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A549、A549/DDP及其各自外泌体之间微小RNA表达谱的比较分析。

Comparative analysis of microRNA expression profiles between A549, A549/DDP and their respective exosomes.

作者信息

Qin Xiaobing, Yu Shaorong, Xu Xiaoyue, Shen Bo, Feng Jifeng

机构信息

Research Center for Clinical Oncology, Nanjing Medical University Affiliated Cancer Hospital, Jiangsu Cancer Hospital and Jiangsu Institute of Cancer Research, Nanjing, Jiangsu Province, China.

Department of Oncology, Xuzhou First People's Hospital, Xuzhou, Jiangsu Province, China.

出版信息

Oncotarget. 2017 Jun 27;8(26):42125-42135. doi: 10.18632/oncotarget.15009.

Abstract

Exosomes were reported to transport bioactive molecules and influence the biology behavior of recipient cells. In order to study the role of exosomal microRNAs in the mechanism of cisplatin resistance to lung cancer cells, we analyzed the expression profiles of microRNAs in A549, A549/DDP cells and their exosomes by microarray. The results showed that a certain proportion of microRNAs were co-expressed in the cells and exosomes. Linear regression analysis showed that the expression of microRNAs in A549 and A549/DDP cells were strongly correlated with those in their respective exosomes. The expression level of 5 microRNAs (miR-197-5p, miR-4443, miR-642a-3p, miR-27b-3p and miR-100-5p) with the most differential expression were verified by qRT-PCR. The results were consistent with those of the microarray. Target gene prediction and pathway analysis discovered that the microRNAs in the intersections may participate in drug resistance. And the prediction of their association with diseases found that most of these microRNAs was associated with lung cancer. We could draw a preliminary conclusion that microRNAs in exosomes may be involved in the drug resistance of lung cancer cells to cisplatin.

摘要

据报道,外泌体可运输生物活性分子并影响受体细胞的生物学行为。为了研究外泌体微小RNA在肺癌细胞顺铂耐药机制中的作用,我们通过微阵列分析了A549、A549/DDP细胞及其外泌体中微小RNA的表达谱。结果表明,一定比例的微小RNA在细胞和外泌体中共同表达。线性回归分析表明,A549和A549/DDP细胞中微小RNA的表达与其各自外泌体中的表达密切相关。通过qRT-PCR验证了差异表达最明显的5种微小RNA(miR-197-5p、miR-4443、miR-642a-3p、miR-27b-3p和miR-100-5p)的表达水平。结果与微阵列结果一致。靶基因预测和通路分析发现,交集处的微小RNA可能参与耐药。对它们与疾病关联的预测发现,这些微小RNA中的大多数与肺癌有关。我们可以初步得出结论,外泌体中的微小RNA可能参与肺癌细胞对顺铂的耐药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7743/5522054/ab6920189a36/oncotarget-08-42125-g001.jpg

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