Investigating the Anticancer Effects of Pleurotus Ostreatus Polysaccharide on G0/G1 Cell Cycle Arrest and Apoptosis in Ehrlich Ascites Carcinoma Cells.

Cancer is one of the leading causes of mortality worldwide. Despite the advancement of cancer treatment by various means including surgery, chemotherapy, etc., cancer is still a challenging disease to manage. This study was undertaken to investigate extraction, purification, structural elucidation, and the potential anti-cancer effects of Pleurotus ostreatus polysaccharide (POP). The anti-cancer activities were performed on the Ehrlich Ascites Carcinoma Cell Line. The results demonstrated that the MW of  POP was154649.8 Da with homopolysaccharide composed of D-glucose units, featuring (1→6)-α-D-Glcp backbone with O-6 branches and T-α-D-Glcp terminations. and the yield was 6.27%. was 6.27%, The antitumor activity assessment demonstrated significant cytotoxicity of POP against Ehrlich Ascites Carcinoma (EAC) cells, with an IC50 of 121.801 µg/mL, supported by LDH release analysis. POP inhibited cell migration, invasion, and colony formation, indicating its potential as an anti-cancer agent. POP elicited the apoptotic activity with the upregulation of Caspase-9 and Bax, and downregulation of Bcl-2. The DNA fragmentation assay further confirmed apoptosis-mediated DNA degradations. Additionally, POP-induced cell cycle arrest at the G0/G1 phase, by altering the expression of p53, Cyclin D, and Cdk4 proteins. So, Pleurotus ostreatus polysaccharide (POP) showed significant cytotoxicity on Ehrlich Ascites Carcinoma cells, indicating potential as an anti-cancer agent.

Dose-response relationship between arsenic exposure and the serum enzymes for liver function tests in the individuals exposed to arsenic: a cross sectional study in Bangladesh.

BACKGROUND: Chronic arsenic exposure has been shown to cause liver damage. However, serum hepatic enzyme activity as recognized on liver function tests (LFTs) showing a dose-response relationship with arsenic exposure has not yet been clearly documented. The aim of our study was to investigate the dose-response relationship between arsenic exposure and major serum enzyme marker activity associated with LFTs in the population living in arsenic-endemic areas in Bangladesh. METHODS: A total of 200 residents living in arsenic-endemic areas in Bangladesh were selected as study subjects. Arsenic concentrations in the drinking water, hair and nails were measured by Inductively Coupled Plasma Mass Spectroscopy (ICP-MS). The study subjects were stratified into quartile groups as follows, based on concentrations of arsenic in the drinking water, as well as in subjects' hair and nails: lowest, low, medium and high. The serum hepatic enzyme activities of alkaline phosphatase (ALP), aspartate transaminase (AST) and alanine transaminase (ALT) were then assayed. RESULTS: Arsenic concentrations in the subjects' hair and nails were positively correlated with arsenic levels in the drinking water. As regards the exposure-response relationship with arsenic in the drinking water, the respective activities of ALP, AST and ALT were found to be significantly increased in the high-exposure groups compared to the lowest-exposure groups before and after adjustments were made for different covariates. With internal exposure markers (arsenic in hair and nails), the ALP, AST and ALT activity profiles assumed a similar shape of dose-response relationship, with very few differences seen in the higher groups compared to the lowest group, most likely due to the temporalities of exposure metrics. CONCLUSIONS: The present study demonstrated that arsenic concentrations in the drinking water were strongly correlated with arsenic concentrations in the subjects' hair and nails. Further, this study revealed a novel exposure- and dose- response relationship between arsenic exposure metrics and serum hepatic enzyme activity. Elevated serum hepatic enzyme activities in the higher exposure gradients provided new insights into arsenic-induced liver toxicity that might be helpful for the early prognosis of arsenic-induced liver diseases.

Optimization of extraction of antioxidant polysaccharide from Pleurotus ostreatus (Jacq.) P. Kumm and its cytotoxic activity against murine lymphoid cancer cell line.

The purpose of this study was to optimize the extraction method for polysaccharide from the fruiting bodies of Pleurotus ostreatus (Jacq.) P. Kumm and to assess the antioxidant and cytotoxic potentials of polysaccharide. In this investigation, polysaccharides from Pleurotus ostreatus (Jacq.) P. Kumm were extricated by utilizing the hot water. One-single factor and response surface methodology was established to optimize the extraction conditions for polysaccharide from Pleurotus ostreatus (Jacq.) P. Kumm. Examination of antioxidant activity of Pleurotus ostreatus polysaccharide (POP) was directed by utilizing 2, 2-diphenyl-1-picrylhydrazyl (DPPH) and 2, 2-azino-bis-3-ethyl-benzothiazoline-6-sulfonic acid (ABTS) techniques. Cytotoxicity of POP was evaluated using an MTT assay. The experimental data were fitted to a quadratic equation utilizing multiple regression investigations, and the ideal conditions were as per the following: water/crude material proportion, 26.04 mL/g; an extraction time of 62.08 minutes; and an extraction temperature 70.5°C. Under such conditions, the polysaccharide yield was 5.32 ± 0.12% with the anticipated yield. POP showed good scavenging activity against DPPH radical (p<0.001, EC50 = 1036.38 µg/mL, R2 = 0.8313) and ABTS radicals (p<0.001, EC50 = 824.37 µg/mL, R2 = 0.8223), with a dose (p<0.001)-and-time (p<0.001) dependent cytotoxic potential on Ehrlich ascites carcinoma cell line in vitro. This demonstrated that polysaccharides (POP) had certain cancer prevention agent exercises. In this manner, these examinations give reference to additionally research and reasonable improvement of Pleurotus ostreatus (Jacq.) P. Kumm polysaccharide and POP may prove a useful therapeutic agent, due to its robust antioxidant and cytotoxic activity.

Evolution of disease and potential biocontrol activity of Trichoderma SP. against Rhizoctonia solani on potato / Potencial do biocontrole por Trichoderma em relação à evolução da doença causada por Rhizoctonia solani em batata

Black scurf and stem canker disease cause by the fungal pathogen of Rhizoctonia solani and it is an economical important disease of potatoes in Bangladesh and throughout the world. This study evaluated the black scurf and stem canker disease development in potato and antagonistic activity of Trichoderma spp. against R. solani. The artificial infections were carried out using the inoculums of R. solani. The treatments (%inoculum) were: T1 (0% inoculum), T2 (5% inoculum), T3 (10% inoculum), T4 (20% inoculum), T5 (50% inoculum), and T6 (100% inoculum). The infection of stem canker and black scurf on progeny tubers increased with increase in inoculum levels. The highest disease incidence and severity was found in T6 (100% inocula). T6 showed the maximum black scurf infected tubers (russet, deformed and sclerotia). The lowest germination percentage, plant height and tuber yield were also obtained in the same treatment (100% inocula). Trichoderma spp reduced the growth of R. solani and the highest growth suppression was noted in isolate TM12. According to antagonistic activity, Trichoderma spp. reduced the growth of R. solani but was not able to stop the pathogen development. This finding showed management of this disease or R. solani invasion requires an integrated approach compared to Trichoderma single approach.

A rizoctoniose ou crosta negra causada por Rhizoctonia solani é a mais importante doença nos campos de batata em Bangladesh, bem como em várias regiões do mundo. Este trabalho avaliou o potencial do biocontrole com Trichoderma spp. e sua ação antagonista contra R. solani em batateira. Realizou-se as avaliações do potencial antagonosta usando inoculação artificial de R. solani. Os tratamentos (% de inóculo) foram: T1 (0% de inóculo), T2 (5% ), T3 (10%), T4 (20%), T5 (50%) , e T6 (100% de inóculo). A infecção de rizoctoniose na haste e crosta negra nos tubérculos aumentou proporcionalmente com o aumento do nível de inóculo. A maior incidência e severidade da doença ocorreu no tratamento 6 (100 % de inóculo), o qual apresentou maior quantidade de tubérculos infectados e deformados com escleródios em sua superfície. A menor porcentagem de germinação e produção de tubérculos também foi encontrada no tratamento 6, o qual também apresentou menor altura de planta. Trichoderma spp reduziu o crescimento de R. solani e a maior atividade de supressão do crescimento foi encontrada pelo isolado TM12. Foi detectada a atividade antagonista de Trichoderma spp. em reduzir o crescimento de R. solani, mas este não inibiu o crescimento total do patógeno. Conclui-se que o manejo da rizoctoniose da batateira por colonização de R. solani necessita táticas de manejo integrado em detrimento do uso isolado do manejo ou biocontrole com Trichoderma spp.

Isolation of stigmasterol and beta-sitosterol from methanolic extract of root bark of Calotropis gigantea (Linn).

Aim of this study is to identify and characterize the bioactive principles from the root bark of Calotropis gigantea. It has wide folk medicinal use. For isolation of the compounds, the dried root bark's powder of Calotropis gigantea were subjected to hot extraction and then the crude methanol (MeOH) extract was fractionated with petroleum ether, chloroform and ethyl acetate. Two compounds were isolated and purified from petroleum ether fraction of crude methanol extract and the structures were determined as stigmasterol and beta-sitosterol by analysis of physical, chemical and spectral characteristics (1D NMR and mass spectrometry).