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LRRN4 and UPK3B Are Markers of Primary Mesothelial Cells

BACKGROUND: Mesothelioma is a highly malignant tumor that is primarily caused by occupational or environmental exposure to asbestos fibers. Despite worldwide restrictions on asbestos usage, further cases are expected as diagnosis is typically 20–40 years after exposure. Once diagnosed there is a ver...

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Autores principales: Kanamori-Katayama, Mutsumi, Kaiho, Ai, Ishizu, Yuri, Okamura-Oho, Yuko, Hino, Okio, Abe, Masaaki, Kishimoto, Takumi, Sekihara, Hisahiko, Nakamura, Yukio, Suzuki, Harukazu, Forrest, Alistair R. R., Hayashizaki, Yoshihide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184985/
https://www.ncbi.nlm.nih.gov/pubmed/21984916
http://dx.doi.org/10.1371/journal.pone.0025391
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author Kanamori-Katayama, Mutsumi
Kaiho, Ai
Ishizu, Yuri
Okamura-Oho, Yuko
Hino, Okio
Abe, Masaaki
Kishimoto, Takumi
Sekihara, Hisahiko
Nakamura, Yukio
Suzuki, Harukazu
Forrest, Alistair R. R.
Hayashizaki, Yoshihide
author_facet Kanamori-Katayama, Mutsumi
Kaiho, Ai
Ishizu, Yuri
Okamura-Oho, Yuko
Hino, Okio
Abe, Masaaki
Kishimoto, Takumi
Sekihara, Hisahiko
Nakamura, Yukio
Suzuki, Harukazu
Forrest, Alistair R. R.
Hayashizaki, Yoshihide
author_sort Kanamori-Katayama, Mutsumi
collection PubMed
description BACKGROUND: Mesothelioma is a highly malignant tumor that is primarily caused by occupational or environmental exposure to asbestos fibers. Despite worldwide restrictions on asbestos usage, further cases are expected as diagnosis is typically 20–40 years after exposure. Once diagnosed there is a very poor prognosis with a median survival rate of 9 months. Considering this the development of early pre clinical diagnostic markers may help improve clinical outcomes. METHODOLOGY: Microarray expression arrays on mesothelium and other tissues dissected from mice were used to identify candidate mesothelial lineage markers. Candidates were further tested by qRTPCR and in-situ hybridization across a mouse tissue panel. Two candidate biomarkers with the potential for secretion, uroplakin 3B (UPK3B), and leucine rich repeat neuronal 4 (LRRN4) and one commercialized mesothelioma marker, mesothelin (MSLN) were then chosen for validation across a panel of normal human primary cells, 16 established mesothelioma cell lines, 10 lung cancer lines, and a further set of 8 unrelated cancer cell lines. CONCLUSIONS: Within the primary cell panel, LRRN4 was only detected in primary mesothelial cells, but MSLN and UPK3B were also detected in other cell types. MSLN was detected in bronchial epithelial cells and alveolar epithelial cells and UPK3B was detected in retinal pigment epithelial cells and urothelial cells. Testing the cell line panel, MSLN was detected in 15 of the 16 mesothelioma cells lines, whereas LRRN4 was only detected in 8 and UPK3B in 6. Interestingly MSLN levels appear to be upregulated in the mesothelioma lines compared to the primary mesothelial cells, while LRRN4 and UPK3B, are either lost or down-regulated. Despite the higher fraction of mesothelioma lines positive for MSLN, it was also detected at high levels in 2 lung cancer lines and 3 other unrelated cancer lines derived from papillotubular adenocarcinoma, signet ring carcinoma and transitional cell carcinoma.
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spelling pubmed-31849852011-10-07 LRRN4 and UPK3B Are Markers of Primary Mesothelial Cells Kanamori-Katayama, Mutsumi Kaiho, Ai Ishizu, Yuri Okamura-Oho, Yuko Hino, Okio Abe, Masaaki Kishimoto, Takumi Sekihara, Hisahiko Nakamura, Yukio Suzuki, Harukazu Forrest, Alistair R. R. Hayashizaki, Yoshihide PLoS One Research Article BACKGROUND: Mesothelioma is a highly malignant tumor that is primarily caused by occupational or environmental exposure to asbestos fibers. Despite worldwide restrictions on asbestos usage, further cases are expected as diagnosis is typically 20–40 years after exposure. Once diagnosed there is a very poor prognosis with a median survival rate of 9 months. Considering this the development of early pre clinical diagnostic markers may help improve clinical outcomes. METHODOLOGY: Microarray expression arrays on mesothelium and other tissues dissected from mice were used to identify candidate mesothelial lineage markers. Candidates were further tested by qRTPCR and in-situ hybridization across a mouse tissue panel. Two candidate biomarkers with the potential for secretion, uroplakin 3B (UPK3B), and leucine rich repeat neuronal 4 (LRRN4) and one commercialized mesothelioma marker, mesothelin (MSLN) were then chosen for validation across a panel of normal human primary cells, 16 established mesothelioma cell lines, 10 lung cancer lines, and a further set of 8 unrelated cancer cell lines. CONCLUSIONS: Within the primary cell panel, LRRN4 was only detected in primary mesothelial cells, but MSLN and UPK3B were also detected in other cell types. MSLN was detected in bronchial epithelial cells and alveolar epithelial cells and UPK3B was detected in retinal pigment epithelial cells and urothelial cells. Testing the cell line panel, MSLN was detected in 15 of the 16 mesothelioma cells lines, whereas LRRN4 was only detected in 8 and UPK3B in 6. Interestingly MSLN levels appear to be upregulated in the mesothelioma lines compared to the primary mesothelial cells, while LRRN4 and UPK3B, are either lost or down-regulated. Despite the higher fraction of mesothelioma lines positive for MSLN, it was also detected at high levels in 2 lung cancer lines and 3 other unrelated cancer lines derived from papillotubular adenocarcinoma, signet ring carcinoma and transitional cell carcinoma. Public Library of Science 2011-10-03 /pmc/articles/PMC3184985/ /pubmed/21984916 http://dx.doi.org/10.1371/journal.pone.0025391 Text en Kanamori-Katayama 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
Kanamori-Katayama, Mutsumi
Kaiho, Ai
Ishizu, Yuri
Okamura-Oho, Yuko
Hino, Okio
Abe, Masaaki
Kishimoto, Takumi
Sekihara, Hisahiko
Nakamura, Yukio
Suzuki, Harukazu
Forrest, Alistair R. R.
Hayashizaki, Yoshihide
LRRN4 and UPK3B Are Markers of Primary Mesothelial Cells
title LRRN4 and UPK3B Are Markers of Primary Mesothelial Cells
title_full LRRN4 and UPK3B Are Markers of Primary Mesothelial Cells
title_fullStr LRRN4 and UPK3B Are Markers of Primary Mesothelial Cells
title_full_unstemmed LRRN4 and UPK3B Are Markers of Primary Mesothelial Cells
title_short LRRN4 and UPK3B Are Markers of Primary Mesothelial Cells
title_sort lrrn4 and upk3b are markers of primary mesothelial cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184985/
https://www.ncbi.nlm.nih.gov/pubmed/21984916
http://dx.doi.org/10.1371/journal.pone.0025391
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