LINC01410 Knockdown Suppresses Cervical Cancer Growth and Invasion via Targeting miR-2467-3p/VOPP1 Axis
Fengjuan Liu, Chuansong Wen Department of Gynecology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou 310006, People’s Republic of ChinaCorrespondence: Chuansong WenDepartment of Gynecology, Affiliated Hangzhou First People’...
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| Format: | Article |
| Language: | English |
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Dove Medical Press
2020-02-01
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| Series: | Cancer Management and Research |
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| Online Access: | https://www.dovepress.com/linc01410-knockdown-suppresses-cervical-cancer-growth-and-invasion-via-peer-reviewed-article-CMAR |
| _version_ | 1818423215776595968 |
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| author | Liu F Wen C |
| author_facet | Liu F Wen C |
| author_sort | Liu F |
| collection | DOAJ |
| description | Fengjuan Liu, Chuansong Wen Department of Gynecology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou 310006, People’s Republic of ChinaCorrespondence: Chuansong WenDepartment of Gynecology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, No. 4 Xueshi Road, Shangcheng District, Hangzhou, Zhejiang 310006, People’s Republic of ChinaTel +86-15867187766Email chuansong_wen@163.comBackground: Long noncoding RNAs have essential roles in human diseases, including cancer. Our work aims to assess the function and mechanisms of LINC01410 in cervical cancer (CC) development.Methods: Expression analyses were performed using qRT-PCR. Proliferation was determined through CCK8 and colony formation assays. Cell migration and invasion were determined by Transwell assay. The interactions among LINC01410, miR-2467-3p and VOPP1 were analyzed via luciferase reporter assay.Results: LINC01410 was upregulated in CC tissues and cell lines. LINC01410 upregulation correlated with poor prognosis. LINC01410 silencing suppressed proliferation, migration and invasion of CC cells. LINC01410 was the sponge for miR-2467. And LINC01410 promoted VOPP1 expression through inhibiting miR-2467.Conclusion: Our findings demonstrated that LINC01410 contributed to CC progression through regulating miR-2467/VOPP1 axis and suggested that LINC01410/miR-2467/VOPP1 cascade may be a potential therapeutic target.Keywords: LINC01410, miR-2467-3p, VOPP1, cervical cancer, progression |
| first_indexed | 2024-12-14T13:38:37Z |
| format | Article |
| id | doaj.art-fdd9d99ea91e4f69b47aa77ab115f1dd |
| institution | Directory Open Access Journal |
| issn | 1179-1322 |
| language | English |
| last_indexed | 2024-12-14T13:38:37Z |
| publishDate | 2020-02-01 |
| publisher | Dove Medical Press |
| record_format | Article |
| series | Cancer Management and Research |
| spelling | doaj.art-fdd9d99ea91e4f69b47aa77ab115f1dd2022-12-21T22:59:31ZengDove Medical PressCancer Management and Research1179-13222020-02-01Volume 1285586151601LINC01410 Knockdown Suppresses Cervical Cancer Growth and Invasion via Targeting miR-2467-3p/VOPP1 AxisLiu FWen CFengjuan Liu, Chuansong Wen Department of Gynecology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou 310006, People’s Republic of ChinaCorrespondence: Chuansong WenDepartment of Gynecology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, No. 4 Xueshi Road, Shangcheng District, Hangzhou, Zhejiang 310006, People’s Republic of ChinaTel +86-15867187766Email chuansong_wen@163.comBackground: Long noncoding RNAs have essential roles in human diseases, including cancer. Our work aims to assess the function and mechanisms of LINC01410 in cervical cancer (CC) development.Methods: Expression analyses were performed using qRT-PCR. Proliferation was determined through CCK8 and colony formation assays. Cell migration and invasion were determined by Transwell assay. The interactions among LINC01410, miR-2467-3p and VOPP1 were analyzed via luciferase reporter assay.Results: LINC01410 was upregulated in CC tissues and cell lines. LINC01410 upregulation correlated with poor prognosis. LINC01410 silencing suppressed proliferation, migration and invasion of CC cells. LINC01410 was the sponge for miR-2467. And LINC01410 promoted VOPP1 expression through inhibiting miR-2467.Conclusion: Our findings demonstrated that LINC01410 contributed to CC progression through regulating miR-2467/VOPP1 axis and suggested that LINC01410/miR-2467/VOPP1 cascade may be a potential therapeutic target.Keywords: LINC01410, miR-2467-3p, VOPP1, cervical cancer, progressionhttps://www.dovepress.com/linc01410-knockdown-suppresses-cervical-cancer-growth-and-invasion-via-peer-reviewed-article-CMARlinc01410mir-2467-3pvopp1cervical cancerprogression |
| spellingShingle | Liu F Wen C LINC01410 Knockdown Suppresses Cervical Cancer Growth and Invasion via Targeting miR-2467-3p/VOPP1 Axis Cancer Management and Research linc01410 mir-2467-3p vopp1 cervical cancer progression |
| title | LINC01410 Knockdown Suppresses Cervical Cancer Growth and Invasion via Targeting miR-2467-3p/VOPP1 Axis |
| title_full | LINC01410 Knockdown Suppresses Cervical Cancer Growth and Invasion via Targeting miR-2467-3p/VOPP1 Axis |
| title_fullStr | LINC01410 Knockdown Suppresses Cervical Cancer Growth and Invasion via Targeting miR-2467-3p/VOPP1 Axis |
| title_full_unstemmed | LINC01410 Knockdown Suppresses Cervical Cancer Growth and Invasion via Targeting miR-2467-3p/VOPP1 Axis |
| title_short | LINC01410 Knockdown Suppresses Cervical Cancer Growth and Invasion via Targeting miR-2467-3p/VOPP1 Axis |
| title_sort | linc01410 knockdown suppresses cervical cancer growth and invasion via targeting mir 2467 3p vopp1 axis |
| topic | linc01410 mir-2467-3p vopp1 cervical cancer progression |
| url | https://www.dovepress.com/linc01410-knockdown-suppresses-cervical-cancer-growth-and-invasion-via-peer-reviewed-article-CMAR |
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