Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/4730
Title: Effects of L-fucose supplementation on the viability of cancer cell lines
Authors: Alif Mazlan, Muhammad
Mat Yusof, Afzan
Lokman Md Isa, Muhammad
Keywords: adenocarcinoma
cancer
cell line
fucose
glycosylation
melanoma
Issue Date: 2020
Abstract: Effects of L-fucose supplementation on the viability of cancer cell lines Muhammad Alif Mazlan 1,2 , Afzan Mat Yusof 1,2 , Muhammad Lokman Md. Isa 1,2* 1 Department of Basic Medical Sciences for Nursing, International Islamic University Malaysia, Pahang 25200, Malaysia 2 Human Molecular and Cellular Biology Research Cluster (iMoleC), International Islamic University Malaysia, Pahang 25200, Malaysia *E-mail: lokman@iium.edu.my Abstract Background: Fucose is a deoxyhexose sugar. While the biological roles of L-fucose remain unclear, the sugar is known to accelerate the malignant potential of cancer cells. Therefore, this study aimed to evaluate the viability pattern of human cancer and normal cell lines treated with fucose. Methods: The human gingival fibroblast (HGF-1), colorectal adenocarcinoma (HT-29) and skin malignant melanoma (A375) cell lines were cultured and treated with fucose at three concentrations of 1, 5, and 10 mg/ml. Cell viability was then measured using (3-(4, 5-dimethylthiazolyl-2)-2, 5diphenyltetrazolium bromide (MTT) assay. The data were analyzed using Statistical Package for the Social Sciences software. Results: The percentage of HGF-1 cell viability showed a rapid decline after day 1 of treatment. HT-29 and A375 were capable of surviving treatment with high fucose concentrations. The data were highly significant at p < 0.001. Conclusion: Whereas a high concentration of fucose is toxic to the HGF-1 cell line, the HT-29 and A375 cell lines could potentially adapt to this condition. Down- or upregulation of certain molecules that could induce or inhibit cell death may explain such adaptation. Further testing of up- and downregulated molecules should be conducted in future work. Keywords: adenocarcinoma, cancer, cell line, fucose, glycosylation, melanoma
URI: http://localhost:8080/xmlui/handle/123456789/4730
Appears in Collections:VOL 24 NO 2 2020

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