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OBJECTIVES
General Objective:
Specific Objectives:
- To explore the the biological significance of agarichusblasae to humanity, its benefits for patients suffering from cancer of the prostate. - To evaluate agarichus-blasaes possible apoptotic properties against cancer cells. - To observe agarichus-blasaes biological relation to liver cancer cell prevention and destruction through thorough laboratory sampling and experimentation. - To conceptualize, if not identify credible agarichusblasaes preparation that will facilitate prostate cancer cell inhibition. - To provide recommendations for the improvement and development of cancer research.
The study will be most significant for the people who are in the lower class especially those who are in the undeveloped regions of the country where medical facilities are least available. It is a fact that Philippines, being a third world country, have very limited resources and goods are overpriced including medical expenses. As a result, many people resort in untested, ineffective, alternative medicine in which side-effects could be fatal. By understanding and evaluating carefully, this research will provide and name a potential effective cure for cancer at a low cost because our country has abundant sources of ABM. Aside from being an addition to other potential cures for cancer, this study will also be significant in discouraging people from using untested substances.
WHY AGARICUS?
It
is best known mushroom in the western world Originating in Brazil Used for CANCER, type 2 diabetes, high cholesterol, liver disease, blood stream disorders, digestive problems Also used to boost the immune system for physical and emotional stress
WHY AGARICUS?
Insufficient
evidence for cancer treatment side effects developing research suggests that taking agaricus mushroom might reduce some effects. Efforts to study the health properties of this tasty mushroom is found to be effective breast cancer inhibitor through animal experiments, but also it is best cancer fighter
WHY AGARICUS?
Even
more astounding for those mice fed with mushroom as a preventative agent, injected with powerful cancer-causing Sarcoma 180, 99.4 % of them showed no tumor.
WHY AGARICUS?
Most
experiments done are in animals, rarely have cell lines At the Medical department of Tokyo University and Tokyo College of Pharmacy ; mice with cancerous tumors were fed with Agaricus mushroom. The cancerous tumors were eliminated in 90% of the mice.
METHODOLOGY
PLANT EXTRACTION
1. The Agaricus blazae were to be grounded into powder and be dried. 2. Dried powder (100 g) of Agarichus-Blazae was extracted in soxhlet apparatus with 1000 ml of 95% ethanol. The soxhelation process was carried out until the solvent was found to be colorless. 3. The dark brown ethanolic extract was then filtered, concentrated using a rotary evaporator.
METHODOLOGY: EXTRACTION
SAMPLE GROUNDED and PULVORIZED EXTRACTION USING SOXHLET APPARATUS
CRUDE EXTRACT
CELL LINE
The cell line will be obtained from Saint Lukes Medical Hospital. The cell will be cultured in a growth medium (pH 7.4) supplemented with 10% Fetal bovine serum (FBS) and antibiotics, penicillin (100 units/ml) and streptomycin sulfate (100 g/ml).
1. Cells will be seeded into 4 wells of a 96-well micro titer plate at 2 x 104 cells per well with 100 l growth medium and then incubated for 24 h at 37 C under 5% CO2. 2. Then the medium will be removed while fresh growth medium containing the agarichus-blasae extract is added at 100, 50 and 25 g/ml (Dependent variable). Water and (anticancer medicine) for your negative and positive control respectively. 3. After 3 days of incubation at 37 C under 5% CO2, the medium will be removed while 0.1 mg/ml MTT [3-(4, 5dimethyl thiazole-2yl) - 2, 5-diphenyl tetrazolium bromide] reagent will be added. 4. After 5 h incubation, the MTT will be removed before adding 100 l DMSO to each well and gently shaken. 5. The absorbance was then determined by ELISA reader at 516 nm. 6. Control wells will receive only the media without the extract.
TEST SAMPLE
POSITIVE CONTROL
NEGATIVE CONTROL
MTT ASSAY
MTT ASSAY
MTT ASSAY
APOPTOTIC ASSAY
TRYPAN
1.
2. 3.
BLUE ASSAY Centrifuge an aliquot of cell suspension . Resuspend the cell pellet in 1 ml PBS or serum-free complete medium Mix 1 part of 0.4% trypan blue and 1 part cell suspension, allow mixture to incubate ~3 min at room temp
TIME SCHEDULE
July Review of literature / planning Submission and consultation of research proposal Finalization of the research proposal August September October November December January February March
TIME SCHEDULE
July August September October November December January February March Experimenta tion time Collection of data Data analysis Finalization of written report Final Oral Defense