4.7 Article

mTOR Inhibition Ablates Cisplatin-Resistant Salivary Gland Cancer Stem Cells

Journal

JOURNAL OF DENTAL RESEARCH
Volume 100, Issue 4, Pages 377-386

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/0022034520965141

Keywords

tumor initiating cell; self-renewal; rapamycin; chemotherapy; targeted therapy; head and neck cancer

Funding

  1. Uehara Memorial Foundation
  2. National Institutes of Health/National Institute of Dental and Craniofacial Research [R01-DE021139, R01-DE023220]
  3. Soda Toyoji Memorial Foundation

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This study demonstrated the therapeutic potential of mTOR inhibitors in targeting cisplatin-resistant cancer stem cells in salivary gland mucoepidermoid carcinoma. Combining mTOR inhibitors with platinum-based chemotherapy may offer a promising treatment strategy for patients with advanced MEC.
Patients with advanced salivary gland mucoepidermoid carcinoma (MEC) are treated with surgery and radiotherapy, as current systemic therapies are largely ineffective. As such, current treatment frequently leads to poor long-term survival due to locoregional recurrence or metastases. We have shown that salivary gland cancer stem cells (CSCs) are resistant to platinum-based chemotherapy and drive tumor progression. The purpose of this study was to investigate the effect of therapeutic inhibition of mTOR (mechanistic target of rapamycin) on resistance of CSCs to cisplatin, a prototypic platinum-based chemotherapeutic agent. Viability assays determined the effect of several inhibitors of PI3k/mTOR signaling (e.g., temsirolimus, BKM120, AZD8055, PF4708671) and/or cisplatin on survival of human MEC cells. The impact of mTOR inhibitors and/or cisplatin on MEC stemness was examined with salisphere assays, flow cytometry for ALDH/CD44 (CSC markers for MEC), and Western blots for Bmi-1 expression (marker of stem cell self-renewal). Salivary gland MEC patient-derived xenografts were used to examine the effect of cisplatin and/or temsirolimus on CSCs in vivo. We observed that cisplatin induced mTOR and S6K1 phosphorylation, increased the number and size of MEC salispheres, and induced Bmi-1 expression and the fraction of CSCs in MEC models in vitro. Cisplatin also increased the fraction of CSCs in vivo. In contrast, mTOR inhibition (e.g., temsirolimus) blocked cisplatin-induced Bmi-1 expression and salisphere formation in vitro. Remarkably, temsirolimus slowed down tumor growth and decreased the fraction of CSCs (P < 0.05) even in presence of cisplatin in a short-term in vivo experiment. Collectively, these results demonstrate that therapeutic inhibition of mTOR ablates cytotoxic-resistant CSCs, and they suggest that a combination of an mTOR inhibitor and platinum-based chemotherapy might be beneficial to patients with salivary gland mucoepidermoid carcinoma.

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