Abstract

ObjectiveRecently, our laboratory identified sensory innervation within head and neck squamous cell carcinomas (HNSCCs) and subsequently defined a mechanism whereby HNSCCs promote their own innervation via the release of exosomes that stimulate neurite outgrowth. Interestingly, we noted that exosomes from human papillomavirus (HPV)-positive cell lines were more effective at promoting neurite outgrowth than those from HPV-negative cell lines. As nearly all cervical tumors are HPV-positive, we hypothesized that these findings would extend to cervical cancer. MethodsWe use an in vitro assay with PC12 cells to quantify the axonogenic potential of cervical cancer exosomes. PC12 cells are treated with cancer-derived exosomes, stained with the pan-neuronal marker (β-III tubulin) and the number of neurites quantified. To assess innervation in cervical cancer, we immunohistochemically stained cervical cancer patient samples for β-III tubulin and TRPV1 (sensory marker) and compared the staining to normal cervix. ResultsHere, we show the presence of sensory nerves within human cervical tumors. Additionally, we show that exosomes derived from HPV-positive cervical cancer cell lines effectively stimulate neurite outgrowth. ConclusionsThese data identify sensory nerves as components of the cervical cancer microenvironment and suggest that tumor- derived exosomes promote their recruitment.

Highlights

  • Cervical cancer, the second most common cancer in women worldwide, accounts for an estimated 260,000 deaths annually [1]

  • We show that exosomes derived from human papillomavirus (HPV)-positive cervical cancer cell lines effectively stimulate neurite outgrowth

  • We observed the intra-tumoral presence of the pan-neuronal marker, β-III tubulin, suggesting that head and neck squamous cell carcinomas (HNSCCs) are innervated [9]

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Summary

Introduction

The second most common cancer in women worldwide, accounts for an estimated 260,000 deaths annually [1]. Tumor innervation is associated with worse clinical outcomes in several solid cancers [4,5,6], emphasizing nerves as microenvironmental factors that may contribute to tumor progression. Our laboratory identified sensory innervation in head and neck squamous cell carcinoma (HNSCC) and showed that HNSCCreleased exosomes, small extracellular vesicles that carry diverse cargo, promote neurite outgrowth and tumor innervation [9]. This effect appeared to be associated with exosomes derived from HPV-positive HNSCC cells [9]. These findings suggest that HPVmediated cellular changes may confer exosomes with an enhanced ability to stimulate neurite outgrowth

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