Abstract

We have recently identified and characterized cancer stem cell (CSC) subpopulations within moderately differentiated buccal mucosal squamous cell carcinoma (MDBMSCC). We hypothesized that these CSCs express components of the renin-angiotensin system (RAS). 3,3'-Diaminobenzidine (DAB) immunohistochemical (IHC) staining was performed on formalin-fixed paraffin-embedded MDBMSCC samples to investigate the expression of the components of the RAS: (pro)renin receptor (PRR), angiotensin converting enzyme (ACE), angiotensin II receptor 1 (ATIIR1), and angiotensin II receptor 2 (ATIIR2). NanoString mRNA gene expression analysis and Western Blotting (WB) were performed on snap-frozen MDBMSCC samples to confirm gene expression and translation of these transcripts, respectively. Double immunofluorescent (IF) IHC staining of these components of the RAS with the embryonic stem cell markers OCT4 or SALL4 was performed to demonstrate their localization in relation to the CSC subpopulations within MDBMSCC. DAB IHC staining demonstrated expression of PRR, ACE, ATIIR1, and ATIIR2 in MDBMSCC. IF IHC staining showed that PRR was expressed by the CSC subpopulations within the tumor nests, the peri-tumoral stroma, and the endothelium of the microvessels within the peri-tumoral stroma. ATIIR1 and ATIIR2 were localized to the CSC subpopulations within the tumor nests and the peri-tumoral stroma, while ACE was localized to the endothelium of the microvessels within the peri-tumoral stroma. WB and NanoString analyses confirmed protein expression and transcription activation of PRR, ACE, and ATIIR1, but not of ATIIR2, respectively. Our novel findings of the presence and localization of PRR, ACE, ATIIR1, and potentially ATIIR2 to the CSC subpopulations within MDBMSCC suggest CSC as a therapeutic target by modulation of the RAS.

Highlights

  • Oral cavity cancer is the sixth most common cancer globally [1, 2] with more than 90% being squamous cell carcinoma (SCC) [2, 3]

  • We have recently demonstrated the presence, within moderately differentiated buccal mucosal squamous cell carcinoma (MDBMSCC), of an EMA+/SOX2+/SALL4+/OCT4+/pSTAT3+/ NANOG+ Cancer stem cells (CSCs) subpopulation within the tumor nests; as well as two separate peri-tumoral stromal populations one expressing EMA−/SOX2+/OCT4+/pSTAT3+/NANOG+ and another expressing EMA−/CD34+/SOX2+/OCT4+/pSTAT3+/ NANOG+ localized to the endothelium of the microvessels [16]

  • This CSC subpopulation may represent a “normal” stem cell population or cells that have undergone an epithelial to mesenchymal transition (EMT) [28], with the endothelial population possibly reflecting the phenomenon of vascular mimicry [29]

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Summary

Introduction

Oral cavity cancer is the sixth most common cancer globally [1, 2] with more than 90% being squamous cell carcinoma (SCC) [2, 3]. 5-year survival for BMSCC remains 50–58%, and the overall survival has only increased by 5% in the past 20 years [1, 4, 6]. This poor prognosis is partly due to late presentation with advanced loco-regional disease and less commonly metastasis to the bone, brain, or liver [5]

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