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Titlebook: Chemokine Receptors in Cancer; Amy M. Fulton Book 2009 Humana Press 2009 angiogenesis.cytokines.metastasis.prostate cancer.tumor

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發(fā)表于 2025-3-21 16:17:01 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Chemokine Receptors in Cancer
編輯Amy M. Fulton
視頻videohttp://file.papertrans.cn/225/224909/224909.mp4
概述Cumulatively, these data indicate that chemokine receptors may serve as biomarkers of tumor behavior as well as potential therapeutic targets.It is an appropriate time to summarize what we do and do n
叢書名稱Cancer Drug Discovery and Development
圖書封面Titlebook: Chemokine Receptors in Cancer;  Amy M. Fulton Book 2009 Humana Press 2009 angiogenesis.cytokines.metastasis.prostate cancer.tumor
描述.Chemokines are a superfamily of low molecular weight cytokines that were initially described based on their ability to induce the directed migration of leukocytes to sites of inflammation or injury. In humans, there are approximately 45 chemokines that bind to 19 G-protein-coupled receptors. In addition to mediating cellular migration, chemokines have now been shown to affect many cellular functions including survival, adhesion, invasion, proliferation, and to regulate circulating chemokine levels. Although chemokine receptors were first described on leukocytes, it is now appreciated that chemokine receptors are also expressed by many other cells including endothelial and epithelial cells...Since the first description of chemokine receptors on malignant cells in 2001, an extensive literature has developed describing the expression and function of chemokine receptors in many malignancies. These studies support the initial hypothesis that malignant cells use chemokine receptors to migrate to distant sites of ligand expression and that expression of certain receptors is associated with a poor prognosis. It has also become apparent that malignancies of different tissues may use a dive
出版日期Book 2009
關(guān)鍵詞angiogenesis; cytokines; metastasis; prostate cancer; tumor
版次1
doihttps://doi.org/10.1007/978-1-60327-267-4
isbn_softcover978-1-61737-885-0
isbn_ebook978-1-60327-267-4Series ISSN 2196-9906 Series E-ISSN 2196-9914
issn_series 2196-9906
copyrightHumana Press 2009
The information of publication is updating

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Kausalgesetz und Willensfreiheitrtance of chemokines in providing navigational cues to migrating cells bearing specific receptors is well-established, how chemokine function is regulated is not so well understood and may be of key importance to the design of new therapeutics for numerous human diseases, particularly for the contro
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Quantenmechanik und Weimarer Republiksses including organogenesis, hematopoiesis, and immunity. Recent evidence has highlighted the role of CXCR4 in a variety of diseases including cancer and WHIM syndrome. Expression of CXCR4 in cancer metastasis appears to be due to dysregulation of the receptor leading to enhanced signaling. CXCR4 w
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Kausalgesetz und Willensfreiheitand trafficking of cells. Hypoxia within the tumor microenvironment plays a role in the upregulation of several chemokine receptors on tumor cells and secretion of different chemokines promoting tumor cell invasion and metastatic spread. Preliminary data from animal models show promising antitumor e
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https://doi.org/10.1007/978-3-322-83700-4 CXCR3 is expressed on activated T cells, B cells, Natural Killer (NK) cells, dendritic cells, mast cells, and endothelial cells, and has now been reported on many malignant cells. There are several CXCR3 variants: CXCR3-A promotes chemotaxis and also plays a role in cell survival, CXCR3-B activatio
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https://doi.org/10.1007/978-3-322-83700-4number of solid tumors as well as in hematopoietic malignancies. Local factors such as hypoxia, cytokines (endothelins), or epigenetic changes may be involved in the upregulation of CCR7 by tumor cells. Through distinct signaling pathways, activation of CCR7 by its cognate ligands, CCL21 or CCL19, p
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