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Journal ArticleDOI

Constitutive activation of metalloproteinase ADAM10 in mantle cell lymphoma promotes cell growth and activates the TNFα/NFκB pathway.

Hanan Armanious, +4 more
- 09 Jun 2011 - 
- Vol. 117, Iss: 23, pp 6237-6246
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TLDR
It is concluded that constitutive activation of ADAM10 contributes to the growth of MCL and therefore inhibition ofADAM10 may be a useful strategy to enhance the response of M CL to other therapeutic agents.
About
This article is published in Blood.The article was published on 2011-06-09. It has received 32 citations till now. The article focuses on the topics: Cyclin D1 & Cell growth.

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Citations
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Journal ArticleDOI

Tetraspanin15 regulates cellular trafficking and activity of the ectodomain sheddase ADAM10

TL;DR: The data show that TSPAN15 is a central modulator of ADAM10-mediated ectodomain shedding and Therapeutic manipulation of its expression levels may be an additional approach to specifically regulate the activity of the amyloid precursor protein alpha-secretase ADAM 10.
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Genotoxic Stress Induces Senescence-Associated ADAM10-Dependent Release of NKG2D MIC Ligands in Multiple Myeloma Cells

TL;DR: The combined use of chemotherapeutic drugs and metalloproteinase inhibitors enhances NK cell–mediated recognition of MM cells, preserving MIC molecules on the cell surface and suggesting that targeting of metalliproteinases in conjunction with chemotherapy could be exploited for NK cell-based immunotherAPEutic approaches, thus contributing to avoid the escape of malignant cells from stress-elicited immune responses.
Journal ArticleDOI

Anti-tumour effects of a specific anti-ADAM17 antibody in an ovarian cancer model in vivo.

TL;DR: D1(A12) has anti-ADAM17 activity in vivo, inhibits shedding of EGFR ligands and has potential for use in EGF ligand-dependent tumours.
Journal ArticleDOI

Physiological functions of the amyloid precursor protein secretases ADAM10, BACE1, and Presenilin

TL;DR: This review attempts to summarize selected aspects of the current view of the multiple roles such proteases play in health and disease.
Journal ArticleDOI

Platelet-Derived Exosomal MicroRNA-25-3p Inhibits Coronary Vascular Endothelial Cell Inflammation Through Adam10 via the NF-κB Signaling Pathway in ApoE-/- Mice.

TL;DR: PLT-Exo overexpressing miR-25-3p attenuates ox-LDL-induced CVEC inflammation in ApoE−/− mouse models of atherosclerosis.
References
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Book

Isolation and characterization

TL;DR: Animal Models and Therapy, Directed Differentiation and Characterization of Genetically Modified Embryonic Stem Cells for Therapy, and Use of Differentiating Embryonics Stem cells in the Parkinsonian Mouse Model are reviewed.
Journal ArticleDOI

NF-κB Controls Cell Growth and Differentiation through Transcriptional Regulation of Cyclin D1

TL;DR: It is shown that NF-κB also promotes cell growth in embryonic fibroblasts, correlating with its regulation of cyclin D1, and is identified as an important transcriptional target of NF-α, revealing a mechanism to explain how NF-β is involved in the early phases of the cell cycle to regulate cell growth and differentiation.
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The ADAMs family of metalloproteases: multidomain proteins with multiple functions

TL;DR: This review will first discuss the properties of each of the domains of the ADAMs, then describe the involvement ofADAMs in selected biological processes, and highlight recent interesting findings suggesting roles for ADams in human disease.
Journal ArticleDOI

The ADAM metalloproteinases.

TL;DR: The ADAM family are fundamental to many control processes in development and homeostasis, and unsurprisingly they are also linked to pathological states when their functions are dysregulated, including cancer, cardiovascular disease, asthma, Alzheimer’s disease.
Journal ArticleDOI

Molecular Diagnosis of Primary Mediastinal B Cell Lymphoma Identifies a Clinically Favorable Subgroup of Diffuse Large B Cell Lymphoma Related to Hodgkin Lymphoma

TL;DR: Gene expression profiling strongly supported a relationship between PMBL and Hodgkin lymphoma: over one third of the genes that were more highly expressed in PMBL than in other DLBCLs were also characteristically expressed in Hodgkinymphoma cells.
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