Sakai Kazuya, Hiradate Yuki, Hara Kenshiro, Tanemura Kentaro
Laboratory of Animal Reproduction and Development, Graduate School of Agricultural Science, Tohoku University, Sendai, Miyagi, Japan.
Biochem Biophys Rep. 2021 Oct 22;28:101160. doi: 10.1016/j.bbrep.2021.101160. eCollection 2021 Dec.
Testicular toxicity is a major concern in cancer chemotherapy and drug development as it can result in infertility; however, there are no effective biomarkers for this adverse effect. To identify new biomarkers, we investigated the expression of small non-coding RNAs (sncRNAs) in a mouse model of doxorubicin (DXR)-induced testicular toxicity. First, we performed small RNA-seq analysis of sperm from DXR-treated or control mice and observed differential expression of many genome-derived sequences. We then performed real-time RT-PCR validation of these sequences and discovered that sncRNA detected by one primers, dxRN_3, showed similar differential expression as that seen in the RNA-seq experiment. These findings suggest that the sncRNAs present in sperm have potential as clinically acceptable biomarkers for testicular toxicity.
睾丸毒性是癌症化疗和药物研发中的一个主要问题,因为它可能导致不育;然而,对于这种不良反应尚无有效的生物标志物。为了识别新的生物标志物,我们在多柔比星(DXR)诱导的睾丸毒性小鼠模型中研究了小非编码RNA(sncRNA)的表达。首先,我们对DXR处理的小鼠或对照小鼠的精子进行了小RNA测序分析,并观察到许多基因组衍生序列的差异表达。然后,我们对这些序列进行了实时RT-PCR验证,发现由一种引物dxRN_3检测到的sncRNA表现出与RNA测序实验中相似的差异表达。这些发现表明,精子中存在的sncRNA有潜力作为临床上可接受的睾丸毒性生物标志物。