An Yongkang, Zhang Shuangxi, Zhang Jing, Yin Qing, Han Haitao, Wu Fang, Zhang Xiangan
The First Affiliated Hospital of Henan University of TCM, Anorectal Disease Clinic, Zhengzhou City, Henan Province 450000, People's Republic of China.
The Affiliated Hospital of Henan Academy of TCM, Nursing Department, Zhengzhou City, Henan Province 450000, People's Republic of China.
Cancer Manag Res. 2020 Jul 20;12:6045-6052. doi: 10.2147/CMAR.S247764. eCollection 2020.
NLIPMT, as a tumor suppressive lncRNA, has only been investigated in breast cancer, while its roles in other types of cancer remain unknown. This study aimed to explore the role of NLIPMT in colorectal cancer (CRC).
Expression levels of NLIPMT and TGF-β1 in two types of CRC tissue (Non-tumor tissues and tumor tissues) were measured and compared by qRT-PCR and paired -test, respectively. Correlations between the expression of NLIPMT and TGF-β1 were analyzed by performing linear regression. The effects of transfections on cell invasion and migration were evaluated by Transwell assays.
We found that NLIPMT was downregulated, while TGF-β1 was upregulated in CRC. In CRC tumor, a negative correlation was found between the expression of NLIPMT and TGF-β1. In CRC cells, overexpression of NLIPMT resulted in downregulation, while silencing of NLIPMT resulted in upregulation of TGF-β1. Analysis of cell invasion and migration showed that overexpression of NLIPMT suppressed the tumor cell invasion and migration. In contrast, overexpression of TGF-β1 could promote CRC cell invasion and migration and also reduce the role of NLIPMT. Through the overall survival evaluation, NLIPMT-high groups of CRC represented better survival rate compared to that of the NLIPMT-low group patients.
The expression of lncRNA NLIPMT was negatively correlated with TGF-β1 in CRC. Overexpression of NLIPMT inhibited the colorectal cancer cell migration and invasion by downregulating TGF-β1. Furthermore, the expression of NLIPMT in CRC patients predicted better prognosis, which suggested that NLIPMT could be considered as a novel diagnosis biomarker.
NLIPMT作为一种肿瘤抑制性长链非编码RNA,仅在乳腺癌中得到研究,而其在其他类型癌症中的作用尚不清楚。本研究旨在探讨NLIPMT在结直肠癌(CRC)中的作用。
分别通过qRT-PCR和配对t检验测量并比较两种类型的CRC组织(非肿瘤组织和肿瘤组织)中NLIPMT和TGF-β1的表达水平。通过线性回归分析NLIPMT和TGF-β1表达之间的相关性。通过Transwell实验评估转染对细胞侵袭和迁移的影响。
我们发现CRC中NLIPMT表达下调,而TGF-β1表达上调。在CRC肿瘤中,NLIPMT和TGF-β1的表达之间呈负相关。在CRC细胞中,NLIPMT过表达导致TGF-β1下调,而NLIPMT沉默导致TGF-β1上调。细胞侵袭和迁移分析表明,NLIPMT过表达抑制肿瘤细胞侵袭和迁移。相反,TGF-β1过表达可促进CRC细胞侵袭和迁移,还可削弱NLIPMT的作用。通过总生存评估,CRC中NLIPMT高表达组患者的生存率高于NLIPMT低表达组。
CRC中lncRNA NLIPMT的表达与TGF-β1呈负相关。NLIPMT过表达通过下调TGF-β1抑制结直肠癌细胞迁移和侵袭。此外,NLIPMT在CRC患者中的表达预示着更好的预后,这表明NLIPMT可被视为一种新型诊断生物标志物。