Human papillomavirus 16 E6 oncoprotein promotes up-regulation of RNA-binding protein Sam68 in head and neck cancer

Head and neck squamous cell carcinoma (HNSCC) are a heterogeneous group of tumors linked to diverse risk factors, such as tobacco and alcohol use, as well as human papillomavirus (HPV) infection. HPV16 E6 and E7 oncoproteins are the main players of cell transformation, with the E6*I isoform increasing during neoplastic progression. The aim of this study was to evaluate the role of cellular splicing factors in the production of E6*I in HPV16-related HNSCC. We have evaluated the levels of splicing factors mRNA (HNRNPA1, HNRNPA2B1, SRSF1, SRSF2, SRSF3, BRM and SAM68) as well as HPV16 E6 and E6*I mRNAs by qPCR in HNSCC as well as in SCC152 and SCC154 cell lines. Overall, 42.4% of HNSCC tested positive for HPV16 DNA, and among these 54% expressed E6*I mRNA. The SRSF3, BRM and SAM68 transcripts were significantly higher in HPV-positive compared to HPV-negative HNSCC (<i>p</i> < 0.05), and SAM68 with HPV16 E6*I transcripts concordantly high in both HNSCC and cell lines (<i>r</i> = 0.7). Transduction of LXSN_E6 in HPV-negative PCA5 cell line induced production of E6*I mRNA and overexpression of Sam68 protein. In addition, silencing of SAM68 in SCC152 caused decrease of E6*I RNA and reduced cell growth at 48 hr after siRNA transfection. Higher expression of splicing factors in association with HPV was also confirmed in HNSCC TCGA dataset. In conclusion, our results suggest an interplay between the splicing machinery and HPV16 E6*I in HNSCC. These new observations are crucial for the development of novel therapeutic strategies based on SAM68 inhibitors.

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Journal
Frontiers in Microbiology
Published
2026-02-05
DOI
https://doi.org/10.3389/fmicb.2026.1657818
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
0.00

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article

Human papillomavirus 16 E6 oncoprotein promotes up-regulation of RNA-binding protein Sam68 in head and neck cancer

Francesco Longo, Sara Amiranda, Luisa Dassi, Andrea Cerasuolo et al.
Frontiers in Microbiology
RNA Research and Splicing
article

Human papillomavirus 16 E6 oncoprotein promotes up-regulation of RNA-binding protein Sam68 in head and neck cancer

Francesco Longo, Sara Amiranda, Luisa Dassi, Andrea Cerasuolo, Gerardo Ferrara, Francesco Perri, Franca Maria Tuccillo, Rossella De Cecio, Patrizia Bonelli, Noemy Starita, Anna Lucia Tornesello, T. Cimmino, Rosalia Anna Rega, Petra Claudia Camilla D’Orsi, Franco Ionna, Maria Lina Tornesello, Franco Maria Buonaguro, Salvatore Gagliarde
article en

Abstract

Head and neck squamous cell carcinoma (HNSCC) are a heterogeneous group of tumors linked to diverse risk factors, such as tobacco and alcohol use, as well as human papillomavirus (HPV) infection. HPV16 E6 and E7 oncoproteins are the main players of cell transformation, with the E6*I isoform increasing during neoplastic progression. The aim of this study was to evaluate the role of cellular splicing factors in the production of E6*I in HPV16-related HNSCC. We have evaluated the levels of splicing factors mRNA (HNRNPA1, HNRNPA2B1, SRSF1, SRSF2, SRSF3, BRM and SAM68) as well as HPV16 E6 and E6*I mRNAs by qPCR in HNSCC as well as in SCC152 and SCC154 cell lines. Overall, 42.4% of HNSCC tested positive for HPV16 DNA, and among these 54% expressed E6*I mRNA. The SRSF3, BRM and SAM68 transcripts were significantly higher in HPV-positive compared to HPV-negative HNSCC (<i>p</i> < 0.05), and SAM68 with HPV16 E6*I transcripts concordantly high in both HNSCC and cell lines (<i>r</i> = 0.7). Transduction of LXSN_E6 in HPV-negative PCA5 cell line induced production of E6*I mRNA and overexpression of Sam68 protein. In addition, silencing of SAM68 in SCC152 caused decrease of E6*I RNA and reduced cell growth at 48 hr after siRNA transfection. Higher expression of splicing factors in association with HPV was also confirmed in HNSCC TCGA dataset. In conclusion, our results suggest an interplay between the splicing machinery and HPV16 E6*I in HNSCC. These new observations are crucial for the development of novel therapeutic strategies based on SAM68 inhibitors.

Frontiers in MicrobiologyVol. 17
Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale" (IT), Scuola Superiore Meridionale (IT)
Ministero della Salute
Good health and well-being
Openalex Percentile: Top 66%
RNA Research and Splicing
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