Department of Bionano Technology, Gachon University, Seongnam-si 13120, Korea.
Gachon Medical Research Institute, Gil Medical Center, Gachon University, Incheon 21565, Korea.
Int J Environ Res Public Health. 2022 Mar 28;19(7):4008. doi: 10.3390/ijerph19074008.
Background: Neoadjuvant chemoradiotherapy (nCRT) prior to surgery is considered standard therapy for locally advanced rectal cancer. Unfortunately, most patients with rectal cancer are resistant to radiotherapy. This might be a genetic cause. The role of certain rectal cancer-causing genes has not been completely elucidated. This study aims to investigate the genes responsible for locally advanced rectal cancer patients not reacting to radiotherapy. Methods: Whole exome sequencing of the DNA samples was performed on the samples. Bioinformatic analysis on the subjects was established. Individual genetic information was screened to identify differently expressed genes that more frequently appeared in non-complete response (NCR) compared to complete response (CR) patients after nCRT. All variations were verified by Sanger sequencing. Results: Genotyping information and pathway analyses of the samples indicated genes such as FLCN, CALML5, and ANTXR1 to be commonly mutated in CR group, whereas genes such as GALNTL14, CNKSR1, ACD, and CUL3 were more commonly mutated in the NCR group. Chi-square test revealed some significant variants (<0.05) such as rs3744124 (FLCN), rs28365986 (ANTXR1), rs10904516 (CALML5), rs3738952 (CUL3), rs13394 and rs2293013 (PIH1D1), rs2274531 (GPA33), rs4963048 (BRSK2), rs17883366 (IL3RA), rs2297575 (PSMD5), rs2288101 (GALNT14), and rs11954652 (DCTN4). Conclusion: Identifying an array of genes that separate NCRs from CRs would lead to finding genetic biomarkers for early detection of rectal cancer patients that are resistant to nCRT. A further investigation to validate the significance of genetic biomarkers to segregate NCRs from CRs should be performed with a larger CRC dataset. Protein expression levels, as well as transcriptomic analysis, would also help us understand the mechanism of how these genes could play a role in preventing radiation therapy to patients. This would be essential to prevent redundant radiation therapy.
术前新辅助放化疗(nCRT)被认为是局部晚期直肠癌的标准治疗方法。不幸的是,大多数直肠癌患者对放疗有耐药性。这可能是遗传原因。某些直肠癌相关基因的作用尚未完全阐明。本研究旨在探讨导致局部晚期直肠癌患者对放疗无反应的基因。
对样本进行全外显子组测序。对受试者进行生物信息学分析。筛选个体遗传信息,以鉴定在 nCRT 后非完全缓解(NCR)患者中较常出现的与完全缓解(CR)患者不同的表达基因。所有变异均通过 Sanger 测序验证。
样本的基因分型信息和通路分析表明,CR 组中常见的基因突变基因如 FLCN、CALML5 和 ANTXR1,而 NCR 组中更常见的基因突变基因如 GALNTL14、CNKSR1、ACD 和 CUL3。卡方检验显示了一些有统计学意义的变异体(<0.05),如 rs3744124(FLCN)、rs28365986(ANTXR1)、rs10904516(CALML5)、rs3738952(CUL3)、rs13394 和 rs2293013(PIH1D1)、rs2274531(GPA33)、rs4963048(BRSK2)、rs17883366(IL3RA)、rs2288101(PSMD5)、rs2288101(GALNT14)和 rs11954652(DCTN4)。
鉴定一组可将 NCR 与 CR 分开的基因,将有助于找到用于早期检测对 nCRT 耐药的直肠癌患者的遗传生物标志物。应使用更大的 CRC 数据集进一步验证遗传生物标志物是否有助于将 NCR 与 CR 分开。蛋白质表达水平以及转录组分析也将帮助我们了解这些基因在阻止患者接受放射治疗方面发挥作用的机制。这对于防止不必要的放射治疗至关重要。