Tian Ye, Sun Changyu, Zhang Limeng, Pan Yuan
Department of Senior Ward, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer; Key Laboratory of Cancer Prevention and Therapy, Tianjin; Tianjin's Clinical Research Center for Cancer, Tianjin 300060, China.
Tianjin Taishan Cancer Hospital & International Personalized Cancer Center, Tianjin 300450, China.
Cancer Biol Med. 2018 May;15(2):157-164. doi: 10.20892/j.issn.2095-3941.2017.0182.
Research has demonstrated that microRNA (miR)-106a is related to cisplatin resistance. We investigated the expression of miR-106a in the serum of patients with non-small cell lung cancer (NSCLC) and their sensitivity to chemotherapy by cisplatin combined with gemcitabine.
Eighty-five NSCLC patients, who completed four cycles of gemcitabine and cisplatin chemotherapy, volunteered for this study and their serum samples were collected. Serum samples from 60 healthy subjects were used as controls. Real-time quantitative polymerase chain reaction (real-time qPCR) was used to quantify the level of miR-106a in the serum. Demographic and survival data of these patients were collected for the analysis.
The expression of miR-106a in the serum of NSCLC patients was significantly higher than that of healthy subjects ( < 0.001). The expression of miR-106a was not correlated with patients' gender, age, tumor size, lymphatic metastasis, and pathological types; but was correlated with patients' tumor staging ( = 0.003). After chemotherapy, serum miR-106a expression decreased in patients. The decrease in miR-106a expression in the chemotherapy-sensitive group was much higher than that in the chemotherapy-resistant group. Survival analysis shows that NSCLC patients with high expression of miR-106a have a poorer prognosis. The overall survival of NSCLC patients in the chemotherapy-sensitive group was significantly higher than that in the chemotherapy-resistant group.
High expression of miR-106a may be involved in the development of NSCLC. MiR-106a has significance in the prognosis of NSCLC. The level of miR-106a in the serum can be a useful parameter in screening for drug resistance during cisplatin-based chemotherapy.
研究表明,微小RNA(miR)-106a与顺铂耐药有关。我们调查了非小细胞肺癌(NSCLC)患者血清中miR-106a的表达及其对顺铂联合吉西他滨化疗的敏感性。
85例完成四个周期吉西他滨和顺铂化疗的NSCLC患者自愿参与本研究,并采集其血清样本。60例健康受试者的血清样本用作对照。采用实时定量聚合酶链反应(实时qPCR)定量血清中miR-106a的水平。收集这些患者的人口统计学和生存数据进行分析。
NSCLC患者血清中miR-106a的表达明显高于健康受试者(<0.001)。miR-106a的表达与患者的性别、年龄、肿瘤大小、淋巴转移和病理类型无关;但与患者的肿瘤分期相关(=0.003)。化疗后,患者血清miR-106a表达下降。化疗敏感组miR-106a表达的下降幅度远高于化疗耐药组。生存分析表明,miR-106a高表达的NSCLC患者预后较差。化疗敏感组NSCLC患者的总生存期明显高于化疗耐药组。
miR-106a的高表达可能参与NSCLC的发生发展。miR-106a对NSCLC的预后具有重要意义。血清中miR-106a的水平可作为基于顺铂化疗期间耐药筛查的有用参数。