Zhang Xiangyan, Wu Jie, Wang Lili, Zhao Han, Li Hong, Duan Yuhe, Li Yujun, Xu Ping, Ran Wenwen, Xing Xiaoming
Department of Pathology, Affiliated Hospital of Qingdao University, Qingdao, China.
Department of Pediatrics, Affiliated Hospital of Qingdao University, Qingdao, China.
PeerJ. 2020 Feb 12;8:e8602. doi: 10.7717/peerj.8602. eCollection 2020.
To investigate the frequency and prognostic role of the human epidermal growth factor receptor 2 gene () and V600E gene mutation in Chinese patients with colorectal cancer (CRC).
Clinicopathological and survival information from 480 patients with stage I-III CRC were reviewed and recorded. amplification was analyzed by immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH), V600E mutation was tested by IHC and Sanger sequencing. The relationship between and V600E mutation status and clinicopathological characteristics and outcomes were determined.
The amplification of and V600E mutation were identified in 27 of 480 (5.63%) and 19 of 480 (3.96%) CRC patients, respectively. amplification significantly correlated with greater bowel wall invasion ( = 0.041) and more advanced TNM stage (I vs. II vs. III; 0 vs 5.78% vs. 7.41%, = 0.013). Patients suffering from tumors with poor differentiation had a higher incidence rate of V600E mutation than those with moderate/well differentiation (7.77% vs 2.92%, = 0.04). amplification was an independent prognostic factor for worse disease-free survival (DFS) (HR = 2.53, 95% CI: 1.21-5.30, = 0.014).
The prevalence of amplification and V600E mutation in stage I-III CRC patients in Chinese was 6% and 4%, respectively, and amplification appeared to be associated with a worse DFS. More comprehensive molecular classification and survival analysis are needed to validate our findings.
探讨人表皮生长因子受体2基因()及V600E基因突变在中国结直肠癌(CRC)患者中的频率及预后作用。
回顾并记录480例I - III期CRC患者的临床病理及生存信息。采用免疫组织化学(IHC)和荧光原位杂交(FISH)分析扩增情况,采用IHC和Sanger测序检测V600E突变。确定与V600E突变状态与临床病理特征及预后的关系。
480例CRC患者中,分别有27例(5.63%)和19例(3.96%)检测到扩增和V600E突变。扩增与更广泛的肠壁侵犯显著相关(= 0.041),且与更晚期的TNM分期相关(I期 vs. II期 vs. III期;0 vs 5.78% vs. 7.41%,= 0.013)。低分化肿瘤患者的V600E突变发生率高于中/高分化患者(7.77% vs 2.92%,= 0.04)。扩增是无病生存期(DFS)较差的独立预后因素(HR = 2.53,95% CI:1.21 - 5.30,= 0.014)。
中国I - III期CRC患者中扩增和V600E突变的发生率分别为6%和4%,且扩增似乎与较差的DFS相关。需要更全面的分子分类和生存分析来验证我们的发现。