Precise Carrier-Free Pt(IV)-Nanobombs for Apoptosis/Ferroptosis Synergistic Tumor Therapy: A New Effective Method to Obtain Good Chemotherapy and Low Toxicity DOI
Xu Guo, Xin Liang, Jiale Liu

и другие.

Journal of Medicinal Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Дек. 16, 2024

The emerged apoptosis/ferroptosis synergistic platinum-based therapy has attracted a lot of attention but is far from clinic use due to high systemic toxicity. Herein, series novel precise carrier-free self-assembled platinum(IV) nanoparticles with lipid regulation effect named FSPNPs (5NPs–8NPs) were constructed via connecting fenofibrate acid (FA) cisplatin or oxaliplatin-derived platinum(IV)-intermediates disulfide bonds. can be stimulated by high-glutathione/ascorbic and acidity environment produce an "explosion-like" cascade release process. Cell-activity showed precision FSPNPs, which accumulated more in tumor cells inhibited cell proliferation. Especially, 5NPs have higher selectivity than cisplatin. downregulated glutathione/glutathione peroxidase 4, increased reactive oxygen species/lipid peroxidation/malondialdehyde, induced DNA damage/S-phase arrest, regulated p53/Bcl-2/Bax trigger the hybrid pathway. released FA derivates docked into peroxisome proliferator-activated receptor α activating cholesterol metabolism destroy membrane integrity. also good biocompatibility superior antitumor activity no observable tissue damage.

Язык: Английский

Ferroptosis-Related Oxaliplatin Resistance in Multiple Cancers: Potential Roles and Therapeutic Implications DOI Creative Commons

Si-Jia Zhong,

Zihan Wang,

Jiaxi Yang

и другие.

Heliyon, Год журнала: 2024, Номер 10(18), С. e37613 - e37613

Опубликована: Сен. 1, 2024

Oxaliplatin (OXA)-based therapy is effective in the treatment of multiple cancers. However, primary or acquired OXA resistance remains an emerging challenge for its clinical application. Ferroptosis iron-dependent mode cell death that has been demonstrated to play essential role chemoresistance many drugs, including OXA. In particular, dysregulation SLC7A11-GPX4, one major antioxidant systems ferroptosis, was found colorectal cancer (CRC) and hepatocellular carcinoma (HCC). addition, Nrf2, upstream regulator GPX4 other factors, also involved CRC HCC. Inhibition SLC7A11-GPX4 Nrf2 by genetic deletion pharmaceutical inhibition could significantly reverse resistance. Long noncoding RNA (lncRNA) participates ferroptosis cells. Specifically, LINC01134 promotes recruitment promoter GPX4, thereby exerting transcriptional regulation which eventually increases sensitivity HCC through upregulation ferroptosis. On hand, a novel lncRNA DACT3-AS1 sensitizes gastric cells miR-181a-5p/sirtuin 1(SIRT1)-mediated Therapies based on combination enhancers provide new therapeutic insights overcome present review, we current understanding ferroptosis-related resistance, highlight pathogenesis chemoresistance, summarize available therapies target enhancing

Язык: Английский

Процитировано

3

Ferroptosis: A new way to intervene in the game between Mycobacterium tuberculosis and macrophages DOI Creative Commons

Wuerken Jumabayi,

Abdusemer Reyimu,

Rongrong Zheng

и другие.

Microbial Pathogenesis, Год журнала: 2024, Номер 197, С. 107014 - 107014

Опубликована: Окт. 11, 2024

Язык: Английский

Процитировано

2

Glutathione dynamics in subcellular compartments and implications for drug development DOI
Hanfeng Lin, Lingfei Wang, Xiqian Jiang

и другие.

Current Opinion in Chemical Biology, Год журнала: 2024, Номер 81, С. 102505 - 102505

Опубликована: Июль 24, 2024

Язык: Английский

Процитировано

2

Ferroptosis, a therapeutic target for cardiovascular diseases, neurodegenerative diseases and cancer DOI Creative Commons
Yinghui Li, Cui-Yun Liu, Bo Fang

и другие.

Journal of Translational Medicine, Год журнала: 2024, Номер 22(1)

Опубликована: Дек. 22, 2024

The identification of ferroptosis represents a pivotal advancement in the field cell death research, revealing an entirely novel mechanism cellular demise and offering new insights into initiation, progression, therapeutic management various diseases. Ferroptosis is predominantly induced by intracellular iron accumulation, lipid peroxidation, or impairments antioxidant defense system, culminating membrane rupture consequent death. Studies have associated with wide range diseases, enhancing our comprehension its underlying mechanisms, we can formulate innovative strategies, thereby providing renewed hope for patients.

Язык: Английский

Процитировано

2

Ferroptosis: Latest evidence and perspectives on plant‐derived natural active compounds mitigating doxorubicin‐induced cardiotoxicity DOI
Boyu Wang,

Jiameng Wang,

Changxing Liu

и другие.

Journal of Applied Toxicology, Год журнала: 2024, Номер unknown

Опубликована: Июль 18, 2024

Abstract Doxorubicin (DOX) is a chemotherapy drug widely used in clinical settings, acting as first‐line treatment for various malignant tumors. However, its use greatly limited by the cardiotoxicity it induces, including doxorubicin‐induced cardiomyopathy (DIC). The mechanisms behind DIC are not fully understood, but potential biological thought to include oxidative stress, inflammation, energy metabolism disorders, mitochondrial damage, autophagy, apoptosis, and ferroptosis. Recent studies have shown that cardiac injury induced DOX closely related Due their high efficacy, availability, low side effects, natural medicine treatments hold strong potential. Currently, medicines been mitigate DOX‐induced ferroptosis ease through functions such antioxidation, iron ion homeostasis correction, lipid regulation, function improvement. Therefore, this review summarizes of regulation plant products, with expectation providing reference future research development inhibitors targeting DIC. This explores (DIC) how products can alleviate inhibiting reducing correcting homeostasis, regulating metabolism, improving function.

Язык: Английский

Процитировано

1

Iron metabolism in doxorubicin-induced cardiotoxicity: From mechanisms to therapies DOI

Hua Ye,

Lin Wu, Yanmei Liu

и другие.

The International Journal of Biochemistry & Cell Biology, Год журнала: 2024, Номер 174, С. 106632 - 106632

Опубликована: Июль 23, 2024

Язык: Английский

Процитировано

1

Mechanisms and Therapeutic Potential of GPX4 in Pain Modulation DOI Creative Commons

Shiwen Fan,

Kaixin Wang,

Tianhao Zhang

и другие.

Pain and Therapy, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 6, 2024

Pain, a complex symptom encompassing both sensory and emotional dimensions, constitutes significant global public health issue. Oxidative stress is pivotal factor in the pathophysiology of pain, with glutathione peroxidase 4 (GPX4) recognized as crucial antioxidant enzyme involved defense mechanisms ferroptosis pathways. This review systematically explores GPX4's functions across various pain models, including neuropathic, inflammatory, low back, cancer-related pain. Specifically, focus includes physiological roles, mechanisms, regulation ferroptosis, involvement signal transduction pathways, metabolic regulation. By summarizing current research, we highlight potential GPX4-targeted therapies management.

Язык: Английский

Процитировано

1

AI in Predictive Toxicology DOI
Bancha Yingngam

Advances in medical technologies and clinical practice book series, Год журнала: 2024, Номер unknown, С. 79 - 134

Опубликована: Сен. 14, 2024

The field of toxicology is undergoing a significant transformation due to the integration artificial intelligence (AI). In addition traditional reliance on empirical studies and animal testing, AI-powered predictive now used predict toxic effects chemicals drugs. This chapter examines role AI in enhancing accuracy, efficiency, breadth toxicological assessments by bridging gap between approaches advanced techniques. It explores various methodologies, such as machine learning, deep neural networks, focusing their application toxicity prediction. Furthermore, this investigates with databases development validation models. also addresses challenges associated toxicology, including data quality, model interpretability, scalability. concludes that despite facing challenges, powerful tool modern analysis.

Язык: Английский

Процитировано

0

H2 protects H9c2 cells from hypoxia/reoxygenation injury by inhibiting the Wnt/CX3CR1 signaling pathway DOI Creative Commons
Jingsheng Wang, Bin Ma, Xue Jiang

и другие.

Medical Gas Research, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 8, 2024

Myocardial ischemia-reperfusion injury is a severe cardiovascular disease, and its treatment prevention are crucial for improving patient prognosis reducing the economic burden. This study aimed to explore impact of hydrogen (H2) on hypoxia/reoxygenation (H/R) in H9c2 cells (derived from rat embryonic heart tissue) induced by peroxide (H2O2) elucidate underlying mechanism. An H/R model was established via exposure 15 μM H2O2 3 hours, followed incubation 5% CO2 atmosphere at 37°C 24 hours. Then, were treated with H2 (50%) 6, 12 or The results demonstrated that exposed subjected presented marked decrease cell survival rate, accompanied morphological alterations, such as curling wrinkling, elevated lactate dehydrogenase levels. Notably, mitigated time-dependent manner, damage observed decreasing Compared group, increased activities antioxidant enzymes, including catalase, superoxide dismutase, glutathione peroxidase, while concurrently level malondialdehyde, an indicator cellular damage. Furthermore, downregulated expression inflammatory cytokines inflammatory-related factors, specifically interleukin-6, high-mobility group box 1, tumor necrosis factor-alpha, Toll-like receptor 4, post-H/R injury. resulted levels proteins associated Wnt/C-X3-C-motif 1 signaling pathway, β-catenin, glycogen synthase kinase-3 beta, adenomatous polyposis coli, Wnt C-X3-C-motif 1. observation suggests potential mechanism protective effects against Therefore, exerts effect H2O2, potentially inhibiting activated pathway. inhibition, turn, prevents generation oxidative stress, cytokines, inflammation-associated factors.

Язык: Английский

Процитировано

0

Vanillic acid attenuates doxorubicin-induced cardiotoxicity by regulating PINK1/Parkin/Mfn2 signaling pathway DOI Creative Commons
Cheng Zhang,

Jiayun Guo,

Yimeng Li

и другие.

Journal of Functional Foods, Год журнала: 2024, Номер 123, С. 106595 - 106595

Опубликована: Ноя. 26, 2024

Язык: Английский

Процитировано

0