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Molecular signatures in IASLC/ATS/ERS classified growth patterns of lung adenocarcinoma

BACKGROUND: The current classification of human lung adenocarcinoma defines five different histological growth patterns within the group of conventional invasive adenocarcinomas. The five growth patterns are characterised by their typical architecture, but also by variable tumor biological behaviour...

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Autores principales: Zabeck, Heike, Dienemann, Hendrik, Hoffmann, Hans, Pfannschmidt, Joachim, Warth, Arne, Schnabel, Philipp A., Muley, Thomas, Meister, Michael, Sültmann, Holger, Fröhlich, Holger, Kuner, Ruprecht, Lasitschka, Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198952/
https://www.ncbi.nlm.nih.gov/pubmed/30352093
http://dx.doi.org/10.1371/journal.pone.0206132
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author Zabeck, Heike
Dienemann, Hendrik
Hoffmann, Hans
Pfannschmidt, Joachim
Warth, Arne
Schnabel, Philipp A.
Muley, Thomas
Meister, Michael
Sültmann, Holger
Fröhlich, Holger
Kuner, Ruprecht
Lasitschka, Felix
author_facet Zabeck, Heike
Dienemann, Hendrik
Hoffmann, Hans
Pfannschmidt, Joachim
Warth, Arne
Schnabel, Philipp A.
Muley, Thomas
Meister, Michael
Sültmann, Holger
Fröhlich, Holger
Kuner, Ruprecht
Lasitschka, Felix
author_sort Zabeck, Heike
collection PubMed
description BACKGROUND: The current classification of human lung adenocarcinoma defines five different histological growth patterns within the group of conventional invasive adenocarcinomas. The five growth patterns are characterised by their typical architecture, but also by variable tumor biological behaviour. AIMS: The aim of this study was to identify specific gene signatures of the five adenocarcinoma growth patterns defined by the joint IASLC/ATS/ERS working group. METHODS: Total RNA from microdissected adenocarcinoma tissue samples of ten lepidic, ten acinar, ten solid, nine papillary, and nine micropapillary tumor portions was isolated and prepared for gene expression analysis. Differential expression of genes was determined using the R package “LIMMA”. The overall significance of each signature was assessed via global test. Gene ontology statistics were analysed using GOstat. For immunohistochemical validation, tissue specimens from 20 tumors with solid and 20 tumors with lepidic growth pattern were used. RESULTS: Microarray analyses between the growth patterns resulted in numerous differentially expressed genes between the solid architecture and other patterns. The comparison of transcriptomic activity in the solid and lepidic patterns revealed 705 up- and 110 downregulated non-redundant genes. The pattern-specific protein expression of Inositol-1,4,5-trisphosphate-kinase-A (ITPKA) and angiogenin by immunohistochemistry confirmed the RNA levels. The strongest differences in protein expression between the two patterns were shown for ITPKA (p = 0.02) and angiogenin (p = 0.113). CONCLUSIONS: In this study growth pattern-specific gene signatures in pulmonary adenocarcinoma were identified and distinct transcriptomic differences between lung adenocarcinoma growth patterns were defined. The study provides valuable new information about pulmonary adenocarcinoma and allows a better assessment of the five adenocarcinoma subgroups.
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spelling pubmed-61989522018-11-19 Molecular signatures in IASLC/ATS/ERS classified growth patterns of lung adenocarcinoma Zabeck, Heike Dienemann, Hendrik Hoffmann, Hans Pfannschmidt, Joachim Warth, Arne Schnabel, Philipp A. Muley, Thomas Meister, Michael Sültmann, Holger Fröhlich, Holger Kuner, Ruprecht Lasitschka, Felix PLoS One Research Article BACKGROUND: The current classification of human lung adenocarcinoma defines five different histological growth patterns within the group of conventional invasive adenocarcinomas. The five growth patterns are characterised by their typical architecture, but also by variable tumor biological behaviour. AIMS: The aim of this study was to identify specific gene signatures of the five adenocarcinoma growth patterns defined by the joint IASLC/ATS/ERS working group. METHODS: Total RNA from microdissected adenocarcinoma tissue samples of ten lepidic, ten acinar, ten solid, nine papillary, and nine micropapillary tumor portions was isolated and prepared for gene expression analysis. Differential expression of genes was determined using the R package “LIMMA”. The overall significance of each signature was assessed via global test. Gene ontology statistics were analysed using GOstat. For immunohistochemical validation, tissue specimens from 20 tumors with solid and 20 tumors with lepidic growth pattern were used. RESULTS: Microarray analyses between the growth patterns resulted in numerous differentially expressed genes between the solid architecture and other patterns. The comparison of transcriptomic activity in the solid and lepidic patterns revealed 705 up- and 110 downregulated non-redundant genes. The pattern-specific protein expression of Inositol-1,4,5-trisphosphate-kinase-A (ITPKA) and angiogenin by immunohistochemistry confirmed the RNA levels. The strongest differences in protein expression between the two patterns were shown for ITPKA (p = 0.02) and angiogenin (p = 0.113). CONCLUSIONS: In this study growth pattern-specific gene signatures in pulmonary adenocarcinoma were identified and distinct transcriptomic differences between lung adenocarcinoma growth patterns were defined. The study provides valuable new information about pulmonary adenocarcinoma and allows a better assessment of the five adenocarcinoma subgroups. Public Library of Science 2018-10-23 /pmc/articles/PMC6198952/ /pubmed/30352093 http://dx.doi.org/10.1371/journal.pone.0206132 Text en © 2018 Zabeck 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
Zabeck, Heike
Dienemann, Hendrik
Hoffmann, Hans
Pfannschmidt, Joachim
Warth, Arne
Schnabel, Philipp A.
Muley, Thomas
Meister, Michael
Sültmann, Holger
Fröhlich, Holger
Kuner, Ruprecht
Lasitschka, Felix
Molecular signatures in IASLC/ATS/ERS classified growth patterns of lung adenocarcinoma
title Molecular signatures in IASLC/ATS/ERS classified growth patterns of lung adenocarcinoma
title_full Molecular signatures in IASLC/ATS/ERS classified growth patterns of lung adenocarcinoma
title_fullStr Molecular signatures in IASLC/ATS/ERS classified growth patterns of lung adenocarcinoma
title_full_unstemmed Molecular signatures in IASLC/ATS/ERS classified growth patterns of lung adenocarcinoma
title_short Molecular signatures in IASLC/ATS/ERS classified growth patterns of lung adenocarcinoma
title_sort molecular signatures in iaslc/ats/ers classified growth patterns of lung adenocarcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198952/
https://www.ncbi.nlm.nih.gov/pubmed/30352093
http://dx.doi.org/10.1371/journal.pone.0206132
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