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Expression of LDL receptor-related proteins (LRPs) in common solid malignancies correlates with patient survival

LDL receptor-related proteins (LRPs) are transmembrane receptors involved in endocytosis, cell-signaling, and trafficking of other cellular proteins. Considerable work has focused on LRPs in the fields of vascular biology and neurobiology. How these receptors affect cancer progression in humans rema...

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Autores principales: Gonias, Steven L., Karimi-Mostowfi, Nicki, Murray, Sarah S., Mantuano, Elisabetta, Gilder, Andrew S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663383/
https://www.ncbi.nlm.nih.gov/pubmed/29088295
http://dx.doi.org/10.1371/journal.pone.0186649
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author Gonias, Steven L.
Karimi-Mostowfi, Nicki
Murray, Sarah S.
Mantuano, Elisabetta
Gilder, Andrew S.
author_facet Gonias, Steven L.
Karimi-Mostowfi, Nicki
Murray, Sarah S.
Mantuano, Elisabetta
Gilder, Andrew S.
author_sort Gonias, Steven L.
collection PubMed
description LDL receptor-related proteins (LRPs) are transmembrane receptors involved in endocytosis, cell-signaling, and trafficking of other cellular proteins. Considerable work has focused on LRPs in the fields of vascular biology and neurobiology. How these receptors affect cancer progression in humans remains largely unknown. Herein, we mined provisional databases in The Cancer Genome Atlas (TCGA) to compare expression of thirteen LRPs in ten common solid malignancies in patients. Our first goal was to determine the abundance of LRP mRNAs in each type of cancer. Our second goal was to determine whether expression of LRPs is associated with improved or worsened patient survival. In total, data from 4,629 patients were mined. In nine of ten cancers studied, the most abundantly expressed LRP was LRP1; however, a correlation between LRP1 mRNA expression and patient survival was observed only in bladder urothelial carcinoma. In this malignancy, high levels of LRP1 mRNA were associated with worsened patient survival. High levels of LDL receptor (LDLR) mRNA were associated with decreased patient survival in pancreatic adenocarcinoma. High levels of LRP10 mRNA were associated with decreased patient survival in hepatocellular carcinoma, lung adenocarcinoma, and pancreatic adenocarcinoma. LRP2 was the only LRP for which high levels of mRNA expression correlated with improved patient survival. This correlation was observed in renal clear cell carcinoma. Insights into LRP gene expression in human cancers and their effects on patient survival should guide future research.
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spelling pubmed-56633832017-11-09 Expression of LDL receptor-related proteins (LRPs) in common solid malignancies correlates with patient survival Gonias, Steven L. Karimi-Mostowfi, Nicki Murray, Sarah S. Mantuano, Elisabetta Gilder, Andrew S. PLoS One Research Article LDL receptor-related proteins (LRPs) are transmembrane receptors involved in endocytosis, cell-signaling, and trafficking of other cellular proteins. Considerable work has focused on LRPs in the fields of vascular biology and neurobiology. How these receptors affect cancer progression in humans remains largely unknown. Herein, we mined provisional databases in The Cancer Genome Atlas (TCGA) to compare expression of thirteen LRPs in ten common solid malignancies in patients. Our first goal was to determine the abundance of LRP mRNAs in each type of cancer. Our second goal was to determine whether expression of LRPs is associated with improved or worsened patient survival. In total, data from 4,629 patients were mined. In nine of ten cancers studied, the most abundantly expressed LRP was LRP1; however, a correlation between LRP1 mRNA expression and patient survival was observed only in bladder urothelial carcinoma. In this malignancy, high levels of LRP1 mRNA were associated with worsened patient survival. High levels of LDL receptor (LDLR) mRNA were associated with decreased patient survival in pancreatic adenocarcinoma. High levels of LRP10 mRNA were associated with decreased patient survival in hepatocellular carcinoma, lung adenocarcinoma, and pancreatic adenocarcinoma. LRP2 was the only LRP for which high levels of mRNA expression correlated with improved patient survival. This correlation was observed in renal clear cell carcinoma. Insights into LRP gene expression in human cancers and their effects on patient survival should guide future research. Public Library of Science 2017-10-31 /pmc/articles/PMC5663383/ /pubmed/29088295 http://dx.doi.org/10.1371/journal.pone.0186649 Text en © 2017 Gonias 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gonias, Steven L.
Karimi-Mostowfi, Nicki
Murray, Sarah S.
Mantuano, Elisabetta
Gilder, Andrew S.
Expression of LDL receptor-related proteins (LRPs) in common solid malignancies correlates with patient survival
title Expression of LDL receptor-related proteins (LRPs) in common solid malignancies correlates with patient survival
title_full Expression of LDL receptor-related proteins (LRPs) in common solid malignancies correlates with patient survival
title_fullStr Expression of LDL receptor-related proteins (LRPs) in common solid malignancies correlates with patient survival
title_full_unstemmed Expression of LDL receptor-related proteins (LRPs) in common solid malignancies correlates with patient survival
title_short Expression of LDL receptor-related proteins (LRPs) in common solid malignancies correlates with patient survival
title_sort expression of ldl receptor-related proteins (lrps) in common solid malignancies correlates with patient survival
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663383/
https://www.ncbi.nlm.nih.gov/pubmed/29088295
http://dx.doi.org/10.1371/journal.pone.0186649
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