New approaches to the understanding of the molecular basis of oral cancer

被引:63
作者
Patel, V [1 ]
Leethanakul, C [1 ]
Gutkind, JS [1 ]
机构
[1] NIDCR, Oral & Pharyngeal Canc Branch, NIH, Bethesda, MD 20892 USA
关键词
genetic alterations; gene expression; CGAP; genomics; proteomics;
D O I
10.1177/10454411010120010401
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Cancers of the oral cavity, salivary glands, larynx, and pharynx, collectively referred to as squamous cell carcinomas of the head and neck (HNSCC), are the sixth most common cancer among men in the developed world. The prognosis of HNSCC patients is still poor, which reflects the fact that although the risk factors for HNSCC are well-recognized, very little is known about the molecular mechanisms responsible for this malignancy. This review describes some of the current efforts and technological advances that have focused on the creation of a complete information infrastructure for genes expressed during squamous cell carcinogenesis. These include: the recently described HNSCC-specific chromosomal alterations (cCAP); the Head and Neck Cancer Genome Anatomy Project (HN-CGAP), whose goal is the systematic identification and cataloguing of known and novel genes expressed during tumor development; and the use of laser-capture microdissection (LCM), which is pivotal for the comprehensive molecular characterization of normal, pre-cancerous, and malignant cells by means of DNA-array technology. The latter provides the means for the analysis of expression patterns of thousands of genes simultaneously. The use of LCM for proteomics and DNA analysis is also included in this review. These revolutionary approaches are likely to have an unprecedented impact on cancer biology, and provide exciting opportunities to unravel the still-unknown mechanisms involved in squamous cell carcinogenesis. They are also expected to provide a molecular blueprint for HNSCC, thus helping to identify suitable markers for the early detection of pre-neoplastic lesions, as well as novel targets for pharmacological intervention in this disease.
引用
收藏
页码:55 / 63
页数:9
相关论文
共 70 条
[1]   Broad patterns of gene expression revealed by clustering analysis of tumor and normal colon tissues probed by oligonucleotide arrays [J].
Alon, U ;
Barkai, N ;
Notterman, DA ;
Gish, K ;
Ybarra, S ;
Mack, D ;
Levine, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (12) :6745-6750
[2]   Expression scanning of an array of growth control genes in human tumor cell lines [J].
Bertucci, F ;
Van Hulst, S ;
Bernard, K ;
Loriod, B ;
Granjeaud, S ;
Tagett, R ;
Starkey, M ;
Nguyen, C ;
Jordan, B ;
Birnbaum, D .
ONCOGENE, 1999, 18 (26) :3905-3912
[3]  
Bockmuhl U, 1998, HEAD NECK-J SCI SPEC, V20, P145, DOI 10.1002/(SICI)1097-0347(199803)20:2<145::AID-HED8>3.0.CO
[4]  
2-2
[5]   CANCER STATISTICS, 1993 [J].
BORING, CC ;
SQUIRES, TS ;
TONG, T .
CA-A CANCER JOURNAL FOR CLINICIANS, 1993, 43 (01) :7-26
[6]  
Bryce SD, 1999, CANCER RES, V59, P2038
[7]  
Califano J, 1996, CANCER RES, V56, P2488
[8]  
Celis JE, 1999, CANCER RES, V59, P3003
[9]   Oncogenic Ras triggers cell suicide through the activation of a caspase-independent cell death program in human cancer cells [J].
Chi, SJ ;
Kitanaka, C ;
Noguchi, K ;
Mochizuki, T ;
Nagashima, Y ;
Shirouzu, M ;
Fujita, H ;
Yoshida, M ;
Chen, WB ;
Asai, A ;
Himeno, M ;
Yokoyama, S ;
Kuchino, Y .
ONCOGENE, 1999, 18 (13) :2281-2290
[10]   Role of K-ras mutations in colorectal carcinoma [J].
Chiang, JM .
CANCER LETTERS, 1998, 126 (02) :179-185