Literature DB >> 25031728

The role of pleomorphic adenoma gene-like 2 in gastrointestinal cancer development, progression, and prognosis.

Bo Liu1, Chong Lu1, Yong-Xi Song1, Peng Gao1, Jing-Xu Sun1, Xiao-Wan Chen1, Mei-Xian Wang2, Yu-Lan Dong2, Hui-Mian Xu1, Zhen-Ning Wang1.   

Abstract

Numerous previous studies have revealed that pleomorphic adenoma gene-like 2 (PLAGL2) is a transcription factor that is active in cancer progression. The aim of this study was to investigate the role of PLAGL2 in the development, progression and prognosis of gastrointestinal cancer. Immunohistochemical analysis revealed that PLAGL2 was expressed in gastrointestinal tumors and adjacent normal tissues. The expression of PLAGL2 was significantly higher in 225 colorectal cancer tissues than in 66 adjacent non-tumor tissues (P = 0.037). However, expression was not significantly different between 286 gastric tumors and 57 adjacent non-tumor tissues (P = 0.352). Moreover, the PLAGL2 expression level significantly correlated with the depth of tumor invasion in colorectal cancer (P = 0.030). However, the PLAGL2 expression level significantly correlated with tumor size in gastric cancer (P = 0.046). Furthermore, we performed survival analyses and found that neither higher nor lower PLAGL2 expression was a prognostic factor in gastrointestinal cancer. Our findings indicate that PALGL2 serves as a tumor oncoprotein in the development and progression of colorectal cancer. However, the role of this protein in the development, progression and prognosis of gastric cancer is uncertain. Further investigation into the molecular mechanisms of PLAGL2 activity in gastrointestinal cancer is warranted.

Entities:  

Keywords:  Gastrointestinal cancer; PLAGL2; immunohistochemistry; prognosis; tumor invasion

Mesh:

Substances:

Year:  2014        PMID: 25031728      PMCID: PMC4097215     

Source DB:  PubMed          Journal:  Int J Clin Exp Pathol        ISSN: 1936-2625


  28 in total

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Journal:  Int J Cancer       Date:  2011-08-30       Impact factor: 7.396

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Journal:  Lung Cancer       Date:  2011-03-11       Impact factor: 5.705

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Authors:  K Kas; M L Voz; K Hensen; E Meyen; W J Van de Ven
Journal:  J Biol Chem       Date:  1998-09-04       Impact factor: 5.157

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Authors:  Gang Zheng; Jinying Ning; Yu-Chung Yang
Journal:  Biochem Biophys Res Commun       Date:  2007-10-11       Impact factor: 3.575

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Journal:  Cancer Res       Date:  2007-11-15       Impact factor: 12.701

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  13 in total

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Journal:  PLoS One       Date:  2016-08-18       Impact factor: 3.240

2.  Pleomorphic adenoma gene like-2 induces epithelial-mesenchymal transition via Wnt/β-catenin signaling pathway in human colorectal adenocarcinoma.

Authors:  Yong-Peng Wang; Peng-Tao Guo; Zhi Zhu; Hao Zhang; Yan Xu; Yu-Ze Chen; Fang Liu; Si-Ping Ma
Journal:  Oncol Rep       Date:  2017-03-02       Impact factor: 3.906

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Authors:  Genyi Qu; Yong Xu; Shaw P Wan; Guang Yang
Journal:  Sci Rep       Date:  2018-04-16       Impact factor: 4.379

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5.  Overexpression of NELFCD promotes colorectal cancer cells proliferation, migration, and invasion.

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6.  Nuclear Tau, p53 and Pin1 Regulate PARN-Mediated Deadenylation and Gene Expression.

Authors:  Jorge Baquero; Sophia Varriano; Martha Ordonez; Pawel Kuczaj; Michael R Murphy; Gamage Aruggoda; Devon Lundine; Viktoriya Morozova; Ali Elhadi Makki; Alejandra Del C Alonso; Frida E Kleiman
Journal:  Front Mol Neurosci       Date:  2019-10-15       Impact factor: 5.639

7.  PLAGL2 promotes the proliferation and migration of gastric cancer cells via USP37-mediated deubiquitination of Snail1.

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9.  DNA-methylation-mediated silencing of miR-486-5p promotes colorectal cancer proliferation and migration through activation of PLAGL2/IGF2/β-catenin signal pathways.

Authors:  Xiangxiang Liu; Xiaoxiang Chen; Kaixuan Zeng; Mu Xu; Bangshun He; Yuqin Pan; Huiling Sun; Bei Pan; Xueni Xu; Tao Xu; Xiuxiu Hu; Shukui Wang
Journal:  Cell Death Dis       Date:  2018-10-10       Impact factor: 8.469

10.  PLAGL2 promotes epithelial-mesenchymal transition and mediates colorectal cancer metastasis via β-catenin-dependent regulation of ZEB1.

Authors:  Liang Wu; Zili Zhou; Shengbo Han; Jinhuang Chen; Zhengyi Liu; Xudan Zhang; Wenzheng Yuan; Jintong Ji; Xiaogang Shu
Journal:  Br J Cancer       Date:  2019-12-12       Impact factor: 7.640

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