M. Heshmati, Nazila Hasani-Reza Abad, Sanaz Pashapour, S. Babashah
{"title":"水飞蓟素对HCT116结肠癌细胞SBDSP1和CASC11基因表达的影响","authors":"M. Heshmati, Nazila Hasani-Reza Abad, Sanaz Pashapour, S. Babashah","doi":"10.5812/jkums-122802","DOIUrl":null,"url":null,"abstract":"Background: Numerous studies have proven that silymarin can fight cancer, but the results remain controversial. Objectives: This study aimed to determine the expression levels of SBDSP1 and CASC11 genes in HCT116 colon cancer cells to evaluate the cytotoxic effects of silymarin. Methods: This study was conducted on HCT 116 cell lines, which were divided into groups treated with 6.25, 12.5, 25, 50, 100, 250, and 500 μg/mL silymarin and control group. The silymarin cytotoxicity was checked using the MTT assay, and the apoptosis induction rate was determined using the annexin (An)-V/PI kit and flow cytometry. The real-time PCR was also used to examine the expression of the CASC11 and SBDSP1 genes. The data were compared using one-way analysis of variance between groups. Results: The cell survival was reduced based on concentration and time, and IC50 concentrations were observed in 30.94, 41.50, and 46.41 μg/mL at 24, 48, and 72 hours, respectively. In addition, the treatment with IC50 concentration significantly increased in apoptosis after 48 hours compared to the control. A decrease in expression of CASC11 and SBDSP1 genes was observed in HCT116 cells treated with IC50 concentrations after 24 and 48 hours. Conclusions: According to the results, silymarin, as an active substance, declines survival, induces apoptosis, and reduces the expression of SBDSP1 and CASC11 genes on the HCT-116 colon cancer cell line based on concentration and time.","PeriodicalId":16201,"journal":{"name":"Journal of Kermanshah University of Medical Sciences","volume":"93 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":"{\"title\":\"Evaluating the Effects of Silymarin on Expressing SBDSP1 and CASC11 Genes in HCT116 Colon Cancer Cells\",\"authors\":\"M. Heshmati, Nazila Hasani-Reza Abad, Sanaz Pashapour, S. Babashah\",\"doi\":\"10.5812/jkums-122802\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Numerous studies have proven that silymarin can fight cancer, but the results remain controversial. Objectives: This study aimed to determine the expression levels of SBDSP1 and CASC11 genes in HCT116 colon cancer cells to evaluate the cytotoxic effects of silymarin. Methods: This study was conducted on HCT 116 cell lines, which were divided into groups treated with 6.25, 12.5, 25, 50, 100, 250, and 500 μg/mL silymarin and control group. The silymarin cytotoxicity was checked using the MTT assay, and the apoptosis induction rate was determined using the annexin (An)-V/PI kit and flow cytometry. The real-time PCR was also used to examine the expression of the CASC11 and SBDSP1 genes. The data were compared using one-way analysis of variance between groups. Results: The cell survival was reduced based on concentration and time, and IC50 concentrations were observed in 30.94, 41.50, and 46.41 μg/mL at 24, 48, and 72 hours, respectively. In addition, the treatment with IC50 concentration significantly increased in apoptosis after 48 hours compared to the control. A decrease in expression of CASC11 and SBDSP1 genes was observed in HCT116 cells treated with IC50 concentrations after 24 and 48 hours. Conclusions: According to the results, silymarin, as an active substance, declines survival, induces apoptosis, and reduces the expression of SBDSP1 and CASC11 genes on the HCT-116 colon cancer cell line based on concentration and time.\",\"PeriodicalId\":16201,\"journal\":{\"name\":\"Journal of Kermanshah University of Medical Sciences\",\"volume\":\"93 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Kermanshah University of Medical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5812/jkums-122802\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Kermanshah University of Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5812/jkums-122802","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Evaluating the Effects of Silymarin on Expressing SBDSP1 and CASC11 Genes in HCT116 Colon Cancer Cells
Background: Numerous studies have proven that silymarin can fight cancer, but the results remain controversial. Objectives: This study aimed to determine the expression levels of SBDSP1 and CASC11 genes in HCT116 colon cancer cells to evaluate the cytotoxic effects of silymarin. Methods: This study was conducted on HCT 116 cell lines, which were divided into groups treated with 6.25, 12.5, 25, 50, 100, 250, and 500 μg/mL silymarin and control group. The silymarin cytotoxicity was checked using the MTT assay, and the apoptosis induction rate was determined using the annexin (An)-V/PI kit and flow cytometry. The real-time PCR was also used to examine the expression of the CASC11 and SBDSP1 genes. The data were compared using one-way analysis of variance between groups. Results: The cell survival was reduced based on concentration and time, and IC50 concentrations were observed in 30.94, 41.50, and 46.41 μg/mL at 24, 48, and 72 hours, respectively. In addition, the treatment with IC50 concentration significantly increased in apoptosis after 48 hours compared to the control. A decrease in expression of CASC11 and SBDSP1 genes was observed in HCT116 cells treated with IC50 concentrations after 24 and 48 hours. Conclusions: According to the results, silymarin, as an active substance, declines survival, induces apoptosis, and reduces the expression of SBDSP1 and CASC11 genes on the HCT-116 colon cancer cell line based on concentration and time.