Zhou Qiyang, Tao Feng, Qiu Liqing, Chen Hanlin, Bao Hua, Wu Xue, Shao Yang, Chi Liangjie, Song Hu
Jiangsu Institute of Medical Device Testing, Nanjing, Jiangsu 210012, China.
Department of Gastrointestinal Surgery, Shaoxing Peopleés Hospital (Shaoxing Hospital, Zhejiang University School of Medicine, Shaoxing, Zhejiang 312000, China.
J Oncol. 2022 Apr 22;2022:1498053. doi: 10.1155/2022/1498053. eCollection 2022.
Gastric cancer is one of the most common and deadly cancer types worldwide, which brings millions of dollars of economic loss each year. Patients diagnosed with early-onset gastric cancer were reported to have a worse prognosis compared to other gastric cancer patients, while the mechanisms behind such phenomenon are unknown. To identify age-dependent somatic alternations in gastric cancer, next-generation sequencing targeting 425 genes was performed on 1688 gastric tumor tissues and corresponding plasma samples. In our study, the microsatellite instability (MSI) and chromosomal instability score (CIS) values increased along with the age of patients, which indicates that older patients display a less genomic stability pattern. The differences of somatic alternations between young and old groups were compared. Somatic mutations CDH1 and copy number gains of FGFR2 were identified to enrich in the younger gastric cancer patients, which may contribute to the worse prognosis of early-onset gastric cancer patients.
胃癌是全球最常见且致命的癌症类型之一,每年造成数百万美元的经济损失。据报道,与其他胃癌患者相比,被诊断为早发性胃癌的患者预后更差,而这种现象背后的机制尚不清楚。为了确定胃癌中与年龄相关的体细胞变化,对1688份胃肿瘤组织及相应血浆样本进行了针对425个基因的二代测序。在我们的研究中,微卫星不稳定性(MSI)和染色体不稳定性评分(CIS)值随患者年龄增加而升高,这表明老年患者呈现出基因组稳定性较低的模式。比较了年轻组和老年组之间体细胞变化的差异。发现体细胞突变CDH1和FGFR2的拷贝数增加在年轻胃癌患者中富集,这可能是早发性胃癌患者预后较差的原因。