Yu Jing, Li Ning, Wang Xin, Ren Hua, Wang Weihu, Wang Shulian, Song Yongwen, Liu Yueping, Li Yexiong, Zhou Xuantong, Luo Aiping, Liu Zhihua, Jin Jing
Department of Radiation Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, People's Republic of China.
The State Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, People's Republic of China.
Oncotarget. 2016 Sep 27;7(39):64233-64243. doi: 10.18632/oncotarget.11649.
Preoperative chemoradiotherapy (pre-CRT) has been represented as the standard treatment for locally advanced rectal cancer (LARC), but large variations of tumor radiation response to CRT have been reported in the clinic. To explore the function of microRNAs as potential therapeutic predictors of pre-CRT pathological response in LARC, we analyzed global miRNA expression in CRT-sensitive and CRT-resistant groups before treatment. MiR-345 was significantly elevated in the CRT-resistant group. Therefore, miR-345 was selected as a candidate for further analysis. We assessed the correlation between the miRNA signatures and the chemoradiotherapeutic response in 20 randomly selected LARC tissue samples (Validation set) and 87 serum samples (Training set) by qRT-PCR. Further, we validated the results in 42 randomly selected LARC serum samples (Validation set). High miR-345 expression was significantly correlated with unfavorable pre-CRT pathological response in tissue and serum. Moreover, low miR-345 levels predicted superior 3-year local recurrence free survival (LRFS). Taken together, circulating serum miR-345 correlates with unfavorable pre-CRT response and poor locoregional control in LARC. It might be a promising biomarker to facilitate patient stratification for personalized treatment.
术前放化疗(pre-CRT)已被视为局部晚期直肠癌(LARC)的标准治疗方法,但临床上已报道肿瘤对放化疗的反应存在很大差异。为了探索微小RNA作为LARC中pre-CRT病理反应潜在治疗预测指标的功能,我们在治疗前分析了CRT敏感组和CRT抵抗组中的整体miRNA表达。miR-345在CRT抵抗组中显著升高。因此,选择miR-345作为进一步分析的候选对象。我们通过qRT-PCR评估了20个随机选择的LARC组织样本(验证组)和87个血清样本(训练组)中miRNA特征与放化疗反应之间的相关性。此外,我们在42个随机选择的LARC血清样本(验证组)中验证了结果。高miR-345表达与组织和血清中不利的pre-CRT病理反应显著相关。此外,低miR-345水平预示着3年局部无复发生存率(LRFS)更高。综上所述,循环血清miR-345与LARC中不利的pre-CRT反应和较差的局部区域控制相关。它可能是一种有前景的生物标志物,有助于患者分层以进行个性化治疗。