4.1 Article

Mammalian target of rapamycin (mTOR) is involved in the survival of cells mediated by chemokine receptor 7 through PI3K/Akt in metastatic squamous cell carcinoma of the head and neck

Journal

BRITISH JOURNAL OF ORAL & MAXILLOFACIAL SURGERY
Volume 48, Issue 4, Pages 291-296

Publisher

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.bjoms.2009.06.007

Keywords

mTOR; CCR7; PI3K; Squamous cell carcinoma of head and neck; Survival

Funding

  1. National Natural Science Foundation of China [30672331]
  2. Scientific Research Starting Foundation for Young Scholars of School of Stomatology, China Medical University [K101593-09-18]

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Metastatic squamous cell carcinoma (SCC) of the head and neck expresses chemokine receptor 7 (CCR7). which activates phosphoinositide-3 kinase (PI3K) to promote invasion and survival of SCC cells in the head and neck. We hypothesised that mammalian target of rapamycin (m-TOR) may be the downstream molecule of the CCR7-PI3K pathway. Results have shown that interaction between CCR7 and its ligand CCL19 induces the phosphorylation of mTOR and its target p70s6k. This phosphorylation is abolished by inhibition of CCR7 and PI3K/Akt, indicating that mTOR is involved in the CCR7-PI3K cascade. The inhibitors of mTOR and CCR7-PI3K also lead to a significant increase in CCL19-induced death, apoptosis, and cell-cycle arrest of metastatic SCC cells in the head and neck. Taken together, our data indicate the important part played by mTOR in CCR7-induced survival of such SCC cells. (C) 2009 The British Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.

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