58 research outputs found

    Tongue Cancer Cell-Derived CCL20 Induced by Interaction With Macrophages Promotes CD163 Expression on Macrophages

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    BackgroundCD163-positive macrophages contribute to the aggressiveness of oral squamous cell carcinoma. We showed in a previous report that CD163-positive macrophages infiltrated not only to the cancer nest but also to its surrounding epithelium, depending on the presence of stromal invasion in tongue carcinogenesis. However, the role of intraepithelial macrophages in tongue carcinogenesis remains unclear. In this study, we assessed the biological behavior of intraepithelial macrophages on their interaction with cancer cells.Materials and MethodsWe established the indirect coculture system (intraepithelial neoplasia model) and direct coculture system (invasive cancer model) of human monocytic leukemia cell line THP-1-derived CD163-positive macrophages with SCC25, a tongue squamous cell carcinoma (TSCC) cell line. Conditioned media (CM) harvested from these systems were analyzed using cytokine array and enzyme-linked immunosorbent assay and extracted a specific upregulated cytokine in CM from the direct coculture system (direct CM). The correlation of both this cytokine and its receptor with various clinicopathological factors were evaluated based on immunohistochemistry using clinical samples from 59 patients with TSCC. Moreover, the effect of this cytokine in direct CM on the phenotypic alterations of THP-1 was confirmed by real-time polymerase chain reaction, western blotting, immunofluorescence, and transwell migration assay.ResultsIt was shown that CCL20 was induced in the direct CM specifically. Interestingly, CCL20 was produced primarily in SCC25. The expression level of CCR6, which is a sole receptor of CCL20, was higher than the expression level of SCC25. Our immunohistochemical investigation showed that CCL20 and CCR6 expression was associated with lymphatic vessel invasion and the number of CD163-positive macrophages. Recombinant human CCL20 induced the CD163 expression and promoted migration of THP-1. We also confirmed that a neutralizing anti-CCL20 antibody blocked the induction of CD163 expression by direct CM in THP-1. Moreover, ERK1/2 phosphorylation was associated with the CCL20-driven induction of CD163 expression in THP-1.ConclusionsTongue cancer cell-derived CCL20 that was induced by interaction with macrophages promotes CD163 expression on macrophages

    Comparative Analyses Define Differences Between Bhd-Associated Renal Tumour and Sporadic Chromophobe Renal Cell Carcinoma

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    BACKGROUND: Birt-Hogg-Dubé (BHD) syndrome, caused by germline alteration of folliculin (FLCN) gene, develops hybrid oncocytic/chromophobe tumour (HOCT) and chromophobe renal cell carcinoma (ChRCC), whereas sporadic ChRCC does not harbor FLCN alteration. To date, molecular characteristics of these similar histological types of tumours have been incompletely elucidated. METHODS: To elucidate renal tumourigenesis of BHD-associated renal tumours and sporadic renal tumours, we conducted whole genome sequencing (WGS) and RNA-sequencing (RNA-seq) of sixteen BHD-associated renal tumours from nine unrelated BHD patients, twenty-one sporadic ChRCCs and seven sporadic oncocytomas. We then compared somatic mutation profiles with FLCN variants and RNA expression profiles between BHD-associated renal tumours and sporadic renal tumours. FINDINGS: RNA-seq analysis revealed that BHD-associated renal tumours and sporadic renal tumours have totally different expression profiles. Sporadic ChRCCs were clustered into two distinct clusters characterized by L1CAM and FOXI1 expressions, molecular markers for renal tubule subclasses. Increased mitochondrial DNA (mtDNA) copy number with fewer variants was observed in BHD-associated renal tumours compared to sporadic ChRCCs. Cell-of-origin analysis using WGS data demonstrated that BHD-associated renal tumours and sporadic ChRCCs may arise from different cells of origin and second hit FLCN alterations may occur in early third decade of life in BHD patients. INTERPRETATION: These data further our understanding of renal tumourigenesis of these two different types of renal tumours with similar histology. FUNDING: This study was supported by JSPS KAKENHI Grants, RIKEN internal grant, and the Intramural Research Program of the National Institutes of Health (NIH), National Cancer Institute (NCI), Center for Cancer Research

    Synthesis of MgO templated mesoporous carbons and its use for capacitor electrode

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    Mesoporous carbons (MPCs) with large specific surface area are synthesized by the heat-treatment and subsequent acid treatment of magnesium citrate. The MPCs obtained are examined as electrode materials for electric double layer capacitor and show the huge gravimetric capacitance with superior rate performance in sulphuric acid electrolyte. The MPCs also realize the larger capacitance than conventional activated carbon in organic electrolyte and extraordinary high retention of capacitance at very low temperature, such as 80% of room temperature value at -60 °C.Se han sintetizado carbones mesoporosos (MPCs) con elevadas superficies específicas mediante tratamiento térmico y posterior tratamiento ácido de citrato de magnesio. Los MPCs obtenidos se han estudiado como electrodos para condensadores de doble capa eléctrica. Estos materiales presentan una capacidad gravimétrica muy elevada y una velocidad de carga-descarga alta en medio ácido sulfúrico. Los MPCs también poseen valores de capacidad en electrolito orgánico mayores que los carbones activados convencionales y presentan una retención de capacidad extraordinariamente alta a muy bajas temperaturas (a una temperatura de -60ºC se obtiene una retención de capacidad en torno al 80% con respecto a la capacidad medida a temperatura ambiente)

    Cationic Rhodium(I) Tetrafluoroborate-Catalyzed         Intramolecular Carbofluorination of Alkenes           via the Activation of a Carbon–Fluorine Bond in Acyl Fluorides

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    C–F bonds of acyl fluorides can be cleaved and added across teth-ered alkenes in the presence of a cationic rhodium(I) tetrafluorobo-rate catalyst. This 1,2-carbofluorination reaction offers a powerful method for the synthesis of tertiary alkyl fluoride derivatives with atom economy of 100%. Mechanistic studies indicate that the concerted action of a rhodium cation and a tetrafluoroborate anion is the key for the success of this catalytic cleavage and formation of C–F bonds in a controlled manner
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