Aberrant activation of the Hedgehog signalling pathway in squamous cell carcinoma of the vulva as a potential target for cancer therapy.
Uddin, Khalil O'Neill, Danielle Kehoe, Sean Ganesan, Raji Dawson, Christopher W
Uddin, Khalil
O'Neill, Danielle
Kehoe, Sean
Ganesan, Raji
Dawson, Christopher W
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Affiliation
University of Birmingham; Birmingham Women's and Children's NHS Foundation Trust; Sandwell and West Birmingham NHS Trust
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Publication date
2021-09-03
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Abstract
In a previous study, we showed that the Hedgehog (Hh) signalling pathway is aberrantly activated in vulval squamous cell carcinoma (VSCC). In this study, we further validated our findings on a prospective cohort of primary VSCC cases, where immunohistochemical staining confirmed that key Hh pathway components were overexpressed in VSCC compared to normal vulval epithelium. We also undertook a series of in vitro studies to determine the extent of Hh pathway activation in VSCC-derived cell lines, and examine the consequences of pathway inhibition on the growth of these cells. We found that of six cell lines tested, four displayed elevated baseline Hh pathway activity that was dependent on SHH ligand, or in one case, a PTCH1 gene mutation. Hh signalling appeared necessary to sustain cell growth, as SHH ligand depletion with Robotikinin or SMO inhibition, either with chemical inhibitors (Itraconazole or LDE-225) or SMO-specific siRNA, attenuated GLI1 activity and cell proliferation in both monolayer and organotypic raft culture. Furthermore, treatment of Hh-dependent cell lines with SMO inhibitors sensitised cells to Cisplatin. Findings from our study offer us the opportunity to explore further the development of targeted chemotherapy for women with VSCC driven by aberrant Hh activation.
Citation
Yap, J. K. W., Uddin, K., Pounds, R., O'Neill, D., Kehoe, S., Ganesan, R., & Dawson, C. W. (2021). Aberrant activation of the Hedgehog signalling pathway in squamous cell carcinoma of the vulva as a potential target for cancer therapy. Scientific reports, 11(1), 17665.
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Article