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经典瞬时受体电位通道蛋白在人非小细胞肺癌组织中的表达

BACKGROUND AND OBJECTIVE: Transient receptor potential canonical (TRPC) proteins, a group of Ca(2+) permeable nonselective cation channels, are thought to constitute store-operated calcium channels (SOCC) and mediate store-operated calcium entry (SOCE) in various cell types. Members of TRPC have bee...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015152/
https://www.ncbi.nlm.nih.gov/pubmed/20681449
http://dx.doi.org/10.3779/j.issn.1009-3419.2010.06.009
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collection PubMed
description BACKGROUND AND OBJECTIVE: Transient receptor potential canonical (TRPC) proteins, a group of Ca(2+) permeable nonselective cation channels, are thought to constitute store-operated calcium channels (SOCC) and mediate store-operated calcium entry (SOCE) in various cell types. Members of TRPC have been found to be involved in abnormal proliferation, differentiation, and growth of cancer cells. The aim of this study is to detect the mRNA and protein expression of TRPC in non-small cell lung cancer (NSCLC). METHODS: Real-time quantitative PCR was performed to screen the expression of TRPC mRNA in NSCLC tissue. Protein expression of TRPC was detected by Western blot. RESULTS: Among the seven family members of TRPC so far identified (TRPC1-7), we detected the expression of TRPC1, TRPC3, TRPC4, TRPC6 mRNA in 24 cases of NSCLC tissue; TRPC2, TRPC5 and TRPC7 mRNA were not detectable. The relative abundance of the expressed TRPC was TRPC1≈TRPC6>TRPC3>TRPC4. Western blot confirmed the protein expression of TRPC1, TRPC3, TRPC4 and TRPC6 in NSCLC tissue. CONCLUSION: Out of the seven members of TRPC, we found TRPC1, TRPC3, TRPC4, TRPC6 mRNA and protein were selectively expressed in human NSCLC tissue. This study could provide a basis for future exploration of the individual role of these TRPC proteins in mediating SOCE and in the progression of lung cancer.
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spelling pubmed-60151522018-07-06 经典瞬时受体电位通道蛋白在人非小细胞肺癌组织中的表达 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: Transient receptor potential canonical (TRPC) proteins, a group of Ca(2+) permeable nonselective cation channels, are thought to constitute store-operated calcium channels (SOCC) and mediate store-operated calcium entry (SOCE) in various cell types. Members of TRPC have been found to be involved in abnormal proliferation, differentiation, and growth of cancer cells. The aim of this study is to detect the mRNA and protein expression of TRPC in non-small cell lung cancer (NSCLC). METHODS: Real-time quantitative PCR was performed to screen the expression of TRPC mRNA in NSCLC tissue. Protein expression of TRPC was detected by Western blot. RESULTS: Among the seven family members of TRPC so far identified (TRPC1-7), we detected the expression of TRPC1, TRPC3, TRPC4, TRPC6 mRNA in 24 cases of NSCLC tissue; TRPC2, TRPC5 and TRPC7 mRNA were not detectable. The relative abundance of the expressed TRPC was TRPC1≈TRPC6>TRPC3>TRPC4. Western blot confirmed the protein expression of TRPC1, TRPC3, TRPC4 and TRPC6 in NSCLC tissue. CONCLUSION: Out of the seven members of TRPC, we found TRPC1, TRPC3, TRPC4, TRPC6 mRNA and protein were selectively expressed in human NSCLC tissue. This study could provide a basis for future exploration of the individual role of these TRPC proteins in mediating SOCE and in the progression of lung cancer. 中国肺癌杂志编辑部 2010-06-20 /pmc/articles/PMC6015152/ /pubmed/20681449 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.06.009 Text en 版权所有©《中国肺癌杂志》编辑部2010 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 临床研究
经典瞬时受体电位通道蛋白在人非小细胞肺癌组织中的表达
title 经典瞬时受体电位通道蛋白在人非小细胞肺癌组织中的表达
title_full 经典瞬时受体电位通道蛋白在人非小细胞肺癌组织中的表达
title_fullStr 经典瞬时受体电位通道蛋白在人非小细胞肺癌组织中的表达
title_full_unstemmed 经典瞬时受体电位通道蛋白在人非小细胞肺癌组织中的表达
title_short 经典瞬时受体电位通道蛋白在人非小细胞肺癌组织中的表达
title_sort 经典瞬时受体电位通道蛋白在人非小细胞肺癌组织中的表达
topic 临床研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015152/
https://www.ncbi.nlm.nih.gov/pubmed/20681449
http://dx.doi.org/10.3779/j.issn.1009-3419.2010.06.009
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