Expression of Modulates the Progression of Mutated Thyroid Cancer Cells

BackgroundWe previously reported the frequent neurofibromatosis 2 (NF2) gene mutations in anaplastic thyroid cancers in association with the BRAFV600E mutation. We aimed to investigate the role of NF2 in thyroid cancer with BRAF mutation.MethodsTo identify the function of NF2 in thyroid cancers, we...

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Main Authors: Mi-Hyeon You, Min Ji Jeon, Tae Yong Kim, Won Bae Kim, Young Kee Shong, Won Gu Kim
Format: Article
Language:English
Published: Academya Publishing Co. 2019-06-01
Series:Endocrinology and Metabolism
Subjects:
Online Access:https://e-enm.org/Synapse/Data/PDFData/2008ENM/enm-34-203.pdf
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spelling doaj-3ceb42b883ce41008c445f3253f4c2f42020-11-25T00:59:03ZengAcademya Publishing Co.Endocrinology and Metabolism2093-596X2093-59782019-06-0134220321210.3803/EnM.2019.34.2.203Expression of Modulates the Progression of Mutated Thyroid Cancer CellsMi-Hyeon YouMin Ji JeonTae Yong KimWon Bae KimYoung Kee ShongWon Gu KimBackgroundWe previously reported the frequent neurofibromatosis 2 (NF2) gene mutations in anaplastic thyroid cancers in association with the BRAFV600E mutation. We aimed to investigate the role of NF2 in thyroid cancer with BRAF mutation.MethodsTo identify the function of NF2 in thyroid cancers, we investigated the changes in cell proliferation, colon formation, migration and invasion of thyroid cancer cells (8505C, BHT101, and KTC-1) with BRAFV600E mutation after overexpression and knock-down of NF2. We also examined how cell proliferation changed when NF2 was mutagenized. Human NF2 expression in papillary thyroid carcinoma (PTC) was analyzed using the The Cancer Genome Atlas (TCGA) data.ResultsFirst, NF2 was overexpressed in 8505C and KTC-1 cells. Compared to control, NF2 overexpressed group of both thyroid cancer cells showed significant inhibition in cell proliferation and colony formation. These results were also confirmed by cell migration and invasion assay. After knock-down of NF2 in 8505C cells, there were no significant changes in cell proliferation and colony formation, compared with the control group. However, after mutagenized S288* and Q470* sites of NF2 gene, the cell proliferation increased compared to NF2 overexpression group. In the analysis of TCGA data, the mRNA expression of NF2 was significantly decreased in PTCs with lateral cervical lymph node (LN) metastasis compared with PTCs without LN metastasis.ConclusionOur study suggests that NF2 might play a role as a tumor suppressor in thyroid cancer with BRAF mutation. More studies are needed to elucidate the mechanism how NF2 acts in thyroid cancer with BRAF mutation.https://e-enm.org/Synapse/Data/PDFData/2008ENM/enm-34-203.pdfNeurofibromatosis 2BRAF, mutationThyroid neoplasmsGenes, tumor suppressor
collection DOAJ
language English
format Article
sources DOAJ
author Mi-Hyeon You
Min Ji Jeon
Tae Yong Kim
Won Bae Kim
Young Kee Shong
Won Gu Kim
spellingShingle Mi-Hyeon You
Min Ji Jeon
Tae Yong Kim
Won Bae Kim
Young Kee Shong
Won Gu Kim
Expression of Modulates the Progression of Mutated Thyroid Cancer Cells
Endocrinology and Metabolism
Neurofibromatosis 2
BRAF, mutation
Thyroid neoplasms
Genes, tumor suppressor
author_facet Mi-Hyeon You
Min Ji Jeon
Tae Yong Kim
Won Bae Kim
Young Kee Shong
Won Gu Kim
author_sort Mi-Hyeon You
title Expression of Modulates the Progression of Mutated Thyroid Cancer Cells
title_short Expression of Modulates the Progression of Mutated Thyroid Cancer Cells
title_full Expression of Modulates the Progression of Mutated Thyroid Cancer Cells
title_fullStr Expression of Modulates the Progression of Mutated Thyroid Cancer Cells
title_full_unstemmed Expression of Modulates the Progression of Mutated Thyroid Cancer Cells
title_sort expression of modulates the progression of mutated thyroid cancer cells
publisher Academya Publishing Co.
series Endocrinology and Metabolism
issn 2093-596X
2093-5978
publishDate 2019-06-01
description BackgroundWe previously reported the frequent neurofibromatosis 2 (NF2) gene mutations in anaplastic thyroid cancers in association with the BRAFV600E mutation. We aimed to investigate the role of NF2 in thyroid cancer with BRAF mutation.MethodsTo identify the function of NF2 in thyroid cancers, we investigated the changes in cell proliferation, colon formation, migration and invasion of thyroid cancer cells (8505C, BHT101, and KTC-1) with BRAFV600E mutation after overexpression and knock-down of NF2. We also examined how cell proliferation changed when NF2 was mutagenized. Human NF2 expression in papillary thyroid carcinoma (PTC) was analyzed using the The Cancer Genome Atlas (TCGA) data.ResultsFirst, NF2 was overexpressed in 8505C and KTC-1 cells. Compared to control, NF2 overexpressed group of both thyroid cancer cells showed significant inhibition in cell proliferation and colony formation. These results were also confirmed by cell migration and invasion assay. After knock-down of NF2 in 8505C cells, there were no significant changes in cell proliferation and colony formation, compared with the control group. However, after mutagenized S288* and Q470* sites of NF2 gene, the cell proliferation increased compared to NF2 overexpression group. In the analysis of TCGA data, the mRNA expression of NF2 was significantly decreased in PTCs with lateral cervical lymph node (LN) metastasis compared with PTCs without LN metastasis.ConclusionOur study suggests that NF2 might play a role as a tumor suppressor in thyroid cancer with BRAF mutation. More studies are needed to elucidate the mechanism how NF2 acts in thyroid cancer with BRAF mutation.
topic Neurofibromatosis 2
BRAF, mutation
Thyroid neoplasms
Genes, tumor suppressor
url https://e-enm.org/Synapse/Data/PDFData/2008ENM/enm-34-203.pdf
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