Mitotic Checkpoint Proteins in Tumorigenesis
Mitotic Checkpoint Proteins in Tumorigenesis
批准号:
6912547
负责人:
FRANK D. MCKEON
金额:
$37.8万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-07-18 至 2007-06-30
关键词:
acetylationbiological signal transductioncarcinogenesiscell cycle proteinscell deathchromosome movementgenetically modified animalshigh performance liquid chromatographyimmunoprecipitationlaboratory mousemass spectrometrymitotic spindle apparatusneoplasm /cancer geneticsneoplastic processp53 gene /proteinphosphorylationprotooncogenetissue /cell culturetumor suppressor proteins
中文摘要
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英文摘要
DESCRIPTION: (provided by applicant) The mitotic checkpoint describes molecular
controls that monitor chromosome segregation, a process that ensures the
faithful transfer of a cell's genome to its progeny. Should any of these steps
fail, the mitotic checkpoint triggers a cell cycle arrest to provide additional
time to complete the process before cell division. Arguably more important to
tumorigenesis, but largely unexplored, is a second function of the mitotic
checkpoint- inducing cell death when division occurs without proper chromosome
segregation. Recently, the mitotic checkpoint has come under increased scrutiny
because many cancer cells show chromosomal aneuploidy, at least some of which
can be explained by a genetically dominant chromosome instability (GIN)
phenotype. This chromosome instability may in fact be acting early in
tumorigenesis to promote the rapid loss and gain of tumor suppressors and
proto-oncogenes, respectively. Taken together, these findings suggest a
critical link between the mitotic checkpoint and cancer pathways.
This is a proposal to decipher the mechanisms underlying the second function of
the mitotic checkpoint, that of killing cells which undergo abnormal chromosome
segregation. Preliminary data support the hypothesis that cells showing
abnormal chromosome segregation are killed in a manner dependent on signaling
from two mitotic checkpoint proteins, BUB1 and MAD3L, to the tumor suppressor
p53. We want to determine how BUB 1 and MAD3L, which appear to monitor
successive phases of chromosome segregation, signal failures and whether both
of these signals act through p53 stabilization. Finally, we will develop murine
models that test the consequences of defects in the mitotic checkpoint on
tumorigenesis, as well as develop models to further decipher the biochemical
pathways between the checkpoint signaling molecules and p53. We anticipate that
these studies will address an important hypothesis for the generation of
cancers and contribute to our understanding and prevention of these diseases.
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海外基金