Tao Ji, Liu Yan-Long, Zhang Gan, Ma Yu-Yan, Cui Bin-Bin, Yang Yan-Mei
Department of Medical Oncology, the Affiliated Tumor Hospital, Harbin Medical University, Harbin, China.
Tumour Biol. 2014 Oct;35(10):9619-25. doi: 10.1007/s13277-014-2220-6. Epub 2014 Jun 27.
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.
Mel-18是多梳蛋白家族(PcG)的成员之一,该家族蛋白是染色质调节因子,在肿瘤发生过程中发挥重要作用。本研究旨在探讨Mel-18在结直肠癌(CRC)患者中的临床及预后意义。为此,采用qRT-PCR和蛋白质免疫印迹法对82例原发性CRC及配对的癌旁黏膜组织样本中Mel-18 mRNA的表达进行评估。我们发现,CRC组织中Mel-18 mRNA的总体表达显著低于癌旁黏膜组织(p = 0.007,Wilcoxon配对符号秩检验)。Mel-18与病理分类(T分类p = 0.003,N分类p < 0.001,M分类p = 0.015)及临床AJCC分期(p < 0.001)呈负相关。此外,Mel-18水平较高的CRC患者无病生存期(DFS)延长(p < 0.001)。多因素分析显示,Mel-18表达降低可能是患者3年DFS的危险因素(HR = 1.895;95%CI 1.032,3.477;p = 0.039)。因此得出结论,Mel-18表达降低可能促进CRC的发生/发展。