Song Jianning, Yin Jie, Bai Zhigang, Zhang Jun, Meng Hua, Cai Jun, Deng Wei, Ma Xuemei, Zhang Zhongtao
Department of General Surgery, Beijing Friendship Hospital, Capital Medical University, Beijing Key Laboratory of Cancer Invasion and Metastasis Research & National Clinical Research Center for Digestive Diseases, 95 Yongan Road, Xi Cheng District, Beijing, 100050, People's Republic of China.
Dig Dis Sci. 2017 May;62(5):1223-1234. doi: 10.1007/s10620-017-4513-2. Epub 2017 Mar 24.
Adjuvant chemotherapy is an important component in the treatment of gastric cancer (GC) patients; however, some patients do not respond to the drugs. We aimed to develop a practical profile based on serum microRNAs (miRNAs) that can be used to predict patients likely to respond to treatment.
Microarrays were used to screen cisplatin-resistant SGC7901/DDP GC cells and the parental SGC7901 cell lines for miRNAs related to chemotherapy sensitivity. The correlation between the expression patterns of identified serum miRNAs and overall survival was confirmed in 68 GC patients. Furthermore, we also validated the signature of the serum miRNAs in an independent cohort of 50 GC patients.
From the screening microarrays, we focused on miR-15a, miR-15b and miR-93 as downregulated miRNAs in the SGC7901/DDP cells and miR-27a, miR-106a and miR-664 as upregulated miRNAs. Only serum miR-106, miR-15a, miR-93 and miR-664 were useful in predicting the prognosis of patients who received adjuvant chemotherapy. We identified a signature of four serum miRNAs (miR-106, miR-15a, miR-93 and miR-664) that, when combined, can be used as a risk score for overall survival. Patients with a higher risk score had worse prognosis (p < 0.05). For the independent cohort of patients, the signature of the four miRNAs predicted prognosis well.
Our data showed that the risk score derived from the four serum miRNAs was closely associated with the overall survival in GC patients who received adjuvant chemotherapy.
辅助化疗是胃癌(GC)患者治疗的重要组成部分;然而,一些患者对这些药物没有反应。我们旨在基于血清微小RNA(miRNA)制定一个实用的特征谱,可用于预测可能对治疗有反应的患者。
使用微阵列筛选顺铂耐药的SGC7901/DDP GC细胞系和亲本SGC7901细胞系中与化疗敏感性相关的miRNA。在68例GC患者中证实了所鉴定血清miRNA的表达模式与总生存期之间的相关性。此外,我们还在一个由50例GC患者组成的独立队列中验证了血清miRNA的特征谱。
通过筛选微阵列,我们关注SGC7901/DDP细胞中下调的miR-15a、miR-15b和miR-93,以及上调的miR-27a、miR-106a和miR-664。只有血清miR-106、miR-15a、miR-93和miR-664可用于预测接受辅助化疗患者的预后。我们鉴定出四种血清miRNA(miR-106、miR-15a、miR-93和miR-664)的特征谱,将其组合时可作为总生存期的风险评分。风险评分较高的患者预后较差(p<0.05)。对于独立的患者队列,这四种miRNA的特征谱能很好地预测预后。
我们的数据表明,源自四种血清miRNA的风险评分与接受辅助化疗的GC患者的总生存期密切相关。