Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add filters








Year range
1.
Chinese journal of integrative medicine ; (12): 644-654, 2023.
Article in English | WPRIM | ID: wpr-982294

ABSTRACT

Chinese medicine (CM) is an important resource for human life understanding and discovery of drugs. However, due to the unclear pharmacological mechanism caused by unclear target, research and international promotion of many active components have made little progress in the past decades of years. CM is mainly composed of multi-ingredients with multi-targets. The identification of targets of multiple active components and the weight analysis of multiple targets in a specific pathological environment, that is, the determination of the most important target is the main obstacle to the mechanism clarification and thus hinders its internationalization. In this review, the main approach to target identification and network pharmacology were summarized. And BIBm (Bayesian inference modeling), a powerful method for drug target identification and key pathway determination was introduced. We aim to provide a new scientific basis and ideas for the development and international promotion of new drugs based on CM.


Subject(s)
Humans , Medicine, Chinese Traditional , Drugs, Chinese Herbal/therapeutic use , Bayes Theorem , Molecular Docking Simulation
2.
Acta Physiologica Sinica ; (6): 565-570, 2018.
Article in Chinese | WPRIM | ID: wpr-687794

ABSTRACT

Son of sevenless homolog 1 (SOS1) protein is a ubiquitously expressed adapter. As a key protein in intracellular signaling, SOS1 plays an important role in many signal transduction pathways, such as Ras and Rac signaling pathways. The abnormal expression or mutation of SOS1 is closely related to clinical diseases. In this article, we review research progress on SOS1 functions and its roles in physiology and pathophysiology.

3.
Acta Physiologica Sinica ; (6): 57-64, 2016.
Article in Chinese | WPRIM | ID: wpr-331682

ABSTRACT

Gab proteins, Grb2 (growth factor receptor binding protein 2)-associated binder, are important scaffolding adapter proteins required by many signaling pathways. In mammals, the Gab proteins mainly consist of Gab1, Gab2 and Gab3, and are involved in the amplification and integration of signal transduction evoked by a variety of extracellular stimuli, including various growth factors and cytokines. They are known to play key roles in many biological processes through the two classical signal pathways, SHP2/RAS/ERK and PI3K/AKT. In this review, we provide an overview of the structure and function of the scaffolding adapter, Gab, with a special focus on its role in tumor, inflammation and cardiovascular diseases.


Subject(s)
Humans , Adaptor Proteins, Signal Transducing , Cardiovascular Diseases , Inflammation , Intercellular Signaling Peptides and Proteins , Neoplasms , Phosphatidylinositol 3-Kinases , Phosphorylation , Signal Transduction
4.
Protein & Cell ; (12): 224-234, 2014.
Article in English | WPRIM | ID: wpr-757507

ABSTRACT

We have recently reported that Ginsenoside Rh2 (G-Rh2) induces the activation of two initiator caspases, caspase-8 and caspase-9 in human cancer cells. However, the molecular mechanism of its death-inducing function remains unclear. Here we show that G-Rh2 stimulated the activation of both caspase-8 and caspase-9 simultaneously in HeLa cells. Under G-Rh2 treatment, membrane death receptors Fas and TNFR1 are remarkably upregulated. However, the induced expression of Fas but not TNFR1 was contributed to the apoptosis process. Moreover, significant increases in Fas expression and caspase-8 activity temporally coincided with an increase in p53 expression in p53-non-mutated HeLa and SK-HEP-1 cells upon G-Rh2 treatment. In contrast, Fas expression and caspase-8 activity remained constant with G-Rh2 treatment in p53-mutated SW480 and PC-3 cells. In addition, siRNA-mediated knockdown of p53 diminished G-Rh2-induced Fas expression and caspase-8 activation. These results indicated that G-Rh2-triggered extrinsic apoptosis relies on p53-mediated Fas over-expression. In the intrinsic apoptotic pathway, G-Rh2 induced strong and immediate translocation of cytosolic BAK and BAX to the mitochondria, mitochondrial cytochrome c release, and subsequent caspase-9 activation both in HeLa and in SW480 cells. p53-mediated Fas expression and subsequent downstream caspase-8 activation as well as p53-independent caspase-9 activation all contribute to the activation of the downstream effector caspase-3/-7, leading to tumor cell death. Taken together, we suggest that G-Rh2 induces cancer cell apoptosis in a multi-path manner and is therefore a promising candidate for anti-tumor drug development.


Subject(s)
Humans , Apoptosis , Caspase 3 , Metabolism , Caspase 8 , Metabolism , Caspase 9 , Metabolism , Cell Line, Tumor , Cell Proliferation , Cytochromes c , Metabolism , Enzyme Activation , Ginsenosides , Chemistry , Pharmacology , HeLa Cells , Inhibitory Concentration 50 , Mitochondria , Metabolism , Protein Transport , Receptors, Death Domain , Metabolism , Receptors, Tumor Necrosis Factor, Type I , Metabolism , Signal Transduction , Tumor Suppressor Protein p53 , Metabolism , Up-Regulation , bcl-2 Homologous Antagonist-Killer Protein , Metabolism , bcl-2-Associated X Protein , Metabolism , fas Receptor , Metabolism
5.
Protein & Cell ; (12): 543-553, 2011.
Article in English | WPRIM | ID: wpr-757067

ABSTRACT

Sequential activation of cyclin-dependent kinases (Cdks) controls mammalian cell cycle. Here we demonstrate that the upregulation of cyclin-dependent kinase 2 (Cdk2) activity coincides with the loss of mitochondrial membrane potential (MMP) in paclitaxel-induced apoptosis. Ectopic expression of the dominant negative Cdk2 (Cdk2-dn) and a specific Cdk2 inhibitor, p21( WAF1/CIP1 ), effectively suppresses the loss of MMP, the release of cytochrome c, and subsequent activation of caspase-3 in paclitaxel-treated cells. Whereas forced activation of Cdk2 by overexpression of cyclin A dramatically promotes these events. We further show that Cdk2 activation status does not interfere with a procedure that lies downstream of cytochrome c release induced by Bax protein. These findings suggest that Cdk2 kinase can regulate apoptosis at earlier stages than mitochondrial permeability transition and cytochrome c release.


Subject(s)
Humans , Antineoplastic Agents, Phytogenic , Pharmacokinetics , Pharmacology , Apoptosis , Cell Cycle , Cyclin-Dependent Kinase 2 , Metabolism , HeLa Cells , Mitochondria , Metabolism , Paclitaxel , Pharmacokinetics , Pharmacology , Permeability , Up-Regulation
6.
Chinese Acupuncture & Moxibustion ; (12): 140-144, 2008.
Article in Chinese | WPRIM | ID: wpr-292890

ABSTRACT

<p><b>OBJECTIVE</b>To assess the therapeutic effect of acupuncture on dementia.</p><p><b>METHODS</b>The literatures of acupuncture for treatment of dementia are comprehensively searched in according with the demands of the evidence-based medicine (EBM), which are collected from relevant domestic medical literature databases in the last ten years. Meta-analysis is conducted on the literatures enrolled.</p><p><b>RESULTS</b>Twenty-two randomized controlled trials are included, among them, 19 trials are carried out by Meta-analysis. The total OR is 3.72 [2.73, 5.07], and the funnel plot is approximately symmetry. It is indicated that the curative effect of acupuncture groups is better than the control groups (Z = 8.32, P < 0.00001).</p><p><b>CONCLUSION</b>Acupuncture therapy is effective on dementia according to the domestic clinical literatures. However, the quality of the studies needs further improving and increasing.</p>


Subject(s)
Aged , Humans , Acupuncture Therapy , Dementia , Therapeutics , Randomized Controlled Trials as Topic
SELECTION OF CITATIONS
SEARCH DETAIL