Cited by 83Cancer-related molecular mechanisms researchMicroRNA in disease regulationCircular RNAs in diseases

The lncRNA UCA1 interacts with miR-182 to modulate glioma proliferation and migration by targeting iASPP

He, Zongze, Wang, Yujue, Huang, Guangfu, Wang, Qi, Zhao, Dongdong, Chen, Longyi·2017·Archives of Biochemistry and Biophysics

Abstract

Long non-coding RNA (lncRNA) urothelial carcinoma associated 1 (UCA1) has been reported to be involved in the development and progression of many types of tumors including breast cancer, gastric cancer, and bladder cancer. However, the exact effects and molecular mechanisms of UCA1 in glioma progression remain unclear up to now. In this study, we firstly found that UCA1 was upregulated in glioma tumor samples and negatively correlated with survival time. Then, we investigated the role of UCA1 in human glioma cell lines. Our results showed that upregulation of lncRNA-UCA1 in glioma tissues and cell lines could promote glioma cell proliferation and migration through interaction with miR-182, and knockdown of UCA1 inhibited the proliferation and migration of human glioma cell. In addition, miR-182 dependent inhibitor of apoptosis-stimulating protein of p53 (iASPP) was required in the regulation of UCA1 induced glioma cell proliferation. Taken together, UCA1 might promote proliferation and migration of glioma, to regulate the tumor growth and metastasis via miR-182 dependent iASPP regulation. Therefore, lncRNA-UCA1 could be regarded as a therapeutic target in human glioma.

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Crossref · 10.1016/j.abb.2017.01.013

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  • Two lncRNAs, H19 and UCA1, regulate glioblastoma progression by interacting with mir-140 and mir-182, respectively.

    “Two lncRNAs, H19 and UCA1, regulate GBM progression by interacting with mir-140 and mir-182, respectively.”

    From The p53 Pathway in Glioblastoma (2018) · cites this paper as [57]

  • H19 and UCA1 reduce the expression and activity of mir-140 and mir-182, and therefore possess p53-dependent oncogenic activity in glioblastoma.

    “H19 and UCA1 reduce the expression and activity of these miRNAs, and therefore possess p53-dependent oncogenic activity in GBM [57,58].”

    From The p53 Pathway in Glioblastoma (2018) · cites this paper as [57]

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Authors
He, Z., Wang, Y., Huang, G., Wang, Q., Zhao, D., & Chen, L.
Affiliations
  • University of Electronic Science and Technology of China (CN)
  • Kailuan General Hospital (CN)
Corresponding author
  • Zhao, Dongdong
  • Chen, Longyi
Venue
Archives of Biochemistry and Biophysics
Publisher
Elsevier BV
Published
2017-06
Volume
623-624
Pages
1-8
ISSN
0003-9861 (ISSN-L)
OpenAlex
W2580761780
Cited by
83
References
43
Citations by year
2026: 1 · 2025: 1 · 2024: 3 · 2023: 5 · 2022: 8 · 2021: 12 · 2020: 9 · 2019: 15 · 2018: 21 · 2017: 8
FWCI
4.88
Type
journal article
Language
en
Open access
closed
Locations
  • Archives of Biochemistry and Biophysics (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Sichuan Provincial Health Department Research Projects (130203)
  • Youth fund of Sichuan Provincial People's Hospital (2015QN18)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Circular RNAs in diseases
Keywords
UCA1, long non-coding RNA, miR-182, iASPP, glioma, cell proliferation, cell migration, metastasis, prognostic factors, therapeutic target, lncRNA-miRNA interaction
MeSH terms
Brain, Brain Neoplasms, Cell Movement, Female, Glioma, Humans, Male, Middle Aged, Repressor Proteins, Gene Expression Regulation, Neoplastic, MicroRNAs, Cell Line, Tumor, Intracellular Signaling Peptides and Proteins, Cell Proliferation, RNA, Long Noncoding

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