Author/Authors :
Ayatollahi, Hossein Mashhad University of Medical Sciences , Tavassoli, Alireza Mashhad University of Medical Sciences , Jafarian, Amir Hossein Mashhad University of Medical Sciences , Alavi, Amin Ghaem Hospital - Mashhad University of Medical Sciences , Shakeri, Sepideh Ghaem Hospital - Mashhad University of Medical Sciences , Shams, Fatemeh Ghaem Hospital - Mashhad University of Medical Sciences , Sheikhi, Maryam Ghaem Hospital - Mashhad University of Medical Sciences , Motamedi Rad, Neda Ghaem Hospital - Mashhad University of Medical Sciences , Sadeghian, Mohammad Hadi Mashhad University of Medical Sciences , Bahrami, Afsane School of Medicine - Mashhad University of Medical Sciences
Abstract :
Background & objective: KRAS mutations are reported in many types of cancers
including pancreas, lung, colon, breast,and gastric (GC). High frequency of KRAS
mutation is observed in the pancreas,colon, and lung cancers; they commonly arise
in codon 12 and 13 of exon 2. Due to the lack of information about the frequency of
KRAS mutations in the Northeast of Iran, the currentstudy aimed at evaluating KRAS
frequency in cases with GC in this region.
Methods: A total of120 formalin-fixed, paraffin-embedded blocks of patients with
GC were assessed. The assays to detect KRAS in codon 12 and13 were obtained
through the peptide nucleic acid (PNA)-clamp.
Results: Totally 87 male and 33 female patients were analyzed in the current study.
The mean age of the subjects was 55years.The most common tumoral fragment was
located on the body with 48 cases (40%) and the less frequent was related to fondues
with six cases (5%).Of the 120 GC samples, 16(13.3%) caseshad codon 12 KRAS
mutation, and 16.7% had codon 13 mutations. There were no significant relationships
between gender,age, and KRAS mutations in the studied specimens.
Conclusion: In conclusion, the overall frequency of KRAS codon 12 and 13 mutations in GC was 30% in the current study population.Frequency of KRAS codon 12
and 13 mutations hadsignificant correlation with tumors location. Different pathogenic mechanismsare suggested for GC according to tumor location. The current study
resultsmay be an important diagnostic tool for physicians managing atrophic gastritis.