Magnitude of stromal hemangiogenesis correlates with histologic subtype of non-Hodgkin's lymphoma.

TitleMagnitude of stromal hemangiogenesis correlates with histologic subtype of non-Hodgkin's lymphoma.
Publication TypeJournal Article
Year of Publication2006
AuthorsRuan J, Hyjek E, Kermani P, Christos PJ, Hooper AT, Coleman M, Hempstead B, Leonard JP, Chadburn A, Rafii S
JournalClin Cancer Res
Volume12
Issue19
Pagination5622-31
Date Published2006 Oct 01
ISSN1078-0432
KeywordsActins, Adult, Aged, Aged, 80 and over, Antigens, CD, Antigens, CD34, Antigens, Differentiation, Myelomonocytic, Burkitt Lymphoma, Female, Humans, Leukemia, Lymphocytic, Chronic, B-Cell, Lymphoma, Follicular, Lymphoma, Large B-Cell, Diffuse, Lymphoma, Non-Hodgkin, Male, Microcirculation, Middle Aged, Muscle, Smooth, Neovascularization, Pathologic, Stromal Cells, Vascular Endothelial Growth Factor A, Vascular Endothelial Growth Factor Receptor-1, Vascular Endothelial Growth Factor Receptor-2
Abstract

PURPOSE: Tumor stromal microenvironment promotes neoplastic growth and angiogenesis. We have previously shown that recruitment of marrow-derived vascular endothelial growth factor receptor-1(+) (VEGFR-1(+)) proangiogenic hematopoietic progenitors contributes instructively and structurally to neoangiogenesis in mouse models. Here, we investigated whether stromal incorporation of CD68(+) hemangiogenic cells and alpha-smooth muscle actin(+) (alpha-SMA(+)) stromal cells correlates with neoangiogenesis and progression in human non-Hodgkin's lymphoma subtypes.

EXPERIMENTAL DESIGN: Spatial localizations of vascular and stromal cells expressing CD34, VEGFR-1, alpha-SMA, and CD68 were examined by immunohistochemistry in 42 cases of non-Hodgkin's lymphoma, including diffuse large B-cell lymphoma, Burkitt lymphoma, follicular lymphoma, and chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), and compared with benign follicular hyperplasia.

RESULTS: Compared with indolent lymphomas, there was a profound increase in recruitment of CD68(+) cells and VEGFR-1(+) neovessels in aggressive subtypes (including those transformed from indolent subtypes), where CD68(+) cells were localized to the perivascular region of neovessels as well as the stromal compartment. The perivascular CD68(+) cells expressed VEGFR-1 and VEGF-A. In contrast, there was a diffuse increase in alpha-SMA incorporation throughout the stromal compartment of indolent subtype of CLL/SLL compared with the scant perivascular pattern in aggressive subtypes. Overall, there was no correlation between CD34(+) microvessel density and lymphoma histologic subtype.

CONCLUSIONS: Heightened stromal hemangiogenesis as marked by infiltration of proangiogenic VEGFR-1(+)CD68(+)VEGF-A(+) cells and their paracrine cross-talk with neovasculature appears to be a distinct feature of aggressive lymphoma, providing novel targets for antiangiogenic therapy, whereas alpha-SMA(+) stromal vascular network may be differentially targeted in CLL/SLL.

DOI10.1158/1078-0432.CCR-06-1204
Alternate JournalClin Cancer Res
PubMed ID17020964
Grant ListHL 075234 / HL / NHLBI NIH HHS / United States
HL 59312 / HL / NHLBI NIH HHS / United States
HL 67839 / HL / NHLBI NIH HHS / United States
K23 RR 016814 / RR / NCRR NIH HHS / United States
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Amy Chadburn, M.D.

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