共 69 条
Modulation of K-Ras-Dependent Lung Tumorigenesis by MicroRNA-21
被引:561
作者:

Hatley, Mark E.
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机构:
Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
Univ Texas SW Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA

Patrick, David M.
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Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA

Garcia, Matthew R.
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机构:
Univ Texas SW Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA

Richardson, James A.
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h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA

Bassel-Duby, Rhonda
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h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA

van Rooij, Eva
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h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA

Olson, Eric N.
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h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
机构:
[1] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
来源:
基金:
美国国家卫生研究院;
关键词:
TUMOR-SUPPRESSOR GENE;
BREAST-CANCER CELLS;
TRANSFORMATION SUPPRESSOR;
EXPRESSION SIGNATURE;
PDCD4;
EXPRESSION;
AP-1;
ACTIVITY;
UP-REGULATION;
MIR-21;
APOPTOSIS;
TARGETS;
D O I:
10.1016/j.ccr.2010.08.013
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Lung cancer is the leading cause of cancer-related deaths in the world, and non-small-cell lung cancer (NSCLC) accounts for 80% of cases. MicroRNA-21 (miR-21) expression is increased and predicts poor survival in NSCLC. Although miR-21 function has been studied in vitro with cancer cell lines, the role of miR-21 in tumor development in vivo is unknown. We utilize transgenic mice with loss-of-function and gain-of-function miR-21 alleles combined with a model of NSCLC to determine the role of miR-21 in lung cancer. We show that overexpression of miR-21 enhances tumorigenesis and that genetic deletion of miR-21 partially protects against tumor formation. MiR-21 drives tumorigenesis through inhibition of negative regulators of the Ras/MEK/ERK pathway and inhibition of apoptosis.
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页码:282 / 293
页数:12
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