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DCE-MRI of Sunitinib-Induced Changes in Tumor Microvasculature and Hypoxia: A Study of Pancreatic Ductal Adenocarcinoma Xenografts.

Authors :
Wegner CS
Hauge A
Simonsen TG
Gaustad JV
Andersen LMK
Rofstad EK
Source :
Neoplasia (New York, N.Y.) [Neoplasia] 2018 Jul; Vol. 20 (7), pp. 734-744. Date of Electronic Publication: 2018 Jun 19.
Publication Year :
2018

Abstract

The purpose of this study was dual: to investigate (a) whether sunitinib may induce changes in tumor microvasculature and hypoxia in pancreatic ductal adenocarcinoma (PDAC) and (b) whether any changes can be detected by DCE-MRI. Sunitinib-treated and untreated control tumors of two PDAC xenograft models (BxPC-3 and Panc-1) were subjected to DCE-MRI before the imaged tumors were prepared for quantitative analysis of immunohistochemical preparations. Pimonidazole was used as a hypoxia marker, and fraction of hypoxic tissue (HF <subscript>Pim</subscript> ), density of CD31-positive microvessels (MVD <subscript>CD31</subscript> ), and density of αSMA-positive microvessels (MVD <subscript>αSMA</subscript> ) were measured. Parametric images of K <superscript>trans</superscript> and v <subscript>e</subscript> were derived from the DCE-MRI data by using the Tofts pharmacokinetic model. BxPC-3 tumors showed increased HF <subscript>Pim</subscript> , decreased MVD <subscript>CD31</subscript> , unchanged MVD <subscript>αSMA</subscript> , and increased vessel maturation index (VMI = MVD <subscript>αSMA</subscript> /MVD <subscript>CD31</subscript> ) after sunitinib treatment. The increase in VMI was seen because sunitinib induced selective pruning rather than maturation of αSMA-negative microvessels. Even though the microvessels in sunitinib-treated tumors were less abnormal than those in untreated tumors, this microvessel normalization did not improve the function of the microvascular network or normalize the tumor microenvironment. In Panc-1 tumors, HF <subscript>Pim</subscript> , MVD <subscript>CD31</subscript> , MVD <subscript>αSMA</subscript> , and VMI were unchanged after sunitinib treatment. Median K <superscript>trans</superscript> increased with increasing MVD <subscript>CD31</subscript> and decreased with increasing HF <subscript>Pim</subscript> , and the correlations were similar for treated and untreated BXPC-3 and Panc-1 tumors. These observations suggest that sunitinib may induce significant changes in the microenvironment of PDACs, and furthermore, that K <superscript>trans</superscript> may be an adequate measure of tumor vascular density and hypoxia in untreated as well as sunitinib-treated PDACs.<br /> (Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1476-5586
Volume :
20
Issue :
7
Database :
MEDLINE
Journal :
Neoplasia (New York, N.Y.)
Publication Type :
Academic Journal
Accession number :
29886124
Full Text :
https://doi.org/10.1016/j.neo.2018.05.006