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Extracellular Vesicle-Mediated Transfer of a Novel Long Noncoding RNA TUC339: A Mechanism of Intercellular Signaling in Human Hepatocellular Cancer
Open accessAbstract
Although the expression of long noncoding RNA (lncRNA) is altered in hepatocellular cancer (HCC), their biological effects are poorly defined. We have identified lncRNA with highly conserved sequences, ultraconserved lncRNA (ucRNA) that are transcribed and altered in expression in HCC. Extracellular vesicles, such as exosomes and microvesicles, are released from tumor cells and can transfer biologically active proteins and RNA across cells. We sought to identify the role of vesicle-mediated transfer of ucRNA as a mechanism by which these novel lncRNA could influence intercellular signaling with potential for environmental modulation of tumor cell behavior. HCC-derived extracellular vesicles could be isolated from cells in culture and taken up by adjacent cells. The expression of several ucRNA was dramatically altered within extracellular vesicles compared to that in donor cells. The most highly significantly expressed ucRNA in HCC cell-derived extracellular vesicles was cloned and identified as a 1,198-bp ucRNA, termed TUC339. TUC339 was functionally implicated in modulating tumor cell growth and adhesion. Suppression of TUC339 by siRNA reduced HCC cell proliferation, clonogenic growth, and growth in soft agar. Thus, intercellular transfer of TUC339 represents a unique signaling mechanism by which tumor cells can promote HCC growth and spread. These findings expand the potential roles of ucRNA in HCC, support the existence of selective mechanisms for lncRNA export from cells,…
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“We also analyzed expression of TUC339, a long non-coding RNA that is selectively released in EV from hepatocellular cancer cells and is foundationally implicated in modulating tumor cell behavior (15).”
From Analysis of Extracellular RNA by Digital PCR (2014) · cites this paper as [15]
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Extracellular vesicle RNA signaling in the liver tumor microenvironment
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Self-citationApoptotic neuron-secreted HN12 inhibits cell apoptosis in Hirschsprung's disease
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Metadata
- Authors
- Kogure, T., Yan, I. K., Lin, W.-L., & Patel, T.
- Affiliations
- Mayo Clinic (US)
- Mayo Clinic in Florida (US)
- Corresponding author
- Patel, T.
- Venue
- Genes & Cancer
- Publisher
- SAGE Publications
- Published
- 2013-07-01
- Volume
- 4
- Issue
- 7-8
- Pages
- 261-272
- ISSN
- 1947-6019 (ISSN-L)
- 1947-6027
- PMC
- PMC3807642
- OpenAlex
- W2118018590
- Cited by
- 303
- References
- 23
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 13 · 2023: 16 · 2022: 28 · 2021: 31 · 2020: 37 · 2019: 32 · 2018: 31 · 2017: 30 · 2016: 37 · 2015: 25 · 2014: 14 · 2013: 1
- FWCI
- 11.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Cancer (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK069370)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- 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
- Keywords
- long non-coding RNA, extracellular vesicles, exosomes, microvesicles, hepatocellular carcinoma, intercellular RNA transfer, tumor cell proliferation, tumor cell adhesion, tumor microenvironment
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