Literature DB >> 24964959

Expression and clinicopathological significance of Mel-18 mRNA in colorectal cancer.

Ji Tao1, Yan-Long Liu, Gan Zhang, Yu-Yan Ma, Bin-Bin Cui, Yan-Mei Yang.   

Abstract

Mel-18 is a member of the polycomb group (PcG) of proteins, which are chromatin regulatory factors that play an important role in oncogenesis. This study was designed to investigate the clinical and prognostic significance of Mel-18 in colorectal cancer (CRC) patients. For this purpose, expression of Mel-18 mRNA was evaluated in 82 primary CRC and paired noncancerous mucosa samples by qRT-PCR and Western blotting. We found that overall Mel-18 mRNA expression in the CRC tissue was significantly lower than in the noncancerous mucosal tissue (p = 0.007, Wilcoxon matched-pairs signed-ranks test). Mel-18 was conversely correlated with the pathological classifications (p = 0.003 for T, p < 0.001 for N, and p = 0.015 for M classifications, respectively) and clinical AJCC stage (p < 0.001). Furthermore, CRC patients with a higher level of Mel-18 showed prolonged disease-free survivals (DFS) (p < 0.001). In multivariate analysis, the diminished Mel-18 expression may be a risk factor for the patients' 3-year DFS (HR = 1.895; 95 % CI 1.032, 3.477; p = 0.039). It was therefore concluded that the lower Mel-18 expression might contribute to the CRC development/progression.

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Year:  2014        PMID: 24964959     DOI: 10.1007/s13277-014-2220-6

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


  35 in total

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3.  Studies on the expression patterns of class I PI3K catalytic subunits and its prognostic significance in colorectal cancer.

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7.  Analysis of Mel-18 expression in prostate cancer tissues and correlation with clinicopathologic features.

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  5 in total

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2.  B-cell specific Moloney leukemia virus insert site 1 and peptidyl arginine deiminase IV positively regulate carcinogenesis and progression of esophageal squamous cell carcinoma.

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Review 3.  Context-dependent actions of Polycomb repressors in cancer.

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4.  Co-inhibition of BMI1 and Mel18 enhances chemosensitivity of esophageal squamous cell carcinoma in vitro and in vivo.

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5.  Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features.

Authors:  Peter D Turnpenny; Michael J Wright; Melissa Sloman; Richard Caswell; Anthony J van Essen; Erica Gerkes; Rolph Pfundt; Susan M White; Nava Shaul-Lotan; Lori Carpenter; G Bradley Schaefer; Alan Fryer; A Micheil Innes; Kirsten P Forbes; Wendy K Chung; Heather McLaughlin; Lindsay B Henderson; Amy E Roberts; Karen E Heath; Beatriz Paumard-Hernández; Blanca Gener; Katherine A Fawcett; Romana Gjergja-Juraški; Daniela T Pilz; Andrew E Fry
Journal:  Am J Hum Genet       Date:  2018-10-18       Impact factor: 11.025

  5 in total

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