Lee Seung Woo, Lee Taekyu, Sul Hae Jung, Park Ki Cheol, Park Joonhong
Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.
Thermo Fisher Scientific Solutions, Seoul 06349, Korea.
J Clin Med. 2021 May 10;10(9):2038. doi: 10.3390/jcm10092038.
We aimed to investigate molecular factors potentially related to the progression of gastric adenoma (GA) to gastric cancer (GC) and compare the mutation characteristics between GC and GA.
We conducted custom gene panel sequencing for 135 GC-related genes and estimated the difference in somatic mutation profiles between 20 GC and 20 GA cases.
A total of 31 somatic mutations, including 22 missense, 3 nonsense, and 6 frameshift mutations, were detected in 17 samples. We estimated an average of 1.8 mutations per sample (range, 1 to 3 mutations), with 12 in GC and 5 in GA. GC tended to have one or more mutated genes ( = 0.0217), as well as higher allele frequencies of mutated genes ( = 0.0003), compared to GA. Likewise, known driver mutations associated with GC tumorigenesis (, , , and ) were identified in half of the GC cases (50%, 10/20; = 0.0002). Only the mutant burden, regardless of gene type, was retained, with an odds ratio of 1.8392 (95% confidence interval (CI), 1.0071 to 3.3588; = 0.0474).
Our study demonstrates that the accumulation of mutant burden contributes to tumorigenesis progression from GA to GC in Korean patients, regardless of the kind of genes. These findings may elucidate the molecular pathogenesis of gastric carcinogenesis and malignant progression.
我们旨在研究可能与胃腺瘤(GA)进展为胃癌(GC)相关的分子因素,并比较GC和GA之间的突变特征。
我们对135个与GC相关的基因进行了定制基因面板测序,并估计了20例GC和20例GA病例之间体细胞突变谱的差异。
在17个样本中检测到总共31个体细胞突变,包括22个错义突变、3个无义突变和6个移码突变。我们估计每个样本平均有1.8个突变(范围为1至3个突变),其中GC中有12个,GA中有5个。与GA相比,GC倾向于有一个或多个突变基因(P = 0.0217),以及突变基因的更高等位基因频率(P = 0.0003)。同样,在一半的GC病例(50%,10/20;P = 0.0002)中鉴定出与GC肿瘤发生相关的已知驱动突变(KRAS、NRAS、BRAF和PIK3CA)。仅保留了突变负担,无论基因类型如何,优势比为1.8392(95%置信区间(CI),1.0071至3.3588;P = 0.0474)。
我们的研究表明,在韩国患者中,无论基因类型如何,突变负担的积累都有助于从GA到GC的肿瘤发生进展。这些发现可能阐明胃癌发生和恶性进展的分子发病机制。