乳腺癌患者20种血清mirna与临床病理变量的关系

Açelya GÖKDENİZ YILDIRIM, Aydın Demiray, Ali Can Koç, H. Şenol, A. Yaren
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引用次数: 0

摘要

确定mirna在乳腺癌发病机制中的作用,可能有助于乳腺癌的诊断和治疗。在本研究中,39例浸润性乳腺癌患者在诊断期间和治疗后检测20种mirna (miR-105、miR-21、miR-141、miR-200a、miR-200b、miR-200c、miR-203、miR-210、miR-375、miR-34a、miR-133a、miR-155、miR-139-5p、miR-143、miR-145、miR-365、miR-299-5p、miR-411、miR-452、miR-17)的血清水平。分析结果发现,局部晚期/转移组血清miR-200c(p=0.030)、miR-375(p=0.045)、miR-34a(p=0.042)水平显著升高。淋巴结受累阳性患者血清miR-141水平(p=0.062)较低,而同一患者组中miR-133a水平(p=0.037)较高。孕激素受体阴性组MiR-105(p=0.015)、miR-203(p=0.015)、miR-375(p=0.033)、miR-145(p=0.025)血清水平显著升高,雌激素受体阴性组MiR-105(p= 0.053)血清水平也显著升高。在人表皮生长因子受体-2阳性患者中,miR-375和miR-133a水平明显升高(p=0.037和p=0.014)。ki-67指数>20%的患者组MiR-143(p=0.009)和miR-145(p=0.017)水平较高。发现2种mirna (miR-133a(p=0.018)和miR-139-5p(p=0.004))在luminal B组患者中显著升高,并按分子亚组分开。9个mirna (miR-105(p=0.0001)、miR-21(p=0.001)、miR-141(p=0.041)、miR-200a(p=0.003)、miR-200b(p=0.0001)、miR-200c(p=0.0001)、miR-203(p=0.0001)、miR-34a(p=0.0001)、miR-452(p=0.018))在治疗后显著升高,5个mirna (miR-155(p=0.0001)、miR-143(p=0.0001)、miR-145(p=0.0001)、miR-365(p=0.0001)、miR-299-5p(p=0.0001))在治疗后显著降低。我们认为mirna可能有助于评估浸润性乳腺癌的随访和预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ASSOCIATION BETWEEN TWENTY SERUM MIRNAS AND CLINICOPATHOLOGICAL VARIABLES IN PATIENTS WITH BREAST CANCER
Determining that miRNAs play a role in breast cancer pathogenesis suggests that it may be useful in the diagnosis and treatment of breast cancer. In this study, 39 patients with invasive breast cancer were diagnosed with serum levels of 20 miRNAs(miR-105, miR-21, miR-141, miR-200a, miR-200b, miR-200c, miR-203, miR-210, miR-375, miR-34a, miR-133a, miR-155, miR-139-5p, miR-143, miR-145, miR-365, miR-299-5p, miR-411, miR-452, miR-17) were analyzed during diagnosis and after treatment. In the analysis results, it is detected that serum levels of miR-200c(p=0.030), miR-375(p=0.045), miR-34a(p=0.042) were significantly higher in the local advanced/metastatic group. Serum level of miR-141(p=0.062) was lower in patients with positive lymph node involvement, whereas miR-133a(p=0.037) levels were higher in the same patient group. MiR-105(p=0.015), miR-203(p=0.015), miR-375(p=0.033), miR-145(p=0.025) serum levels were significantly higher in the progesterone receptor negative group, likewise miR-105(p=0.053) levels were high in the estrogen receptor negative patient group. The high levels of miR-375 and miR-133a were noticeable in human epidermal growth factor receptor-2 positive patients(p=0.037 and p=0.014, respectively). MiR-143(p=0.009) and miR-145(p=0.017) levels were observed to be higher in the patient group with a ki-67 index>20%. It was found that 2 miRNAs(miR-133a(p=0.018) and miR-139-5p(p=0.004)) were significantly higher in patients in the luminal B group, which were separated by molecular subgroups. Nine of miRNAs that evaluated(miR-105(p=0.0001), miR-21(p=0.001), miR-141(p=0.041), miR-200a(p=0.003), miR-200b(p=0.0001), miR-200c(p=0.0001), miR-203(p=0.0001), miR-34a(p=0.0001), miR-452(p=0.018)) significantly increased after treatment and 5 of the miRNAs(miR-155(p=0.0001), miR-143(p=0.0001), miR-145(p=0.0001), miR-365(p=0.0001), miR-299-5p(p=0.0001)) were significantly reduced after treatment. We think that miRNAs may help in evaluating the follow-up and prognosis of invasive breast cancer.
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