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Long noncoding RNA SNHG3 promotes malignant phenotypes in cervical cancer cells via association with YAP1
被引:8
作者:
Zhu, Hongyu
[1
]
Zhu, Chenyu
[2
]
Feng, Xiang
[3
]
Luo, Youzhen
[1
]
机构:
[1] China Three Gorges Univ, Gynecol Ward 2, Coll Clin Med Sci 1, Yichang Cent Peoples Hosp, Yichang 443003, Hubei, Peoples R China
[2] China Three Gorges Univ, Yichang Cent Peoples Hosp, Gastrointestinal Surg, Coll Clin Med Sci 1, Yichang 443003, Hubei, Peoples R China
[3] China Three Gorges Univ, Yichang Cent Peoples Hosp, Obstet Dept, Coll Clin Med Sci 1, Yichang 443003, Hubei, Peoples R China
来源:
关键词:
Protein stability;
Proliferation;
Migration;
Invasion;
MIGRATION;
INVASION;
D O I:
10.1007/s13577-021-00644-7
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Long non-coding RNA (LncRNA) Small Nucleolar RNA Host Gene 3 (SNHG3) is involved in the occurrence and development of various cancers. However, the exact function and mechanism of SNHG3 in cervical cancer (CC) are still unclear. In this context, we identified a significant increase of SNHG3 expression in CC tissues. Upregulation of SNHG3 expression was associated with advanced FIGO stage and metastasis, and indicated poor overall survival of the CC patients. Functionally, SNHG3 enhanced the proliferation, migration and invasion of CC cells in vitro, and facilitated CC growth in vivo. Further investigation uncovered that SNHG3 interacted with oncoprotein YAP1, thus suppressing its degradation. Additionally, SNHG3 modulated the transcription of several target genes of YAP1. The oncogenic role of SNHG3 was partially attributable to YAP1. Taken together, our research revealed the prognostic and functional roles for SNHG3 in CC, suggesting that SNHG3 could serve as a biomarker for prognosis and a therapeutic target for CC.
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页码:320 / 332
页数:13
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