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REGULATORY ROLE OF RAC AND CDC42 ON TUMOR METASTASIS

REGULATORY ROLE OF RAC AND CDC42 ON TUMOR METASTASIS
RAC和CDC42对肿瘤转移的调节作用
批准号:
6377633
负责人:
SURANGANIE DHARMAWARDHANE
金额:
$11.25万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-05-01 至 2003-04-30

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DESCRIPTION: (Adapted from the investigator's abstract) Delineation of the molecular mechanisms of directed motility is important for understanding the processes of cancer metastasis and invasion. The processes underlying the migration of primary tumor cells to ectopic sites involve the reorganization of the actin cytoskeleton. Several factors that regulate changes in the actin cytoskeleton of motile cells have been identified, however, the signaling molecules that direct the de novo polymerization of actin and its ultimate spatial and dynamic organization need to be clarified. Several members of the Rho family of small GTPases (Rho, Rac and Cdc42) have been identified as key signal transducers that link cell surface receptors to the actin cytoskeleton. We aim to test the hypothesis that Rac and Cdc42 are important regulators of breast cancer cell metastasis. Our research plan involves general strategy of using molecular genetics approach in combination with cellular and biochemical techniques. The construction of stable transfectants of human and rat mammary carcinoma cells with dominant active, dominant negative, and effector domain mutations of Rac and Cdc42 will be performed. We will evaluate the effect of activating or inactivating Rac and Cdc42 on breast cancer metastasis. These transfectants will be characterized by cellular, biochemical, and histopathological analysis. The metastatic potential of the transfected breast cancer cells expressing mutant Rac and Cdc42 will be assessed following injection into rats (rat mammary carcinomas) and nude mice (human mammary carcinomas). This research is expected to establish Rac and/or Cdc42 as important mediators of cancer metastasis. Our long-term goal is to delineate the signaling cascades mediated by Rac and/or Cdc42 that underlie invasion and metastasis. Identifying such key regulators of directed migration is expected to increase knowledge of the cellular and molecular basis of metastasis and may also lead to novel approaches in cancer therapy.
期刊论文(4)
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科研奖励(0)
会议论文
In vitro analysis of the invasive phenotype of SUM 149, an inflammatory breast cancer cell line.
对炎症性乳腺癌细胞系的侵入性表型的体外分析。
DOI: 10.1186/1475-2867-5-11
发表时间: 2005-04-27
期刊: CANCER CELL INTERNATIONAL
影响因子: 5.8
作者: [Hoffmeyer, Michaela R., Wall, Kristin M., Dharmawardhane, Suranganie F.]
通讯作者: Dharmawardhane, Suranganie F.
DOI: 10.1186/bcr1329
发表时间: 2005
期刊: Breast cancer research : BCR
影响因子: --
作者: [Baugher PJ, Krishnamoorthy L, Price JE, Dharmawardhane SF]
通讯作者: Dharmawardhane SF
MBQ-167 derivatives as antimetastatic cancer agents.
Molecular targets of soy isoflavones in breast cancer progression
CANCER RESEARCH CENTER
  • 批准号:
    8166211
  • 项目类别:
  • 资助金额:
    $18.74万
  • 财政年份:
    2010
  • 负责人:
    SURANGANIE DHARMAWARDHANE
  • 依托单位:
Targeting breast cancer progression
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