Special Issues
Table of Content

Bioactive Natural Components as Regulators of Cellular Pathways and Disease Progression

Submission Deadline: 31 July 2026 View: 475 Submit to Special Issue

Guest Editors

Assoc. Prof. Mantang Qiu

Email: drmantangqiu@gmail.com

Affiliation: Department of Thoracic Surgery, Thoracic Oncology Institute, Peking University People's Hospital, Beijing, 100044, China

Homepage:

Research Interests: molecular oncology, tumor microenvironment, noncoding rna and circular rna, cancer metabolism, biomarkers and therapeutic targets, rna-based therapeutics, cellular signalling and disease regulation, translational cancer research

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Assist. Prof. Yunhan Ji

Email: yunhan.ji@shsmu.edu.cn

Affiliation: Department of Orthopedics, Tongren Hospital Shanghai Jiao Tong University School of Medicine, Shanghai, 200336, China

Homepage:

Research Interests: orthopaedic regeneration, bone and joint rehabilitation, inflammatory regulation in musculoskeletal disorders, bioactive materials and natural compounds, cellular signalling in tissue repair, oxidative stress and bone metabolism, translational musculoskeletal medicine, regenerative therapeutics and biomaterials

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Summary

Natural bioactive compounds have become a cornerstone in modern biomedical research due to their potential to provide safer and more effective alternatives to conventional drugs. Derived from plants, marine organisms, fungi, and microorganisms, these components—including alkaloids, flavonoids, terpenoids, and polyphenols—exhibit diverse pharmacological effects such as anti-inflammatory, antioxidant, antimicrobial, and anticancer activities. Their ability to modulate cellular and subcellular signaling pathways, regulate gene and protein expression, and influence key cellular behaviors (such as proliferation, apoptosis, autophagy, and differentiation) provides mechanistic insights into their therapeutic potential.

Recent research has shed light on the molecular mechanisms by which these bioactive natural components and their synthetic derivatives regulate oxidative stress, suppress inflammatory mediators, modulate gene expression, and interfere with disease-associated signalling cascades. Particular attention is now directed toward elucidating how these compounds act at the cellular level to influence intracellular signaling networks, protein modifications, transcriptional regulation, and intercellular communication. Advances in isolation, structural characterization, and formulation have further enhanced their therapeutic efficacy, selectivity, and bioavailability. However, for meaningful biological interpretation, it is essential that these findings be supported by mechanistic studies conducted in cellular or subcellular models. This growing evidence base highlights the need for continued exploration of natural products and their active constituents through mechanistic studies that reveal the cellular basis of disease modulation.

This special issue welcomes original research articles, reviews, and short communications focused on the cellular, molecular, and biochemical aspects of bioactive natural components and their roles in modulating disease processes.

1. Scope of the Special Issue
This issue aims to highlight innovative contributions related to:
• Pharmacological activities of natural product extracts and bioactive molecules investigated through cellular and molecular experiments
• Isolation and characterization of therapeutic monomeric compounds linked to mechanistic studies at the cell level
• Cellular and molecular mechanisms of action in regulating inflammatory, oxidative, metabolic, and oncogenic pathways
• Studies using cell lines, primary cells, or organoids to elucidate the signaling pathways affected by bioactive compounds
• Mechanistic validation of in vivo findings using cell-based assays
• Preclinical and clinical studies evaluating disease-specific therapeutic efficacy when supported by cell-level mechanistic evidence
• Synergistic interactions between natural compounds and conventional drugs demonstrated through modulation of intracellular signaling cascades
• Exploration of protein–protein interactions, post-translational modifications, and gene regulatory mechanisms affected by natural products
• Advances in formulation, delivery systems, and bioavailability enhancement only when directly linked to cellular uptake, intracellular trafficking, or mechanistic effects
• Toxicological assessment, safety profiling, and regulatory perspectives supported by molecular or cellular mechanistic insights

2. Target Diseases May Include (but are not limited to):
• Cancer and tumor suppression via modulation of cellular proliferation, apoptosis, and autophagy pathways
• Neurodegenerative disorders (e.g., Alzheimer's, Parkinson's disease) through regulation of neuronal survival signaling and oxidative stress pathways
• Cardiovascular diseases with a focus on endothelial and myocardial cell mechanisms
• Metabolic syndromes (e.g., diabetes, obesity) through cellular regulation of insulin signaling and lipid metabolism
• Autoimmune and chronic inflammatory diseases by dissecting cell-type-specific inflammatory responses
• Infectious diseases and antimicrobial resistance with mechanistic insights into host–pathogen interactions at the cellular level


Keywords

bioactive natural compounds, cellular signalling pathways, disease modulation, mechanistic studies, anti-inflammatory activity, antioxidant effects, apoptosis and autophagy, drug–natural compound interactions

Published Papers


  • Open Access

    REVIEW

    Gut Microbiota-Derived Exosomes Are Unique Natural Nanocarriers for Therapeutics

    Ibrahim M. Ibrahim, Shadab Md
    BIOCELL, DOI:10.32604/biocell.2026.077548
    (This article belongs to the Special Issue: Bioactive Natural Components as Regulators of Cellular Pathways and Disease Progression)
    Abstract Gut microbiota-derived exosomes (MDEs) have emerged as a novel class of drug delivery and are secreted by bacteria, fungi, and archaea in the human microbiota within the human intestinal ecosystem and possess inherent biocompatibility and lower immunogenicity, enabling seamless integration within host intestinal and systemic bioenvironments. This review elucidates the cellular and molecular mechanisms governing MDE function, explaining how their unique lipid bilayer composition facilitates cellular entry via receptor-mediated endocytosis and membrane fusion. This review discusses how gut MDEs traverse biological barriers, such as the blood-brain barrier and intestinal mucosa, by modulating tight junction proteins… More >

    Graphic Abstract

    Gut Microbiota-Derived Exosomes Are Unique Natural Nanocarriers for Therapeutics

  • Open Access

    ARTICLE

    Research on the Mechanism of Gallic Acid Inhibiting Ferroptosis and Delaying IgA Nephropathy by Regulating the MAPK Signaling Pathway through DUSP1

    Qiguo Wang, Qin Wang, Wen Ye, Qin Feng, Ting Wang
    BIOCELL, DOI:10.32604/biocell.2026.075633
    (This article belongs to the Special Issue: Bioactive Natural Components as Regulators of Cellular Pathways and Disease Progression)
    Abstract Objectives: IgA nephropathy (IgAN) is a common primary glomerulonephritis with limited treatment options. Gallic acid (GA) has demonstrated renal protective effects, but its precise mechanisms against IgAN remain incompletely elucidated. This study aims to reveal the molecular mechanism by which GA exerts a renal protective effect on IgAN. Methods: Transcriptomics and network pharmacology were combined in an integrative manner. The GSE175759 dataset’s differentially expressed genes (DEGs) were filtered out. SwissTargetPrediction and Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) were used to forecast GA’s goals. Core targets and pathways were obtained by functional… More >

  • Open Access

    ARTICLE

    Lycium Barbarum Polysaccharides Upregulate Trx2 in Schwann Cells through ESR1 to Repair Sciatic Nerve Injury in Rats

    Guoxu Ma, Yonglu Huang, Fan Gong, Jianke Wu, Yi Ding, Ziyang Zhang, Xiaoliang Li, Jian Gao, Tingting Dang, Bowen Zhang
    BIOCELL, DOI:10.32604/biocell.2026.078402
    (This article belongs to the Special Issue: Bioactive Natural Components as Regulators of Cellular Pathways and Disease Progression)
    Abstract Objectives: Sciatic nerve injury (SNI) impairs quality of life, and Lycium barbarum polysaccharides (LBP) may exert therapeutic effects via regulating Schwann cell (SC) mitochondrial stability, though the mechanism remains unclear. The study aimed to elucidate the therapeutic mechanisms of LBP in mitigating sciatic nerve injury by protecting Schwann cells via the estrogen receptor 1 (ESR1)/thioredoxin 2 (Trx2) pathway. Methods: An in vitro SNI model was established by inducing RSC96 cells with H2O2. Cell counting kit-8 (CCK8) assay, enzyme-linked immunosorbent assay (ELISA), Western blot, reactive oxygen species (ROS) and adenosine triphosphate (ATP) quantification, and mitochondrial membrane potential (MMP) detection were… More >

  • Open Access

    ARTICLE

    Anti-Inflammatory Effects of Veratramine against Lipopolysaccharide-Induced Inflammation

    Gyuri Han, Yun Hee Jeong, Ga Eun Kim, Jong-Sup Bae
    BIOCELL, DOI:10.32604/biocell.2026.075139
    (This article belongs to the Special Issue: Bioactive Natural Components as Regulators of Cellular Pathways and Disease Progression)
    Abstract Objectives: Plant-derived bioactive molecules are increasingly recognized as valuable therapeutic resources for managing diverse pathological conditions, particularly those involving vascular inflammation. This study aimed to determine whether veratramine (VRT), a naturally occurring steroidal alkaloid found in Veratrum species of the Liliaceae family, attenuates LPS-induced vascular and pulmonary inflammation by upregulating heme oxygenase-1 (HO-1) and modulating the Nrf2, nuclear factor (NF)-κB, and signal transducer and activator of transcription (STAT1) signaling pathways. Methods: The study assessed the modulatory effects of VRT on HO-1, cyclooxygenase-2 (COX-2), and inducible nitric oxide synthase (iNOS) in LPS-activated human umbilical vein endothelial cells… More >

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