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Antibacterial effect of alpha-mangostin from Garcinia mangostana. L against oral streptococci and staphylococci biofilms: a systematic review Praptiningsih, Rahmawati Sri; Siswomihardjo, Widowati; Jonarta, Alma Linggar; Yulianto, Heribertus Dedy Kusuma; Syifa, Liftia Layyinatus; Rochmah, Yayun Siti; Ichwan, Solachuddin Jauhari Arief
Padjadjaran Journal of Dentistry Vol 36, No 2 (2024): July 2024
Publisher : Universitas Padjadjaran

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/pjd.vol36no2.53957

Abstract

ABSTRACTIntroduction: Interactions among competing bacteria, which inhibit each other's growth to maintain the balance of microorganisms in the biofilm, can influence oral cavity homeostasis. Natural products contain compounds with the potential to combat various diseases, including caries. Alpha-mangostin from Garcinia mangostana. L exhibits antibacterial properties against oral streptococci and staphylococci, acting through several mechanisms, including the disruption of peptidoglycan, which ultimately leads to cell brittleness and rupture. This study aims to assess the impact of antibacterial alpha-mangostin on oral streptococci and staphylococci biofilm. Methods: The research methodology employed secondary data collection through a systematic review study. We conducted searches across databases including PubMed, ScienceDirect, and Google Scholar to identify Indonesian and English references encompassing textbooks, research findings, reviews, and internet articles relevant to the topic published between 2014 and 2024. Following a thorough screening process, we selected articles deemed pertinent for inclusion in the review. Subsequently, these articles underwent evaluation for full-text accessibility, language compatibility, and availability of information from the respective journals, resulting in the selection of 20 articles. Results: Analysis was carried out on 20 articles. Ten articles described the effects of alpha-mangostin's inhibit oral biofilm, 6 articles discussed the effects of alpha-mangostin's antibacterial activity against Streptococcus mutans and Streptococcus sanguis, 3 article state mechanism alpha-mangostin inhibit membrane enzymes such as F(H+)-ATPase and the phosphoenolpyruvate-sucrose phosphotransferase system on Staphylococcus aureus. Additionally, one article described inhibition mechanisms of aldolase, glyceraldehyde-3-phosphate dehydrogenase, and lactic dehydrogenase on Staphylococcus epidermidis. Conclusion: Alpha-mangostin inhibits and disrupts biofilm defense mechanisms. It possesses antimicrobial properties effective against oral streptococci and staphylococci, including Streptococcus mutans, Streptococcus sanguis, Staphylococcus aureus and Staphylococcus epidermidis. These properties operate through various mechanisms, including enhancing the permeability of bacterial cell walls, ultimately leading to bacterial cell death.KEYWORDSOral biofilm, alpha-mangostin, oral streptococci, staphylococci
Molecular docking analysis between anti-apoptosis EGFR and four coumarins, and four carbazole alkaloids: in silico study Afriza, Dhona; Suriyah, Wastuti Hidayati; Ichwan, Solachuddin Jauhari Arief; Knights, Joe
Padjadjaran Journal of Dentistry Vol 36, No 1 (2024): March 2024
Publisher : Universitas Padjadjaran

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/pjd.vol36no1.52467

Abstract

Introduction: The anti-apoptotic protein EGFR is typically overexpressed in the majority of head and neck squamous cell carcinomas (HNSCC) and has been targeted for genetic therapy. The Clausena excavata plant is an evergreen shrub that has been widely used for various disease therapies, including cancer. Coumarin and carbazole alkaloids are the plant's primary active ingredients. This study aims to determine the molecular interaction between EGFR and several coumarins (clauslactone E, dentatin, nordentatin, clausenidin) and carbazole alkaloids (7- hydroxyheptaphylline, clausine E, 2,7 - dimethoxy - 9H - carbazole - 3- carbaldehyde,and 2,7 – dimethoxy - 9H - carbazole – 3-carboxylic acid). Methods: This research was carried out in silico using the molecular docking method. Molecular docking analysis was performed using AutoDock Vina, AutoDockTools 1.5.6., Pymol, and Discovery Studio Biovia 2021. The three-dimensional structure of the EGFR protein was retrieved from the RCSB Protein Data Bank. Ligands were obtained from the PubChem Compound Database. The comparison ligand was doxorubicin. Molecular docking results were analyzed based on binding affinity, amino acid interactions, visualization of docking results, and Lipinski's rule of five. Results: All of the investigated ligands with the EGFR receptor had strong binding affinity (-6.8 and -8.3 kcal/mol), almost the same as the comparison ligand (-8.2 kcal/mol). Each interaction also produced a different number of amino acid residues. Conclusion: These four coumarin compounds and four carbazole alkaloid compounds are considered potential EGFR inhibitors and anticancer candidates.KeywordMolecular docking, anticancer, oncogene protein, natural compunds
Curcuma xanthorrhiza Rhizome Extract Induces Apoptosis in HONE-1 Nasopharyngeal Cancer Cells Through Bid Ranggaini, Dewi; Sandra, Ferry; Halim, Johni; Ichwan, Solachuddin Jauhari Arief; Djamil, Melanie Sadono
The Indonesian Biomedical Journal Vol 15, No 1 (2023)
Publisher : The Prodia Education and Research Institute (PERI)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.18585/inabj.v15i1.2217

Abstract

BACKGROUND: Curcuma xanthorrhiza rhizomes have been demonstrated to have anticancer properties toward various types of cancer cells. The effect of C. xanthorrhiza rhizome extract (CXRE) on nasopharyngeal cancer (NPC) cells, including HONE-1 cell line has not been elucidated yet. Therefore, the effect of CXRE on the apoptosis of HONE-1 cells and its possible underlying mechanism are necessary to be explored.METHODS: C. xanthorrhiza rhizomes were minced, dried, extracted with distilled ethanol, filtered, and evaporated to produce CXRE. HONE-1 cells were seeded, starved, and treated with dimethyl sulfoxide (DMSO), Doxorubicin, or various concentrations of CXRE. Treated HONE-1 cells were stained with 4',6'-diamidino-2-phenylindole (DAPI) and the number of viable cells was counted. HONE-1 cells were also collected, lysed, and further processed for immunoblotting analysis to measure Bid activity.RESULTS: The number of viable HONE-1 cells decreased in concentration- and time-dependent manner. The number of viable cells in 50 and 250 μg/mL CXRE-treated groups were significantly lower compared with that in the DMSO-treated group after 24 h. At 48 h incubation period, the number of viable cells in 10, 50 and 250 μg/mL CXRE-treated groups were significantly lower compared with that in the DMSO-treated group. The number of viable cells in 250 μg/mL CXRE-treatment group was not significantly different compared with that in the Doxorubicin-treated group after 48 h. Bid expression levels in CXRE-treated groups were lower compared with that in the DMSO-treated group.CONCLUSION: CXRE could induce apoptosis via Bid activation, hence reducing the viability of HONE-1 cells.KEYWORDS: Curcuma xanthorrhiza, nasopharyngeal cancer, HONE-1 cells, apoptosis, Bid