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首页> 外文期刊>American Journal of Translational Research >Elevated levels of both microRNA 378 (miR-378) and kallikrein-related peptidase 4 (KLK4) mRNA are associated with an unfavorable prognosis in triple-negative breast cancer
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Elevated levels of both microRNA 378 (miR-378) and kallikrein-related peptidase 4 (KLK4) mRNA are associated with an unfavorable prognosis in triple-negative breast cancer

机译:microRNA 378(miR-378)和Kallikrein相关的肽酶4(KLK4)mRNA的升高水平与三阴性乳腺癌的不利预后有关

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Triple-negative breast cancer (TNBC) patients have the worst outcome among all breast cancer subtypes. In oral squamous carcinoma cells, miR-378 was reported to target the mRNA of kallikrein-related peptidase 4 (KLK4), resulting in inhibition of cell proliferation, migration and invasion, induction of apoptosis, and reduction of tumor growth in vivo . Similarly, a miR-378/KLK4 axis has been proposed in prostate cancer. Here, we analyzed the correlation between miR-378 and KLK4 mRNA expression and determined the prognostic impact of both factors in TNBC. miR-378 and KLK4 mRNA expression levels were determined by quantitative PCR in tumor tissue of TNBC patients (n=103) and correlated with clinical parameters and patients’ survival. There was no significant correlation between miR-378 and KLK4 mRNA expression. In univariate Cox regression analysis, elevated miR-378 expression was significantly associated with shortened disease-free survival (DFS, P=0.047) and overall survival (OS, P=0.031), high KLK4 mRNA levels were linked to a worse DFS (P=0.033). Combination of KLK4 mRNA and miR-378 (KLK4+miR-378, low/low versus high and/or high) allowed even better discrimination between favorable and unfavorable prognosis (DFS, P=0.008; OS, P=0.025). In multivariable analysis, miR-378 and KLK4+miR-378 expression remained independent predictive factors for DFS (P=0.014, P=0.010, respectively) and OS (P=0.016, P=0.049, respectively), while KLK4 mRNA only showed a trend towards significance for DFS (P=0.061). Our findings suggest that in TNBC there is no significant impact of miR-378 on KLK4 expression. Both factors, miR-378 and, to a lesser extent, KLK4 mRNA represent unfavorable prognostic markers in TNBC patients.
机译:三重阴性乳腺癌(TNBC)患者在所有乳腺癌亚型中具有最糟糕的结果。在口腔鳞状癌细胞中,据报道miR-378靶向Kallikrein相关的肽酶4(KLK4)的mRNA,导致抑制细胞增殖,迁移和侵袭,诱导细胞凋亡和体内肿瘤生长的降低。类似地,在前列腺癌中提出了MIR-378 / KLK4轴。这里,我们分析了MiR-378和KLK4 mRNA表达之间的相关性,并确定了两种因素在TNBC中的预后影响。通过TNBC患者的肿瘤组织中的定量PCR测定miR-378和KLK4 mRNA表达水平,并与临床参数和患者存活相关。 miR-378和KLK4 mRNA表达之间没有显着的相关性。在单变量的Cox回归分析中,升高的miR-378表达与缩短无疾病存活(DFS,P = 0.047)和总存活(OS,P = 0.031)显着相关,高KLK4 mRNA水平与更差的DFS相关联(P. = 0.033)。 KLK4 mRNA和miR-378的组合(KLK4 + miR-378,低/低与高和/或高)允许在有利和不利的预后(DFS,P = 0.008; OS,P = 0.025)之间更好地辨别。在多变量分析中,miR-378和Klk4 + miR-378表达仍然是DFS的独立预测因子(P = 0.014,P = 0.010,分别)和OS(分别为0.016,P = 0.049),而KLK4 mRNA仅显示对DFS意义的趋势(P = 0.061)。我们的研究结果表明,在TNBC中,MIR-378对KLK4表达没有显着影响。因素,miR-378和较小程度,KLK4 mRNA代表TNBC患者的不利预后标志物。

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