Identification of genes differentially over-expressed in lung squamous cell carcinoma using combination of cDNA subtraction and microarray analysis

被引:88
作者
Wang, T
Hopkins, D
Schmidt, C
Silva, S
Houghton, R
Takita, H
Repasky, E
Reed, SG
机构
[1] Corixa Corp, Dept Tumor Antigen Discovery, Seattle, WA 98104 USA
[2] Roswell Pk Canc Ctr, Dept Surg, Buffalo, NY 14263 USA
[3] Roswell Pk Canc Ctr, Dept Immunol, Buffalo, NY 14263 USA
关键词
lung squamous cell carcinoma (LSCC); microarray; cDNA subtraction; connexin; 26; plakophilin; 1; keratin;
D O I
10.1038/sj.onc.1203457
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In order to develop effective vaccine products against human cancer, we are interested in identifying genes over-expressed in tumor cells. Through a combination of cDNA library subtraction and microarray technology, we identified seventeen genes preferentially expressed in lung squamous cell carcinoma, including four novel genes. To date, expression profiles of these genes were confirmed by Northern and/or real-time analysis, and several genes were also found to be expressed in head and neck squamous tumors. Thus, these combined methods represent a high throughput approach for identifying tumor specific genes. Furthermore, the report of characterization on these genes will allow them to be exploited for their diagnostic, prognostic, and therapeutic potentials including immunotherapy and antibody based anticancer therapy.
引用
收藏
页码:1519 / 1528
页数:10
相关论文
共 31 条
[1]   AUTOANTIBODIES AGAINST A NOVEL EPITHELIAL CADHERIN IN PEMPHIGUS-VULGARIS, A DISEASE OF CELL-ADHESION [J].
AMAGAI, M ;
KLAUSKOVTUN, V ;
STANLEY, JR .
CELL, 1991, 67 (05) :869-877
[2]  
Brechot JM, 1997, EUR J CANCER, V33, P385, DOI 10.1016/S0959-8049(96)00498-4
[3]  
Davidson LA, 1996, J PATHOL, V178, P398
[4]  
DeRisi J, 1996, NAT GENET, V14, P457
[5]   Exploring the metabolic and genetic control of gene expression on a genomic scale [J].
DeRisi, JL ;
Iyer, VR ;
Brown, PO .
SCIENCE, 1997, 278 (5338) :680-686
[6]   Dominant-negative abrogation of connexin-mediated cell growth control by mutant connexin genes [J].
DuflotDancer, A ;
Mesnil, M ;
Yamasaki, H .
ONCOGENE, 1997, 15 (18) :2151-2158
[7]   LIBRARY SUBTRACTION OF INVITRO CDNA LIBRARIES TO IDENTIFY DIFFERENTIALLY EXPRESSED GENES IN SCRAPIE INFECTION [J].
DUGUID, JR ;
DINAUER, MC .
NUCLEIC ACIDS RESEARCH, 1990, 18 (09) :2789-2792
[8]   IDENTIFICATION OF AN IMMUNODOMINANT PEPTIDE OF HER-2/NEU PROTOONCOGENE RECOGNIZED BY OVARIAN TUMOR-SPECIFIC CYTOTOXIC T-LYMPHOCYTE LINES [J].
FISK, B ;
BLEVINS, TL ;
WHARTON, JT ;
IOANNIDES, CG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (06) :2109-2117
[9]   PGP9.5 as a candidate tumor marker for non-small-cell lung cancer [J].
Hibi, K ;
Westra, WH ;
Borges, M ;
Goodman, S ;
Sidransky, D ;
Jen, J .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (03) :711-715
[10]  
Hibi K, 1998, CANCER RES, V58, P5690