disseminated breast cancer cells acquire a highly malignant and aggressive metastatic phenotype during metastatic latency in the bone乳腺癌细胞获得高度恶性和传播积极的转移表型在转移性骨延迟.pdfVIP
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disseminated breast cancer cells acquire a highly malignant and aggressive metastatic phenotype during metastatic latency in the bone乳腺癌细胞获得高度恶性和传播积极的转移表型在转移性骨延迟
Disseminated Breast Cancer Cells Acquire a Highly
Malignant and Aggressive Metastatic Phenotype during
Metastatic Latency in the Bone
1 2 1 3 1
Carolyn G. Marsden , Mary Jo Wright , Latonya Carrier , Krzysztof Moroz , Brian G. Rowan *
1 Department of Structural and Cellular Biology, The Louisiana Cancer Research Consortium, Tulane University Health Sciences Center, New Orleans, Louisiana, United
States of America, 2 Department of Surgery, The Louisiana Cancer Research Consortium, Tulane University School of Medicine, New Orleans, Louisiana, United States of
America, 3 Section of Surgical Pathology and Cytopathology, Louisiana Cancer Research Consortium, Tulane University School of Medicine, New Orleans, Louisiana, United
States of America
Abstract
Background: Disseminated tumor cells (DTCs) in the bone marrow may exist in a dormant state for extended periods of
time, maintaining the ability to proliferate upon activation, engraft at new sites, and form detectable metastases. However,
understanding of the behavior and biology of dormant breast cancer cells in the bone marrow niche remains limited, as well
as their potential involvement in tumor recurrence and metastasis. Therefore, the purpose of this study was to investigate
the tumorigenicity and metastatic potential of dormant disseminated breast cancer cells (prior to activation) in the bone
marrow.
Methodology/Principal Findings: Total bone marrow, isolated from mice previously injected with tumorspheres into the
mammary fat pad, was injected into the mammary fat pad of NUDE mice. As a negative control, bone marrow isolated from
non-injected mice was injected into the mammary fat pad of NUDE mice. The resultant tumors were analyzed by
immunohistochemistry for
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