Long noncoding RNA LINC00284 facilitates cell proliferation in papillary thyroid cancer via impairing miR-3127-5p targeted E2F7 suppression

Abstract Accumulating evidence has suggested that long noncoding RNAs (lncRNAs) exert crucial modulation roles in the biological behaviors of multiple malignancies. Nonetheless, the specific function of lncRNA LINC00284 in papillary thyroid cancer (PTC) remains not fully understood. The objective of...

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Main Authors: Bin Zhou, Yugang Ge, Qing Shao, Liyi Yang, Xin Chen, Guoqin Jiang
Format: Article
Language:English
Published: Nature Publishing Group 2021-06-01
Series:Cell Death Discovery
Online Access:https://doi.org/10.1038/s41420-021-00551-8
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author Bin Zhou
Yugang Ge
Qing Shao
Liyi Yang
Xin Chen
Guoqin Jiang
author_facet Bin Zhou
Yugang Ge
Qing Shao
Liyi Yang
Xin Chen
Guoqin Jiang
author_sort Bin Zhou
collection DOAJ
description Abstract Accumulating evidence has suggested that long noncoding RNAs (lncRNAs) exert crucial modulation roles in the biological behaviors of multiple malignancies. Nonetheless, the specific function of lncRNA LINC00284 in papillary thyroid cancer (PTC) remains not fully understood. The objective of this research was to explore the influence of LINC00284 in PTC and elucidate its potential mechanism. The Cancer Genome Atlas (TCGA), gene expression omnibus (GEO) datasets were used to analyze LINC00284 expression differences in thyroid cancer and normal samples, followed by the verification of qRT-PCR in our own PTC and adjacent non-tumor tissues. The impacts of LINC00284 on PTC cell growth were detected in vitro via CCK-8, colony formation, EdU assays, and in vivo via a xenograft tumor model. Bioinformatics analyses and biological experiments were conducted to illuminate the molecular mechanism. We found that LINC00284 expression was remarkably increased in PTC tissues and its overexpression was closely correlated with larger tumor size. In addition, silencing LINC00284 could effectively attenuate PTC cell proliferation, induce apoptosis and G1 arrest in vitro, as well as suppress tumorigenesis in mouse xenografts. Mechanistic investigations showed that LINC00284 acted as a competing endogenous RNA (ceRNA) for miR-3127-5p, thus resulting in the disinhibition of its endogenous target E2F7. In short, our findings indicated that LINC00284–miR-3127-5p–E2F7 axis exerted oncogenic properties in PTC and may offer a new promising target for the diagnosis and therapy of PTC.
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spelling doaj.art-12819bb0c9134f12b9d8a9f0176195c72022-12-21T21:55:09ZengNature Publishing GroupCell Death Discovery2058-77162021-06-017111110.1038/s41420-021-00551-8Long noncoding RNA LINC00284 facilitates cell proliferation in papillary thyroid cancer via impairing miR-3127-5p targeted E2F7 suppressionBin Zhou0Yugang Ge1Qing Shao2Liyi Yang3Xin Chen4Guoqin Jiang5Department of General Surgery, The Second Affiliated Hospital of Soochow UniversityDepartment of Thyroid and Breast Surgery, The Affiliated Jiangyin Hospital of Southeast University Medical CollegeDepartment of Thyroid and Breast Surgery, The Affiliated Jiangyin Hospital of Southeast University Medical CollegeDepartment of Thyroid and Breast Surgery, The Affiliated Jiangyin Hospital of Southeast University Medical CollegeDepartment of Thyroid and Breast Surgery, The Affiliated Jiangyin Hospital of Southeast University Medical CollegeDepartment of General Surgery, The Second Affiliated Hospital of Soochow UniversityAbstract Accumulating evidence has suggested that long noncoding RNAs (lncRNAs) exert crucial modulation roles in the biological behaviors of multiple malignancies. Nonetheless, the specific function of lncRNA LINC00284 in papillary thyroid cancer (PTC) remains not fully understood. The objective of this research was to explore the influence of LINC00284 in PTC and elucidate its potential mechanism. The Cancer Genome Atlas (TCGA), gene expression omnibus (GEO) datasets were used to analyze LINC00284 expression differences in thyroid cancer and normal samples, followed by the verification of qRT-PCR in our own PTC and adjacent non-tumor tissues. The impacts of LINC00284 on PTC cell growth were detected in vitro via CCK-8, colony formation, EdU assays, and in vivo via a xenograft tumor model. Bioinformatics analyses and biological experiments were conducted to illuminate the molecular mechanism. We found that LINC00284 expression was remarkably increased in PTC tissues and its overexpression was closely correlated with larger tumor size. In addition, silencing LINC00284 could effectively attenuate PTC cell proliferation, induce apoptosis and G1 arrest in vitro, as well as suppress tumorigenesis in mouse xenografts. Mechanistic investigations showed that LINC00284 acted as a competing endogenous RNA (ceRNA) for miR-3127-5p, thus resulting in the disinhibition of its endogenous target E2F7. In short, our findings indicated that LINC00284–miR-3127-5p–E2F7 axis exerted oncogenic properties in PTC and may offer a new promising target for the diagnosis and therapy of PTC.https://doi.org/10.1038/s41420-021-00551-8
spellingShingle Bin Zhou
Yugang Ge
Qing Shao
Liyi Yang
Xin Chen
Guoqin Jiang
Long noncoding RNA LINC00284 facilitates cell proliferation in papillary thyroid cancer via impairing miR-3127-5p targeted E2F7 suppression
Cell Death Discovery
title Long noncoding RNA LINC00284 facilitates cell proliferation in papillary thyroid cancer via impairing miR-3127-5p targeted E2F7 suppression
title_full Long noncoding RNA LINC00284 facilitates cell proliferation in papillary thyroid cancer via impairing miR-3127-5p targeted E2F7 suppression
title_fullStr Long noncoding RNA LINC00284 facilitates cell proliferation in papillary thyroid cancer via impairing miR-3127-5p targeted E2F7 suppression
title_full_unstemmed Long noncoding RNA LINC00284 facilitates cell proliferation in papillary thyroid cancer via impairing miR-3127-5p targeted E2F7 suppression
title_short Long noncoding RNA LINC00284 facilitates cell proliferation in papillary thyroid cancer via impairing miR-3127-5p targeted E2F7 suppression
title_sort long noncoding rna linc00284 facilitates cell proliferation in papillary thyroid cancer via impairing mir 3127 5p targeted e2f7 suppression
url https://doi.org/10.1038/s41420-021-00551-8
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