author_facet Ji, Li
Li, Xue
Ji, Li
Li, Xue
author Ji, Li
Li, Xue
spellingShingle Ji, Li
Li, Xue
Journal of Cellular Physiology
Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
Cell Biology
Clinical Biochemistry
Physiology
author_sort ji, li
spelling Ji, Li Li, Xue 0021-9541 1097-4652 Wiley Cell Biology Clinical Biochemistry Physiology http://dx.doi.org/10.1002/jcp.28853 <jats:title>Abstract</jats:title><jats:p>Tumor suppressor long noncoding RNA maternally expressed gene 3 (lncRNA MEG3) exists in various cancers. Nonetheless, the functions of lncRNA MEG3 in choriocarcinoma (CC) are still not well studied. We explored the effects of lncRNA MEG3 on human CC JEG‐3 and BeWo cells. lncRNA MEG3 was overexpressed, and the effects of lncRNA MEG3 on cell viability, proliferation, apoptosis, migration, and invasion were assessed by the cell counting kit‐8 assay, western blot analysis, flow cytometry (plus western blot analysis), and transwell assay (plus western blot analysis), respectively. Then, the expression level of miR‐211 was detected by real‐time quantitative polymerase chain reaction. After that, the effects of dysregulated microRNA‐211 (miR‐211) with overexpressing lncRNA MEG3 on JEG‐3 cells and BeWo cells were testified. Western blot analysis was used to study the involvements of the signaling pathways in the lncRNA MEG3‐associated modulation. We found that lncRNA MEG3 upregulation reduced cell viability, inhibited proliferation, migration and invasion, and promoted apoptosis. Expression of miR‐211 was upregulated after lncRNA MEG3 overexpression. Effects of lncRNA MEG3 overexpression were augmented by miR‐211 overexpression, while they were declined by miR‐211 silencing. Phosphorylated levels of PI3K, AKT, and AMP‐activated protein kinase (AMPK) were decreased by lncRNA MEG3 overexpression via regulation of miR‐211. To sum up, lncRNA MEG3 could repress proliferation, migration and invasion, and promote apoptosis of JEG‐3 and BeWo cells through upregulating miR‐211. The PI3K/AKT and AMPK pathways were inhibited by lncRNA MEG3 overexpression via regulation of miR‐211.</jats:p> <i>Retracted</i>: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211 Journal of Cellular Physiology
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title Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_unstemmed Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_full Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_fullStr Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_full_unstemmed Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_short Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_sort <i>retracted</i>: long noncoding rna meg3 is a tumor suppressor in choriocarcinoma by upregulation of microrna‐211
topic Cell Biology
Clinical Biochemistry
Physiology
url http://dx.doi.org/10.1002/jcp.28853
publishDate 2019
physical 22911-22920
description <jats:title>Abstract</jats:title><jats:p>Tumor suppressor long noncoding RNA maternally expressed gene 3 (lncRNA MEG3) exists in various cancers. Nonetheless, the functions of lncRNA MEG3 in choriocarcinoma (CC) are still not well studied. We explored the effects of lncRNA MEG3 on human CC JEG‐3 and BeWo cells. lncRNA MEG3 was overexpressed, and the effects of lncRNA MEG3 on cell viability, proliferation, apoptosis, migration, and invasion were assessed by the cell counting kit‐8 assay, western blot analysis, flow cytometry (plus western blot analysis), and transwell assay (plus western blot analysis), respectively. Then, the expression level of miR‐211 was detected by real‐time quantitative polymerase chain reaction. After that, the effects of dysregulated microRNA‐211 (miR‐211) with overexpressing lncRNA MEG3 on JEG‐3 cells and BeWo cells were testified. Western blot analysis was used to study the involvements of the signaling pathways in the lncRNA MEG3‐associated modulation. We found that lncRNA MEG3 upregulation reduced cell viability, inhibited proliferation, migration and invasion, and promoted apoptosis. Expression of miR‐211 was upregulated after lncRNA MEG3 overexpression. Effects of lncRNA MEG3 overexpression were augmented by miR‐211 overexpression, while they were declined by miR‐211 silencing. Phosphorylated levels of PI3K, AKT, and AMP‐activated protein kinase (AMPK) were decreased by lncRNA MEG3 overexpression via regulation of miR‐211. To sum up, lncRNA MEG3 could repress proliferation, migration and invasion, and promote apoptosis of JEG‐3 and BeWo cells through upregulating miR‐211. The PI3K/AKT and AMPK pathways were inhibited by lncRNA MEG3 overexpression via regulation of miR‐211.</jats:p>
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author Ji, Li, Li, Xue
author_facet Ji, Li, Li, Xue, Ji, Li, Li, Xue
author_sort ji, li
container_issue 12
container_start_page 22911
container_title Journal of Cellular Physiology
container_volume 234
description <jats:title>Abstract</jats:title><jats:p>Tumor suppressor long noncoding RNA maternally expressed gene 3 (lncRNA MEG3) exists in various cancers. Nonetheless, the functions of lncRNA MEG3 in choriocarcinoma (CC) are still not well studied. We explored the effects of lncRNA MEG3 on human CC JEG‐3 and BeWo cells. lncRNA MEG3 was overexpressed, and the effects of lncRNA MEG3 on cell viability, proliferation, apoptosis, migration, and invasion were assessed by the cell counting kit‐8 assay, western blot analysis, flow cytometry (plus western blot analysis), and transwell assay (plus western blot analysis), respectively. Then, the expression level of miR‐211 was detected by real‐time quantitative polymerase chain reaction. After that, the effects of dysregulated microRNA‐211 (miR‐211) with overexpressing lncRNA MEG3 on JEG‐3 cells and BeWo cells were testified. Western blot analysis was used to study the involvements of the signaling pathways in the lncRNA MEG3‐associated modulation. We found that lncRNA MEG3 upregulation reduced cell viability, inhibited proliferation, migration and invasion, and promoted apoptosis. Expression of miR‐211 was upregulated after lncRNA MEG3 overexpression. Effects of lncRNA MEG3 overexpression were augmented by miR‐211 overexpression, while they were declined by miR‐211 silencing. Phosphorylated levels of PI3K, AKT, and AMP‐activated protein kinase (AMPK) were decreased by lncRNA MEG3 overexpression via regulation of miR‐211. To sum up, lncRNA MEG3 could repress proliferation, migration and invasion, and promote apoptosis of JEG‐3 and BeWo cells through upregulating miR‐211. The PI3K/AKT and AMPK pathways were inhibited by lncRNA MEG3 overexpression via regulation of miR‐211.</jats:p>
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id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9qY3AuMjg4NTM
imprint Wiley, 2019
imprint_str_mv Wiley, 2019
institution DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14
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spelling Ji, Li Li, Xue 0021-9541 1097-4652 Wiley Cell Biology Clinical Biochemistry Physiology http://dx.doi.org/10.1002/jcp.28853 <jats:title>Abstract</jats:title><jats:p>Tumor suppressor long noncoding RNA maternally expressed gene 3 (lncRNA MEG3) exists in various cancers. Nonetheless, the functions of lncRNA MEG3 in choriocarcinoma (CC) are still not well studied. We explored the effects of lncRNA MEG3 on human CC JEG‐3 and BeWo cells. lncRNA MEG3 was overexpressed, and the effects of lncRNA MEG3 on cell viability, proliferation, apoptosis, migration, and invasion were assessed by the cell counting kit‐8 assay, western blot analysis, flow cytometry (plus western blot analysis), and transwell assay (plus western blot analysis), respectively. Then, the expression level of miR‐211 was detected by real‐time quantitative polymerase chain reaction. After that, the effects of dysregulated microRNA‐211 (miR‐211) with overexpressing lncRNA MEG3 on JEG‐3 cells and BeWo cells were testified. Western blot analysis was used to study the involvements of the signaling pathways in the lncRNA MEG3‐associated modulation. We found that lncRNA MEG3 upregulation reduced cell viability, inhibited proliferation, migration and invasion, and promoted apoptosis. Expression of miR‐211 was upregulated after lncRNA MEG3 overexpression. Effects of lncRNA MEG3 overexpression were augmented by miR‐211 overexpression, while they were declined by miR‐211 silencing. Phosphorylated levels of PI3K, AKT, and AMP‐activated protein kinase (AMPK) were decreased by lncRNA MEG3 overexpression via regulation of miR‐211. To sum up, lncRNA MEG3 could repress proliferation, migration and invasion, and promote apoptosis of JEG‐3 and BeWo cells through upregulating miR‐211. The PI3K/AKT and AMPK pathways were inhibited by lncRNA MEG3 overexpression via regulation of miR‐211.</jats:p> <i>Retracted</i>: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211 Journal of Cellular Physiology
spellingShingle Ji, Li, Li, Xue, Journal of Cellular Physiology, Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211, Cell Biology, Clinical Biochemistry, Physiology
title Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_full Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_fullStr Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_full_unstemmed Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_short Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
title_sort <i>retracted</i>: long noncoding rna meg3 is a tumor suppressor in choriocarcinoma by upregulation of microrna‐211
title_unstemmed Retracted: Long noncoding RNA MEG3 is a tumor suppressor in choriocarcinoma by upregulation of microRNA‐211
topic Cell Biology, Clinical Biochemistry, Physiology
url http://dx.doi.org/10.1002/jcp.28853