kruppel样因子4 (KLF-4)在结直肠癌中的抑瘤作用。

D. Xiu, Y. Chen, L. Liu, H. Yang, G. F. Liu
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引用次数: 8

摘要

kruppel样因子(KLFs)是一组转录调节因子,最近被发现对各种胃肠道癌症具有肿瘤抑制功能。本研究旨在探讨KLF-4在结直肠癌(crc)中的表达模式及其预后价值。通过免疫组织化学分析、实时定量聚合酶链反应和western blotting检测结直肠癌组织中KLF-4的水平。采用卡方检验评价KLF-4表达与临床病理特征的相关性。Kaplan-Meier分析评估KLF-4在结直肠癌患者中的预后价值。此外,我们评估了KLF-4敲低对CRC HT-29细胞增殖的影响。我们的研究结果显示,KLF-4在31个CRC样本中显著下调,这些样本来自具有淋巴转移、肿瘤细胞低分化和肿瘤复发等更多恶性特征的CRC患者。发现低KLF-4组的结直肠癌患者总生存率降低,无病生存时间缩短。此外,转染siRNA- klf -4的HT-29细胞与转染对照siRNA的细胞相比,增殖能力增强。综上所述,较低的KLF-4表达与CRC患者的恶性CRC状态及预后不良相关。此外,KLF-4的抑制促进了CRC细胞的体外增殖。这些结果为KLF-4在结直肠癌中的肿瘤抑制作用提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumor-suppressive role of Kruppel-like factor 4 (KLF-4) in colorectal cancer.
Kruppel-like factors (KLFs) are a group of transcriptional regulators that have recently been identified to exhibit tumor-suppressive function against various gastrointestinal cancers. The present study aims to investigate the expression patterns and prognostic value of KLF-4 in colorectal cancers (CRCs). KLF-4 levels in CRC tissues were examined via immunohistochemistry analysis, real-time quantitative polymerase chain reaction, and western blotting. The chi-square test was performed to evaluate the correlation between KLF-4 expression and the clinicopathological characteristics. Kaplan-Meier analysis was performed to assess the prognostic value of KLF-4 in CRC patients. In addition, we evaluated the effect of KLF-4 knockdown on the proliferation of CRC HT-29 cells. Our results showed significant downregulation of KLF-4 in 31 CRC samples, collected from CRC patients showing more malignant characteristics such as lymphatic metastasis, low tumor cell differentiation, and tumor recurrence. CRC patients in the low KLF-4 group were found to have reduced overall survival and decreased disease-free survival time. Moreover, HT-29 cells transfected with siRNA-KLF-4 showed increased proliferation compared to those transfected with control siRNA. In summary, lower KLF-4 expression was correlated with malignant CRC status and poor prognosis in CRC patients. Moreover, KLF-4 suppression promoted the proliferation of CRC cells in vitro. These results provide novel insights into the tumor suppressive role of KLF-4 in CRC.
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