Temporal Heterogeneity in Blood Supply in Human Tumor Xenografts

Temporal heterogeneities in tumor blood supply were studied by using a recently developed first-pass imaging technique. First-pass imaging movies of A-07-GFP human tumor xenografts growing in window chambers were recorded at a frame rate of ∼9 fps and a spatial resolution of 10.8 x 10.8 µm2 after a...

Full description

Bibliographic Details
Main Authors: Kjetil G. Brurberg, Jon-Vidar Gaustad, Camilla S. Mollatt, Einar K. Rofstad
Format: Article
Language:English
Published: Elsevier 2008-07-01
Series:Neoplasia: An International Journal for Oncology Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1476558608800115
_version_ 1828310154053943296
author Kjetil G. Brurberg
Jon-Vidar Gaustad
Camilla S. Mollatt
Einar K. Rofstad
author_facet Kjetil G. Brurberg
Jon-Vidar Gaustad
Camilla S. Mollatt
Einar K. Rofstad
author_sort Kjetil G. Brurberg
collection DOAJ
description Temporal heterogeneities in tumor blood supply were studied by using a recently developed first-pass imaging technique. First-pass imaging movies of A-07-GFP human tumor xenografts growing in window chambers were recorded at a frame rate of ∼9 fps and a spatial resolution of 10.8 x 10.8 µm2 after a bolus of 155-kDa tetramethylrhodamine isothiocyanate-labeled dextran had been administered intravenously. Each tumor was subjected to imaging thrice, with 20 minutes between each repetition. Highly specific maps of the vascular network and blood supply time (BST) images (i.e., images of the time from when arterial blood enters a tumor through the main supplying artery until it reaches a vessel segment within the tumor) were produced from the movies. The tumors had one to three supplying arterioles and showed substantial temporal heterogeneity in BST. Homogeneous changes in BST in the entire vascular network were seen in tumors supplied by one arteriole. Blood supply time fluctuations in tumor subregions were observed in tumors having two or three supplying arterioles. In addition, individual vessel segments frequently showed significant changes in BST with time. High-magnification transmission microscopy imaging substantiated that BST changes could be a consequence of arterial/arteriolar vasomotor activity, vessel wall compression, varying flow rate, and vascular stasis.
first_indexed 2024-04-13T15:40:08Z
format Article
id doaj.art-b7a865a1ddf348e0a8b6ac24d663f4a0
institution Directory Open Access Journal
issn 1476-5586
1522-8002
language English
last_indexed 2024-04-13T15:40:08Z
publishDate 2008-07-01
publisher Elsevier
record_format Article
series Neoplasia: An International Journal for Oncology Research
spelling doaj.art-b7a865a1ddf348e0a8b6ac24d663f4a02022-12-22T02:41:10ZengElsevierNeoplasia: An International Journal for Oncology Research1476-55861522-80022008-07-0110772773510.1593/neo.08388Temporal Heterogeneity in Blood Supply in Human Tumor XenograftsKjetil G. BrurbergJon-Vidar GaustadCamilla S. MollattEinar K. RofstadTemporal heterogeneities in tumor blood supply were studied by using a recently developed first-pass imaging technique. First-pass imaging movies of A-07-GFP human tumor xenografts growing in window chambers were recorded at a frame rate of ∼9 fps and a spatial resolution of 10.8 x 10.8 µm2 after a bolus of 155-kDa tetramethylrhodamine isothiocyanate-labeled dextran had been administered intravenously. Each tumor was subjected to imaging thrice, with 20 minutes between each repetition. Highly specific maps of the vascular network and blood supply time (BST) images (i.e., images of the time from when arterial blood enters a tumor through the main supplying artery until it reaches a vessel segment within the tumor) were produced from the movies. The tumors had one to three supplying arterioles and showed substantial temporal heterogeneity in BST. Homogeneous changes in BST in the entire vascular network were seen in tumors supplied by one arteriole. Blood supply time fluctuations in tumor subregions were observed in tumors having two or three supplying arterioles. In addition, individual vessel segments frequently showed significant changes in BST with time. High-magnification transmission microscopy imaging substantiated that BST changes could be a consequence of arterial/arteriolar vasomotor activity, vessel wall compression, varying flow rate, and vascular stasis.http://www.sciencedirect.com/science/article/pii/S1476558608800115
spellingShingle Kjetil G. Brurberg
Jon-Vidar Gaustad
Camilla S. Mollatt
Einar K. Rofstad
Temporal Heterogeneity in Blood Supply in Human Tumor Xenografts
Neoplasia: An International Journal for Oncology Research
title Temporal Heterogeneity in Blood Supply in Human Tumor Xenografts
title_full Temporal Heterogeneity in Blood Supply in Human Tumor Xenografts
title_fullStr Temporal Heterogeneity in Blood Supply in Human Tumor Xenografts
title_full_unstemmed Temporal Heterogeneity in Blood Supply in Human Tumor Xenografts
title_short Temporal Heterogeneity in Blood Supply in Human Tumor Xenografts
title_sort temporal heterogeneity in blood supply in human tumor xenografts
url http://www.sciencedirect.com/science/article/pii/S1476558608800115
work_keys_str_mv AT kjetilgbrurberg temporalheterogeneityinbloodsupplyinhumantumorxenografts
AT jonvidargaustad temporalheterogeneityinbloodsupplyinhumantumorxenografts
AT camillasmollatt temporalheterogeneityinbloodsupplyinhumantumorxenografts
AT einarkrofstad temporalheterogeneityinbloodsupplyinhumantumorxenografts