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Circulating giant macrophages as a potential biomarker of solid tumors
Author(s) -
Daniel L. Adams,
Stuart S. Martin,
R. Katherine Alpaugh,
Monica S. Charpentier,
Susan Tsai,
Raymond C. Bergan,
Irene Ogden,
William J. Catàlona,
Saranya Chumsri,
Cha-Mei Tang,
Massimo Cristofanilli
Publication year - 2014
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1320198111
Subject(s) - intravasation , extravasation , circulating tumor cell , biomarker , liquid biopsy , microvesicles , metastasis , cancer , cancer cell , cancer research , macrophage , medicine , pathology , biology , microrna , gene , biochemistry , in vitro
Tumor-associated macrophages (TAMs) derived from primary tumors are believed to facilitate circulating tumor cell (CTC) seeding of distant metastases, but the mechanisms of these processes are poorly understood. Although many studies have focused on the migration of CTCs, less attention has been given to TAMs that, like CTCs, derive from tumor sites. Using precision microfilters under low-flow conditions, we isolated circulating cancer-associated macrophage-like cells (CAMLs) from the peripheral blood of patients with breast, pancreatic, or prostate cancer. CAMLs, which are not found in healthy individuals, were found to express epithelial, monocytic, and endothelial protein markers and were observed bound to CTCs in circulation. These data support the hypothesis that disseminated TAMs can be used as a biomarker of advanced disease and suggest that they have a participatory role in tumor cell migration.

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