Breast Cancer Cell Colonization of the Human Bone Marrow Adipose Tissue Niche

BACKGROUND/OBJECTIVES: Bone is a preferred site of breast cancer metastasis, suggesting the presence of tissue-specific features that attract and promote the outgrowth of breast cancer cells. We sought to identify parameters of human bone tissue associated with breast cancer cell osteotropism and co...

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Main Authors: Zach S. Templeton, Wen-Rong Lie, Weiqi Wang, Yael Rosenberg-Hasson, Rajiv V. Alluri, John S. Tamaresis, Michael H. Bachmann, Kitty Lee, William J. Maloney, Christopher H. Contag, Bonnie L. King
Format: Article
Language:English
Published: Elsevier 2015-12-01
Series:Neoplasia: An International Journal for Oncology Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1476558615001426
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spelling doaj-3adf2171ed224d0584acf7772b1113402020-11-24T23:21:55ZengElsevierNeoplasia: An International Journal for Oncology Research1476-55861522-80022015-12-01171284986110.1016/j.neo.2015.11.005Breast Cancer Cell Colonization of the Human Bone Marrow Adipose Tissue NicheZach S. Templeton0Wen-Rong Lie1Weiqi Wang2Yael Rosenberg-Hasson3Rajiv V. Alluri4John S. Tamaresis5Michael H. Bachmann6Kitty Lee7William J. Maloney8Christopher H. Contag9Bonnie L. King10Department of Pediatrics, 150E Clark Center, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5427EMD Millipore Corporation, 14 Research Park Drive, St Charles, MO 63304-5618Department of Immunology, Fairchild Science Building, D033, 299 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5124Department of Immunology, Fairchild Science Building, D033, 299 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5124Department of Pediatrics, 150E Clark Center, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5427Department of Biomedical Data Science, Room T101F, Redwood Building, 150 Governor's Lane, Stanford University School of Medicine, Stanford, CA 94305-5405Department of Pediatrics, 150E Clark Center, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5427Cell Sciences Imaging Facility, Beckman Center (B050B), Stanford University School of Medicine, Stanford, CA 94305-5301Department of Orthopaedic Surgery, 450 Broadway Street, Pavillion C, 4th Floor, Stanford University School of Medicine, Redwood City, CA 94063-6342Department of Pediatrics, 150E Clark Center, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5427Department of Pediatrics, 150E Clark Center, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5427BACKGROUND/OBJECTIVES: Bone is a preferred site of breast cancer metastasis, suggesting the presence of tissue-specific features that attract and promote the outgrowth of breast cancer cells. We sought to identify parameters of human bone tissue associated with breast cancer cell osteotropism and colonization in the metastatic niche. METHODS: Migration and colonization patterns of MDA-MB-231-fLuc-EGFP (luciferase-enhanced green fluorescence protein) and MCF-7-fLuc-EGFP breast cancer cells were studied in co-culture with cancellous bone tissue fragments isolated from 14 hip arthroplasties. Breast cancer cell migration into tissues and toward tissue-conditioned medium was measured in Transwell migration chambers using bioluminescence imaging and analyzed as a function of secreted factors measured by multiplex immunoassay. Patterns of breast cancer cell colonization were evaluated with fluorescence microscopy and immunohistochemistry. RESULTS: Enhanced MDA-MB-231-fLuc-EGFP breast cancer cell migration to bone-conditioned versus control medium was observed in 12/14 specimens (P = .0014) and correlated significantly with increasing levels of the adipokines/cytokines leptin (P = .006) and IL-1β (P = .001) in univariate and multivariate regression analyses. Fluorescence microscopy and immunohistochemistry of fragments underscored the extreme adiposity of adult human bone tissues and revealed extensive breast cancer cell colonization within the marrow adipose tissue compartment. CONCLUSIONS: Our results show that breast cancer cells migrate to human bone tissue-conditioned medium in association with increasing levels of leptin and IL-1β, and colonize the bone marrow adipose tissue compartment of cultured fragments. Bone marrow adipose tissue and its molecular signals may be important but understudied components of the breast cancer metastatic niche.http://www.sciencedirect.com/science/article/pii/S1476558615001426
collection DOAJ
language English
format Article
sources DOAJ
author Zach S. Templeton
Wen-Rong Lie
Weiqi Wang
Yael Rosenberg-Hasson
Rajiv V. Alluri
John S. Tamaresis
Michael H. Bachmann
Kitty Lee
William J. Maloney
Christopher H. Contag
Bonnie L. King
spellingShingle Zach S. Templeton
Wen-Rong Lie
Weiqi Wang
Yael Rosenberg-Hasson
Rajiv V. Alluri
John S. Tamaresis
Michael H. Bachmann
Kitty Lee
William J. Maloney
Christopher H. Contag
Bonnie L. King
Breast Cancer Cell Colonization of the Human Bone Marrow Adipose Tissue Niche
Neoplasia: An International Journal for Oncology Research
author_facet Zach S. Templeton
Wen-Rong Lie
Weiqi Wang
Yael Rosenberg-Hasson
Rajiv V. Alluri
John S. Tamaresis
Michael H. Bachmann
Kitty Lee
William J. Maloney
Christopher H. Contag
Bonnie L. King
author_sort Zach S. Templeton
title Breast Cancer Cell Colonization of the Human Bone Marrow Adipose Tissue Niche
title_short Breast Cancer Cell Colonization of the Human Bone Marrow Adipose Tissue Niche
title_full Breast Cancer Cell Colonization of the Human Bone Marrow Adipose Tissue Niche
title_fullStr Breast Cancer Cell Colonization of the Human Bone Marrow Adipose Tissue Niche
title_full_unstemmed Breast Cancer Cell Colonization of the Human Bone Marrow Adipose Tissue Niche
title_sort breast cancer cell colonization of the human bone marrow adipose tissue niche
publisher Elsevier
series Neoplasia: An International Journal for Oncology Research
issn 1476-5586
1522-8002
publishDate 2015-12-01
description BACKGROUND/OBJECTIVES: Bone is a preferred site of breast cancer metastasis, suggesting the presence of tissue-specific features that attract and promote the outgrowth of breast cancer cells. We sought to identify parameters of human bone tissue associated with breast cancer cell osteotropism and colonization in the metastatic niche. METHODS: Migration and colonization patterns of MDA-MB-231-fLuc-EGFP (luciferase-enhanced green fluorescence protein) and MCF-7-fLuc-EGFP breast cancer cells were studied in co-culture with cancellous bone tissue fragments isolated from 14 hip arthroplasties. Breast cancer cell migration into tissues and toward tissue-conditioned medium was measured in Transwell migration chambers using bioluminescence imaging and analyzed as a function of secreted factors measured by multiplex immunoassay. Patterns of breast cancer cell colonization were evaluated with fluorescence microscopy and immunohistochemistry. RESULTS: Enhanced MDA-MB-231-fLuc-EGFP breast cancer cell migration to bone-conditioned versus control medium was observed in 12/14 specimens (P = .0014) and correlated significantly with increasing levels of the adipokines/cytokines leptin (P = .006) and IL-1β (P = .001) in univariate and multivariate regression analyses. Fluorescence microscopy and immunohistochemistry of fragments underscored the extreme adiposity of adult human bone tissues and revealed extensive breast cancer cell colonization within the marrow adipose tissue compartment. CONCLUSIONS: Our results show that breast cancer cells migrate to human bone tissue-conditioned medium in association with increasing levels of leptin and IL-1β, and colonize the bone marrow adipose tissue compartment of cultured fragments. Bone marrow adipose tissue and its molecular signals may be important but understudied components of the breast cancer metastatic niche.
url http://www.sciencedirect.com/science/article/pii/S1476558615001426
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