miR-362-3p suppresses ovarian cancer by inhibiting LRP8

Background: Ovarian cancer is one of the most common female cancers, with a high incidence worldwide. Aberrant expression of low‐density lipoprotein (LDL) receptor‐related protein 8 (LRP8) and microRNA (miR)-362-3p is involved in the pathogenesis of different cancers. Methods: We aimed to elucidate...

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Autores principales: Chun Li, Yi Yang, Huimin Wang, Yu Song, Huan Huang
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Lenguaje:EN
Publicado: Elsevier 2022
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Acceso en línea:https://doaj.org/article/67c2494b59f3474daa2912d4ad9714d4
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spelling oai:doaj.org-article:67c2494b59f3474daa2912d4ad9714d42021-11-28T04:29:52ZmiR-362-3p suppresses ovarian cancer by inhibiting LRP81936-523310.1016/j.tranon.2021.101284https://doaj.org/article/67c2494b59f3474daa2912d4ad9714d42022-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S1936523321002758https://doaj.org/toc/1936-5233Background: Ovarian cancer is one of the most common female cancers, with a high incidence worldwide. Aberrant expression of low‐density lipoprotein (LDL) receptor‐related protein 8 (LRP8) and microRNA (miR)-362-3p is involved in the pathogenesis of different cancers. Methods: We aimed to elucidate the underlying mechanism of the miR-362-3p-LRP8 axis in ovarian cancer. Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was used to examine miR-362-3p and LRP8 expression in ovarian cancer tissues and cells. The luciferase assay was used to determine the relationship between miR-362-3p and LRP8. The function of overexpression of miR-362-3p and LRP8 was determined by assessing the cell viability using the cell counting kit 8 (CCK-8) assay, proliferation using 5′‑bromo-2′-deoxyuridine (BrdU) assay, migration using wound healing assay, invasion using transwell assay, and the protein expression levels of matrix metalloproteinase (MMP)-2, MMP9, and integrin α5 or β1 using western blotting assays in ovarian cancer cells. Results: miR-362-3p expression levels were decreased in ovarian cancer tissues and cells and negatively correlated with LRP8 levels. Overexpression of miR-362-3p dramatically repressed cell growth. Furthermore, overexpression of LRP8 significantly facilitated the proliferation, migration, and invasion of ovarian cancer cells, which counteracted the inhibitory effect of miR-362-3p on ovarian cancer cell growth. Conclusions: We reported that miR-362-3p hampered cell growth by repressing LRP8 expression in ovarian cancer cells. Our results provide new insights into ovarian cancer, involving both miR-362-3p and LRP8, which can be used as potential biomarkers for the treatment of ovarian cancer.Chun LiYi YangHuimin WangYu SongHuan HuangElsevierarticlemiR-362-3pLOvarian cancerGrowthCancer treatmentNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENTranslational Oncology, Vol 15, Iss 1, Pp 101284- (2022)
institution DOAJ
collection DOAJ
language EN
topic miR-362-3p
L
Ovarian cancer
Growth
Cancer treatment
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle miR-362-3p
L
Ovarian cancer
Growth
Cancer treatment
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Chun Li
Yi Yang
Huimin Wang
Yu Song
Huan Huang
miR-362-3p suppresses ovarian cancer by inhibiting LRP8
description Background: Ovarian cancer is one of the most common female cancers, with a high incidence worldwide. Aberrant expression of low‐density lipoprotein (LDL) receptor‐related protein 8 (LRP8) and microRNA (miR)-362-3p is involved in the pathogenesis of different cancers. Methods: We aimed to elucidate the underlying mechanism of the miR-362-3p-LRP8 axis in ovarian cancer. Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was used to examine miR-362-3p and LRP8 expression in ovarian cancer tissues and cells. The luciferase assay was used to determine the relationship between miR-362-3p and LRP8. The function of overexpression of miR-362-3p and LRP8 was determined by assessing the cell viability using the cell counting kit 8 (CCK-8) assay, proliferation using 5′‑bromo-2′-deoxyuridine (BrdU) assay, migration using wound healing assay, invasion using transwell assay, and the protein expression levels of matrix metalloproteinase (MMP)-2, MMP9, and integrin α5 or β1 using western blotting assays in ovarian cancer cells. Results: miR-362-3p expression levels were decreased in ovarian cancer tissues and cells and negatively correlated with LRP8 levels. Overexpression of miR-362-3p dramatically repressed cell growth. Furthermore, overexpression of LRP8 significantly facilitated the proliferation, migration, and invasion of ovarian cancer cells, which counteracted the inhibitory effect of miR-362-3p on ovarian cancer cell growth. Conclusions: We reported that miR-362-3p hampered cell growth by repressing LRP8 expression in ovarian cancer cells. Our results provide new insights into ovarian cancer, involving both miR-362-3p and LRP8, which can be used as potential biomarkers for the treatment of ovarian cancer.
format article
author Chun Li
Yi Yang
Huimin Wang
Yu Song
Huan Huang
author_facet Chun Li
Yi Yang
Huimin Wang
Yu Song
Huan Huang
author_sort Chun Li
title miR-362-3p suppresses ovarian cancer by inhibiting LRP8
title_short miR-362-3p suppresses ovarian cancer by inhibiting LRP8
title_full miR-362-3p suppresses ovarian cancer by inhibiting LRP8
title_fullStr miR-362-3p suppresses ovarian cancer by inhibiting LRP8
title_full_unstemmed miR-362-3p suppresses ovarian cancer by inhibiting LRP8
title_sort mir-362-3p suppresses ovarian cancer by inhibiting lrp8
publisher Elsevier
publishDate 2022
url https://doaj.org/article/67c2494b59f3474daa2912d4ad9714d4
work_keys_str_mv AT chunli mir3623psuppressesovariancancerbyinhibitinglrp8
AT yiyang mir3623psuppressesovariancancerbyinhibitinglrp8
AT huiminwang mir3623psuppressesovariancancerbyinhibitinglrp8
AT yusong mir3623psuppressesovariancancerbyinhibitinglrp8
AT huanhuang mir3623psuppressesovariancancerbyinhibitinglrp8
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