The present data confirm that PA and MEC are the most common benign and malignant SGTs. However, it is important to consider that differences in tumor types may be influenced by whether a tumor derives from a medical or a dental service.

Fatty acid synthase (FASN) is the enzyme responsible for the endogenous synthesis of the saturated fatty acid palmitate. In contrast to most normal cells, malignant cells depend on FASN activity for growth and survival. In fact, FASN is overexpressed in a variety of human cancers including cutaneous melanoma, in which its levels of expression are associated with a poor prognosis and depth of invasion. Here, we show that the specific inhibition of FASN activity by the antiobesity drug Orlistat or siRNA is able to significantly reduce proliferation and promote apoptosis in the mouse metastatic melanoma cell line B16-F10. These results prompted us to verify the effect of FASN inhibition on the metastatic process in a model of spontaneous melanoma metastasis, in which B16-F10 cells injected in the peritoneal cavity of C57BL/6 mice metastasize to the mediastinal lymph nodes. We observed that mice treated with Orlistat 48 hr after the inoculation of B16-F10 cells exhibited a 52% reduction in the number of mediastinal lymph node metastases, in comparison with the control animals. These results suggest that FASN activity is essential for B16-F10 melanoma cell proliferation and survival while its inactivation by Orlistat significantly reduces their metastatic spread. The chemical inhibition of FASN activity could have a potential benefit in association with the current chemotherapy for melanoma. ' 2008 Wiley-Liss, Inc.Key words: melanoma; fatty acid synthase; metastasis; Orlistat; B16-F10 cells Endogenous fatty acid synthesis from the small carbon precursors acetyl-CoA and malonyl-CoA is dependent on the activity of fatty acid synthase (FASN, EC2.3.1.85). In most of the cells, FASN is downregulated by the dietary fatty acids, with exception of lipogenic tissues as liver, lactating breast, fetal lung and adipose tissue.1,2 Recent studies provide compelling evidence that neoplastic lipogenesis is essential for cancer cell survival. In fact, several human epithelial malignancies, such as those of prostate, breast, ovary, bladder, lung, stomach and oral cavity, melanoma as well as soft tissue sarcomas overexpress FASN. [3][4][5][6][7][8][9][10][11][12][13][14][15][16] For some of these tumors, such as prostate, breast and ovarian cancers and melanoma, 4,5,9,12 FASN overexpression has also been associated with a poor prognosis. Experimental studies have shown that FASN inhibition reduces cell proliferation by blocking DNA replication during S-phase, induces apoptosis, [17][18][19][20] and decrease the size of prostate, ovarian and breast cancer xenografts. 3,21,22 In addition, the inhibition of FASN activity has a chemopreventive effect in the breast cancer transgenic neu-N mouse model. 23 Orlistat (tetrahydrolipstatin) is an irreversible inhibitor of pancreatic and gastric lipases clinically used because of its antiobesity properties that also blocks the activity of the thioesterase domain of FASN. 24 In fact, FASN inhibition by Orlistat reduces proliferation and promotes apoptosis in prostate, breast and stomach cancer cel...

A significant association between the BD model and outcome of OSCC patients was observed, indicating this new histopathological grading system as a possible prognostic tool.

An important role has been attributed to cancerassociated fibroblasts (CAFs) in the tumorigenesis of oral squamous cell carcinoma (OSCC), the most common tumor of the oral cavity. Previous studies demonstrated that CAFsecreted molecules promote the proliferation and invasion of OSCC cells, inducing a more aggressive phenotype. In this study, we searched for differences in the secretome of CAFs and normal oral fibroblasts (NOF) using mass spectrometrybased proteomics and biological network analysis. Comparison of the secretome profiles revealed that upregulated proteins involved mainly in extracellular matrix organization and disassembly and collagen metabolism. Among the upregulated proteins were fibronectin type III domain-containing 1 (FNDC1), serpin peptidase inhibitor type 1 (SERPINE1), and stanniocalcin 2 (STC2), the upregulation of which was validated by quantitative PCR and ELISA in an independent set of CAF cell lines. The transition of transforming growth factor beta 1 (TGF-β1)-mediating NOFs into CAFs was accompanied by significant upregulation of FNDC1, SERPINE1, and STC2, confirming the participation of these proteins in the CAF-derived secretome. Type I collagen, the main constituent of the connective tissue, was also associated with several upregulated biological processes. The immunoexpression of type I collagen N-terminal propeptide (PINP) was significantly correlated in vivo with CAFs in the tumor front and was associated with significantly shortened survival of OSCC patients. Presence of CAFs in the tumor stroma was also an independent prognostic factor for OSCC disease-free survival. These results demonstrate the value of secretome profiling for evaluating the role of CAFs in the tumor microenvironment and identify potential novel therapeutic targets such as FNDC1, SERPINE1, and STC2. Furthermore, type I collagen expression by CAFs, represented by PINP levels, may be a prognostic marker of OSCC outcome.Electronic supplementary material The online version of this article

Considering the possible loss of cylinders during immunohistochemical reactions, 2.0-mm TMAs in duplicate are a more reliable approach for pleomorphic adenoma immunohistochemical study.