This review underscores the emerging theme that deregulated PCP signaling contributes to tumorigenesis, providing new potential targets for cancer therapy. [Mol Cancer Ther 2009;8(8):2103-9]“
“Aims: In this study, we evaluated whether catechins could inhibit the expression of pro-inflammatory mediators induced by dental caries-related bacteria, Streptococci, or pathogen-associated molecular patterns (PAMPs) stimulation in human FRAX597 dental pulp fibroblasts (HDPF). We further determined the mechanisms

of the anti-inflammatory activity of catechins.\n\nMain methods: Streptococci or PAMP-stimulated HDPF were treated with catechin, and then the expression and production of pro-inflammatory mediators were determined by RT-PCR and ELISA. Furthermore, the signal transduction pathways activated with toll-like receptor (TLR)2 ligand were assessed by Immunoblot and ELISA using blocking assay with specific inhibitors.\n\nKey findings: Increased expressions of pro-inflammatory mediators are found in inflamed dental pulp, especially in HDPF. We recently reported that dental pulpal innate immune responses may mainly result from the predominantly-expressed TLR2 signaling. Catechins, polyphenolic compounds GPCR & G Protein in green tea, exert protective and healing effects through multiple mechanisms, including antioxidative and anti-inflammatory effects. However, there

are no reports concerning the effects of catechins on dental pulp. In this study, we demonstrated that the up-regulated expressions of IL-8 or PGE(2) in Streptococci or PAMP-stimulated HDPF were inhibited by catechins, (-)-epicatechin gallate (ECG) and (-)-epigallocatechin selleckchem gallate (EGCG). In TLR2 ligand-stimulated HDPF, specific inhibitors of extracellular signal regulated kinase (ERK)1/2, p38, c-jun NH(2)-terminal kinase (SAP/JNK), NF-kappa B or catechins markedly reduced the level of pro-inflammatory mediators and the phosphorylation of these signal

transduction molecules was suppressed by catechins.\n\nSignificance: These findings suggest that catechins might be useful therapeutically as an anti-inflammatory modulator of dental pulpal inflammation. (C) 2010 Elsevier Inc. All rights reserved.”
“The complete molecule of title compound, C58H58P4, is generated by a crystallographic twofold rotation axis that passes through the center of the C(methine)-C(methine) bond of length 1.582 (4) angstrom The C-P bond lengths are 1.8824 (19) and 1.8991 (19) angstrom. The P-C-P angle of 109.69 (9)degrees is essentially equal to the expected value of 109.5 degrees for a tetrahedral C atom. Although the C(methine) P-C(aromatic) bond angles range from 102.67 (9) to 107.04 (9)degrees, the C(aromatic)-P-C(aromatic) bond angles of 96.72 (9) and 97.29 (9)degrees are significantly smaller.