Insights into the role of components of the tumor microenvironment in oral carcinoma call for new therapeutic approaches |
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Authors: | Tuula Salo Marilena Vered Ibrahim O. Bello Pia Nyberg Carolina Cavalcante Bitu Ayelet Zlotogorski Hurvitz Dan Dayan |
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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 |
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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. |
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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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