Mutational analyses of the BRAF, KRAS, and PIK3CA genes in oral squamous cell carcinoma

被引:31
作者
Bruckman, Karl C. [2 ,3 ]
Schoenleben, Frank [4 ,5 ]
Qiu, Wanglong [4 ]
Woo, Victoria L. [6 ]
Su, Gloria H. [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Otolaryngol Head & Neck Surg, New York, NY 10032 USA
[2] Columbia Univ, Med Ctr, Coll Dent Med, New York, NY USA
[3] Thomas Jefferson Univ Hosp, Dept Oral & Maxillofacial Surg, Philadelphia, PA 19107 USA
[4] Columbia Univ, Med Ctr, Dept Otolaryngol Head & Neck Surg, New York, NY USA
[5] Univ Erlangen Nurnberg, Dept Vasc Surg, Erlangen, Germany
[6] Columbia Univ, Med Ctr, Div Oral Pathol, Coll Dent Med, New York, NY USA
来源
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTOLOGY | 2010年 / 110卷 / 05期
关键词
H-RAS ONCOGENE; HIGH-FREQUENCY; HUMAN CANCER; HEAD; NECK; ACTIVATION; AMPLIFICATION; EXPRESSION; UNCOMMON; PATHWAY;
D O I
10.1016/j.tripleo.2010.05.002
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives. The development of oral squamous cell carcinoma (OSCC) is a complex, multistep process. To date, numerous oncogenes and tumor-suppressor genes have been implicated in oral carcinogenesis. Of particular interest in this regard are genes involved in cell cycling and apoptosis, such BRAF, KRAS, and PIK3CA genes. Study design. Mutations of BRAF, KRAS, and PIK3CA were evaluated by direct genomic sequencing of exons 1 of KRAS, 11 and 15 of BRAF, and 9 and 20 of PIK3CA in OSCC specimens. Results. Both BRAF and KRAS mutations were detected with a mutation frequency of 2% (1/42). PIK3CA mutations were detected at 3% (1/35). Conclusions. This is the first report implicating BRAF mutation in OSCC. Our study supports that mutations in the BRAF, KRAS, and PIK3CA genes make at least a minor contribution to OSCC tumorigenesis, and pathway-specific therapies targeting these 2 pathways should be considered for OSCC in a subset of patients with these mutations. (Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2010; 110: 632-637)
引用
收藏
页码:632 / 637
页数:6
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