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长链非编码 RNA PlncRNA-1 通过调控 PI3K/Akt 信号通路促进结直肠癌细胞的进展。

Long Noncoding RNA PlncRNA-1 Promotes Colorectal Cancer Cell Progression by Regulating the PI3K/Akt Signaling Pathway.

机构信息

The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, P.R. China.

Department of Oncology, The People's Hospital of Zhengzhou, Zhengzhou, Henan, P.R. China.

出版信息

Oncol Res. 2018 Mar 5;26(2):261-268. doi: 10.3727/096504017X15031557924132. Epub 2017 Aug 23.

DOI:10.3727/096504017X15031557924132
PMID:28835319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7844685/
Abstract

Accumulating evidence has indicated that long noncoding RNA (lncRNA) PlncRNA-1 plays an important regulatory role in cancers. However, the expression and biological functions of PlncRNA-1 in colorectal cancer (CRC) are still unclear. In the present study, we determined the expression of PlncRNA-1 in CRC and explored the function of PlncRNA-1 on CRC cell progression. The results showed that PlncRNA-1 was significantly increased in CRC tissues and cell lines; high PlncRNA-1 expression was associated with depth of invasion, lymph node metastasis, and TNM stage of CRC patients. Kaplan-Meier curve analysis showed that patients with high PlncRNA-1 expression had a poor overall survival. PlncRNA-1 knockdown remarkably reduced cell proliferation, migration, and invasion and promoted cell apoptosis in vitro. In vivo xenograft experiments showed that PlncRNA-1 inhibition significantly suppressed tumor growth. Finally, we used an agonist (740Y-P) of the PI3K/Akt signaling pathway; function assays showed that PlncRNA-1 exerted its effects by targeting the PI3K/Akt signaling pathway in CRC. Taken together, our data suggested that PlncRNA-1 might act as an oncogene in CRC progression and serve as a potential biomarker and therapeutic target for the treatment of CRC.

摘要

越来越多的证据表明,长非编码 RNA(lncRNA)PlncRNA-1 在癌症中发挥着重要的调控作用。然而,PlncRNA-1 在结直肠癌(CRC)中的表达和生物学功能仍不清楚。在本研究中,我们测定了 PlncRNA-1 在 CRC 中的表达情况,并探讨了 PlncRNA-1 对 CRC 细胞进展的功能。结果表明,PlncRNA-1 在 CRC 组织和细胞系中显著上调;高 PlncRNA-1 表达与 CRC 患者的浸润深度、淋巴结转移和 TNM 分期相关。Kaplan-Meier 曲线分析显示,高 PlncRNA-1 表达的患者总体生存率较差。PlncRNA-1 敲低显著减少了细胞增殖、迁移和侵袭,并促进了细胞凋亡。体内异种移植实验表明,PlncRNA-1 抑制显著抑制了肿瘤生长。最后,我们使用了 PI3K/Akt 信号通路的激动剂(740Y-P);功能分析表明,PlncRNA-1 通过靶向 CRC 中的 PI3K/Akt 信号通路发挥作用。综上所述,我们的数据表明,PlncRNA-1 可能在 CRC 进展中作为癌基因发挥作用,并可作为 CRC 治疗的潜在生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/3d6556e82fb6/OR-26-261-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/a2bf74264be6/OR-26-261-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/f8b121f7aa3b/OR-26-261-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/b8cc49c1443c/OR-26-261-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/8da2a50ceb57/OR-26-261-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/3d6556e82fb6/OR-26-261-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/a2bf74264be6/OR-26-261-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/f8b121f7aa3b/OR-26-261-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/b8cc49c1443c/OR-26-261-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/8da2a50ceb57/OR-26-261-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d206/7844685/3d6556e82fb6/OR-26-261-g005.jpg

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