CYTOKINES AS ENDOGENOUS MEDIATORS OF CANCER CACHEXIA
细胞因子作为癌症恶病质的内源性介质
基本信息
- 批准号:3196887
- 负责人:
- 金额:$ 12.02万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1990
- 资助国家:美国
- 起止时间:1990-07-01 至 1995-04-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Anorexia, weight loss and cachexia are the most visibly recognizable
symptoms associated with cancer. However, the causes of cancer cachexia
remain unknown. This application proposes that the anorexia, losses of
lean tissue and body fat, and the hepatic acute phase response in patients
or experimental animals with cancer can be attributed in part to an
inappropriate or excessive production of cytokines, including interleukin-1
alpha or beta (IL-1), tumor necrosis factor-alpha (TNF-alpha/cachectin)
and/or interleukin-6 (interferon-beta2). Experimental evidence suggests
that either the tumor itself or tumor-infiltrating macrophages and other
accessory cells, blood monocytes, or macrophages contained in organs of the
reticuloendothelial system may be spontaneously releasing one or more of
these cytokines. Therefore, in this application, cytokine production (IL-
1. TNF-alpha and IL-6) will be evaluated directly in the tumors of
cachectic mice and of weight-losing patients by measuring both the quantity
of cytokine-specific mRNA and immune reactive protein present, and from
organs of the reticuloendothelial system of tumor-bearing mice. In
addition, to determine whether the production of one or more of these
cytokines is contributing directly to the development of cancer cachexia,
specific neutralizing polyclonal and monoclonal antibodies directed against
these cytokines and/or their tissue receptors will be administered in vivo
to tumor-bearing mice in order to determine whether blocking the actions of
these cytokines can either reduce the severity of or prevent the
development of cancer cachexia. Thus, the specific goal of this
application is to determine whether tumor specific or associated cytokine
production are common findings in experimental and human cancer, whether
the cytokines are of tumor or host origin, and finally, whether the host
changes in food intake, carcass protein and fat composition, and hepatic
acute phase response can be attributed to the inappropriate production of
these cytokines.
厌食症、体重减轻和恶病质是最明显的
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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LYLE L MOLDAWER其他文献
LYLE L MOLDAWER的其他文献
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{{ truncateString('LYLE L MOLDAWER', 18)}}的其他基金
Stratifying Patient Immune Endotypes in Sepsis (SPIES Study)
脓毒症患者免疫内型分层(SPIES 研究)
- 批准号:
10439853 - 财政年份:2020
- 资助金额:
$ 12.02万 - 项目类别:
Stratifying Patient Immune Endotypes in Sepsis (SPIES Study)
脓毒症患者免疫内型分层(SPIES 研究)
- 批准号:
10651650 - 财政年份:2020
- 资助金额:
$ 12.02万 - 项目类别:
Stratifying Patient Immune Endotypes in Sepsis (SPIES Study)
脓毒症患者免疫内型分层(SPIES 研究)
- 批准号:
10042541 - 财政年份:2020
- 资助金额:
$ 12.02万 - 项目类别:
Stratifying Patient Immune Endotypes in Sepsis (SPIES Study)
脓毒症患者免疫内型分层(SPIES 研究)
- 批准号:
10254395 - 财政年份:2020
- 资助金额:
$ 12.02万 - 项目类别:
Administrative Supplement: Stratifying Patient Immune Endotypes in Sepsis (SPIES Study)
行政补充:脓毒症患者免疫内型分层(SPIES 研究)
- 批准号:
10683437 - 财政年份:2020
- 资助金额:
$ 12.02万 - 项目类别:
Validation of a Genomics Based Prognostic in Severe Trauma
严重创伤中基于基因组学的预后验证
- 批准号:
8668117 - 财政年份:2013
- 资助金额:
$ 12.02万 - 项目类别:
Validation of a Genomics Based Prognostic in Severe Trauma
严重创伤中基于基因组学的预后验证
- 批准号:
9061719 - 财政年份:2013
- 资助金额:
$ 12.02万 - 项目类别:
Validation of a Genomics Based Prognostic in Severe Trauma
严重创伤中基于基因组学的预后验证
- 批准号:
8427852 - 财政年份:2013
- 资助金额:
$ 12.02万 - 项目类别:
Inflammation and Repair as Determinants of Hemodialysis Fistula Maturation
炎症和修复是血液透析瘘成熟的决定因素
- 批准号:
8450880 - 财政年份:2011
- 资助金额:
$ 12.02万 - 项目类别:
Inflammation and Repair as Determinants of Hemodialysis Fistula Maturation
炎症和修复是血液透析瘘成熟的决定因素
- 批准号:
8093245 - 财政年份:2011
- 资助金额:
$ 12.02万 - 项目类别:
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