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Investigation of Free S-Glycidol Compound Cytotoxicity Mechanism in<br />

Human Colon Cell Line (Hct 116) Via Mapk Pathway<br />

Nanthini Ravi<br />

Supervisor: Dr. Nurul Huda Binti Abdul Kadir @Abdul Rahman<br />

Bachelor of Science (Biological Sciences)<br />

School of Fundamental Science<br />

Human Colorectal Cancer is classified as the third most common cancer in both men<br />

and women although the risk is slightly lower in woman. Free S Glycidol Compound<br />

cytotoxicity was investigated against Human Colon Cell Lines (HCT-116). The cytotoxic<br />

effect of HCT-116 cells were evaluated by using AlamarBlue ® assay. The compound<br />

showed significant potential to reduce the viability of the HCT-116 cells with exclusive<br />

50% inhibition concentration (IC50) on each time of the treatments (IC50: 4.30mM<br />

after 24 hours; 0.656mM after 48 hours; 0.398mM after 72 hours). GAPDH, ERK1/2,<br />

p-ERK, BCL-2, CASPACE-3 mitogen-activated protein kinase (MAPK) was detected<br />

using Western blot technique and our results had shown that the protein expression<br />

of treated HCT-116 with S Glycidol compound for CASPACE-3 was down-regulated for<br />

both 24 and 48 hours indicating no apoptosis involved although BCL-2 shows preapoptotic<br />

expression at 24 hours, suggesting that cell death event was initially<br />

triggered but underwent homeostasis. In line, with the result of protein expression of<br />

CASPACE-3, there is no induction of apoptosis via ROS generation after treated for 24<br />

hours, thus suggesting that the cell death event does not occur after the treatment<br />

with Free S Glycidol Compound.<br />

392 | U M T U N D E R G R A D U A T E R E S E A R C H D A Y 2018

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