Estradiol regulates miR-135b and mismatch repair gene expressions via estrogen receptor-β in colorectal cells.

Estrogen has anti-colorectal cancer effects which are thought to be mediated by mismatch repair gene (MMR) activity. Estrogen receptor (ER) expression is associated with microRNA (miRNA) expression in ER-positive tumors. However, studies of direct link between estrogen (especially estradiol E2), miRNA expression, and MMR in colorectal cancer (CRC) have not been done. In this study, we first evaluated the effects of estradiol (E2) and its antagonist ICI182,780 on the expression of miRNAs (miR-31, miR-155 and miR-135b) using COLO205, SW480 and MCF-7 cell lines, followed by examining the association of tissue miRNA expression and serum E2 levels using samples collected from 18 colorectal cancer patients. E2 inhibited the expressions of miRNAs in COLO205 cells, which could be reversed by E2 antagonist ICI 182.780. The expression of miR-135b was inversely correlated with serum E2 level and ER-β mRNA expression in CRC patients' cancer tissues. There were significant correlations between serum E2 level and expression of ER-β, miR-135b, and MMR in colon cancer tissue. This study suggests that the effects of estrogen on MMR function may be related to regulating miRNA expression via ER-β, which may be the basis for the anti-cancer effect in colorectal cells

A SMART WIDE-AREA MONITORING SYSTEM BASED ON COGNITIVE RADIO

ABSTRAC

2,4-Dibromo-6-[(hydroxyimino)methyl]phenol

In the title compound, C7H5Br4NO2, intra­molecular O—H⋯N hydrogen bonds are observed. In the crystal structure, inter­molecular O—H⋯O hydrogen bonds link the mol­ecules into dimers

Different Effects of Six Antibiotics and Ten Traditional Chinese Medicines on Shiga Toxin Expression by Escherichia coli

This study compared the effects of ten types of traditional Chinese medicines (TCMs) and six different antibiotics on E. coli O157:H7 Shiga toxin gene (stx2) mRNA expression level based on real-time PCR and the expression level of Stx toxin using an ELISA quantitative assay. We also compared their effects on the induction of the SOS response. The results clearly indicated that all ten TCMs had negative results in the SOS response induction test, while most TCMs did not increase the levels of stx2 mRNA and the Stx toxin. Some TCMs did increase the mRNA levels of the stx2 gene and the Stx toxin level, but their increases were much lower than those caused by antibiotics. With the exception of cefotaxime, the six antibiotics increased the Stx toxin level and increased the stx2 gene mRNA level. With the exceptions of cefotaxime and tetracycline, the antibiotics increased the SOS induction response. These results suggest that TCMs may have advantages compared with antibiotics, when treating E. coli O157:H7; TCMs did not greatly increase Stx toxin production and release

catena-Poly[[(diaqua­calcium)-bis­(μ-2-fluorobenzoato)-1′:1κ3 O:O,O′;1:1′′κ3 O,O′:O] 2,2′-bipyridine hemi­solvate]

In the title compound, {[Ca(C7H4FO2)2(H2O)2]·0.5C10H8N2}n, the CaII atom is coordinated by eigth O atoms from four 2-fluoro­benzoate ligands and two water mol­ecules, resulting in a distorted CaO8 square-anti­prismatic coordination environment. The 2-fluoro­benzoate ligand bridges two symmetry-related CaII atoms, giving rise to a chain structure extending along [100]. The distances between the Ca atom and its two symmetry-related counterparts are 4.054 (2) and 4.106 (2) Å. The polymeric chains are connected by classical O—H⋯N hydrogen bonds into a layer structure parallel to (010). The layers are connected by non-classical C—H⋯F hydrogen bonds into a three-dimensional supra­molecular structure. O—H⋯O and C—H⋯O inter­actions also occur. The uncoordinated 2,2′-bipyridine mol­ecule is located on a centre of symmetry at the mid-point of the bond between the two heterocycles. One of the two benzene rings is disordered over two sites with occupancy factors of 0.60 and 0.40

4,4-Diacetyl­hepta­nedinitrile

The asymmetric unit of the title compound, C11H14N2O2, contains one half-mol­ecule as the central C atom of the mol­ecule lies on a twofold rotation axis. In the crystal structure, weak inter­molecular C—H⋯N hydrogen bonds link the mol­ecules into zigzag chains along c

Research on Effects of the Thermal Stimulation by Moxibustion at Different Temperatures on Cardiac Function in Rats and on Mast Cells in the Local Site of Moxibustion

Objective. To observe effects of the thermal stimulation by moxibustion at different temperatures on cardiac function in brachycardia rat model and on mast cells in the local site of moxibustion at the Ximen Acupoint and to compare the differences of the effects of moxibustion at different temperatures. Method. Establish the brachycardia rat model with propranolol and observe effects of the thermal stimulation by moxibustion at different temperatures (38°C and 46°C). Results. The thermal stimulation by moxibustion at 2 temperatures may increase HR, MAP, LVSP, and +dp/dtmax and reduce t-dp/dtmax in brachycardia rats; the 46°C moxibustion group shows greater regulating effects on cardiac function in rats than that in the 38°C moxibustion group (P<0.05). The thermal stimulation by moxibustion at 2 temperatures may promote degranulation of mast cells in the local site of moxibustion at the Ximen Acupoint; the degranulation rate in the 46°C moxibustion group is higher than that in the 38°C moxibustion group (P<0.05). Conclusion. There is a certain association between the effect on the target organ and the effect in the local site of moxibustion. The moxibustion effect possibly resulted from local mast cells degranulation and different thermoreceptors activated by the thermal stimulation at different temperatures