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The clinical significance of forkhead box protein A1 and its role in colorectal cancer

机译:叉头盒蛋白A1的临床意义及其在结直肠癌中的作用

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Forkhead box protein A1 (FOXA1) is a transcription factor; recent studies have reported that FOXA1 has an oncogenic or tumor suppressive role in human malignancies, and its expression is associated with the prognosis of patients with cancer. However, further studies are required to determine the clinical significance of FOXA1 and its role in colorectal cancer (CRC). In the present study, FOXA1 expression was detected in 90 samples of CRC tissues and matched noncancerous tissues using immunohistochemistry. In these cases, FOXA1 expression was detected in 57.8% (52/90) of the CRC samples, whereas only 37.8% (34/90) of the noncancerous specimens exhibited a positive FOXA1 signal. In addition, the present study demonstrated that the mRNA expression levels of FOXA1 were significantly increased in CRC tissues compared with in matched tumor-adjacent tissues. Furthermore, the positive expression of FOXA1 was associated with poor clinicopathological characteristics of CRC, including poor tumor differentiation, large tumor size, lymph node metastases and advanced tumor-node-metastasis tumor stage. Notably, patients with CRC with positive FOXA1 expression exhibited a significantly reduced 5-year survival rate compared with those with negative FOXA1 expression. Multivariate Cox regression analysis revealed that FOXA1 expression was an independent prognostic indicator for patients with CRC. In addition, FOXA1 knockdown evidently inhibited cell proliferation and induced apoptosis in SW480 and HCT116 CRC cells. Notably, FOXA1 knockdown also prominently reduced the expression of yes-associated protein (YAP) in SW480 and HCT116 cells. In conclusion, the results of the present study indicated that FOXA1 may be considered a potential prognostic marker, and may promote tumor growth of CRC by upregulating YAP expression.
机译:叉头盒蛋白A1(FOXA1)是一种转录因子。最近的研究报道FOXA1在人类恶性肿瘤中具有致癌或抑癌作用,其表达与癌症患者的预后有关。但是,需要进一步的研究来确定FOXA1的临床意义及其在结直肠癌(CRC)中的作用。在本研究中,使用免疫组织化学法在90个CRC组织和匹配的非癌组织样本中检测到FOXA1表达。在这些情况下,在57.8%(52/90)的CRC样本中检测到FOXA1表达,而在非癌样本中只有37.8%(34/90)的FOXA1阳性。此外,本研究表明,与匹配的肿瘤相邻组织相比,CRC组织中FOXA1的mRNA表达水平显着增加。此外,FOXA1的阳性表达与CRC较差的临床病理特征有关,包括较差的肿瘤分化,较大的肿瘤大小,淋巴结转移和晚期的淋巴结转移肿瘤阶段。值得注意的是,与FOXA1表达阴性的患者相比,FOXA1表达阳性的CRC患者的5年生存率显着降低。多变量Cox回归分析显示FOXA1表达是CRC患者的独立预后指标。此外,FOXA1敲低明显抑制SW480和HCT116 CRC细胞中的细胞增殖并诱导凋亡。值得注意的是,FOXA1敲低还显着降低了SW480和HCT116细胞中yes关联蛋白(YAP)的表达。总之,本研究的结果表明FOXA1可能被认为是潜在的预后标志物,并可能通过上调YAP表达来促进CRC的肿瘤生长。

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