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MRGD, a MAS-related G-protein Coupled Receptor, Promotes Tumorigenisis and Is Highly Expressed in Lung Cancer
To elucidate the function of MAS-related GPCR, member D (MRGD) in cancers, we investigated the in vitro and in vivo oncogenic function of MRGD using murine fibroblast cell line NIH3T3 in which MRGD is stably expressed. The expression pattern of MRGD in clinical samples was also analyzed. We found th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3370999/ https://www.ncbi.nlm.nih.gov/pubmed/22715397 http://dx.doi.org/10.1371/journal.pone.0038618 |
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author | Nishimura, Satoko Uno, Makiko Kaneta, Yasuyuki Fukuchi, Keisuke Nishigohri, Haruyuki Hasegawa, Jun Komori, Hironobu Takeda, Shigeki Enomoto, Katsuhiko Nara, Futoshi Agatsuma, Toshinori |
author_facet | Nishimura, Satoko Uno, Makiko Kaneta, Yasuyuki Fukuchi, Keisuke Nishigohri, Haruyuki Hasegawa, Jun Komori, Hironobu Takeda, Shigeki Enomoto, Katsuhiko Nara, Futoshi Agatsuma, Toshinori |
author_sort | Nishimura, Satoko |
collection | PubMed |
description | To elucidate the function of MAS-related GPCR, member D (MRGD) in cancers, we investigated the in vitro and in vivo oncogenic function of MRGD using murine fibroblast cell line NIH3T3 in which MRGD is stably expressed. The expression pattern of MRGD in clinical samples was also analyzed. We found that overexpression of MRGD in NIH3T3 induced focus formation and multi-cellular spheroid formation, and promoted tumors in nude mice. In other words, overexpression of MRGD in NIH3T3 induced the loss of contact inhibition, anchorage-independent growth and in vivo tumorigenesis. Furthermore, it was found that the ligand of MRGD, beta-alanine, enhanced spheroid formation in MRGD-expressing NIH3T3 cells. From investigation of clinical cancer tissues, we found high expression of MRGD in several lung cancers by immunohistochemistry as well as real time PCR. Based on these results, MRGD could be involved in tumorigenesis and could also be a novel anticancer drug target. |
format | Online Article Text |
id | pubmed-3370999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33709992012-06-19 MRGD, a MAS-related G-protein Coupled Receptor, Promotes Tumorigenisis and Is Highly Expressed in Lung Cancer Nishimura, Satoko Uno, Makiko Kaneta, Yasuyuki Fukuchi, Keisuke Nishigohri, Haruyuki Hasegawa, Jun Komori, Hironobu Takeda, Shigeki Enomoto, Katsuhiko Nara, Futoshi Agatsuma, Toshinori PLoS One Research Article To elucidate the function of MAS-related GPCR, member D (MRGD) in cancers, we investigated the in vitro and in vivo oncogenic function of MRGD using murine fibroblast cell line NIH3T3 in which MRGD is stably expressed. The expression pattern of MRGD in clinical samples was also analyzed. We found that overexpression of MRGD in NIH3T3 induced focus formation and multi-cellular spheroid formation, and promoted tumors in nude mice. In other words, overexpression of MRGD in NIH3T3 induced the loss of contact inhibition, anchorage-independent growth and in vivo tumorigenesis. Furthermore, it was found that the ligand of MRGD, beta-alanine, enhanced spheroid formation in MRGD-expressing NIH3T3 cells. From investigation of clinical cancer tissues, we found high expression of MRGD in several lung cancers by immunohistochemistry as well as real time PCR. Based on these results, MRGD could be involved in tumorigenesis and could also be a novel anticancer drug target. Public Library of Science 2012-06-08 /pmc/articles/PMC3370999/ /pubmed/22715397 http://dx.doi.org/10.1371/journal.pone.0038618 Text en Nishimura 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 Nishimura, Satoko Uno, Makiko Kaneta, Yasuyuki Fukuchi, Keisuke Nishigohri, Haruyuki Hasegawa, Jun Komori, Hironobu Takeda, Shigeki Enomoto, Katsuhiko Nara, Futoshi Agatsuma, Toshinori MRGD, a MAS-related G-protein Coupled Receptor, Promotes Tumorigenisis and Is Highly Expressed in Lung Cancer |
title | MRGD, a MAS-related G-protein Coupled Receptor, Promotes Tumorigenisis and Is Highly Expressed in Lung Cancer |
title_full | MRGD, a MAS-related G-protein Coupled Receptor, Promotes Tumorigenisis and Is Highly Expressed in Lung Cancer |
title_fullStr | MRGD, a MAS-related G-protein Coupled Receptor, Promotes Tumorigenisis and Is Highly Expressed in Lung Cancer |
title_full_unstemmed | MRGD, a MAS-related G-protein Coupled Receptor, Promotes Tumorigenisis and Is Highly Expressed in Lung Cancer |
title_short | MRGD, a MAS-related G-protein Coupled Receptor, Promotes Tumorigenisis and Is Highly Expressed in Lung Cancer |
title_sort | mrgd, a mas-related g-protein coupled receptor, promotes tumorigenisis and is highly expressed in lung cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3370999/ https://www.ncbi.nlm.nih.gov/pubmed/22715397 http://dx.doi.org/10.1371/journal.pone.0038618 |
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