Cargando…

3131 ONCOSTREAMS: NOVEL DYNAMICS PATHOLOGICAL MULTICELLULAR STRUCTURES INVOLVED IN GLIOBLATOMA GROWTH AND INVASION

OBJECTIVES/SPECIFIC AIMS: Oncostreams represent a novel growth pattern of GBM. In this study we uncovered the cellular and molecular mechanism that regulates the oncostreams function in GBM growth and invasion. METHODS/STUDY POPULATION: We studied oncostreams organization and function using genetica...

Descripción completa

Detalles Bibliográficos
Autores principales: Comba, Andrea, Dunn, Patrick, Argento, Anna E, Kadiyala, Padma, Motsch, Sebastien, Kish, Phillip, Kahana, Alon, Zamler, Daniel, Muraszko, Karin, Castro, Maria G, Lowenstein, Pedro R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798800/
http://dx.doi.org/10.1017/cts.2019.253
_version_ 1783460140361449472
author Comba, Andrea
Dunn, Patrick
Argento, Anna E
Kadiyala, Padma
Motsch, Sebastien
Kish, Phillip
Kahana, Alon
Zamler, Daniel
Muraszko, Karin
Castro, Maria G
Lowenstein, Pedro R
author_facet Comba, Andrea
Dunn, Patrick
Argento, Anna E
Kadiyala, Padma
Motsch, Sebastien
Kish, Phillip
Kahana, Alon
Zamler, Daniel
Muraszko, Karin
Castro, Maria G
Lowenstein, Pedro R
author_sort Comba, Andrea
collection PubMed
description OBJECTIVES/SPECIFIC AIMS: Oncostreams represent a novel growth pattern of GBM. In this study we uncovered the cellular and molecular mechanism that regulates the oncostreams function in GBM growth and invasion. METHODS/STUDY POPULATION: We studied oncostreams organization and function using genetically engineered mouse gliomas models (GEMM), mouse primary patient derived GBM model and human glioma biopsies. We evaluated the molecular landscape of oncostreams by laser capture microdissection (LCM) followed by RNA-Sequencing and bioinformatics analysis. RESULTS/ANTICIPATED RESULTS: Oncostreams are multicellular structures of 10-20 cells wide and 2-400 μm long. They are distributed throughout the tumors in mouse and human GBM. Oncostreams are heterogeneous structures positive for GFAP, Nestin, Olig2 and Iba1 cells and negative for Neurofilament. Using GEMM we found a negative correlation between oncostream density and animal survival. Moreover, examination of patient’s glioma biopsies evidenced that oncostreams are present in high grade but no in low grade gliomas. This suggests that oncostreams may play a role in tumor malignancy. Our data also indicated that oncostreams aid local invasion of normal brain. Transcriptome analysis of oncostreams revealed 43 differentially expressed (DE) genes. Functional enrichment analysis of DE genes showed that “collagen catabolic processes”, “positive regulation of cell migration”, and “extracellular matrix organization” were the most over-represented GO biological process. Network analysis indicated that Col1a1, ACTA2, MMP9 and MMP10 are primary target genes. These genes were also overexpressed in more malignant tumors (WT-IDH) compared to the less malignant (IDH1- R132H) tumors. Confocal time lapse imagining of 3D tumor slices demonstrated that oncostreams display a collective motion pattern within gliomas that has not been seen before. DISCUSSION/SIGNIFICANCE OF IMPACT: In summary, oncostreams are anatomically and molecularly distinctive, regulate glioma growth and invasion, display collective motion and are regulated by the extracellular matrix. We propose oncostreams as novel pathological markers valuable for diagnosis, prognosis and designing therapeutics for GBM patients.
format Online
Article
Text
id pubmed-6798800
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Cambridge University Press
record_format MEDLINE/PubMed
spelling pubmed-67988002019-10-28 3131 ONCOSTREAMS: NOVEL DYNAMICS PATHOLOGICAL MULTICELLULAR STRUCTURES INVOLVED IN GLIOBLATOMA GROWTH AND INVASION Comba, Andrea Dunn, Patrick Argento, Anna E Kadiyala, Padma Motsch, Sebastien Kish, Phillip Kahana, Alon Zamler, Daniel Muraszko, Karin Castro, Maria G Lowenstein, Pedro R J Clin Transl Sci Mechanistic Basic to Clinical OBJECTIVES/SPECIFIC AIMS: Oncostreams represent a novel growth pattern of GBM. In this study we uncovered the cellular and molecular mechanism that regulates the oncostreams function in GBM growth and invasion. METHODS/STUDY POPULATION: We studied oncostreams organization and function using genetically engineered mouse gliomas models (GEMM), mouse primary patient derived GBM model and human glioma biopsies. We evaluated the molecular landscape of oncostreams by laser capture microdissection (LCM) followed by RNA-Sequencing and bioinformatics analysis. RESULTS/ANTICIPATED RESULTS: Oncostreams are multicellular structures of 10-20 cells wide and 2-400 μm long. They are distributed throughout the tumors in mouse and human GBM. Oncostreams are heterogeneous structures positive for GFAP, Nestin, Olig2 and Iba1 cells and negative for Neurofilament. Using GEMM we found a negative correlation between oncostream density and animal survival. Moreover, examination of patient’s glioma biopsies evidenced that oncostreams are present in high grade but no in low grade gliomas. This suggests that oncostreams may play a role in tumor malignancy. Our data also indicated that oncostreams aid local invasion of normal brain. Transcriptome analysis of oncostreams revealed 43 differentially expressed (DE) genes. Functional enrichment analysis of DE genes showed that “collagen catabolic processes”, “positive regulation of cell migration”, and “extracellular matrix organization” were the most over-represented GO biological process. Network analysis indicated that Col1a1, ACTA2, MMP9 and MMP10 are primary target genes. These genes were also overexpressed in more malignant tumors (WT-IDH) compared to the less malignant (IDH1- R132H) tumors. Confocal time lapse imagining of 3D tumor slices demonstrated that oncostreams display a collective motion pattern within gliomas that has not been seen before. DISCUSSION/SIGNIFICANCE OF IMPACT: In summary, oncostreams are anatomically and molecularly distinctive, regulate glioma growth and invasion, display collective motion and are regulated by the extracellular matrix. We propose oncostreams as novel pathological markers valuable for diagnosis, prognosis and designing therapeutics for GBM patients. Cambridge University Press 2019-03-27 /pmc/articles/PMC6798800/ http://dx.doi.org/10.1017/cts.2019.253 Text en © The Association for Clinical and Translational Science 2019 http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (http://creativecommons.org/licenses/by-ncnd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is unaltered and is properly cited. The written permission of Cambridge University Press must be obtained for commercial re-use or in order to create a derivative work.
spellingShingle Mechanistic Basic to Clinical
Comba, Andrea
Dunn, Patrick
Argento, Anna E
Kadiyala, Padma
Motsch, Sebastien
Kish, Phillip
Kahana, Alon
Zamler, Daniel
Muraszko, Karin
Castro, Maria G
Lowenstein, Pedro R
3131 ONCOSTREAMS: NOVEL DYNAMICS PATHOLOGICAL MULTICELLULAR STRUCTURES INVOLVED IN GLIOBLATOMA GROWTH AND INVASION
title 3131 ONCOSTREAMS: NOVEL DYNAMICS PATHOLOGICAL MULTICELLULAR STRUCTURES INVOLVED IN GLIOBLATOMA GROWTH AND INVASION
title_full 3131 ONCOSTREAMS: NOVEL DYNAMICS PATHOLOGICAL MULTICELLULAR STRUCTURES INVOLVED IN GLIOBLATOMA GROWTH AND INVASION
title_fullStr 3131 ONCOSTREAMS: NOVEL DYNAMICS PATHOLOGICAL MULTICELLULAR STRUCTURES INVOLVED IN GLIOBLATOMA GROWTH AND INVASION
title_full_unstemmed 3131 ONCOSTREAMS: NOVEL DYNAMICS PATHOLOGICAL MULTICELLULAR STRUCTURES INVOLVED IN GLIOBLATOMA GROWTH AND INVASION
title_short 3131 ONCOSTREAMS: NOVEL DYNAMICS PATHOLOGICAL MULTICELLULAR STRUCTURES INVOLVED IN GLIOBLATOMA GROWTH AND INVASION
title_sort 3131 oncostreams: novel dynamics pathological multicellular structures involved in glioblatoma growth and invasion
topic Mechanistic Basic to Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798800/
http://dx.doi.org/10.1017/cts.2019.253
work_keys_str_mv AT combaandrea 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion
AT dunnpatrick 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion
AT argentoannae 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion
AT kadiyalapadma 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion
AT motschsebastien 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion
AT kishphillip 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion
AT kahanaalon 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion
AT zamlerdaniel 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion
AT muraszkokarin 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion
AT castromariag 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion
AT lowensteinpedror 3131oncostreamsnoveldynamicspathologicalmulticellularstructuresinvolvedinglioblatomagrowthandinvasion