Literature DB >> 27494742

microRNA-214 Governs Lung Cancer Growth and Metastasis by Targeting Carboxypeptidase-D.

Xiaojian Zhao1, Caiping Lu2, Weiwei Chu1, Yaxiao Zhang1, Bing Zhang1, Qiang Zeng1, Renfeng Wang1, Zhe Li1, Baolei Lv1, Jiabao Liu1.   

Abstract

Lung cancer is one of the most malignant cancers with a high metastatic potential. The purpose of this study was to study the role and the underlying mechanism of miR-214 in lung cancer progression. The expression of miR-214 in normal lung and lung cancer tissue was analyzed by quantitative real-time PCR analysis. Furthermore, H1299 cells were infected with miR-214 lentivirus, and the effect of infection on cell viability and migration was analyzed. Carboxypeptidase-D (CPD), as a potential target of miR-214, was characterized in either normal lung or lung cancer tissues. The interaction of CPD expression with the tumor suppressing effect of miR-214 was characterized. We demonstrated that low miR-214 expression is a hallmark of lung cancer, especially high-grade and metastatic cancer. In vitro studies in H1299 cells confirmed that low miR-214 expression is associated with enhanced proliferation and migratory abilities. Similarly, CPD overexpression coincides with high-grade lung cancer and the CPD overexpression could reverse the inhibitory effects of miR-214. miR-214 is a tumor suppressor in lung cancer. miR-214 inhibits lung cancer progression by targeting CPD. The miR-214-CPD axis may be a therapeutic axis for lung cancer patients.

Entities:  

Keywords:  carboxypeptidase-D; lung cancer; metastasis; miR-214

Mesh:

Substances:

Year:  2016        PMID: 27494742     DOI: 10.1089/dna.2016.3398

Source DB:  PubMed          Journal:  DNA Cell Biol        ISSN: 1044-5498            Impact factor:   3.311


  8 in total

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Authors:  Xiaofeng Chen; Jiangyuan Du; Rui Jiang; Ling Li
Journal:  Am J Transl Res       Date:  2018-04-15       Impact factor: 4.060

2.  Knockdown of differentiation antagonizing non-protein coding RNA exerts anti-tumor effect by up-regulating miR-214 in endometrial carcinoma.

Authors:  Jingli Sun; Shaofeng Gao; Cuihua Lu
Journal:  Mol Cell Biochem       Date:  2019-06-03       Impact factor: 3.396

3.  Discovery of Mechanism-Based Inactivators for Human Pancreatic Carboxypeptidase A from a Focused Synthetic Library.

Authors:  Sebastián A Testero; Carla Granados; Daniel Fernández; Pablo Gallego; Giovanni Covaleda; David Reverter; Josep Vendrell; Francesc X Avilés; Irantzu Pallarès; Shahriar Mobashery
Journal:  ACS Med Chem Lett       Date:  2017-09-22       Impact factor: 4.345

4.  miR-214-3p promotes the proliferation, migration and invasion of osteosarcoma cells by targeting CADM1.

Authors:  Haiqing Cai; Mingyuan Miao; Zhigang Wang
Journal:  Oncol Lett       Date:  2018-06-08       Impact factor: 2.967

5.  AGO2 promotes tumor progression in KRAS-driven mouse models of non-small cell lung cancer.

Authors:  Jean Ching-Yi Tien; Seema Chugh; Andrew E Goodrum; Yunhui Cheng; Rahul Mannan; Yuping Zhang; Lisha Wang; Vijaya L Dommeti; Xiaoming Wang; Alice Xu; Jennifer Hon; Carson Kenum; Fengyun Su; Rui Wang; Xuhong Cao; Sunita Shankar; Arul M Chinnaiyan
Journal:  Proc Natl Acad Sci U S A       Date:  2021-05-18       Impact factor: 11.205

Review 6.  miRNA Regulation of Glutathione Homeostasis in Cancer Initiation, Progression and Therapy Resistance.

Authors:  Barbara Marengo; Alessandra Pulliero; Alberto Izzotti; Cinzia Domenicotti
Journal:  Microrna       Date:  2020

7.  MicroRNA‑214 suppresses the viability, migration and invasion of human colorectal carcinoma cells via targeting transglutaminase 2.

Authors:  Huiguo Shan; Xuefeng Zhou; Chuanjun Chen
Journal:  Mol Med Rep       Date:  2019-06-03       Impact factor: 2.952

8.  microRNA-214 suppresses the growth of cervical cancer cells by targeting EZH2.

Authors:  Yanling Yang; Yang Liu; Guilin Li; Lei Li; Peng Geng; Hongjuan Song
Journal:  Oncol Lett       Date:  2018-08-24       Impact factor: 2.967

  8 in total

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