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Uncaria Gambir Roxb (Bajakah) Effects on tumor growth, apoptosis, inflammation, and angiogenesis of DMBA-Induced mammary carcinoma in rat: An immunohistochemistry study
Author(s):
1. Prabudi Prabudi: Department of Surgical Oncology Hasan Basry Hospital, South Kalimantan
2. Nia Kania: Department of Pathology Anatomy, Faculty of Medicine and Health Sciences, Lambung Mangkurat University, Ulin General Hospital, Banjarmasin, South Kalimantan
3. Eko Suhartono: Department of Medical Chemistry/Biochemistry, Faculty of Medicine and Health Sciences, Lambung Mangkurat University, Banjarbaru, South Kalimantan
4. Didik Dwi Sanyoto: Departement of Biomedical, Anatomy Division, Faculty of Medicine and Health Sciences, Lambung Mangkurat University, Banjarmasin, Indonesia
Abstract:
Objective: To investigate the antitumor effects of U. Gambir extract on 7, 12-dimethylbenz [a] anthracene (DMBA)-induced mammary carcinoma in Wistar rats. Methodology: This experimental study included 30 female rats divided in five groups receiving different U. Gambir extracts at 200 mg/kg, 600 mg/kg, 1000 mg/kg body weight (BW), and positive control (capecitabine 65mg/kg BW). Apoptosis, inflammation, and angiogenesis induction were assessed by immunohistochemistry, and quantifying biomarkers caspase-3, NF-KB, and VEGFR-2 expressions using the Histoscore method. Statistical analyses included one-way ANOVA (tumor volume) with Bonferroni post hoc and chi-square tests for biomarker expression. Results: The 600 mg/kg BW U. Gambir group exhi-bited significant tumor growth inhibition (p0.05). VEGFR-2 expression is no different compared to the control group. Conclusions: These findings suggest that U. Gambir extracts have antitumor activity by decreasing tumor volume. However, further research is essential to def-ine the mechanistic pathways and identify active com-ponents.
Page(s): 762-765
DOI: DOI not available
Published: Journal: Rawal Medical Journal, Volume: 50, Issue: 3, Year: 2025
Keywords:
Breast Cancer , caspase3 , NFkB , U Gambir , tumor growth , VEGFR2
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