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低氧上调肺腺癌细胞中Annexin A1的表达

BACKGROUND AND OBJECTIVE: The growth of tumor often faced up with lackness of blood and oxygen, and it has been reported that Annexin A1 may be involved in tumor. The aim of this investigation is to explore the characteristics of expression of Annexin A1 in lung adenocarcinoma A549 cells after hypox...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000123/
https://www.ncbi.nlm.nih.gov/pubmed/22613333
http://dx.doi.org/10.3779/j.issn.1009-3419.2012.05.05
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collection PubMed
description BACKGROUND AND OBJECTIVE: The growth of tumor often faced up with lackness of blood and oxygen, and it has been reported that Annexin A1 may be involved in tumor. The aim of this investigation is to explore the characteristics of expression of Annexin A1 in lung adenocarcinoma A549 cells after hypoxia. METHODS: A549 cells were exposured to either normoxia (21%O(2)) or hypoxia (1%O(2)) condition for 4 h, 12 h, 24 h. The expressions of Annexin A1 mRNA levels were measured by RT-PCR. The expressions of Annexin 1 protein were investigaged by Western blot. The relative content of reactive oxygen species (ROS) were assayed by special kit. The expressions of nuclear translocation of NF-κB was assayed by Western blot; After been treated with ROS scavenger NAC and PDTC, the levels of Annexin 1 protein of A549 cells were measured by Western blot. RESULTS: Compared with normoxia group, the Annexin A1 mRNA in hypoxia group increased after 4 h, and then decreased gradually; Moreover, Annexin 1 protein levels of A549 cells were also increased when treated with hypoxia. An increaing of ROS production in cells exprosed to hypoxia was detected. NAC and PDTC inhibited hypoxia-induced Annexin A1 increase. CONCLUSION: Hypoxia upregulates the expression of Annexin A1 in lung adenocarcinoma A549 cells, in which process ROS-NF-κB may paticipate in.
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spelling pubmed-60001232018-07-06 低氧上调肺腺癌细胞中Annexin A1的表达 Zhongguo Fei Ai Za Zhi 基础研究 BACKGROUND AND OBJECTIVE: The growth of tumor often faced up with lackness of blood and oxygen, and it has been reported that Annexin A1 may be involved in tumor. The aim of this investigation is to explore the characteristics of expression of Annexin A1 in lung adenocarcinoma A549 cells after hypoxia. METHODS: A549 cells were exposured to either normoxia (21%O(2)) or hypoxia (1%O(2)) condition for 4 h, 12 h, 24 h. The expressions of Annexin A1 mRNA levels were measured by RT-PCR. The expressions of Annexin 1 protein were investigaged by Western blot. The relative content of reactive oxygen species (ROS) were assayed by special kit. The expressions of nuclear translocation of NF-κB was assayed by Western blot; After been treated with ROS scavenger NAC and PDTC, the levels of Annexin 1 protein of A549 cells were measured by Western blot. RESULTS: Compared with normoxia group, the Annexin A1 mRNA in hypoxia group increased after 4 h, and then decreased gradually; Moreover, Annexin 1 protein levels of A549 cells were also increased when treated with hypoxia. An increaing of ROS production in cells exprosed to hypoxia was detected. NAC and PDTC inhibited hypoxia-induced Annexin A1 increase. CONCLUSION: Hypoxia upregulates the expression of Annexin A1 in lung adenocarcinoma A549 cells, in which process ROS-NF-κB may paticipate in. 中国肺癌杂志编辑部 2012-05-20 /pmc/articles/PMC6000123/ /pubmed/22613333 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.05.05 Text en 版权所有©《中国肺癌杂志》编辑部2012 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
低氧上调肺腺癌细胞中Annexin A1的表达
title 低氧上调肺腺癌细胞中Annexin A1的表达
title_full 低氧上调肺腺癌细胞中Annexin A1的表达
title_fullStr 低氧上调肺腺癌细胞中Annexin A1的表达
title_full_unstemmed 低氧上调肺腺癌细胞中Annexin A1的表达
title_short 低氧上调肺腺癌细胞中Annexin A1的表达
title_sort 低氧上调肺腺癌细胞中annexin a1的表达
topic 基础研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000123/
https://www.ncbi.nlm.nih.gov/pubmed/22613333
http://dx.doi.org/10.3779/j.issn.1009-3419.2012.05.05
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