Post-transcriptional suppression of G protein-coupled receptor 15 (GPR15) by microRNA-1225 inhibits proliferation, migration, and invasion of human colorectal cancer cells.

The G protein-coupled receptors (GPRs) have been shown to regulate several cancer related processes. The aberrant expression of GPRs has been linked to the development of several cancers. The present study was designed to examine the expression and decipher the role of GPR15 in the development of human colorectal cancer. The results revealed GPR15 to be significantly (P < 0.05) upregulated in colorectal cancer cells. The silencing of GPR15 inhibited the growth of the colorectal cancer cells via induction of apoptosis. Induction of apoptosis in colorectal cancer cells was associated increase in Bax and decrease in Bcl-2 expression. The silencing of GPR-15 also caused a significant (P < 0.05) decline in the migration and invasion of the colorectal cancer cells. Bioinformatic analysis and luciferase assay revealed that the expression of GPR15 to be post-transcriptionally regulated by microRNA-1225 (miR-1225). The expression of miR-1225 was found to significantly (P < 0.05) downregulated in colorectal cancer cells and its overexpression caused suppression of GPR15 and inhibited the proliferation of the colorectal cancer cells. Nonetheless, overexpression of GPR15 could avoid the growth inhibitory effects of miR-1225. The results suggest that the GPR15/miR-1225 axis play an important role in the development of colon rectal cancer and exhibit therapeutic implications for its treatment.

Effect of sodium hyaluronate-arboxycellulose membrane (Seprafilm®) on postoperative small bowel obstruction: A meta-analysis.

BACKGROUND: This meta-analysis was performed to evaluate the effect of Seprafilm® on postoperative small bowel obstruction. METHODS: A literature search was conducted in the PubMed and EMBASE databases through August 2020. The pooled risk ratios as well as the corresponding 95% confidence intervals were calculated using RevMan 5.3 software. RESULTS: A total of 9 clinical control trials involving 4,351 patients (2,123 in the Seprafilm® group and 2,228 in the control group) were included. The overall analysis showed that the pooled risk ratio was 0.45 (95% confidence interval = 0.34-0.60; P < .00001), indicating that the risk of postoperative small bowel obstruction can be significantly decreased by the application of Seprafilm®. Similarly, an obvious effect of Seprafilm® on reducing the rate of postoperative small bowel obstruction was also shown in the subgroup analyses by population (adult participants), study design (randomized control study or nonrandomized control study), region (Japan or Korea), follow-up duration (2 years or 5 years), and sheet number of Seprafilm® (1 sheet or >1 sheet). CONCLUSION: In conclusion, the use of Seprafilm® is beneficial for decreasing the rate of postoperative small bowel obstruction.

Doxorubicin loaded liposomes for lung tumor targeting: in vivo cell line study in human lung cancer.

PURPOSE: In the present investigation the hydrophilic drug doxorubicin (DOX) was successfully incorporated with the drug carrier GE11 which serves as marker for tumor cells in non small cell lung cancer(NSCLC) to form the liposomal formulation. METHODS: The formulation was fabricated in two steps: one being the preparation of liposomal formulation using reverse phase evaporation method and second is synthesis of DSPE-PEG 2000 - GE 11complex. RESULTS: Thus prepared liposomes when evaluated via scanning electron spectroscopy showed smooth and spherical surface with particle size ranging between 102±0.3 to 120±0.5 nm. The percent encapsulation efficiency was 65.34 with highest drug release of 98% up to 45 h. The cytotoxic study revealed the non-toxic nature of carrier protein (i.e. GE11). The microbiological study has shown the antibiotic efficiency of liposomal formulation to be comparable with pure drug. In vivo cellular uptake study showed efficiency of GE11 protein in accumulation in tumor cells. The study conducted in mice showed more reduction in tumor size with liposomal formulation (312 mm3) than with pure drug (540 mm3). CONCLUSION: DOX loaded liposomes with GE11 as carriers were successfully formulated by using reverse phase evaporation method. The prepared liposomal formulation was found to be most effective in combating cancer cells when compared to pure drug.