ROLE OF A NEW ETS FACTOR, PDEF, IN PROSTATE CANCER
ROLE OF A NEW ETS FACTOR, PDEF, IN PROSTATE CANCER
批准号:
6633648
负责人:
TOWIA A. LIBERMANN
金额:
$25.14万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-04-01 至 2006-03-31
关键词:
androgen receptor athymic mouse enzyme activity gel mobility shift assay gene induction /repression hormone related neoplasm /cancer human tissue male mitogen activated protein kinase neoplasm /cancer genetics neoplastic process neoplastic transformation oncoproteins prostate neoplasms prostate specific antigen transcription factor
中文摘要
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英文摘要
DESCRIPTION: Prostate cancer has become the most common solid cancer in older
men. Although androgen ablation therapy, surgery and radiation therapy are
effective for the treatment of local prostate cancer, there is no effective
treatment available for patients with metastatic androgen-independent disease.
The poor prognosis for androgen-independent advanced prostate cancer reflects
in part the lack of knowledge about the tumor's basic biology. In particular,
very little is known about the molecular mechanisms that trigger the conversion
of an initially androgen-dependent cancer to androgen-independence. Our goal is
to understand the role of a novel prostate epithelium-specific transcription
factor, PDEF (Prostate Derived Ets Factor), a member of the Ets transcription
factor/oncogene family in human prostate cancer. PDEF is expressed in the
luminal epithelial cells of normal human prostate and preliminary results
indicate that PDEF expression is elevated in cancerous portions of the
prostate. PDEF acts independently of androgen as a strong transcriptional
enhancer of the PSA and PSMA promoter, two diagnostic markers used for
monitoring androgen-dependent and -independent prostate cancer. Activated MAP
kinases drastically enhance PDEF mediated transcriptional activation. PDEF also
interacts and cooperates with the androgen receptor in inducing expression of
the PSA gene. Thus, our hypothesis is that PDEF bypasses or activates the
androgen receptor and thereby contributes to the progression from an initially
androgen-dependent prostate cancer to an androgen-independent cancer. We
propose to determine the role of this novel member of the Ets family in
prostate cancer formation and progression and the possibility to use this new
factor as another diagnostic tool and as a potential therapeutic target. Thus,
the specific aims are:
Specific Aim #1. Does PDEF play a crucial role in prostate cancer development
or progression?
Specific Aim #2. Is PDEF a critical regulator of prostate-specific PSA gene
expression?
Specific Aim #3. Can PDEF activity explain the conversion of prostate cancer
cells to androgen-independence? Due to the importance of the Ets family in
regulation of various tissue- and differentiation-specific genes and due to the
direct implication of several members of the Ets family in various human
cancers, PDEF is expected to play a role in prostate epithelial cell
transformation or prostate cancer progression.
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