KRAS, BRAF, EGFR and HER2 gene status in a Spanish population of colorectal cancer

被引:32
作者
Herreros-Villanueva, Marta [1 ]
Rodrigo, Maximiliano [2 ]
Claver, Manuel [2 ]
Muniz, Pilar [3 ]
Lastra, Enrique [4 ]
Garcia-Giron, Carlos [4 ]
Jesus Coma del Corral, Maria [1 ]
机构
[1] Hosp Gen Yague, Unidad Invest, Burgos 09005, Spain
[2] Hosp Gen Yague, Serv Anat Patol, Burgos 09005, Spain
[3] Univ Burgos, Dept Bioquim, Burgos 09005, Spain
[4] Hosp Gen Yague, Serv Oncol, Burgos 09005, Spain
关键词
EGFR; HER2; KRAS; BRAF; Colorectal cancer; Mutation; GROWTH-FACTOR RECEPTOR; PHASE-III TRIAL; CLINICAL-RESPONSE; RAS MUTATIONS; CETUXIMAB; PLUS; AMPLIFICATION; PANITUMUMAB; THERAPY; CHEMOTHERAPY;
D O I
10.1007/s11033-010-0232-x
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
To evaluate the KRAS, BRAF, EGFR, and HER2 gene status in colorectal cancer by novel techniques and evaluate whether anti-HER2 therapies could be offered in the treatment of these patients. There are conflicting data on the prevalence of BRAF mutations and EGFR and HER2 gene amplification in colorectal KRAS wild type patients. In our study we tried to evaluate these expressions and their relationship to future treatment assays. Clinical-pathological data and paraffin-embedded specimens were collected from 186 patients who underwent colorectal resections at General Yague Hospital in Burgos, Spain. KRAS and BRAF status was analyzed by real-time PCR in all patients. EGFR and HER2/NEU gene amplification was detected using fluorescent in situ hybridisation technique (FISH) in 38 KRAS and BRAF wild type patients. KRAS mutations were present in 48% of the colorectal cancer patients. BRAF mutations were present in 6.25% of the KRAS wild type patients. EGFR and HER2 gene amplification was observed in 5.3% and 26.3%, respectively, of KRAS and BRAF wild type colorectal cancer patients. HER2, but not EGFR gene amplification, was frequently observed in KRAS and BRAF wild type colorectal cancer patients. These data indicate that HER2 amplification could be one of the genes to be considered in the therapeutic management of colorectal cancer.
引用
收藏
页码:1315 / 1320
页数:6
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