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In-silico studies on evaluating the liver-protective effectiveness of a polyherbal formulation in preventing hepatocellular carcinoma progression.

作者信息

Kalath Haritha, Vishwakarma Riya, Banjan Bhavya, Ramakrishnan Krishnapriya, Koshy Abel John, Raju Rajesh, Rehman Niyas, Revikumar Amjesh

机构信息

Centre for Integrative Omics Data Science (CIODS), Yenepoya (Deemed to be University), Mangalore, 575018 Karnataka India.

Kerala Genome Data Centre, Kerala Development and Innovation Strategic Council, Vazhuthacaud, Thiruvananthapuram, 695014 Kerala India.

出版信息

In Silico Pharmacol. 2024 Nov 19;12(2):109. doi: 10.1007/s40203-024-00285-2. eCollection 2024.


DOI:10.1007/s40203-024-00285-2
PMID:39569037
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11574239/
Abstract

UNLABELLED: Liv-52, an herbal formulation consisting of seven distinct plants and Mandur Bhasma, is recognized for its hepatoprotective, anti-inflammatory, and antioxidant properties. To investigate the pharmacological potential of each phytochemical from these plants, we conducted ADMET analysis, molecular docking, and molecular dynamic simulations to identify potent molecules capable of inhibiting the interaction between Alpha-fetoprotein (AFP) and Cysteine aspartyl protease 3 (Caspase-3/CASP3). In our study, we have used molecular docking of all the compounds against AFP and filtered them on the basis of ADME properties. Among the compounds analyzed, (-) Syringaresinol from , exhibited good binding interactions with AFP, the highest binding free energy, and maintained stability throughout the simulation along with favorable drug likeness properties based on ADME and Toxicity analysis. These findings have strongly indicated that (-) Syringaresinol is a potential inhibitor of AFP, providing a promising therapeutic avenue for hepatocellular carcinoma (HCC) treatment by inhibiting the interaction between AFP and CASP3, thereby reinstating normal CASP3 activity. Further in vitro studies are imperative to validate the therapeutic efficacy of (-) Syringaresinol as an AFP inhibitor, potentially impeding the progression of HCC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40203-024-00285-2.

摘要

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本文引用的文献

[1]
Targeting AFP-RARβ complex formation: a potential strategy for treating AFP-positive hepatocellular carcinoma.

Mol Divers. 2025-4

[2]
Etiologically Significant microRNAs in Hepatitis B Virus-Induced Hepatocellular Carcinoma.

OMICS. 2024-6

[3]
Preparation and investigation of a novel combination of loaded, arabinoxylan-cross-linked β-cyclodextrin nanosponges for the treatment of cancer: , , and evaluation.

Front Pharmacol. 2023-12-6

[4]
Hepatitis B Virus Modulated Transcriptional Regulatory Map of Hepatic Cellular MicroRNAs.

OMICS. 2023-12

[5]
studies of active compounds and their role in thyroid peroxidase activity.

J Biomol Struct Dyn. 2024

[6]
screening and identification of potential drug-like compounds for dengue-associated thrombocytopenia from leaf extracts.

J Biomol Struct Dyn. 2024-7

[7]
Prognostic Scores and Survival Rates by Etiology of Hepatocellular Carcinoma: A Review.

J Clin Med Res. 2023-4

[8]
IMPPAT 2.0: An Enhanced and Expanded Phytochemical Atlas of Indian Medicinal Plants.

ACS Omega. 2023-2-23

[9]
Plant-derived natural products and combination therapy in liver cancer.

Front Oncol. 2023-2-14

[10]
The Role of Alpha-Fetoprotein (AFP) in Contemporary Oncology: The Path from a Diagnostic Biomarker to an Anticancer Drug.

Int J Mol Sci. 2023-1-28

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