Results 1 to 10 of about 8,294 (131)

Targeting the NR3C1-ACSL4 Axis Triggers Ferroptosis to Overcome Radioresistance in Prostate Cancer. [PDF]

open access: yesCancer Sci
The glucocorticoid receptor NR3C1 drives prostate cancer radioresistance by upregulating ACSL4. High ACSL4 levels create a lipid metabolic vulnerability. The clinical agent DHA synergizes with ACSL4 to induce lipid peroxidation and ferroptosis, effectively overcoming radioresistance.
Yang J   +7 more
europepmc   +2 more sources

Development of a Disease-Specific Virtual Malaria Population for Physiologically-Based Pharmacokinetic Modeling. [PDF]

open access: yesCPT Pharmacometrics Syst Pharmacol
ABSTRACT Malaria remains a major global health challenge, with an urgent need for new therapies to combat the evolving resistance to anti‐malarial treatments. Physiologically‐based pharmacokinetic (PBPK) modeling offers a promising approach to accurately predict PK, optimize dosing strategies, reduce development time and cost, and de‐risk the ...
Ding J, Pei Q, Hoglund RM, Tarning J.
europepmc   +2 more sources

Effects of dietary dihydroartemisinin on growth performance, meat quality, and antioxidant capacity in broiler chickens

open access: yesPoultry Science
This study aimed to investigate the effects of dietary dihydroartemisinin on the growth performance, meat quality, and antioxidant capacity of broiler chickens.
Hao Zhang, Jingfei Zhang
exaly   +3 more sources

Development of R 8 modified epirubicin–dihydroartemisinin liposomes for treatment of non-small-cell lung cancer

open access: yesArtificial Cells, Nanomedicine and Biotechnology, 2019
Presently, there are no few anticancer drugs that have been used clinically due to their poor targeting ability, short half-life period, non-selective distributions, generation of vasculogenic mimicry (VM) channels, high metastasis, and high recurrence ...
Xuetao Li, Rui-Jun Ju
exaly   +3 more sources

Dihydroartemisinin-piperaquine plus sulfadoxine-pyrimethamine versus either drug alone for intermittent preventive treatment of malaria in pregnancy: A double-blind, randomized, controlled phase 3 trial from Uganda. [PDF]

open access: yesPLoS Medicine
BackgroundTo mitigate adverse consequences of malaria in pregnancy, the World Health Organization recommends intermittent preventive treatment of malaria in pregnancy (IPTp) with sulfadoxine-pyrimethamine.
Abel Kakuru   +18 more
doaj   +2 more sources

Artemisia annua and A. afra Teas, Artemisinin, and Dihydroartemisinin Differentially Regulate ROS and Fibrosis-Associated Phenotypes in Human Dermal Fibroblasts [PDF]

open access: yesMolecules
Fibrosis is driven by persistent fibroblast activation, oxidative stress, myofibroblast differentiation, and extracellular matrix remodeling, yet available antifibrotic therapies remain limited.
Samuel Isife   +4 more
doaj   +2 more sources

The effects of polysaccharides from Inonotus obliquus, artemisinin, and dihydroartemisinin on the reproductive system of male mice infected with Neospora caninum [PDF]

open access: yesFrontiers in Veterinary Science
The present study investigated the protective effects of Inonotus obliquus polysaccharides (IOPs), artemisinin, and dihydroartemisinin (DHA) on Neospora caninum-induced damage of the reproductive system in male BALB/c mice.
Jianhao Zhao   +11 more
doaj   +2 more sources

Self-assembled dihydroartemisinin nanoparticles as a platform for cervical cancer chemotherapy

open access: yesDrug Delivery, 2020
Dihydroartemisinin (DHA) is a potent anti-cancer drug that has limited clinical applications due to poor water solubility and low bioavailability. We designed a biodegradable poly(ethylene glycol) methyl ether-poly(ε-caprolactone) (MPEG-PCL) micelle ...
Biqiong Wang, Shaozhi Fu, Zhouxue Wu
exaly   +2 more sources

Dihydroartemisinin exerts its anticancer activity through depleting cellular iron via transferrin receptor-1. [PDF]

open access: yesPLoS ONE, 2012
Artemisinin and its main active metabolite dihydroartemisinin, clinically used antimalarial agents with low host toxicity, have recently shown potent anticancer activities in a variety of human cancer models.
Qian Ba   +9 more
doaj   +1 more source

Design, Synthesis and Anti-Lung Cancer Evaluation of 1, 2, 3-Triazole Tethered Dihydroartemisinin-Isatin Hybrids

open access: yesFrontiers in Pharmacology, 2021
A series of 1,2,3-triazole tethered dihydroartemisinin-isatin hybrids 8a-c and 9a-k were designed and synthesized. Their antiproliferative activity against A549, doxorubicin-resistant A549 (A549/DOX) as well as cisplatin-resistant A549 (A549/DDP) lung ...
Haodong Hou   +4 more
doaj   +1 more source

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