Antioxidative and ROS-dependent apoptotic effects of Roxb. stem against human lung cancer: network pharmacology and experimental validation.

Abdelbaset Mohamed Elasbali, Waleed Abu Al-Soud, Afnan Elayyan Mousa Elayyan, Hassan H Alhassan, Corina Danciu, Elyasa Mustafa Elfaki, Salem Hussain Alharethi, Bandar Alharbi, Hamad H Alanazi, Mohamed El Mohtadi, Mitesh Patel, Mohd Adnan

Journal: Journal of biomolecular structure & dynamics 2024;42(21):11651-11676

PMID: 37776015

Abstract

Lung cancer remains a formidable global health challenge, necessitating the exploration of novel therapeutic approaches. This study investigates the potential of Roxb. stem extract as an anticancer agent against human lung cancer, focusing on its antioxidative and ROS-dependent apoptotic effects. Utilizing a combination of network pharmacology and in-vitro experimental validation, we delineate the multifaceted molecular mechanisms underlying the observed effects. The antioxidant potential of stem extract was evaluated by the 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2-azinobis (3-ethyl-benzothiazoline-6-sulfonic acid) (ABTS) and ferric reducing/antioxidant power (FRAP), hydroxyl free radical scavenging, reactive nitrogen oxide scavenging and super oxide anion radical scavenging assays. Furthermore, the antiproliferative and proapoptotic effect of stem extract was evaluated against A549 lung adenocarcinoma cell line using the consecrated sulforhodamine B (SBR) and Annexin V-PI assays. Additionally, the mitochondrial membrane potential (MMP) and the total reactive oxygen species (ROS) estimation assays were performed. As a result, network pharmacology analysis revealed a complex interaction network between the bioactive constituents of and key proteins implicated in lung cancer progression. The stem extract showed dose-dependent antioxidant activity against DPPH (IC - 87.38 µg/mL), reactive nitrogen oxide (IC - 318.34 µg/mL), FRAP (IC - 359.96 µg/mL), hydroxy free radicals (IC - 526.12 µg/mL) than ABTS (IC - 698.45 µg/mL) and super oxide anion (IC - 892.71 µg/mL) as well as cytotoxic activity against A549 cells (IC - 436.80 µg/mL). Observations of morphological features in treated cells have revealed hallmark of apoptosis properties. Furthermore, as a result of treatment with stem extract, ROS generation and mitochondrial depolarization were increased in A549 cells, suggesting that this treatment has significant apoptotic properties. . These findings highlight the potential utility of this natural extract as an innovative therapeutic strategy for lung cancer treatment. The integration of network pharmacology and experimental validation enhances our understanding of the underlying mechanisms and provide the way for further translational research.Communicated by Ramaswamy H. Sarma.

Address: Department of Clinical Laboratory Science, College of Applied Sciences-Qurayyat, Jouf University, Qurayyat, Saudi Arabia.; Department of Clinical Laboratory Science, College of Applied Sciences-Sakaka, Jouf University, Sakaka, Saudi Arabia.; Department of Pharmacognosy, Faculty of Pharmacy, "Victor Babes" University of Medicine and Pharmacy, Timisoara, Romania.; Department of Biological Science, College of Arts and Science, Najran University, Najran, Saudi Arabia.; Department of Clinical Laboratory, College of Applied Medical Sciences, University of Hail, Hail, Saudi Arabia.; Department of Biology, Edge Hill University, Ormskirk, UK.; Research and Development Cell, Department of Biotechnology, Parul Institute of Applied Sciences, Parul University, Vadodara, India.; Department of Biology, College of Science, University of Hail, Hail, Saudi Arabia.
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