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Exosomal transcript cargo and functional correlation with HNSCC patients’ survival

Authors :
Joni Yadav
Apoorva Chaudhary
Tanya Tripathi
Divya Janjua
Udit Joshi
Nikita Aggarwal
Arun Chhokar
Chetkar Chandra Keshavam
Anna Senrung
Alok Chandra Bharti
Source :
BMC Cancer, Vol 24, Iss 1, Pp 1-23 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

Abstract

Abstract Background HPV status in a subset of HNSCC is linked with distinct treatment outcomes. Present investigation aims to elucidate the distinct clinicopathological features of HPV-positive and HPV-negative HNSCC and investigate their association with the HNSCC patient survival. Materials and methods The total RNA of exosomes from HPV-positive (93VU147T) and HPV-negative (OCT-1) HNSCC cells was isolated, and the transcripts were estimated using Illumina HiSeq X. The expression of altered transcripts and their clinical relevance were further analyzed using publicly available cancer transcriptome data from The Cancer Genome Atlas (TCGA). Results Transcriptomic analyses identified 3785 differentially exported transcripts (DETs) in HPV-positive exosomes compared to HPV-negative exosomes. DETs that regulate the protein machinery, cellular redox potential, and various neurological disorder-related pathways were over-represented in HPV-positive exosomes. TCGA database revealed the clinical relevance of altered transcripts. Among commonly exported abundant transcripts, SGK1 and MAD1L1 showed high expression, which has been correlated with poor survival in HNSCC patients. In the top 20 DETs of HPV-negative exosomes, high expression of FADS3, SGK3, and TESK2 correlated with poor survival of the HNSCC patients in the TCGA database. Conclusion Overall, our study demonstrates that HPV-positive and HPV-negative cells’ exosomes carried differential transcripts cargo that may be related to pathways associated with neurological disorders. Additionally, the altered transcripts identified have clinical relevance, correlating with patient survival in HNSCC, thereby highlighting their potential as biomarkers and as therapeutic targets.

Details

Language :
English
ISSN :
14712407
Volume :
24
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Cancer
Publication Type :
Academic Journal
Accession number :
edsdoj.04664fb90ad845f480cdab138b5f692a
Document Type :
article
Full Text :
https://doi.org/10.1186/s12885-024-12759-9