumorigenesis by Targeting PIK3CA in Non-Small Cell Lung Cancer.微小RNA-142-5p通过靶向磷脂酰肌醇-4,5-二磷酸3-激酶催化亚基α抑制非小细胞肺癌的肿瘤发生
Cell Physiol Biochem. 2017;43(6):2505-2515. doi: 10.1159/000484459. Epub 2017 Oct 31.
5
Low PTEN levels and PIK3CA mutations predict resistance to neoadjuvant lapatinib and trastuzumab without chemotherapy in patients with HER2 over-expressing breast cancer.低水平的 PTEN 和 PIK3CA 突变预示着曲妥珠单抗联合拉帕替尼新辅助治疗 HER2 过表达乳腺癌时,即使不联合化疗,也会产生耐药性。
Breast Cancer Res Treat. 2018 Feb;167(3):731-740. doi: 10.1007/s10549-017-4533-9. Epub 2017 Nov 7.
6
PTEN Physically Interacts with and Regulates E2F1-mediated Transcription in Lung Cancer.PTEN 与 E2F1 相互作用并调节肺癌中的转录。
Cell Cycle. 2018;17(8):947-962. doi: 10.1080/15384101.2017.1388970. Epub 2018 May 31.
7
Both plasma and tumor tissue miR-146a high expression correlates with prolonged overall survival of surgical patients with intrahepatic cholangiocarcinoma.血浆和肿瘤组织中miR-146a的高表达均与肝内胆管癌手术患者的总生存期延长相关。
Medicine (Baltimore). 2017 Nov;96(44):e8267. doi: 10.1097/MD.0000000000008267.
8
PTEN deficiency sensitizes endometrioid endometrial cancer to compound PARP-PI3K inhibition but not PARP inhibition as monotherapy.PTEN 缺失使子宫内膜样子宫内膜癌对联合 PARP-PI3K 抑制敏感,但对 PARP 抑制作为单药治疗不敏感。
Oncogene. 2018 Jan 18;37(3):341-351. doi: 10.1038/onc.2017.326. Epub 2017 Sep 25.
9
LncRNA-CCAT1 Promotes Migration, Invasion, and EMT in Intrahepatic Cholangiocarcinoma Through Suppressing miR-152.长链非编码RNA-CCAT1通过抑制miR-152促进肝内胆管癌的迁移、侵袭和上皮-间质转化
Dig Dis Sci. 2017 Nov;62(11):3050-3058. doi: 10.1007/s10620-017-4759-8. Epub 2017 Sep 18.
10
Histopathological evidence of neoplastic progression of von Meyenburg complex to intrahepatic cholangiocarcinoma.先天性肝内胆管错构瘤向肝内胆管癌肿瘤进展的组织病理学证据。
Hum Pathol. 2017 Sep;67:217-224. doi: 10.1016/j.humpath.2017.08.004. Epub 2017 Aug 18.

增强的血浆miR-142-5p通过靶向PTEN促进肝内胆管癌进展。

Enhanced plasma miR-142-5p promotes the progression of intrahepatic cholangiocarcinoma via targeting PTEN.

作者信息

Wei Guifen, Yuan Yiting, He Xinzhong, Jin Liming, Jin Di

机构信息

Department of Hepatobiliary and Pancreatic Surgery, The First People's Hospital of Tongxiang, Tongxiang, Zhejiang 314500, P.R. China.

出版信息

Exp Ther Med. 2019 May;17(5):4190-4196. doi: 10.3892/etm.2019.7438. Epub 2019 Mar 26.

DOI:10.3892/etm.2019.7438
PMID:31007750
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6468441/
Abstract

The aim of the present study was to evaluate the expression and specific role of microRNA (miR)-142-5p in the progression of intrahepatic cholangiocarcinoma (ICC). Reverse transcription-quantitative polymerase chain reaction was performed to evaluate miR-142-5p expression in patients with ICC and healthy control subjects. The results revealed that plasma miR-142-5p was significantly increased in patients with ICC compared with the control group. Furthermore, miR-142-5p was also increased in ICC tissues compared with adjacent non-neoplastic tissues. Compared with patients with Ta-T1 stage ICC, miR-142-5p was significantly elevated in patients with ICC ≥T2 stage. Patients with ICC at G3 stage had much higher plasma miR-142-5p levels compared with those at G1/2 stage. Receiver operating characteristic analysis indicated that miR-142-5p could be used as a biomarker to differentiate patients with ICC from healthy controls. Kaplan-Meier analysis demonstrated that plasma miR-142-5p was negatively correlated with survival in patients with ICC. A dual luciferase reporter assay indicated that miR-142-5p significantly suppressed the relative luciferase activity of pmirGLO-PTEN-3' untranslated region compared with the control group. In summary, the results of the present study provide novel data indicating that plasma miR-142-5p is significantly upregulated in patients with ICC. miR-142-5p may therefore have potential as a biomarker for screening patients with ICC from healthy controls.

摘要

本研究的目的是评估微小RNA(miR)-142-5p在肝内胆管癌(ICC)进展中的表达及特定作用。采用逆转录定量聚合酶链反应来评估ICC患者和健康对照者中miR-142-5p的表达。结果显示,与对照组相比,ICC患者血浆中的miR-142-5p显著升高。此外,与相邻的非肿瘤组织相比,ICC组织中的miR-142-5p也升高。与Ta-T1期ICC患者相比,ICC≥T2期患者的miR-142-5p显著升高。G3期ICC患者的血浆miR-142-5p水平明显高于G1/2期患者。受试者工作特征分析表明,miR-142-5p可作为区分ICC患者与健康对照者的生物标志物。Kaplan-Meier分析表明,血浆miR-142-5p与ICC患者的生存率呈负相关。双荧光素酶报告基因检测表明,与对照组相比,miR-142-5p显著抑制了pmirGLO-PTEN-3'非翻译区的相对荧光素酶活性。总之,本研究结果提供了新的数据,表明ICC患者血浆中的miR-142-5p显著上调。因此,miR-142-5p可能有潜力作为从健康对照者中筛选ICC患者的生物标志物。