Comparison of KRAS Mutation Tests in Colorectal Cancer Patients

被引:11
|
作者
Hancer, Veysel Sabri [1 ]
Buyukdogan, Murat [2 ]
Turkmen, Ilknur [3 ]
Bassullu, Nuray [3 ]
Altug, Tuncay [1 ]
Diz-Kucukkaya, Reyhan [4 ]
Bulbul-Dogusoy, Gulen [3 ]
Demir, Gokhan [5 ]
机构
[1] Istanbul Bilim Univ, Dept Med Biol & Genet, Fac Med, TR-34394 Istanbul, Turkey
[2] Gayrettepe Florence Nightingale Hosp, Genet Dis Diag Ctr, Istanbul, Turkey
[3] Istanbul Bilim Univ, Dept Pathol, Fac Med, TR-34394 Istanbul, Turkey
[4] Istanbul Bilim Univ, Div Hematol, Fac Med, TR-34394 Istanbul, Turkey
[5] Istanbul Bilim Univ, Div Med Oncol, Fac Med, TR-34394 Istanbul, Turkey
关键词
RAS; THERAPY; EGFR; SPECIMENS;
D O I
10.1089/gtmb.2011.0027
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
The KRAS pathway and studies evaluating KRAS as a prognostic marker in colorectal cancer are discussed along with advances in KRAS gene mutation testing. Highly sensitive real-time polymerase chain reaction (PCR) methods were developed for this purpose. We examined the applicability of direct sequencing and two real-time PCR methods in the diagnosis of KRAS mutations. We used real-time PCR and direct sequencing-based methods to determine applicability of these KRAS mutation tests in 64 colorectal cancers. The two DNA samples found to be mutation positive by real-time PCR were analyzed again after diluting 100-fold. The results were the same. When we applied the same strategy for the direct sequencing, even a 10-fold dilution did not show the mutations. Therefore, we found that sequencing may not be informative when there are only a few mutant cells in the tumor. KRAS mutation screening on formalin-fixed, paraffin-embedded DNA is very efficient with real-time PCR methods in comparison to direct sequencing. The development and adoption of guidelines for KRAS mutation testing are crucial for success.
引用
收藏
页码:831 / 834
页数:4
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