{"title":"补充L-聚焦对癌细胞活力的影响","authors":"Muhammad Alif Mazlan, A. M. Yusof, M. Isa","doi":"10.7454/msk.v24i2.1185","DOIUrl":null,"url":null,"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. Downor upregulation of certain molecules that could induce or inhibit cell death may explain such adaptation. Further testing of upand downregulated molecules should be conducted in future work.","PeriodicalId":51994,"journal":{"name":"Makara Journal of Health Research","volume":"337 1","pages":"1"},"PeriodicalIF":0.3000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of L-fucose supplementation on the viability of cancer cell lines\",\"authors\":\"Muhammad Alif Mazlan, A. M. Yusof, M. Isa\",\"doi\":\"10.7454/msk.v24i2.1185\",\"DOIUrl\":null,\"url\":null,\"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. Downor upregulation of certain molecules that could induce or inhibit cell death may explain such adaptation. Further testing of upand downregulated molecules should be conducted in future work.\",\"PeriodicalId\":51994,\"journal\":{\"name\":\"Makara Journal of Health Research\",\"volume\":\"337 1\",\"pages\":\"1\"},\"PeriodicalIF\":0.3000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Makara Journal of Health Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7454/msk.v24i2.1185\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Makara Journal of Health Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7454/msk.v24i2.1185","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
摘要
背景:焦糖是一种脱氧己糖。虽然L-病灶的生物学作用尚不清楚,但已知这种糖可以加速癌细胞的恶性潜能。因此,本研究旨在评估人类癌细胞和正常细胞系在聚焦作用下的生存模式。方法:培养人牙龈成纤维细胞(HGF-1)、结直肠腺癌(HT-29)和皮肤恶性黑色素瘤(A375)细胞系,并以1、5、10 mg/ml三种浓度进行聚焦处理。然后用(3-(4,5 -二甲基噻唑-2)- 2,5二苯基溴化四唑(MTT)法测定细胞活力。使用Statistical Package for Social Sciences软件对数据进行分析。结果:治疗第1天HGF-1细胞存活率迅速下降。HT-29和A375在高聚焦浓度下均能存活。数据高度显著,p < 0.001。结论:高浓度的聚焦对HGF-1细胞系是有毒的,而HT-29和A375细胞系可能适应这种情况。可以诱导或抑制细胞死亡的某些分子的下调或上调可以解释这种适应。在今后的工作中,需要对上调和下调的分子进行进一步的检测。
Effects of L-fucose supplementation on the viability of cancer cell lines
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. Downor upregulation of certain molecules that could induce or inhibit cell death may explain such adaptation. Further testing of upand downregulated molecules should be conducted in future work.