Discipline of Genetics, Department of Morphology and Genetics, Federal University of São Paulo, São Paulo, Brazil.
Discipline of Gastroenterology, Department of Medicine, Federal University of São Paulo, São Paulo, Brazil.
Anticancer Res. 2022 Sep;42(9):4381-4394. doi: 10.21873/anticanres.15938.
BACKGROUND/AIM: Previous studies from our research group have shown that trisomy 8 and the amplification of the 8q24.21 region is very frequent in gastric cancer (GC). Little is known about the role of most genes located in this region. Thus, the aim of this study was to understand the possible impact of transcriptional alterations and copy number variation (CNV) of four genes located in the 8q24.21 region - FAM49B, FAM84B, GSDMC and miR-5194 - in GC.
Fifty-one to 85 matched pairs of tumoral and adjacent non-tumoral gastric tissues, from patients with primary GC, were used to analyze gene expression and CNV of the selected genes. We also included 29 H. pylori negative and gastritis negative gastric mucosa tissues from individuals without cancer obtained by endoscopy, as control samples.
The expression of FAM49B, GSDMC and miR-5194 was higher in both tumoral and adjacent non-tumoral samples compared to the negative control. The expression of FAM84B showed no significant difference between tumoral samples and negative controls. However, the expression of FAM84B in the adjacent non-tumoral samples was higher compared to negative control and tumoral samples. Moreover, the higher expression of GSDMC was associated with T3 and T4 tumors, with tumors on stage III and IV and with advanced tumors. Higher copy numbers of FAM49B and GSDMC were associated with intestinal tumor type and with moderately or well-differentiated tumors. Higher copy number of FAM84B was associated with moderately or well-differentiated tumors. Furthermore, the expression of all four genes was positively correlated.
All four genes are upregulated in GC and may play an important role in these neoplasms. GSDMC expression was associated with more aggressive tumors.
背景/目的:本研究小组之前的研究表明,8 号染色体三体和 8q24.21 区域的扩增在胃癌(GC)中非常常见。然而,位于该区域的大多数基因的作用却知之甚少。因此,本研究的目的是了解位于 8q24.21 区域的四个基因 - FAM49B、FAM84B、GSDMC 和 miR-5194 - 的转录改变和拷贝数变异(CNV)对 GC 的可能影响。
使用 51 至 85 对来自原发性 GC 患者的肿瘤和相邻非肿瘤胃组织的配对样本,分析选定基因的基因表达和 CNV。我们还包括了 29 份来自内窥镜检查的无癌症个体的 H. pylori 阴性和胃炎阴性胃黏膜组织作为对照样本。
与阴性对照相比,FAM49B、GSDMC 和 miR-5194 在肿瘤和相邻非肿瘤样本中的表达均升高。FAM84B 在肿瘤样本中的表达与阴性对照之间无显著差异。然而,在相邻非肿瘤样本中,FAM84B 的表达高于阴性对照和肿瘤样本。此外,GSDMC 的高表达与 T3 和 T4 肿瘤、III 和 IV 期肿瘤以及晚期肿瘤相关。FAM49B 和 GSDMC 的较高拷贝数与肠型肿瘤和中或高分化肿瘤相关。FAM84B 的较高拷贝数与中或高分化肿瘤相关。此外,这四个基因的表达呈正相关。
这四个基因在 GC 中均上调,可能在这些肿瘤中发挥重要作用。GSDMC 的表达与侵袭性更强的肿瘤相关。