Literature DB >> 24521741

Relationship between tumor and peripheral blood NPRL2 mRNA levels in patients with colorectal adenoma and colorectal cancer.

Ai-yun Liu1, Dian-Ggang Liu2, Ya-ju Du1, Feng-hua Pei1, Guang Yang3, Bing-rong Liu1, Hui-tao Zhang1, Xin-hong Wang1, Yu-jing Fan1, Ying-zhun Chen4, Yang Jiang5, Jing Chen1.   

Abstract

NPRL2 is a tumor suppressor gene involved in the progression of human cancer. The present study investigated whether NPRL2 expression correlates with colorectal cancer (CRC) progression. Colorectal tissue and peripheral blood samples were obtained from 62 patients with CRC, 38 patients with colorectal adenomas and 51 normal controls. NPRL2 mRNA levels in tissue samples and blood were measured using quantitative real-time PCR. NPRL2 protein expression was determined by immunohistochemistry. NPRL2 protein expression in CRCs was significantly lower than in the adenomas or normal colorectal tissue. NPRL2 mRNA expression was significantly decreased in adenomas compared with normal controls (P<0.0001) and it was further decreased in colorectal tumors compared with adenomas (P<0.0001). NPRL2 mRNA levels expression correlated with tumor stage. In addition, NPRL2 mRNA levels in the blood correlated with the levels detected in tumors. Furthermore, receiver operating characteristic (ROC) analysis showed that NPRL2 expression in blood could distinguish colorectal adenomas and CRCs from normal controls. NPRL2 mRNA expression in CRC tumor tissues and peripheral blood correlated with colorectal tumor progression. Based on our findings, we can conclude that NPRL2 mRNA blood levels could be a potentially useful marker for the detection of early stage adenomas and CRCs.

Entities:  

Keywords:  DNA mismatch repair; adenoma; biological markers; colorectal carcinoma; intensive tumor suppressor gene; nitrogen permease regulator-like 2

Mesh:

Substances:

Year:  2014        PMID: 24521741      PMCID: PMC4026070          DOI: 10.4161/cbt.28016

Source DB:  PubMed          Journal:  Cancer Biol Ther        ISSN: 1538-4047            Impact factor:   4.742


  27 in total

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Authors:  J M D Wheeler
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Journal:  Cancer Res       Date:  2006-10-01       Impact factor: 12.701

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Journal:  Cancer Res       Date:  2002-05-01       Impact factor: 12.701

4.  Expression of candidate chromosome 3p21.3 tumor suppressor genes and down-regulation of BLU in some esophageal squamous cell carcinomas.

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5.  The 630-kb lung cancer homozygous deletion region on human chromosome 3p21.3: identification and evaluation of the resident candidate tumor suppressor genes. The International Lung Cancer Chromosome 3p21.3 Tumor Suppressor Gene Consortium.

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Authors:  Paul W Schenk; Mariel Brok; Antonius W M Boersma; Jourica A Brandsma; Hans Den Dulk; Herman Burger; Gerrit Stoter; Jaap Brouwer; Kees Nooter
Journal:  Mol Pharmacol       Date:  2003-08       Impact factor: 4.436

7.  Functional characterization of the candidate tumor suppressor gene NPRL2/G21 located in 3p21.3C.

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Journal:  Cancer Res       Date:  2004-09-15       Impact factor: 12.701

Review 8.  Epidemiology, treatment and chemoprevention in colorectal cancer.

Authors:  P Rougier; E Mitry
Journal:  Ann Oncol       Date:  2003       Impact factor: 32.976

9.  Optimal markers for real-time quantitative reverse transcription PCR detection of circulating tumor cells from melanoma, breast, colon, esophageal, head and neck, and lung cancers.

Authors:  Liqiang Xi; Daniel G Nicastri; Talal El-Hefnawy; Steven J Hughes; James D Luketich; Tony E Godfrey
Journal:  Clin Chem       Date:  2007-05-24       Impact factor: 8.327

10.  Decreased expression of the FOXO3a gene is associated with poor prognosis in primary gastric adenocarcinoma patients.

Authors:  Xiao-bo Yang; Jing-jing Zhao; Chun-yu Huang; Qi-jing Wang; Ke Pan; Dan-dan Wang; Qiu-zhong Pan; Shan-shan Jiang; Lin Lv; Xiang Gao; Huang-wei Chen; Jia-yin Yao; Min Zhi; Jian-chuan Xia
Journal:  PLoS One       Date:  2013-10-23       Impact factor: 3.240

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  5 in total

Review 1.  SEA you later alli-GATOR--a dynamic regulator of the TORC1 stress response pathway.

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Journal:  J Cell Sci       Date:  2015-05-01       Impact factor: 5.285

2.  Functional characterization of the nitrogen permease regulator-like-2 candidate tumor suppressor gene in colorectal cancer cell lines.

Authors:  Ai-Yun Liu; Ming-Na Liu; Feng-Hua Pei; Jing Chen; Xin-Hong Wang; Dan Liu; Ya-Ju Du; Bing-Rong Liu
Journal:  Mol Med Rep       Date:  2015-06-03       Impact factor: 2.952

3.  Overexpression of Nitrogen Permease Regulator Like-2 (NPRL2) Enhances Sensitivity to Irinotecan (CPT-11) in Colon Cancer Cells by Activating the DNA Damage Checkpoint Pathway.

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Journal:  Med Sci Monit       Date:  2018-03-09

4.  Nitrogen Permease Regulator-Like-2 Exhibited Anti-Tumor Effects And Enhanced The Sensitivity Of Colorectal Cancer Cells To Oxaliplatin And 5-Fluorouracil.

Authors:  Aiyun Liu; Jiutao Qiao; Liyuan He; Zhangmeng Liu; Jing Chen; Fenghua Pei; Yaju Du
Journal:  Onco Targets Ther       Date:  2019-10-18       Impact factor: 4.147

5.  Bioinformatics analysis of the prognostic and immunotherapeutic significance of NPRL2 in stomach adenocarcinoma.

Authors:  Yilin Pi; Yuning Zhan; Jitao Song; Xin Jin; Jing Chen
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  5 in total

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