HPV+ve/−ve oral-tongue cancer stem cells: A potential target for relapse-free therapy

•Tongue squamous cell carcinoma (TSCC) is most aggressive and highly prevalent subtype of head and neck cancer.•Majority of tobacco users are HPV−ve and have bad prognosis while HPV+ve TSCCs not using tobacco show better prognosis.•Tongue cancer stem cells (TCSCs) are resistant to chemo-radio therap...

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Veröffentlicht in:Translational oncology 2021-01, Vol.14 (1), p.100919, Article 100919
Hauptverfasser: Gupta, Shilpi, Kumar, Prabhat, Das, Bhudev C.
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Sprache:eng
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Zusammenfassung:•Tongue squamous cell carcinoma (TSCC) is most aggressive and highly prevalent subtype of head and neck cancer.•Majority of tobacco users are HPV−ve and have bad prognosis while HPV+ve TSCCs not using tobacco show better prognosis.•Tongue cancer stem cells (TCSCs) are resistant to chemo-radio therapy and responsible for cancer relapse.•Targeting TCSCs may provide efficient therapeutic strategy for relapse-free survival of TSCC patients. The tongue squamous cell carcinoma (TSCC) is a highly prevalent head and neck cancer often associated with tobacco and/or alcohol abuse or high-risk human papillomavirus (HR-HPV) infection. HPV positive TSCCs present a unique mechanism of tumorigenesis as compared to tobacco and alcohol-induced TSCCs and show a better prognosis when treated. The poor prognosis and/or recurrence of TSCC is due to presence of a small subpopulation of tumor-initiating tongue cancer stem cells (TCSCs) that are intrinsically resistant to conventional chemoradio-therapies enabling cancer to relapse. Therefore, targeting TCSCs may provide efficient therapeutic strategy for relapse-free survival of TSCC patients. Indeed, the development of new TCSC targeting therapeutic approaches for the successful elimination of HPV+ve/−ve TCSCs could be achieved either by targeting the self-renewal pathways, epithelial mesenchymal transition, vascular niche, nanoparticles-based therapy, induction of differentiation, chemoradio-sensitization of TCSCs or TCSC-derived exosome-based drug delivery and inhibition of HPV oncogenes or by regulating epigenetic pathways. In this review, we have discussed all these potential approaches and highlighted several important signaling pathways/networks involved in the formation and maintenance of TCSCs, which are targetable as novel therapeutic targets to sensitize/eliminate TCSCs and to improve survival of TSCC patients. [Display omitted]
ISSN:1936-5233
1936-5233
DOI:10.1016/j.tranon.2020.100919