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Main Authors: Rahman, Noor, Zafar, Humaira, Rajendran, Thirugnanasambandam, Sharif, Ruby, Almehdi, Ahmed, Tul-Wahab, Atia, Sheikh, Sumbla, Choudhary, M Iqbal
Format: Artículo científico
Language:en
Published: Computers in biology and medicine 2026
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Online Access:https://pubmed.ncbi.nlm.nih.gov/41633277/
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author Rahman, Noor
Zafar, Humaira
Rajendran, Thirugnanasambandam
Sharif, Ruby
Almehdi, Ahmed
Tul-Wahab, Atia
Sheikh, Sumbla
Choudhary, M Iqbal
author_facet Rahman, Noor
Zafar, Humaira
Rajendran, Thirugnanasambandam
Sharif, Ruby
Almehdi, Ahmed
Tul-Wahab, Atia
Sheikh, Sumbla
Choudhary, M Iqbal
Rahman, Noor
Zafar, Humaira
Rajendran, Thirugnanasambandam
Sharif, Ruby
Almehdi, Ahmed
Tul-Wahab, Atia
Sheikh, Sumbla
Choudhary, M Iqbal
collection PubMed - marine biology
contents Exploring natural products as Bcl-2 inhibitors for acute myeloid leukemia therapy using In vitro, STD-NMR spectroscopy, and In silico approaches. Rahman, Noor Zafar, Humaira Rajendran, Thirugnanasambandam Sharif, Ruby Almehdi, Ahmed Tul-Wahab, Atia Sheikh, Sumbla Choudhary, M Iqbal Humans Leukemia, Myeloid, Acute Proto-Oncogene Proteins c-bcl-2 HL-60 Cells Molecular Docking Simulation Biological Products Apoptosis Magnetic Resonance Spectroscopy Antineoplastic Agents Molecular Dynamics Simulation Cell Proliferation Gossypol Acute myeloid leukemia (AML) is the predominant form of acute leukemia, affecting elderly individuals, typically diagnosed at an average age of 68 years. AML cells rely on the Bcl-2 protein for their survival. Overexpression of Bcl-2 protein in various cancer types renders it as a potential candidate for targeted therapies. The present study aimed to identify natural compounds as Bcl-2 inhibitors using in vitro, biophysical, and integrated computational approaches. The MTT assay was performed for cell proliferation, followed by apoptosis and gene expression analysis. STD-NMR spectroscopy, molecular docking and molecular dynamics simulations were performed for protein-ligand interactions. In the in vitro anti-proliferative assay, three natural compounds, gossypol (1), camptothecin (2), and jaceidin (3), were found active against the HL-60 cell line with IC concentrations of 1.634 ± 0.072, 0.137 ± 0.029, and 13.492 ± 2.292 μM, respectively. These compounds triggered apoptosis and decreased cellular viability in a dose-dependent manner. The gene expression analysis of Bax, Bcl-2, and Caspase 3 in HL-60 cells revealed that these compounds induce apoptosis by regulating essential apoptotic genes. Among the three identified potential hits, only gossypol (1) was buffer soluble and subjected to STD-NMR experiment to evaluate its protein-ligand interactions. Furthermore, molecular docking, binding free energies and MD simulation analyses demonstrated stable interactions of these compounds with the Bcl-2 protein. The three natural products showed potent to significant activity, effectively inducing apoptosis in the HL-60 cell line. Hence, this study identifies three potential lead candidates for drug discovery against Bcl-2-related cancers after further mechanistic and pre-clinical studies.
format Artículo científico
id pubmed_41633277
institution PubMed
language en
publishDate 2026
publisher Computers in biology and medicine
record_format pubmed
spellingShingle Exploring natural products as Bcl-2 inhibitors for acute myeloid leukemia therapy using In vitro, STD-NMR spectroscopy, and In silico approaches.
Rahman, Noor
Zafar, Humaira
Rajendran, Thirugnanasambandam
Sharif, Ruby
Almehdi, Ahmed
Tul-Wahab, Atia
Sheikh, Sumbla
Choudhary, M Iqbal
Humans
Leukemia, Myeloid, Acute
Proto-Oncogene Proteins c-bcl-2
HL-60 Cells
Molecular Docking Simulation
Biological Products
Apoptosis
Magnetic Resonance Spectroscopy
Antineoplastic Agents
Molecular Dynamics Simulation
Cell Proliferation
Gossypol
Exploring natural products as Bcl-2 inhibitors for acute myeloid leukemia therapy using In vitro, STD-NMR spectroscopy, and In silico approaches. Rahman, Noor Zafar, Humaira Rajendran, Thirugnanasambandam Sharif, Ruby Almehdi, Ahmed Tul-Wahab, Atia Sheikh, Sumbla Choudhary, M Iqbal Humans Leukemia, Myeloid, Acute Proto-Oncogene Proteins c-bcl-2 HL-60 Cells Molecular Docking Simulation Biological Products Apoptosis Magnetic Resonance Spectroscopy Antineoplastic Agents Molecular Dynamics Simulation Cell Proliferation Gossypol Acute myeloid leukemia (AML) is the predominant form of acute leukemia, affecting elderly individuals, typically diagnosed at an average age of 68 years. AML cells rely on the Bcl-2 protein for their survival. Overexpression of Bcl-2 protein in various cancer types renders it as a potential candidate for targeted therapies. The present study aimed to identify natural compounds as Bcl-2 inhibitors using in vitro, biophysical, and integrated computational approaches. The MTT assay was performed for cell proliferation, followed by apoptosis and gene expression analysis. STD-NMR spectroscopy, molecular docking and molecular dynamics simulations were performed for protein-ligand interactions. In the in vitro anti-proliferative assay, three natural compounds, gossypol (1), camptothecin (2), and jaceidin (3), were found active against the HL-60 cell line with IC concentrations of 1.634 ± 0.072, 0.137 ± 0.029, and 13.492 ± 2.292 μM, respectively. These compounds triggered apoptosis and decreased cellular viability in a dose-dependent manner. The gene expression analysis of Bax, Bcl-2, and Caspase 3 in HL-60 cells revealed that these compounds induce apoptosis by regulating essential apoptotic genes. Among the three identified potential hits, only gossypol (1) was buffer soluble and subjected to STD-NMR experiment to evaluate its protein-ligand interactions. Furthermore, molecular docking, binding free energies and MD simulation analyses demonstrated stable interactions of these compounds with the Bcl-2 protein. The three natural products showed potent to significant activity, effectively inducing apoptosis in the HL-60 cell line. Hence, this study identifies three potential lead candidates for drug discovery against Bcl-2-related cancers after further mechanistic and pre-clinical studies.
title Exploring natural products as Bcl-2 inhibitors for acute myeloid leukemia therapy using In vitro, STD-NMR spectroscopy, and In silico approaches.
topic Humans
Leukemia, Myeloid, Acute
Proto-Oncogene Proteins c-bcl-2
HL-60 Cells
Molecular Docking Simulation
Biological Products
Apoptosis
Magnetic Resonance Spectroscopy
Antineoplastic Agents
Molecular Dynamics Simulation
Cell Proliferation
Gossypol
url https://pubmed.ncbi.nlm.nih.gov/41633277/