共 50 条
The Association of MicroRNA Expression with Prognosis and Progression in Early-Stage, Non-Small Cell Lung Adenocarcinoma: A Retrospective Analysis of Three Cohorts
被引:164
作者:

Saito, Motonobu
论文数: 0 引用数: 0
h-index: 0
机构:
NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
Fukushima Med Univ, Dept Organ Regulatory Surg, Sch Med, Fukushima, Japan NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Schetter, Aaron J.
论文数: 0 引用数: 0
h-index: 0
机构:
NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Mollerup, Steen
论文数: 0 引用数: 0
h-index: 0
机构:
Natl Inst Occupat Hlth, Sect Toxicol, Dept Chem & Biol Working Environm, Oslo, Norway NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Kohno, Takashi
论文数: 0 引用数: 0
h-index: 0
机构:
Natl Canc Ctr, Res Inst, Div Biol, Tokyo 104, Japan NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Skaug, Vidar
论文数: 0 引用数: 0
h-index: 0
机构:
Natl Inst Occupat Hlth, Sect Toxicol, Dept Chem & Biol Working Environm, Oslo, Norway NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Bowman, Elise D.
论文数: 0 引用数: 0
h-index: 0
机构:
NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Mathe, Ewy A.
论文数: 0 引用数: 0
h-index: 0
机构:
NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Takenoshita, Seiichi
论文数: 0 引用数: 0
h-index: 0
机构:
Fukushima Med Univ, Dept Organ Regulatory Surg, Sch Med, Fukushima, Japan NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Yokota, Jun
论文数: 0 引用数: 0
h-index: 0
机构:
Natl Canc Ctr, Res Inst, Div Biol, Tokyo 104, Japan NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Haugen, Aage
论文数: 0 引用数: 0
h-index: 0
机构:
Natl Inst Occupat Hlth, Sect Toxicol, Dept Chem & Biol Working Environm, Oslo, Norway NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Harris, Curtis C.
论文数: 0 引用数: 0
h-index: 0
机构:
NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
机构:
[1] NCI, Human Carcinogenesis Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] Natl Inst Occupat Hlth, Sect Toxicol, Dept Chem & Biol Working Environm, Oslo, Norway
[3] Fukushima Med Univ, Dept Organ Regulatory Surg, Sch Med, Fukushima, Japan
[4] Natl Canc Ctr, Res Inst, Div Biol, Tokyo 104, Japan
基金:
美国国家卫生研究院;
关键词:
TUMOR-SUPPRESSOR GENE;
PREDICTS SURVIVAL;
MIR-21;
CANCER;
PROMOTES;
OVEREXPRESSION;
METASTASIS;
SIGNATURE;
PROFILES;
INVASION;
D O I:
10.1158/1078-0432.CCR-10-2961
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Purpose: There is increasing evidence that altered microRNA expression is associated with tumor progression and survival in cancer patients. We tested if the expression of specific microRNAs was associated with prognosis and disease progression in early-stage lung adenocarcinoma. Experimental Design: The expression of miR-21, miR-17, and miR-155 was measured by quantitative RT-PCR in tissues from 317 non-small cell lung cancer (NSCLC) patients that originated from Maryland, Norway, and Japan. Kaplan-Meier and Cox regression analysis evaluated associations of microRNA expression with cancer-specific mortality and disease-free survival. Results: Elevated miR-21 (HR 2.06, 1.13-3.75), miR-17 (HR 2.00, 1.10-3.61), and miR-155 (HR 2.37, 1.27-4.42) was associated with worse cancer-specific mortality in the Maryland cohort. These were evaluated in two additional cohorts and only miR-21 was associated with worse cancer-specific mortality in the Norwegian cohort (HR 2.78, 1.22-6.31) and worse relapse-free survival in the Japanese cohort (HR 2.82, 1.57-5.07). More advanced stage tumors expressed significantly higher levels of miR-21 compared with TNM stage I tumors. TNM stage I patients were evaluated separately and high levels of miR-21 was associated with worse cancer-specific mortality (HR 2.16, 1.11-4.21) and relapse-free survival (3.40, 1.57-7.36) independent of other clinical factors. Conclusions: This is the first study to report that increased miR-21 expression is associated with disease progression and survival in stage I lung cancer. This suggests that expression of miR-21 may contribute to lung carcinogenesis and serve as a therapeutic target or early-stage prognostic biomarker for lung adenocarcinoma. Clin Cancer Res; 17(7); 1875-82. (C) 2011 AACR.
引用
收藏
页码:1875 / 1882
页数:8
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机构: Washington Univ, Sch Med, Alvin J Siteman Canc Ctr, Div Oncol, St Louis, MO 63110 USA

Govindan, Ramaswamy
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Washington Univ, Sch Med, Alvin J Siteman Canc Ctr, Div Oncol, St Louis, MO 63110 USA Washington Univ, Sch Med, Alvin J Siteman Canc Ctr, Div Oncol, St Louis, MO 63110 USA

Pfeifer, John
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Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA Washington Univ, Sch Med, Alvin J Siteman Canc Ctr, Div Oncol, St Louis, MO 63110 USA
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Esquela-Kerscher, A
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Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA

Slack, FJ
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Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA