DCDC2 inhibits hepatic stellate cell activation and ameliorates CCl4-induced liver fibrosis by suppressing Wnt/β-catenin signaling DOI Creative Commons
Qingqing Liu,

Jing Chen,

Tao Ma

et al.

Scientific Reports, Journal Year: 2024, Volume and Issue: 14(1)

Published: April 24, 2024

Liver fibrosis, as a consequence of chronic liver disease, involves the activation hepatic stellate cell (HSC) caused by various injuries. Emerging evidence suggests that HSC during an inflammatory state can lead to abnormal accumulation extracellular matrix (ECM). Investigating novel strategies inhibit and proliferation holds significant importance for treatment fibrosis. As member doublecortin domain-containing family, domain containing 2 (DCDC2) mutations neonatal sclerosing cholangitis, but its involvement in fibrosis remains unclear. Therefore, this study aims elucidate role DCDC2 Our findings revealed reduction expression both human fibrotic tissues carbon tetrachloride (CCl

Language: Английский

Role of lactate and lactate metabolism in liver diseases (Review) DOI Creative Commons
Shun Yao,

Hongyu Chai,

Ting Tao

et al.

International Journal of Molecular Medicine, Journal Year: 2024, Volume and Issue: 54(1)

Published: May 20, 2024

Lactate is a byproduct of glycolysis, and before the Warburg effect was revealed (in which glucose can be fermented in presence oxygen to produce lactate) it considered metabolic waste product. At present, lactate not only recognized as substrate that provides energy, but also signaling molecule regulates cellular functions under pathophysiological conditions. Lactylation, post‑translational modification, involved development various diseases, including inflammation tumors. Liver disease major health challenge worldwide. In normal liver, there net uptake caused by gluconeogenesis, exhibiting higher clearance rate compared with any other organ. Therefore, abnormalities metabolism lead liver disease, metabolism‑related genes used for predicting prognosis disease. Targeting production, regulating transport modulating lactylation may potential treatment approaches However, currently systematic review summarizes role diseases. present review, diseases fibrosis, non‑alcoholic fatty acute failure hepatocellular carcinoma summarized aim provide insights future research.

Language: Английский

Citations

12

Progress in clinical and basic research of fuzheng Huayu formula for the treatment of liver fibrosis DOI
Grace Zhou, Yadong Fu, Jiamei Chen

et al.

Journal of Ethnopharmacology, Journal Year: 2024, Volume and Issue: 327, P. 118018 - 118018

Published: March 5, 2024

Language: Английский

Citations

9

Cutting-edge insights into liver fibrosis: advanced therapeutic strategies and future perspectives using engineered mesenchymal stem cell-derived exosomes DOI Creative Commons
Manar A. Didamoony, Ayman A. Soubh, Lamiaa A. Ahmed

et al.

Drug Delivery and Translational Research, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 24, 2025

Abstract Liver fibrosis is still a serious health concern worldwide, and there increasing interest in mesenchymal stem cells (MSCs) with tremendous potential for treating this disease because of their regenerative paracrine effects. Recently, many researches have focused on using the released exosomes (EXOs) from to treat liver rather than parent themselves. MSC-derived EXOs (MSC-EXOs) demonstrated favourable outcomes similar cell treatment terms regenerative, immunomodulatory, anti-apoptotic, anti-oxidant, anti-necroptotic, anti-inflammatory anti-fibrotic actions several models fibrosis. are superior terms, including lower immunogenicity risk tumour formation. However, maintaining stability efficacy after vivo transplantation remains major challenge clinical applicability. Therefore, strategies been applied engineering, such as parental modification or modifying directly achieve optimum performance Herein, we discuss underlying mechanisms an overview available therapies, among them EXOs. We also summarise recent developments improving effectiveness advantages limitations these approaches upcoming applications. Graphical

Language: Английский

Citations

1

Amelioration of liver fibrosis with autologous macrophages induced by IL-34-based condition DOI Creative Commons

Yuichi Igarashi,

Haruka Wada,

Masato Muto

et al.

Inflammation and Regeneration, Journal Year: 2025, Volume and Issue: 45(1)

Published: Jan. 24, 2025

Language: Английский

Citations

1

Total Sanghuangporus vaninii extract inhibits hepatocyte ferroptosis and intestinal microbiota disturbance to attenuate liver fibrosis in mice DOI
Siqi Gao,

Xingxing Wang,

Qiuying Xu

et al.

Journal of Ethnopharmacology, Journal Year: 2025, Volume and Issue: unknown, P. 119571 - 119571

Published: Feb. 1, 2025

Language: Английский

Citations

1

Recent Advancements in Antifibrotic Therapies for Regression of Liver Fibrosis DOI Creative Commons
Anshika Jangra, Ashish Kothari,

Phulen Sarma

et al.

Cells, Journal Year: 2022, Volume and Issue: 11(9), P. 1500 - 1500

Published: April 29, 2022

Cirrhosis is a severe form of liver fibrosis that results in the irreversible replacement tissue with scar liver. Environmental toxicity, infections, metabolic causes, or other genetic factors including autoimmune hepatitis can lead to chronic injury and result inflammation fibrosis. This activates myofibroblasts secrete ECM proteins, resulting formation fibrous scars on Fibrosis regression possible through removal pathophysiological causes as well elimination activated myofibroblasts, reabsorption tissue. To date, wide range antifibrotic therapies has been tried tested, varying degrees success. These include use growth factors, cytokines, miRNAs, monoclonal antibodies, stem-cell-based approaches, approaches target ECM. The positive preclinical clinical studies raise prospect viable alternative transplantation near future. present review provides synopsis recent treatment modalities for cirrhosis, brief summary trials have conducted date.

Language: Английский

Citations

33

Self-homing nanocarriers for mRNA delivery to the activated hepatic stellate cells in liver fibrosis DOI Creative Commons
Mahmoud A. Younis, Yusuke Sato, Yaser Hosny Ali Elewa

et al.

Journal of Controlled Release, Journal Year: 2022, Volume and Issue: 353, P. 685 - 698

Published: Dec. 15, 2022

Language: Английский

Citations

33

Design, synthesis, molecular docking and biological evaluation of new carbazole derivatives as anticancer, and antioxidant agents DOI Creative Commons
İrfan Çapan, Mohammed Hawash, Nidal Jaradat

et al.

BMC Chemistry, Journal Year: 2023, Volume and Issue: 17(1)

Published: June 16, 2023

Abstract Background The carbazole skeleton is an important structural motif occurring naturally or synthesized chemically and has antihistaminic, antioxidant, antitumor, antimicrobial, anti-inflammatory activities. Objectives This study aimed to design synthesize a novel series of derivatives evaluate their antiproliferative antioxidant Methods compounds were characterized utilizing HRMS, 1 H-, 13 C APT -NMR, assessed for anticancer, antifibrotic, effects reference biomedical procedures. In addition, the AutoDock Vina application was used perform in-silico docking computations. Results A in current study. Compounds 10 11 found have stronger effect than 2 – 5 against HepG2, HeLa, MCF7 cancer cell lines with IC 50 values 7.68, 10.09, 6.44 µM, respectively. Moreover, compound 9 showed potent activity HeLa value 7.59 µM. However, except , all moderate activities CaCo-2 range 43.7–187.23 All these compared positive control anticancer drug 5-Fluorouracil (5-FU). most anti-fibrotic compound, cellular viability LX-2 57.96% at µM concentration comparison 5-FU. 4 1.05 ± 0.77 5.15 1.01 Conclusion Most promising antiproliferative, antifibrotic biological effects, further in-vivo investigations are needed approve disapprove results.

Language: Английский

Citations

22

Insights on drug and gene delivery systems in liver fibrosis DOI Creative Commons
Kunj Vyas, Mayur M. Patel

Asian Journal of Pharmaceutical Sciences, Journal Year: 2023, Volume and Issue: 18(2), P. 100779 - 100779

Published: Jan. 29, 2023

Complications of the liver are amongst world's worst diseases. Liver fibrosis is first stage problems, while cirrhosis last stage, which can lead to death. The creation effective anti-fibrotic drug delivery methods appears critical due liver's metabolic capacity for drugs and presence insurmountable physiological impediments in way targeting. Recent breakthroughs agents have substantially assisted fibrosis; nevertheless, working mechanism medications not fully understood, there a need design systems that well-understood aid cirrhosis. Nanotechnology-based regarded be but they been adequately researched delivery. As result, capability nanoparticles hepatic was explored. Another approach targeted delivery, considerably improve efficacy if designed target stellate cells (HSCs). We addressed numerous strategies HSCs, eventually fibrosis. Recently genetics proved useful, delivering genetic material place also investigated where different techniques depicted. To summarize, this review paper sheds light on most recent gene-based nano lately shown useful treatment

Language: Английский

Citations

20

Reprogramming activated hepatic stellate cells by siRNA-loaded nanocarriers reverses liver fibrosis in mice DOI Creative Commons
Mahmoud A. Younis, Yusuke Sato, Yaser Hosny Ali Elewa

et al.

Journal of Controlled Release, Journal Year: 2023, Volume and Issue: 361, P. 592 - 603

Published: Aug. 17, 2023

Language: Английский

Citations

20