Publikasi Scopus 2024 per tanggal 31 Mei 2024 (409 artikel)

Ridwan S.; Bahtiar A.; Sukmawati D.; Siriamompun S.
Ridwan, Salbiah (57861088800); Bahtiar, Anton (35365874400); Sukmawati, Dewi (55615650900); Siriamompun, Sirithon (58933973000)
57861088800; 35365874400; 55615650900; 58933973000
Clofazimine attenuates colitis-associated colon cancer through β-catenin signaling pathway in the AOM/DSS mice models
2024
Journal of Applied Pharmaceutical Science
14
3
71
80
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Department of Clinical Pharmacy, Sekolah Tinggi Ilmu Kesehatan (STIKes), Medika Nurul Islam, Sigli, Indonesia; Department of Pharmacology and Toxicology, Faculty of Pharmacy, Universitas Indonesia, Depok, Indonesia; Department of Histology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Department of Food Technology and Nutrition, Faculty of Technology, Research Unit of Thai Food Innovation, Mahasarakham University, Kantharawichai, Thailand
Ridwan S., Department of Clinical Pharmacy, Sekolah Tinggi Ilmu Kesehatan (STIKes), Medika Nurul Islam, Sigli, Indonesia; Bahtiar A., Department of Pharmacology and Toxicology, Faculty of Pharmacy, Universitas Indonesia, Depok, Indonesia; Sukmawati D., Department of Histology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Siriamompun S., Department of Food Technology and Nutrition, Faculty of Technology, Research Unit of Thai Food Innovation, Mahasarakham University, Kantharawichai, Thailand
Clofazimine can suppress tumor growth both in vitro and in vivo, making it a potential anticancer candidate. However, until now, the molecular mechanism of clofazimine in inhibiting cancer is not fully known. This study aims to analyze the possible mechanism of clofazimine in attenuating colitis-associated colon cancer (CAC) observed in the wnt/β-catenin signaling pathway. This study used male Balb/c (n = 36) mice which were randomly divided into six groups: normal control, negative control, curative group [dose of 0.2, 0.4, and 0.8 mg/20 g body weight (BW), respectively], and preventive group dose of 0.4 mg/day 20 g BB. Azoxymethane and dextran sodium sulfate (AOM/DSS) were used to induce colitis-related colon cancer. The enzyme-linked immunosorbent assay (ELISA) approach was used to assess the expression levels of caspase-3 and IL-1. H&E staining was used for histological investigation, followed by immunohistochemistry for catenin and axin-2 expression. The ELISA analysis showed that the curative dose of clofazimine 0.8 mg/20 g BW had lower IL-1β, β-catenin, axin-2, and caspase-3 expression compared to the AOM/DSS group. Histological analysis showed that clofazimine attenuates the inflammatory score compared to the AOM/DSS-only group. The best damage score reduction occurred in the curative dose group of 0.8 mg/kg BW and the preventive dose of 0.4 mg/20 g BW. The protein expression of β-catenin and axin-2 showed that the AOM/DSS-induced group had higher expression than the normal group. Decreased expression of both proteins was seen in a curative dose of clofazimine 0.8 mg/kg BW. Our study indicated that clofazimine has the potential to inhibit the growth of CAC in part through attenuation of the β-catenin signaling pathway, which includes attenuation of IL-1P, β-catenin, and axin-2 expression, followed with improvement in tissue damage. © 2024 Salbiah Ridwan et al. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/). All Rights Reserved.
AOM/DSS model; clofazimine; Colitis-associated colon cancer; Wnt/β-catenin signaling
Axin 2; azoxymethane; beta catenin; caspase 3; catenin; clofazimine; dextran sulfate; interleukin 1; interleukin 1beta; unclassified drug; animal model; animal tissue; antineoplastic activity; Article; cancer inhibition; canonical Wnt signaling; cell infiltration; chemoprophylaxis; colitis; colon cancer; colon weight; controlled study; dysplasia; enzyme linked immunosorbent assay; erythema; histopathology; immunohistochemistry; inflammation; male; mortality rate; mouse; nonhuman; protein expression; scoring system
Direktorat Riset and Pengembangan, Universitas Indonesia, DRPM UI, (NKB-586/UN2.RST/HKP.05.00/2023); Direktorat Riset and Pengembangan, Universitas Indonesia, DRPM UI
This research is funded by the Directorate of Research and Development, Universitas Indonesia, under Hibah PUTI 2023 (Grant No. NKB-586/UN2.RST/HKP.05.00/2023).
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