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Suppression of Lung Tumorigenesis by Leucine Zipper/EF Hand–Containing Transmembrane-1
BACKGROUND: Leucine zipper/EF hand-containing transmembrane-1 (LETM1) encodes for the human homologue of yeast Mdm38p, which is a mitochondria-shaping protein of unclear function. However, a previous study demonstrated that LETM1 served as an anchor protein for complex formation between mitochondria...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2932724/ https://www.ncbi.nlm.nih.gov/pubmed/20824095 http://dx.doi.org/10.1371/journal.pone.0012535 |
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author | Hwang, Soon-Kyung Piao, Longzhen Lim, Hwang-Tae Minai-Tehrani, Arash Yu, Kyeong-Nam Ha, Youn-Cheol Chae, Chan-Hee Lee, Kee-Ho Beck, George R. Park, Jongsun Cho, Myung-Haing |
author_facet | Hwang, Soon-Kyung Piao, Longzhen Lim, Hwang-Tae Minai-Tehrani, Arash Yu, Kyeong-Nam Ha, Youn-Cheol Chae, Chan-Hee Lee, Kee-Ho Beck, George R. Park, Jongsun Cho, Myung-Haing |
author_sort | Hwang, Soon-Kyung |
collection | PubMed |
description | BACKGROUND: Leucine zipper/EF hand-containing transmembrane-1 (LETM1) encodes for the human homologue of yeast Mdm38p, which is a mitochondria-shaping protein of unclear function. However, a previous study demonstrated that LETM1 served as an anchor protein for complex formation between mitochondria and ribosome, and regulated mitochondrial biogenesis. METHODOLOGY/PRINCIPAL FINDINGS: Therefore, we examine the possibility that LETM1 may function to regulate mitochondria and lung tumor growth. In this study, we addressed this question by studying in the effect of adenovirus-mediated LETM1 in the lung cancer cell and lung cancer model mice. To investigate the effects of adenovirus-LETM1 in vitro, we infected with adenovirus-LETM1 in A549 cells. Additionally, in vivo effects of LETM1 were evaluated on K-ras (LA1) mice, human non-small cell lung cancer model mice, by delivering the LETM1 via aerosol through nose-only inhalation system. The effects of LETM1 on lung cancer growth and AMPK related signals were evaluated. Adenovirus-mediated overexpression of LETM1 could induce destruction of mitochondria of lung cancer cells through depleting ATP and AMPK activation. Furthermore, adenoviral-LETM1 also altered Akt signaling and inhibited the cell cycle while facilitating apoptosis. Theses results demonstrated that adenovirus-LETM1 suppressed lung cancer cell growth in vitro and in vivo. CONCLUSIONS/SIGNIFICANCE: Adenovirus-mediated LETM1 may provide a useful target for designing lung tumor prevention and treatment. |
format | Text |
id | pubmed-2932724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29327242010-09-07 Suppression of Lung Tumorigenesis by Leucine Zipper/EF Hand–Containing Transmembrane-1 Hwang, Soon-Kyung Piao, Longzhen Lim, Hwang-Tae Minai-Tehrani, Arash Yu, Kyeong-Nam Ha, Youn-Cheol Chae, Chan-Hee Lee, Kee-Ho Beck, George R. Park, Jongsun Cho, Myung-Haing PLoS One Research Article BACKGROUND: Leucine zipper/EF hand-containing transmembrane-1 (LETM1) encodes for the human homologue of yeast Mdm38p, which is a mitochondria-shaping protein of unclear function. However, a previous study demonstrated that LETM1 served as an anchor protein for complex formation between mitochondria and ribosome, and regulated mitochondrial biogenesis. METHODOLOGY/PRINCIPAL FINDINGS: Therefore, we examine the possibility that LETM1 may function to regulate mitochondria and lung tumor growth. In this study, we addressed this question by studying in the effect of adenovirus-mediated LETM1 in the lung cancer cell and lung cancer model mice. To investigate the effects of adenovirus-LETM1 in vitro, we infected with adenovirus-LETM1 in A549 cells. Additionally, in vivo effects of LETM1 were evaluated on K-ras (LA1) mice, human non-small cell lung cancer model mice, by delivering the LETM1 via aerosol through nose-only inhalation system. The effects of LETM1 on lung cancer growth and AMPK related signals were evaluated. Adenovirus-mediated overexpression of LETM1 could induce destruction of mitochondria of lung cancer cells through depleting ATP and AMPK activation. Furthermore, adenoviral-LETM1 also altered Akt signaling and inhibited the cell cycle while facilitating apoptosis. Theses results demonstrated that adenovirus-LETM1 suppressed lung cancer cell growth in vitro and in vivo. CONCLUSIONS/SIGNIFICANCE: Adenovirus-mediated LETM1 may provide a useful target for designing lung tumor prevention and treatment. Public Library of Science 2010-09-02 /pmc/articles/PMC2932724/ /pubmed/20824095 http://dx.doi.org/10.1371/journal.pone.0012535 Text en Hwang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hwang, Soon-Kyung Piao, Longzhen Lim, Hwang-Tae Minai-Tehrani, Arash Yu, Kyeong-Nam Ha, Youn-Cheol Chae, Chan-Hee Lee, Kee-Ho Beck, George R. Park, Jongsun Cho, Myung-Haing Suppression of Lung Tumorigenesis by Leucine Zipper/EF Hand–Containing Transmembrane-1 |
title | Suppression of Lung Tumorigenesis by Leucine Zipper/EF Hand–Containing Transmembrane-1 |
title_full | Suppression of Lung Tumorigenesis by Leucine Zipper/EF Hand–Containing Transmembrane-1 |
title_fullStr | Suppression of Lung Tumorigenesis by Leucine Zipper/EF Hand–Containing Transmembrane-1 |
title_full_unstemmed | Suppression of Lung Tumorigenesis by Leucine Zipper/EF Hand–Containing Transmembrane-1 |
title_short | Suppression of Lung Tumorigenesis by Leucine Zipper/EF Hand–Containing Transmembrane-1 |
title_sort | suppression of lung tumorigenesis by leucine zipper/ef hand–containing transmembrane-1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2932724/ https://www.ncbi.nlm.nih.gov/pubmed/20824095 http://dx.doi.org/10.1371/journal.pone.0012535 |
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