نتایج جستجو برای: cytotoxicity mechanism

تعداد نتایج: 605553  

Journal: :Infection and immunity 2004
James G Smedley Bruce A McClane

Clostridium perfringens enterotoxin (CPE) has a unique mechanism of action that results in the formation of large, sodium dodecyl sulfate-resistant complexes involving tight junction proteins; those complexes then induce plasma membrane permeability alterations in host intestinal epithelial cells, leading to cell death and epithelial desquamation. Previous deletion and point mutational studies ...

2016
Luciana Miato Gonçalves Silva Camila Aparecida Alves da Silva Aline da Silva Rodolfo Paula Vieira Raquel Agnelli Mesquita-Ferrari José Carlos Cogo Stella Regina Zamuner

BACKGROUND Snakebites is a neglected disease and in Brazil is considered a serious health problem, with the majority of the snakebites caused by the genus Bothrops. Antivenom therapy and other first-aid treatments do not reverse local myonecrose which is the main sequel caused by the envenomation. Several studies have shown the effectiveness of low level laser (LLL) therapy in reducing local my...

2017
Yu-Guo Yuan Yan-Hong Wang Hui-Hui Xing Sangiliyandi Gurunathan

BACKGROUND Graphene and graphene-related materials have gained substantial interest from both academia and industry for the development of unique nanomaterials for biomedical applications. Graphene oxide (GO) and silver nanoparticles (AgNPs) are a valuable platform for the development of nanocomposites, permitting the combination of nanomaterials with different physical and chemical properties ...

2013
Yong Bae Kim Hei-Cheul Jeung Inhye Jeong Kyunghwa Lee Sun Young Rha Hyun Cheol CHUNG Gwi Eon Kim

Sorafenib, an orally available multikinase inhibitor, combined with radiation has shown potential as an anticancer treatment in an in vitro and in vivo colon cancer model. In this study, we investigated the mechanism of enhancement of radiation-induced cytotoxicity by sorafenib in colorectal cancer. The effects of sorafenib on radiation-induced cytotoxicity of DLD-1 and HT-29 were evaluated via...

The advent of combination therapy unprecedentedly shifted the paradigm of cancer treatment by reconstructing the conventional protocols. By identifying the anti-tumoral activity for different natural products, recent interest has focused on inventing the combined-modality strategies in order to increase the cure rates of cancer, while reducing the toxic side effects of current intensive regimen...

Journal: :Cosmetics 2023

The invention and use of chelating purification products directed at atmospheric particulate matter 2.5 (PM2.5) are beneficial in preventing cytotoxicity bodily harm. However, natural plant active compounds that minimize the adverse effect PM2.5 rarely reported. Chlorella pyrenoidosa extracts (CPEs), a nutritional supplement derived from vulgaris, have been shown to antioxidant anti-inflammator...

2011
Qin Liu Peter A. Rice Sanjay Ram Dan M. Granoff Peter T. Beernink Jutamas Shaughnessy Emily M. Braga

2003
HOWARD B. KESSLER

Human monocytes stimulated with phorbol myristate acetate were able to rapidly destroy autologous erythrocte targets. Monocyte-mediated cytotoxicity was related to phorbol myristate acetate concentration and monocyte number. Purified preparations of lymphocytes were incapable of mediating erytlrocyte lysis in this system. The ability of phorbol myristate acetate-stimulated monocytes to lyse ery...

Background and Objectives: Transition metal complexes possess a variety of biological and pharmacological activities, such as antitumor, antimicrobial, anti-inflammatory, anti-diabetic, and free radical scavenging. Many studies have been carried out on platinum-based chemotherapy agents, however, most attention has been paid to non-platinum metal-based agents in order to find different metal comp...

Journal: :Cancer research 1994
W T van der Graaf E G de Vries H Timmer-Bosscha G J Meersma G Mesander E Vellenga N H Mulder

The multidrug resistance (MDR) modulators amiodarone (AM), cyclosporin A (CsA), and PSC 833 were tested for their potential to modulate cytotoxicity of doxorubicin (DOX), vincristine (VCR), and mitoxantrone (MX) in a sensitive human small cell lung carcinoma cell line GLC4, in its DOX-resistant non-P-glycoprotein subline GLC4-Adr, and in its cisplatin-resistant subline GLC4-CDDP. GLC4-Adr, in w...

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