Transcriptome analysis of cervical cancer exosomes and detection of HPVE6*I transcripts in exosomal RNA

微泡 外科肿瘤学 转录组 宫颈癌 小RNA 核糖核酸 外体 医学 计算生物学 癌症研究 生物 癌症 肿瘤科 基因表达 基因 内科学 遗传学
作者
Anjali Bhat,Joni Yadav,Kulbhushan Thakur,Nikita Aggarwal,Arun Chhokar,Tanya Tripathi,Tejveer Singh,Mohit Jadli,Veeramohan Veerapandian,Alok C. Bharti
出处
期刊:BMC Cancer [Springer Nature]
卷期号:22 (1) 被引量:18
标识
DOI:10.1186/s12885-022-09262-4
摘要

Abstract Background Exosomes play a key role in cell-to-cell communication and are integral component of the tumor microenvironment. Recent observations suggest transfer of RNA through tumor-derived exosomes that can potentially translate into regulatory proteins in the recipient cells. Role of cervical cancer-derived exosomes and their transcript cargo is poorly understood. Materials and methods The total RNA of exosomes from HPV-positive (SiHa and HeLa) and HPV-negative (C33a) cervical cancer cell lines were extracted and the transcripts were estimated using Illumina HiSeq X. Further, validation of HPV transcripts were performed using RT-PCR. Results 3099 transcripts were found to be differentially-exported in HPV-positive vs. HPV-negative exosomes ( p value <0.05). Analysis of top 10 GO terms and KEGG pathways showed enrichment of transcripts belonging to axon guidance and tumor innervation in HPV-positive exosomes. Among top 20 overexpressed transcripts, EVC2, LUZP1 and ANKS1B were the most notable due to their involvement in Hh signaling, cellular migration and invasion, respectively. Further, low levels of HPV-specific reads were detected. RT-PCR validation revealed presence of E6*I splice variant of HPV18 in exosomal RNA of HeLa cells. The E6*I transcripts were consistently retained in exosomes obtained from HeLa cells undergoing 5-FU and cisplatin-induced oxidative stress. Conclusion Our data suggests the enrichment of poly-A RNA transcripts in the exosomal cargo of cervical cancer cells, which includes pro-tumorigenic cellular RNA and viral transcripts such as HPV E6, which may have clinical utility as potential exosomal biomarkers of cervical cancer.

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