Gong Weiwei, Zhu Caixia, Liu Yueyang, Muckenhuber Alexander, Bronger Holger, Scorilas Andreas, Kiechle Marion, Dorn Julia, Magdolen Viktor, Dreyer Tobias
Clinical Research Unit, Department of Obstetrics and Gynecology, Technical University of Munich Germany.
Department of Hematology-Oncology, Guangzhou Women and Children's Medical Center Guangzhou, People's Republic of China.
Am J Transl Res. 2021 Mar 15;13(3):1594-1606. eCollection 2021.
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 . 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.
三阴性乳腺癌(TNBC)患者在所有乳腺癌亚型中预后最差。在口腔鳞状癌细胞中,据报道miR-378靶向激肽释放酶相关肽酶4(KLK4)的mRNA,导致细胞增殖、迁移和侵袭受到抑制,诱导细胞凋亡,并减少肿瘤生长。同样,在前列腺癌中也提出了miR-378/KLK4轴。在此,我们分析了miR-378与KLK4 mRNA表达之间的相关性,并确定了这两个因素对TNBC的预后影响。通过定量PCR测定了TNBC患者(n = 103)肿瘤组织中miR-378和KLK4 mRNA的表达水平,并将其与临床参数和患者生存率相关联。miR-378与KLK4 mRNA表达之间无显著相关性。在单变量Cox回归分析中,miR-378表达升高与无病生存期(DFS,P = 0.047)和总生存期(OS,P = 0.031)缩短显著相关,KLK4 mRNA水平高与较差的DFS相关(P = 0.033)。KLK4 mRNA和miR-378的组合(KLK4+miR-378,低/低与高和/或高)能够更好地区分预后良好和不良情况(DFS,P = 0.008;OS,P = 0.025)。在多变量分析中,miR-378和KLK4+miR-378表达仍然是DFS(分别为P = 0.014,P = 0.010)和OS(分别为P = 0.016,P = 0.049)的独立预测因素,而KLK4 mRNA仅显示出对DFS有显著意义的趋势(P = 0.061)。我们的研究结果表明,在TNBC中miR-378对KLK4表达无显著影响。miR-378以及在较小程度上KLK4 mRNA这两个因素均代表TNBC患者不良的预后标志物。