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  • Open Access

    ARTICLE

    Targeting Dynamin-Related Protein 1 and Glucose Metabolism Reverses Acquired Resistance to Sorafenib in Liver Cancer

    Jinhui Che1,2, Zhiyuan Chen1, Feng Zhang3,4, Shuo Zhu2, Shengya Cao5, Ou Li1, Rong Li4,*, Jun Zheng3,4,*, Yubin Liu1,*

    Oncology Research, Vol.34, No.7, 2026, DOI:10.32604/or.2026.067443 - 16 June 2026

    Abstract Objective: Advanced liver cancer, a highly lethal and increasingly prevalent malignancy, frequently develops sorafenib resistance, with aberrant mitochondrial dynamics and metabolism implicated in its pathogenesis. This study aimed to investigate their interplay and assess combination therapies against sorafenib-resistant liver cancer. Methods: Mitochondrial morphology was assessed using immunofluorescent staining. Besides, the mitochondrial metabolic profile was evaluated by measuring the oxygen consumption rate, glucose uptake, and lactate production. Dynamin-related protein 1 (Drp1) expression was determined through immunohistochemical staining, western blotting, and reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Cell counting, colony formation, and cell cycle assays were conducted to… More >

  • Open Access

    ARTICLE

    12-O-Tetradecanoylphorbol-13-Acetate Inhibits TGF-β1-Induced Proliferation and Fibrosis in LX-2 Hepatic Stellate Cells by Regulating both YAP and AKT Activities

    Moo Hyun Kim1, Yongdae Yoon2, Chang Wan Kim1, Jun-Won Lee3, Bhupendra Regmi2, Saher Fatima2, Moon Young Kim2,3, Soon Koo Baik2,3, Pil Young Jung1,*, Young Woo Eom2,*

    BIOCELL, Vol.50, No.6, 2026, DOI:10.32604/biocell.2026.076364 - 09 June 2026

    Abstract Background: Although transforming growth factor-β (TGF-β) drives hepatic stellate cell activation and fibrogenesis, the mechanisms by which 12-O-tetradecanoylphorbol-13-acetate (TPA) modulates these processes in TGF-β1-activated hepatic stellate cells remain to be determined. Therefore, we investigated whether TPA alleviates fibrosis in TGF-β1-treated hepatic stellate cells and regulates both canonical and non-canonical pathways. Further, we assessed whether inhibitors of these pathways similarly affect proliferation and fibrosis in LX-2 cells. Methods: LX-2 hepatic stellate cells were used as the experimental model. Cells were treated with TPA, TGF-β, or TGF-β plus TPA, and Yes-associated protein (YAP) and protein kinase B (PKB;… More >

  • Open Access

    REVIEW

    Emerging Role of ACOD1/Itaconate in Cancer: Bridging Metabolic Reprogramming and Signaling in the Tumor Microenvironment

    Xing-Guo Li1,2,3,#, Lu-Kai Wang4,#, Fu-Ming Tsai5, Hsueh-Chun Wang1,*

    BIOCELL, Vol.50, No.6, 2026, DOI:10.32604/biocell.2026.075492 - 09 June 2026

    Abstract Itaconate, produced by aconitate decarboxylase 1 (ACOD1, also known as IRG1), acts as a key immunometabolite that inhibits succinate dehydrogenase (SDH) and can engage reduction-oxidation (redox)-sensitive signaling programs. This review summarizes the emerging, context-dependent roles of the ACOD1-itaconate axis in cancer, while critically distinguishing between the effects of endogenous itaconate and its cell-permeable derivatives. In tumor cells, endogenous ACOD1 expression or uptake via solute carrier family 13 member 3 (SLC13A3) alters oxidative phosphorylation and glycolysis. In the tumor microenvironment, myeloid-derived itaconate contributes to immune tolerance by reducing dendritic-cell cross-priming and limiting CD8+ T-cell metabolic activity. Moreover, More >

  • Open Access

    ARTICLE

    PD-1 Blockade Reduces Parasite Load and Restores Anti-Parasitic Immunity in Murine Visceral Leishmaniasis

    Xuechun Liao1,#, Xiaoxiao Chen2,#, Shulan Wei1, Qiong Li1, Yanqin Zhao1, Yuying Xiao1, Qi Zhou1, Jianping Chen1,*, Jinlei He1,*

    BIOCELL, Vol.50, No.5, 2026, DOI:10.32604/biocell.2026.077240 - 13 May 2026

    Abstract Objective: Immune checkpoint blockade holds therapeutic potential in visceral leishmaniasis; its underlying mechanism remains unclear. This study aimed to investigate the therapeutic potential and underlying immune mechanisms of Programmed cell death protein 1 (PD-1) blockade in experimental visceral leishmaniasis. Methods: BALB/c mice infected with Leishmania donovani received anti-PD-1 antibody at 35–44 days post-infection. Parasite burden in target organs, serum antibodies, hepatopathology, and transcriptome of the liver were analyzed. T cell exhaustion, activation, apoptosis, and inflammation genes were quantified in target organs. Results: PD-1 blockade reduced splenic parasite load (reduction rate = 82.6%, ***p < 0.001), enhanced hepatic granulomatous… More > Graphic Abstract

    PD-1 Blockade Reduces Parasite Load and Restores Anti-Parasitic Immunity in Murine Visceral Leishmaniasis

  • Open Access

    ARTICLE

    Dioscin Regulates Mitochondrial Autophagy and Cell Cycle to Promote Pulpal Stem Cell Differentiation and Mineralization

    Zhiye Zhou1,2, Jianan Chen3, Qiang Zhu3,*

    BIOCELL, Vol.50, No.5, 2026, DOI:10.32604/biocell.2026.076758 - 13 May 2026

    Abstract Background: Human dental pulp stem cells (hDPSCs) are promising for dental tissue regeneration. Dioscin (Dio), a natural compound, has various biological activities, but its effects on hDPSCs are unclear. This study aims to systematically elucidate the effects of Dio on promoting the osteogenic differentiation of hDPSCs and the underlying molecular mechanisms. Methods: Characterized hDPSCs were treated with Dio. Cell viability, proliferation, osteogenic differentiation (alkaline phosphatase (ALP) activity, Alizarin Red S (ARS)), and migration (Transwell) were assessed. Mitophagy (fluorescence, Western blot for PTEN-induced kinase 1 (PINK1), parkin RBR E3 ubiquitin-protein ligase (PRKN), microtubule-associated protein 1 light chain… More > Graphic Abstract

    Dioscin Regulates Mitochondrial Autophagy and Cell Cycle to Promote Pulpal Stem Cell Differentiation and Mineralization

  • Open Access

    REVIEW

    Role of Protein Misfolding in Human Kidney Diseases

    Sebastián Jaurreteche1,2,*, María Luana Brajkovic2, María Victoria Del Rosal2, Graciela Venera3, Carlos Daniel De la Vega Elena4

    BIOCELL, Vol.50, No.5, 2026, DOI:10.32604/biocell.2026.073790 - 13 May 2026

    Abstract Protein misfolding has emerged as a central mechanism in the pathogenesis of human kidney diseases. Normally, proteins achieve their native conformation through highly regulated folding processes in the endoplasmic reticulum (ER) and cytoplasm, assisted by molecular chaperones and quality-control pathways. However, genetic variants, environmental stressors, or cellular overload can destabilize this system, resulting in unfolded or misfolded proteins that trigger aggregation, amyloid formation, endoplasmic reticulum stress, and activation of the unfolded protein response (UPR). These events may ultimately lead to loss of function, gain of toxic function, and apoptosis. This review summarizes the structural basis… More >

  • Open Access

    REVIEW

    Biostimulants in Modern Agriculture: A Comprehensive Review with Emphasis on Protein Hydrolysates

    Matthew Starr1, Lori Unruh-Snyder1,*, Luke Gatiboni1, Koralalage Jayaratne2

    Phyton-International Journal of Experimental Botany, Vol.95, No.4, 2026, DOI:10.32604/phyton.2026.072898 - 28 April 2026

    Abstract Biostimulants, categorized as microbial or non-microbial, including humic substances, seaweed extracts, chitosan, or protein hydrolysates (PHs), have gained significant attention in modern agriculture for their ability to enhance crop productivity, improve nutrient use efficiency, and increase resilience to abiotic and biotic stresses, while reducing dependence on conventional agrochemicals. This review synthesizes the historical development, classification, mechanisms of action, and agronomic benefits of biostimulants, with a particular emphasis on PHs, which are mixtures of amino acids, peptides, and polypeptides derived from plant or animal proteins through enzymatic, chemical, or thermal hydrolysis. The concept of biostimulants has… More >

  • Open Access

    ARTICLE

    Elucidating the Potential Targets and Mechanisms of Bisphenol A-Induced Prostate Cancer Based on Network Toxicology and Molecular Docking Analyses

    Ashuai Du1,#, Dianbin Guo2,#, Dongbo Yuan3,#, Kai Li4, Yuanyuan Luo4, Songsong Tan3, Xuchao Dai4, Bo Yu5, Wanxiang You6, Junjie Zhao7, Bo Yan3, Kehua Jiang3,*, Xiaofei Fan2,*, Jianguo Zhu3,*,*

    Oncology Research, Vol.34, No.5, 2026, DOI:10.32604/or.2026.076716 - 22 April 2026

    Abstract Background: Bisphenol A (BPA) is a widely used industrial chemical and endocrine-disrupting compound, and accumulating evidence suggests that it may contribute to prostate cancer progression; however, the underlying molecular mechanisms remain incompletely elucidated. This study aimed to elucidate the molecular targets and signaling pathways underlying BPA-induced prostate cancer progression. Methods: In this study, an integrated strategy combining network toxicology, molecular docking, and molecular dynamics simulations was employed to identify potential BPA-related targets and signaling pathways involved in prostate cancer. Candidate targets were retrieved from public databases, followed by protein-protein interaction network analysis to screen key… More >

  • Open Access

    ARTICLE

    Elevated C-Reactive Protein as a Potential Biomarker for Neurological Adverse Events in Immune Checkpoint Inhibitor Therapy: A Prospective Cohort Study

    Laura Duzzi1,#,*, Nora Möhn1,#, Emily Narten1, Janin Thomas1, Susann Mahjoub1, Lea Grote-Levi1, Konstantin Jendretzky1, Sandra Nay1, Felix Konen1, Jonas Wiegmann2, Gernot Beutel2, Tabea Fröhlich2, Benjamin-Alexander Bollmann3, Thomas Wirth4, Imke von Wasielewski5, Florian H. Heidel2, Ralf Gutzmer5,6, Thomas Skripuletz1,§, Philipp Ivanyi2,§, the ICOG (Immune Cooperative Oncology Group)-Investigators7

    Oncology Research, Vol.34, No.5, 2026, DOI:10.32604/or.2026.074095 - 22 April 2026

    Abstract Objectives: Since 2011, immune checkpoint inhibitors (ICI) have transformed the treatment of various cancers. However, our understanding of the autoimmune adverse events, particularly those affecting the nervous system, remains limited. These adverse events can cause significant disability or even death, yet there are currently no established guidelines or biomarkers to aid diagnosis and treatment. With this study, we aim to gain a deeper understanding of neurological adverse events and investigate potential predictive biomarkers. Methods: Between 19 December 2019 and 21 August 2021, 150 out of 543 ICI-treated cancer patients were eligible for our prospective monocentric… More >

  • Open Access

    REVIEW

    Multidimensional Regulatory Network of YAP1 Driving Malignant Progression in Esophageal Cancer: Molecular Mechanisms and Targeted Therapy: A Review

    Jun-Hui Chen1, Si-Run Du1, Chang Liu1, Bei-Bei Liu1, Hai-Ying Xu2, Xin-Ying Ji2, Bo Feng3, Chun-Zheng Ma3, Jun-Hui Guo3,*

    Oncology Research, Vol.34, No.5, 2026, DOI:10.32604/or.2026.073484 - 22 April 2026

    Abstract Esophageal cancer (EC) ranks among the most lethal gastrointestinal malignancies. Due to challenges in early diagnosis, molecular heterogeneity, and therapeutic resistance, patient prognosis remains extremely poor, necessitating the development of novel biomarkers and therapeutic targets. As a core effector of the Hippo signaling pathway, the potential significance of Yes-associated protein 1 (YAP1) has garnered increasing attention. This paper aims to systematically summarize the multi-omics research, molecular mechanisms, and preclinical/translational evidence for YAP1, covering its activation pathways, biological functions, clinical significance, and therapeutic strategies. We elucidated YAP1’s multidimensional regulatory network in EC, including Hippo-dependent and -independent mechanisms, cross-regulation… More >

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