2012 ©
             Publication
Journal Publication
Research Title Preliminary investigation into the anticancer potential of phytochemical isothiocyanates against cholangiocarcinoma 
Date of Distribution 23 May 2024 
Conference
     Title of the Conference งานประชุมวิชาการประจำปีสมาคมเภสัชวิทยาแห่งประเทศไทยครั้งที่ 45 (The 45th Pharmacological and Therapeutic Society of Thailand Annual Meeting) 
     Organiser ภาควิชาเภสัชวิทยา คณะแพทยศาสตร์ศิริราชพยาบาล มหาวิทยาลัยมหิดล อาคารศรีสวรินทิรา ชั้น 12 เลขที่ 2 ถนนวังหลัง เขตบางกอกน้อย กรุงเทพฯ 10700 
     Conference Place Mandarin Hotel Banakok 
     Province/State กรุงเทพมหานครฯ 
     Conference Date 15 May 2024 
     To 17 May 2024 
Proceeding Paper
     Volume 2024 
     Issue 45 
     Page 23 
     Editors/edition/publisher  
     Abstract Cholangiocarcinoma (CCA) is an aggressive malignancy due to a difficult diagnosis, limited treatment options, and chemotherapy resistance. New therapeutic strategies are necessary to improve CCA patients' survival and quality of life. Isothiocyanates (ITCs) are phytochemical compounds in cruciferous vegetables like broccoli, cabbage, and Brussels sprouts. These compounds gained interest owing to their potential health benefits. ITCs display potent anticancer, antioxidant, and anti-inflammatory properties, inhibiting tumor progression and metastasis. Unfortunately, limited information is available regarding the role of ITC in the CCA's anticancer effect. The present study investigated the potential impact of three ITCs (sulforaphane, sulforaphane, and iberin) on the growth of the CCA cell line (KKU-452). Cell viability and cell cycle analysis were evaluated by sulforhodamine-B assay (SRB) and propidium iodide (PI) staining, respectively. The results showed that ITCs decreased cell viability in KKU-452 cells in a dose- and time-dependent manner. IC50 of sulforaphane, sulforaphene, and iberin were 18.232.06, 17.014.77, and 23.635.02 mM, respectively, after 24 h treatment, and 11.450.8, 10.840.95 and 13.601.11 mM, respectively, after 48 h treatment. In addition, ITCs induced cell cycle arrest at G1 and G2/M phases at 12 h and 24 h. Additional experiments are necessary to illustrate the potential of ITCs against CCA and to understand the underlying mechanisms. 
Author
655070043-5 Mr. NANTHAWUT BUACHABAN [Main Author]
Medicine Master's Degree

Peer Review Status มีผู้ประเมินอิสระ 
Level of Conference ชาติ 
Type of Proceeding Abstract 
Type of Presentation Poster 
Part of thesis true 
Presentation awarding false 
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