Literature DB >> 22844381

Expression of miR-21, miR-31, miR-96 and miR-135b is correlated with the clinical parameters of colorectal cancer.

Xin Min Xu1, Jian Chang Qian, Zhou Lu Deng, Zhe Cai, Tao Tang, Peng Wang, Ke Hua Zhang, Jian-Ping Cai.   

Abstract

The aim of this study was to determine the expression of miR-21, miR-31, miR-96 and miR-135b in 52 paired colorectal cancer (CRC) tissues and to analyze the correlation between microRNAs (miRNAs) and clinicopathological features. We developed a quantification method that relies on a standard plot, constructed from known concentrations of standards, in order to measure the number of miRNAs. In addition to this, we analyzed the expression levels of miR-21, miR-31, miR-96 and miR-135b in 52 cases of primary CRC and corresponding normal mucosal tissue using real-time PCR with SYBR-Green I. An independent sample t-test was used to compare the differential expression between tumor tissues and normal mucosal tissues. The Mann-Whitney U and Kruskall-Wallis tests were used to compare the correlation between miRNA expression levels and clinicopathological features. The expression of miR-21, miR-31, miR-96 and miR-135b was upregulated in the CRC tissues compared to normal mucosal tissues (P<0.05). Furthermore, miR-21 and miR-135b were positively correlated with the clinical stage (P=0.048 and P=0.029, respectively), while miR-96 and miR-135b were correlated with liver metastasis (P=0.006 and P=0.013, respectively). Our results suggest that miR-21, miR-31, miR-96 and miR-135b may function in the process of CRC development and progression. miR-135b levels in particular may correlate with the degree of malignancy.

Entities:  

Year:  2012        PMID: 22844381      PMCID: PMC3402725          DOI: 10.3892/ol.2012.714

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


  33 in total

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2.  MicroRNA in cancer prognosis.

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4.  Cancer statistics, 2010.

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7.  Reduced accumulation of specific microRNAs in colorectal neoplasia.

Authors:  Michael Z Michael; Susan M O' Connor; Nicholas G van Holst Pellekaan; Graeme P Young; Robert J James
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Journal:  J Biol Chem       Date:  2007-03-15       Impact factor: 5.157

9.  Altered expression of miR-21, miR-31, miR-143 and miR-145 is related to clinicopathologic features of colorectal cancer.

Authors:  O Slaby; M Svoboda; P Fabian; T Smerdova; D Knoflickova; M Bednarikova; R Nenutil; R Vyzula
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  56 in total

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Review 2.  MicroRNAs in colorectal cancer as markers and targets: Recent advances.

Authors:  Jing-Jia Ye; Jiang Cao
Journal:  World J Gastroenterol       Date:  2014-04-21       Impact factor: 5.742

3.  Pilot Study of Serum MicroRNA-21 as a Diagnostic and Prognostic Biomarker in Egyptian Breast Cancer Patients.

Authors:  Eman A Toraih; Eman A Mohammed; Sherif Farrag; Nevene Ramsis; Somaya Hosny
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4.  MicroRNAs 185, 96, and 223 repress selective high-density lipoprotein cholesterol uptake through posttranscriptional inhibition.

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Journal:  Mol Cell Biol       Date:  2013-03-04       Impact factor: 4.272

5.  Effects of Lactobacillus acidophilus and Bifidobacterium bifidum Probiotics on the Expression of MicroRNAs 135b, 26b, 18a and 155, and Their Involving Genes in Mice Colon Cancer.

Authors:  Zahra Heydari; Mahdi Rahaie; Ali Mohammad Alizadeh; Shahram Agah; Solmaz Khalighfard; Sahar Bahmani
Journal:  Probiotics Antimicrob Proteins       Date:  2019-12       Impact factor: 4.609

6.  miR-182 and miR-135b Mediate the Tumorigenesis and Invasiveness of Colorectal Cancer Cells via Targeting ST6GALNAC2 and PI3K/AKT Pathway.

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7.  Overexpression of microRNA-96-5p inhibits autophagy and apoptosis and enhances the proliferation, migration and invasiveness of human breast cancer cells.

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Journal:  Oncol Lett       Date:  2017-04-11       Impact factor: 2.967

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9.  MicroRNA-135b acts as a tumor promoter by targeting the hypoxia-inducible factor pathway in genetically defined mouse model of head and neck squamous cell carcinoma.

Authors:  Lu Zhang; Zhi-Jun Sun; Yansong Bian; Ashok B Kulkarni
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10.  miR-21 inhibitor suppresses proliferation and migration of nasopharyngeal carcinoma cells through down-regulation of BCL2 expression.

Authors:  Yumei Li; Limei Yan; Wenyu Zhang; Hui Wang; Wei Chen; Nan Hu; Hesheng Ou
Journal:  Int J Clin Exp Pathol       Date:  2014-05-15
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