Expression profiles of non-small cell lung cancers on cDNA microarrays: Identification of genes for prediction of lymph-node metastasis and sensitivity to anti-cancer drugs

被引:0
|
作者
Takefumi Kikuchi
Yataro Daigo
Toyomasa Katagiri
Tatsuhiko Tsunoda
Koichi Okada
Soji Kakiuchi
Hitoshi Zembutsu
Yoichi Furukawa
Masafumi Kawamura
Koichi Kobayashi
Kohzoh Imai
Yusuke Nakamura
机构
[1] Laboratory of Molecular Medicine,First Department of Internal Medicine
[2] Human Genome Center,Division of General Thoracic Surgery, Department of Surgery
[3] Institute of Medical Science,undefined
[4] The University of Tokyo,undefined
[5] Sapporo Medical University,undefined
[6] Laboratory for Medical Informatics,undefined
[7] SNP Research Center,undefined
[8] Riken (Institute of Physical and Chemical Research),undefined
[9] School of Medicine,undefined
[10] Keio University,undefined
来源
Oncogene | 2003年 / 22卷
关键词
non-small cell lung cancer; gene-expression profile; chemosensitivity; lymph-node metastasis;
D O I
暂无
中图分类号
学科分类号
摘要
To investigate genes involved in pulmonary carcinogenesis and those related to sensitivity of nonsmall cell lung cancers (NSCLCs) to therapeutic drugs, we performed cDNA microarray analysis of 37 NSCLCs after laser-capture microdissection of cancer cells from primary tumors. A clustering algorithm applied to the expression data easily distinguished two major histological types of non-small cell lung cancer, adenocarcinoma and squamous cell carcinoma. Subsequent analysis of the 18 adenocarcinomas identified 40 genes whose expression levels could separate cases with lymph-node metastasis from those without metastasis. In addition, we compared the expression data with measurements of the sensitivity of surgically dissected NSCLC specimens to six anti-cancer drugs (docetaxel, paclitaxel, irinotecan, cisplatin, gemcitabine, and vinorelbine), as measured by the CD-DST (collagen gel droplet embedded culture-drug sensitivity test) method. We found significant associations between expression levels of dozens of genes and chemosensitivity of NSCLCs. Our results provide valuable information for eventually identifying predictive markers and novel therapeutic target molecules for this type of cancer.
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页码:2192 / 2205
页数:13
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