Publication: High frequency of KRAS codon 146 and FBXW7 mutations in Thai patients with stage II-III colon cancer
Issued Date
2019-01-01
Resource Type
ISSN
2476762X
15137368
15137368
Other identifier(s)
2-s2.0-85071742558
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Asian Pacific Journal of Cancer Prevention. Vol.20, No.8 (2019), 2319-2326
Suggested Citation
Krittiya Korphaisarn, Ananya Pongpaibul, Ekkapong Roothumnong, Khontawan Pongsuktavorn, Lucksamon Thamlikitkul, Tauangtham Anekpuritanang, Naravat Poungvarin, Wanna Thongnoppakhun, Manop Pithukpakorn High frequency of KRAS codon 146 and FBXW7 mutations in Thai patients with stage II-III colon cancer. Asian Pacific Journal of Cancer Prevention. Vol.20, No.8 (2019), 2319-2326. doi:10.31557/APJCP.2019.20.8.2319 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/50327
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
High frequency of KRAS codon 146 and FBXW7 mutations in Thai patients with stage II-III colon cancer
Other Contributor(s)
Abstract
© 2019 Asian Pacific Organization for Cancer Prevention. Background: KRAS, NRAS, and BRAF gene mutations are the most clinically relevant and frequently reported in colorectal cancer (CRC). Although data on these genes are frequently reported in several counties, data specific to these genes among Thai population are scarce. The aim of this study was to investigate and identify molecular alterations associated with colon cancer in Thai population, and to determine the impact of these genetic aberrations on clinical outcome. Methods: DNA from 108 archived formalin-fixed, paraffin-embedded (FFPE) tissue samples that histologically confirmed adenocarcinoma of stage II-III colon cancer between 2010 and 2012 at Siriraj Hospital (Bangkok, Thailand) were extracted. Gene mutational analysis was performed by next-generation sequencing (NGS) using an Oncomine Solid Tumor DNA kit (Thermo Fisher Scientific, Inc., Waltham, MA, USA). Results: A total of 22 somatic gene mutations were detected. The mutation frequency observed in KRAS, NRAS, BRAF, PIK3CA, and FBXW7 mutations was 47.2%, 1.9%, 1.9%, 12%, and 14.8%, respectively. KRAS mutation codon 12, 13, 59, 61, 117, and 146 mutations were identified in 29.6%, 8.3%, 1.8%, 0.9%, 0.0%, and 8.3%, respectively. KRAS Exon 4 had better DFS compared with Exon 2 and 3. Conclusions: This study is the first to comprehensively report hotspot mutations using NGS in Thai colon cancer patients. The most commonly identified gene mutation frequencies among Thai patients (KRAS, NRAS, BRAF, TP53, and PIK3CA) were similar to the gene mutation frequencies reported in Western population, except for subgroup of KRAS codon 146 and FBXW7 mutations that had a slightly higher frequency.