Laboratorio de Inmunología, Centro Universitario de Ciencias Biológicas y Agropecuarias, Universidad de Guadalajara, Zapopan, México.
Departamento de Clínicas, Centro Universitario de los Altos, Universidad de Guadalajara, Tepatitlán de Morelos, México.
J Clin Pathol. 2020 Feb;73(2):107-111. doi: 10.1136/jclinpath-2019-206128. Epub 2019 Aug 30.
KDM1A/LSD1 and ZNF217 are involved in a protein complex that participates in transcriptional regulation. has been analysed in numerous cancers and its amplification has been associated with advanced stages of disease; however, a similar role for has not been uncovered. In this study, we estimated the number of and gene copies in tissue samples from patients diagnosed with colorectal cancer (CRC), as well as its association with clinicopathological features in patients with CRC.
Paraffin-embedded tumour samples from 50 patients with CRC with a histopathological diagnosis of CRC were included. The number of copies of and genes was determined by fluorescence in situ hybridisation (FISH). We also analysed the association between copy numbers of selected genes and clinicopathological data based on multivariate analysis.
Deletion of the gene occurred in 19 samples (38%), whereas gene amplification was identified in 11 samples (22%). We found a significant association between lymph node metastasis or advanced tumour stage and gene deletion (p value=0.0003 and p value=0.011, respectively).
gene deletion could be considered a novel prognostic biomarker of late-stage CRC.
KDM1A/LSD1 和 ZNF217 参与参与转录调控的蛋白质复合物。在许多癌症中都对其进行了分析,其扩增与疾病的晚期阶段相关;然而,尚未发现 具有类似作用。在这项研究中,我们估计了组织样本中 和 基因拷贝数在诊断为结直肠癌(CRC)的患者中的数量,以及其与 CRC 患者的临床病理特征的关联。
纳入了 50 例经组织病理学诊断为 CRC 的 CRC 患者的石蜡包埋肿瘤样本。通过荧光原位杂交(FISH)确定 和 基因的拷贝数。我们还根据多变量分析分析了选定基因的拷贝数与临床病理数据之间的关联。
19 例(38%)样本中发生了 基因缺失,而 11 例(22%)样本中存在 基因扩增。我们发现淋巴结转移或晚期肿瘤分期与 基因缺失之间存在显著相关性(p 值=0.0003 和 p 值=0.011)。
基因缺失可被视为晚期 CRC 的新型预后生物标志物。