Hypoxic Tumor Microenvironments Reduce Collagen I Fiber Density

Although the mechanisms through which hypoxia influences several phenotypic characteristics such as angiogenesis, selection for resistance to apoptosis, resistance to radiation and chemotherapy, and increased invasion and metastasis are well characterized, the relationship between tumor hypoxia and...

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Main Authors: Samata M. Kakkad, Meiyappan Solaiyappan, Brian O’Rourke, Ioannis Stasinopoulos, Ellen Ackerstaff, Venu Raman, Zaver M. Bhujwalla, Kristine Glunde
Format: Article
Language:English
Published: Elsevier 2010-08-01
Series:Neoplasia: An International Journal for Oncology Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1476558610800624
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spelling doaj-dce6bd824bc04ac1bced16bb67e484b62020-11-25T00:03:46ZengElsevierNeoplasia: An International Journal for Oncology Research1476-55861522-80022010-08-0112860861710.1593/neo.10344Hypoxic Tumor Microenvironments Reduce Collagen I Fiber DensitySamata M. Kakkad0Meiyappan Solaiyappan1Brian O’Rourke2Ioannis Stasinopoulos3Ellen Ackerstaff4Venu Raman5Zaver M. Bhujwalla6Kristine Glunde7JHU ICMIC Program, Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, USAJHU ICMIC Program, Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, USAInstitute of Molecular Cardiobiology, The Johns Hopkins University School of Medicine, Baltimore, MD, USAJHU ICMIC Program, Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, USAJHU ICMIC Program, Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, USAJHU ICMIC Program, Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, USAJHU ICMIC Program, Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, USAJHU ICMIC Program, Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, USA Although the mechanisms through which hypoxia influences several phenotypic characteristics such as angiogenesis, selection for resistance to apoptosis, resistance to radiation and chemotherapy, and increased invasion and metastasis are well characterized, the relationship between tumor hypoxia and components of the extracellular matrix (ECM) is relatively unexplored. The collagen I (Col1) fiber matrix of solid tumors is the major structural part of the ECM. Col1 fiber density can increase tumor initiation, progression, and metastasis, with cancer cell invasion occurringalong radially aligned Col1 fibers. Here we have investigated the influence of hypoxia on Col1 fiber density in solid breast and prostate tumor models. Second harmonic generation (SHG) microscopy was used to detect differences in Col1 fiber density and volume between hypoxic and normoxic tumor regions. Hypoxic regions were detected by fluorescence microscopy, using tumors derived from human breast and prostate cancer cell lines stably expressing enhanced green fluorescent protein (EGFP) under transcriptional control of the hypoxia response element. In-house fiber analysis software was used to quantitatively analyze Col1 fiber density and volume from the SHG microscopy images. Normoxic tumor regions exhibited a dense mesh of Col1 fibers. In contrast, fewer and structurally altered Col1 fibers were detected in hypoxic EGFP-expressing tumor regions. Microarray gene expression analyses identified increased expression of lysyl oxidase and reduced expression of some matrix metal loproteases in hypoxic compared with normoxic cancer cells. These results suggest that hypoxia mediates Col1 fiber restructuring in tumors, which may impact delivery of macromolecular agents as well as dissemination of cells. http://www.sciencedirect.com/science/article/pii/S1476558610800624
collection DOAJ
language English
format Article
sources DOAJ
author Samata M. Kakkad
Meiyappan Solaiyappan
Brian O’Rourke
Ioannis Stasinopoulos
Ellen Ackerstaff
Venu Raman
Zaver M. Bhujwalla
Kristine Glunde
spellingShingle Samata M. Kakkad
Meiyappan Solaiyappan
Brian O’Rourke
Ioannis Stasinopoulos
Ellen Ackerstaff
Venu Raman
Zaver M. Bhujwalla
Kristine Glunde
Hypoxic Tumor Microenvironments Reduce Collagen I Fiber Density
Neoplasia: An International Journal for Oncology Research
author_facet Samata M. Kakkad
Meiyappan Solaiyappan
Brian O’Rourke
Ioannis Stasinopoulos
Ellen Ackerstaff
Venu Raman
Zaver M. Bhujwalla
Kristine Glunde
author_sort Samata M. Kakkad
title Hypoxic Tumor Microenvironments Reduce Collagen I Fiber Density
title_short Hypoxic Tumor Microenvironments Reduce Collagen I Fiber Density
title_full Hypoxic Tumor Microenvironments Reduce Collagen I Fiber Density
title_fullStr Hypoxic Tumor Microenvironments Reduce Collagen I Fiber Density
title_full_unstemmed Hypoxic Tumor Microenvironments Reduce Collagen I Fiber Density
title_sort hypoxic tumor microenvironments reduce collagen i fiber density
publisher Elsevier
series Neoplasia: An International Journal for Oncology Research
issn 1476-5586
1522-8002
publishDate 2010-08-01
description Although the mechanisms through which hypoxia influences several phenotypic characteristics such as angiogenesis, selection for resistance to apoptosis, resistance to radiation and chemotherapy, and increased invasion and metastasis are well characterized, the relationship between tumor hypoxia and components of the extracellular matrix (ECM) is relatively unexplored. The collagen I (Col1) fiber matrix of solid tumors is the major structural part of the ECM. Col1 fiber density can increase tumor initiation, progression, and metastasis, with cancer cell invasion occurringalong radially aligned Col1 fibers. Here we have investigated the influence of hypoxia on Col1 fiber density in solid breast and prostate tumor models. Second harmonic generation (SHG) microscopy was used to detect differences in Col1 fiber density and volume between hypoxic and normoxic tumor regions. Hypoxic regions were detected by fluorescence microscopy, using tumors derived from human breast and prostate cancer cell lines stably expressing enhanced green fluorescent protein (EGFP) under transcriptional control of the hypoxia response element. In-house fiber analysis software was used to quantitatively analyze Col1 fiber density and volume from the SHG microscopy images. Normoxic tumor regions exhibited a dense mesh of Col1 fibers. In contrast, fewer and structurally altered Col1 fibers were detected in hypoxic EGFP-expressing tumor regions. Microarray gene expression analyses identified increased expression of lysyl oxidase and reduced expression of some matrix metal loproteases in hypoxic compared with normoxic cancer cells. These results suggest that hypoxia mediates Col1 fiber restructuring in tumors, which may impact delivery of macromolecular agents as well as dissemination of cells.
url http://www.sciencedirect.com/science/article/pii/S1476558610800624
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