In this study, the expression, clinicopathological correlates and prognostic value of HMGCR expression in colorectal cancer was examined.\n\nFindings: Immunohistochemical expression of HMGCR was assessed in tissue microarrays with primary tumours from 557 incident cases of colorectal cancer in the Malmo Diet and Cancer Study. Pearson’s Chi Square test was applied to explore the associations between HMGCR expression and clinicopathological factors and other investigative biomarkers. Kaplan Meier analysis and Cox proportional hazards modeling were used AP24534 to assess the relationship between HMGCR expression and cancer-specific survival (CSS) according to negative vs positive HMGCR expression. A total number of
535 (96.0%) tumours were suitable for analysis, of which 61 (11.4%) were HMGCR negative. Positive cytoplasmic HMGCR expression was associated with distant metastasis-free disease at diagnosis (p = 0.002), lack of vascular invasion (p = 0.043), microsatellite-instability (p = 0.033), expression of cyclin D1 (p = <0.001) and p21 (p = <0.001). Positive HMGCR
expression was significantly associated with a prolonged CSS in unadjusted Cox regression analysis in the entire cohort (HR = 1.79; 95% RG-7112 in vivo CI 1.20-2.66) and in Stage III-IV disease (HR = 1.71; 95% CI 1.09-2.68), but not after adjustment for established clinicopathological parameters.\n\nConclusions: Findings from this prospective cohort study demonstrate that HMGCR is differentially expressed in colorectal cancer and that positive expression is associated with favourable tumour characteristics and a prolonged survival in unadjusted analysis. The utility of HMGCR as a predictor of response to neoadjuvant or adjuvant statin treatment in colorectal cancer merits further study.\n\nVirtual slides: The virtual slides for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/2115647072103464.”
“In this study, the chemical composition of Torreya nucifera essential oil (TEO) and its biological Entinostat inhibitor activities were analyzed. TEO was obtained by steam distillation from leaves collected from Jeju Island and analyzed using gas chromatography (GC)-flame ionization
detection (FID) and GC-MS. dl-Limonene (30.1%), delta-3-carene (15.37%) and alpha-pinene (11.5%) were the major components in TEO. The antibacterial and anti-inflammatory activities of TEO against skin pathogens have not previously been reported. Thus, we assessed the antibacterial activities of TEO using the disk diffusion method. TEO showed excellent antibacterial activities against Propionibacterium acnes, Propionibacterium granulosum, Malassezia furfur, Staphylococcus epidermidis and Candida albicans. The minimum inhibitory concentration (MIC) of TEO against these skin pathogens ranged from 2.5 to 20.0 mu L mL(-1). In addition, TEO reduced the LPS-induced secretion of interleukin-1 beta (IL-1 beta), IL-6, NO and PGE(2) in RAW 264.7 cells, indicating that it has anti-inflammatory effects.