Roudi Raheleh, Barodabi Mahboubeh, Madjd Zahra, Roviello Giandomenico, Corona Silvia Paola, Panahei Mahshid
Oncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Department of Cell Systems and Anatomy, University of Texas Health San Antonio, San Antonio, TX, USA.
Mol Cell Oncol. 2020 Jul 14;7(5):1788366. doi: 10.1080/23723556.2020.1788366. eCollection 2020.
Colorectal cancer (CRC) is one of the most important malignancies and causes of cancer-related deaths worldwide. Cancer stem cell markers identification could be helpful to acquire important prognostic information and develop new treatment regimens. This study aimed to evaluate the expression of OCT4 and NANOG in CRC patients and their clinical significance. Totally 359 CRC samples were stained for OCT4 and NANOG expression using tissue microarray. The correlation between their expression and clinical and pathological features was explored. The majority of CRC cases showed low-level expression of OCT4 (80%) and NANOG (75%). Lower expression of OCT4 was more often detected in CRC cases with no vascular involvement ( = .01). Also, a trend found between low level of OCT4 expression and absence of distant metastasis or lymph node involvement ( = .07 and = .09, respectively). Surprisingly, a significant positive correlation was observed between NANOG expression and cellular differentiation ( = .05). Our combined analysis demonstrated that OCT4 /NANOG phenotype has frequently seen in colorectal cancer cases with no vascular invasion ( = .05). Our observations indicated that higher expression of OCT4 and NANOG can confer malignant and aggressive behavior to CRC. Evaluation of the co-expression of these cancer stem cell markers can serve a new diagnostic and prognostic approach in CRC patients. These findings also suggested that simultaneous expression of OCT4 and NANOG can be considered as a therapeutic marker for targeted therapy of CRC, especially in advanced stages.
结直肠癌(CRC)是全球最重要的恶性肿瘤之一,也是癌症相关死亡的主要原因。癌症干细胞标志物的鉴定有助于获取重要的预后信息并开发新的治疗方案。本研究旨在评估OCT4和NANOG在CRC患者中的表达及其临床意义。使用组织芯片对359例CRC样本进行OCT4和NANOG表达染色。探讨了它们的表达与临床病理特征之间的相关性。大多数CRC病例显示OCT4(80%)和NANOG(75%)低水平表达。在无血管侵犯的CRC病例中更常检测到OCT4低表达(P = 0.01)。此外,在OCT4低表达与无远处转移或淋巴结受累之间发现一种趋势(分别为P = 0.07和P = 0.09)。令人惊讶的是,观察到NANOG表达与细胞分化之间存在显著正相关(P = 0.05)。我们的综合分析表明,OCT4/NANOG表型在无血管侵犯的结直肠癌病例中很常见(P = 0.05)。我们的观察结果表明,OCT4和NANOG的高表达可赋予CRC恶性和侵袭性行为。评估这些癌症干细胞标志物的共表达可为CRC患者提供一种新的诊断和预后方法。这些发现还表明,OCT4和NANOG的同时表达可被视为CRC靶向治疗的治疗标志物,尤其是在晚期。