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不同转移潜能人大细胞肺癌细胞株转移相关microRNAs的筛选研究

BACKGROUND AND OBJECTIVE: MicroRNAs (miRNAs) regulate a wide range of cancer-associated processes, including cell division, proliferation, cell cycle, apoptosis, angiogenesis, invasion, and metastasis. A microarray was performed to analyze metastasis-related miRNAs with different metastastic potenti...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999993/
https://www.ncbi.nlm.nih.gov/pubmed/22104216
http://dx.doi.org/10.3779/j.issn.1009-3419.2011.11.01
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collection PubMed
description BACKGROUND AND OBJECTIVE: MicroRNAs (miRNAs) regulate a wide range of cancer-associated processes, including cell division, proliferation, cell cycle, apoptosis, angiogenesis, invasion, and metastasis. A microarray was performed to analyze metastasis-related miRNAs with different metastastic potentials and to further elucidate their mechanism in the large-cell lung cancer cell lines. METHODS: L9981 and NL9980 cells were harvested, and total RNA was extracted for CY3. RNA hybridization was then performed on the chip with marked miRNAs. MiRNAs with significantly different expression were selected through statistical analysis. A real-time polymerase chain reaction (PCR) was employed to validate the results of the microarray, and target genes were predicted using bioinformatics. RESULTS: Expressions of 22 miRNAs were significantly different in the L9981/NL9980 cell lines. Compared with the NL9980, 13 miRNAs were upregulated in the L9981 cell lines, whereas 9 miRNAs were downregulated. The result of miR-125a-3p expression based on real-time PCR was consistent with the microarray. Insulin-like growth factor 2 might be a target gene of miR-125a-3p. CONCLUSION: The metastatic miRNA profile in large-cell lung cancer was successfully screened out.
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spelling pubmed-59999932018-07-06 不同转移潜能人大细胞肺癌细胞株转移相关microRNAs的筛选研究 Zhongguo Fei Ai Za Zhi 基础研究 BACKGROUND AND OBJECTIVE: MicroRNAs (miRNAs) regulate a wide range of cancer-associated processes, including cell division, proliferation, cell cycle, apoptosis, angiogenesis, invasion, and metastasis. A microarray was performed to analyze metastasis-related miRNAs with different metastastic potentials and to further elucidate their mechanism in the large-cell lung cancer cell lines. METHODS: L9981 and NL9980 cells were harvested, and total RNA was extracted for CY3. RNA hybridization was then performed on the chip with marked miRNAs. MiRNAs with significantly different expression were selected through statistical analysis. A real-time polymerase chain reaction (PCR) was employed to validate the results of the microarray, and target genes were predicted using bioinformatics. RESULTS: Expressions of 22 miRNAs were significantly different in the L9981/NL9980 cell lines. Compared with the NL9980, 13 miRNAs were upregulated in the L9981 cell lines, whereas 9 miRNAs were downregulated. The result of miR-125a-3p expression based on real-time PCR was consistent with the microarray. Insulin-like growth factor 2 might be a target gene of miR-125a-3p. CONCLUSION: The metastatic miRNA profile in large-cell lung cancer was successfully screened out. 中国肺癌杂志编辑部 2011-11-20 /pmc/articles/PMC5999993/ /pubmed/22104216 http://dx.doi.org/10.3779/j.issn.1009-3419.2011.11.01 Text en 版权所有©《中国肺癌杂志》编辑部2011 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 基础研究
不同转移潜能人大细胞肺癌细胞株转移相关microRNAs的筛选研究
title 不同转移潜能人大细胞肺癌细胞株转移相关microRNAs的筛选研究
title_full 不同转移潜能人大细胞肺癌细胞株转移相关microRNAs的筛选研究
title_fullStr 不同转移潜能人大细胞肺癌细胞株转移相关microRNAs的筛选研究
title_full_unstemmed 不同转移潜能人大细胞肺癌细胞株转移相关microRNAs的筛选研究
title_short 不同转移潜能人大细胞肺癌细胞株转移相关microRNAs的筛选研究
title_sort 不同转移潜能人大细胞肺癌细胞株转移相关micrornas的筛选研究
topic 基础研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999993/
https://www.ncbi.nlm.nih.gov/pubmed/22104216
http://dx.doi.org/10.3779/j.issn.1009-3419.2011.11.01
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