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Insights into the role of components of the tumor microenvironment in oral carcinoma call for new therapeutic approaches
Authors:Tuula Salo  Marilena Vered  Ibrahim O. Bello  Pia Nyberg  Carolina Cavalcante Bitu  Ayelet Zlotogorski Hurvitz  Dan Dayan
Affiliation:1. Department of Diagnostics and Oral Medicine, Institute of Dentistry, University of Oulu, and Medical Research Center, Oulu, Finland;2. Oulu University Central Hospital, Oulu, Finland;3. Institute of Dentistry, University of Helsinki, Helsinki, Finland;4. Institute of Pathology, The Chaim Sheba Medical Center, Tel Hashomer, Ramat Gan, Israel;5. Department of Oral Pathology and Oral Medicine, School of Dentistry, Tel Aviv University, Tel Aviv 69978, Israel;6. Department of Oral Medicine and Diagnostic Sciences, King Saud University, Riyadh, Saudi Arabia;g Department of Oral and Maxillofacial Surgery, Rabin Medical Center, Beilinson Campus, Petah Tikva, Israel
Abstract:
The research on oral cancer has focused mainly on the cancer cells, their genetic changes and consequent phenotypic modifications. However, it is increasingly clear that the tumor microenvironment (TME) has been shown to be in a dynamic state of inter-relations with the cancer cells. The TME contains a variety of components including the non-cancerous cells (i.e., immune cells, resident fibroblasts and angiogenic vascular cells) and the ECM milieu [including fibers (mainly collagen and fibronectin) and soluble factors (i.e., enzymes, growth factors, cytokines and chemokines)]. Thus, it is currently assumed that TME is considered a part of the cancerous tissue and the functionality of its key components constitutes the setting on which the hallmarks of the cancer cells can evolve. Therefore, in terms of controlling a malignancy, one should control the growth, invasion and spread of the cancer cells through modifications in the TME components. This mini review focuses on the TME as a diagnostic approach and reports the recent insights into the role of different TME key components [such as carcinoma-associated fibroblasts (CAFs) and inflammation (CAI) cells, angiogenesis, stromal matrix molecules and proteases] in the molecular biology of oral carcinoma. Furthermore, the impact of TME components on clinical outcomes and the concomitant need for development of new therapeutic approaches will be discussed.
Keywords:αSMA, alpha smooth muscle actin   4NQO, 4-nitroquinoline-1-oxide   ADAMTS, a disintegrin and metalloproteinase with thrombospondin motif   bFGF, basic fibroblast growth factor   BM, basement membrane   BMMSCs, bone marrow-derived mesenchymal stem cells   CAF, cancer-associated fibroblast   CAI, cancer-associated inflammation   CCL5, chemokine (C&ndash  C motif) ligand 5   CD163+, cluster of differentiation 163   CD44, cluster of differentiation 44   CD80, cluster of differentiation 80   CTLs, cytotoxic T lymphocytes   ECM, extracellular matrix   EGF, epidermal growth factor   EMMPRIN, extracellular matrix metalloproteinase inducer   EMT, epithelial&ndash  mesenchymal transition   FGFs, fibroblast growth factors   Foxp3+, forkhead box P3   FSP-1, fibroblast specific protein-1   HGF, hepatocyte growth factor   HIF, hypoxia induced factor   HNSCC, head and neck squamous cell carcinoma   IGF-1, insulin-like growth factor-1   IL-8, interleukin-8   LHR, lymphocytic host response   LOX, lysyl oxidase   MDSCs, myeloid-derived suppressor cells   MET, mesenchymal&ndash  epithelial transformation   MMPs, matrix metalloproteinases   MT1-MMPs, transmembrane type 1 matrix metalloproteinases   NC1, noncollagenous domain 1   NF-kB, nuclear factor kappa B   NK cells, natural killer cells   OSCC, oral squamous cell carcinoma   PINP, procollagen type I N-terminal propeptide   PDGF, platelet-derived growth factor   PDGFR, platelet-derived growth factor receptor   ROS, reactive oxygen species   SCC, squamous cell carcinoma   SDF-1, stromal derived factor-1   TAM, tumor-associated macrophage   TGF-β1, transforming growth factor β-1   TIMPs, tissue inhibitor of metalloproteinases   TME, tumor microenvironment   TNF-α, tumor necrosis factor alpha   Tregs, regulatory T cells   VEGF, vascular endothelial growth factor   WPOI, worst pattern of invasion
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