TIE2-expressing monocytes and M2-polarized macrophages impact survival and correlate with angiogenesis in adenocarcinoma of the pancreas

M2-polarized tumor-associated macrophages (TAMs) and TIE2-expressing monocytes (TEMs) are associated with angiogenesis and have been identified as a potential prognostic marker in several solid tumors, including hepatobiliary malignancies. However, little is known regarding their influence on tumor...

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Veröffentlicht in:Oncotarget 2018-07, Vol.9 (51), p.29715-29726
Hauptverfasser: Atanasov, Georgi, Pötner, Charlotte, Aust, Gabriela, Schierle, Katrin, Dietel, Corinna, Benzing, Christian, Krenzien, Felix, Bartels, Michael, Eichfeld, Uwe, Schmelzle, Moritz, Bahra, Marcus, Pascher, Andreas, Wiltberger, Georg
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Sprache:eng
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Zusammenfassung:M2-polarized tumor-associated macrophages (TAMs) and TIE2-expressing monocytes (TEMs) are associated with angiogenesis and have been identified as a potential prognostic marker in several solid tumors, including hepatobiliary malignancies. However, little is known regarding their influence on tumor progression and patient survival in pancreatic ductal adenocarcinoma (PDAC). Patients with tumors characterized by the presence of CD163 TAMs or TEMs in TCA or TIF, respectively, showed a significantly decreased 1-, 3- and 5-year overall and recurrence-free survival compared to patients without CD163 TAMs or TEMs (all < 0.05). Patients with TEMs in TCA showed a higher incidence of tumor recurrence ( < 0.05). Furthermore, the presence of CD163 TAMs was associated with a higher tumor MVD ( < 0.05). Presence of M2-polarized TAMs and TEMs is associated with a decreased overall and recurrence-free survival of patients with PDAC. The localization and density of CD163 M2-polarized TAMs and TEMs were quantified in the tumor central area (TCA) and tumor-infiltrating front (TIF) in human PDAC tissue ( = 106) and correlated to clinicopathological characteristics, tumor recurrence rates and patient survival. In parallel, tumor microvascular density (MVD) and the density of angiopoietin-positive tumor cells were quantified. Statistical analysis was performed using SPSS software.
ISSN:1949-2553
1949-2553
DOI:10.18632/oncotarget.25690