Dynamics of microvascular remodelling during tumor growth in bone.

Standard

Dynamics of microvascular remodelling during tumor growth in bone. / Fuhrhop, Ina; Schröder, Malte; Rafnsdóttir, Svanheidur Loa; Viezens, Lennart; Rüther, Wolfgang; Hansen-Algenstaedt, Nils; Schäfer, Christian.

In: J ORTHOP RES, Vol. 28, No. 1, 1, 2010, p. 27-31.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Fuhrhop, I, Schröder, M, Rafnsdóttir, SL, Viezens, L, Rüther, W, Hansen-Algenstaedt, N & Schäfer, C 2010, 'Dynamics of microvascular remodelling during tumor growth in bone.', J ORTHOP RES, vol. 28, no. 1, 1, pp. 27-31. <http://www.ncbi.nlm.nih.gov/pubmed/19642113?dopt=Citation>

APA

Fuhrhop, I., Schröder, M., Rafnsdóttir, S. L., Viezens, L., Rüther, W., Hansen-Algenstaedt, N., & Schäfer, C. (2010). Dynamics of microvascular remodelling during tumor growth in bone. J ORTHOP RES, 28(1), 27-31. [1]. http://www.ncbi.nlm.nih.gov/pubmed/19642113?dopt=Citation

Vancouver

Fuhrhop I, Schröder M, Rafnsdóttir SL, Viezens L, Rüther W, Hansen-Algenstaedt N et al. Dynamics of microvascular remodelling during tumor growth in bone. J ORTHOP RES. 2010;28(1):27-31. 1.

Bibtex

@article{1fb82ac1bef04479a0b2285e1e998f97,
title = "Dynamics of microvascular remodelling during tumor growth in bone.",
abstract = "Microcirculatory properties of tumors have been shown to play a pivotal role in tumor progression and inefficacy of therapies. Although the influence of the microenvironment on angiogenesis has been intensively investigated in soft tissue tumors, little is known about the microvascular properties in bone metastasis. To determine the impact of the bone microenvironment on tumor growth and microcirculation we performed intravital microscopy using the {"}femur window{"} after implantation of red-fluorescent-protein-transduced breast cancer cells into the femura of severe-combined-immunodeficient mice. Tumor size, functional vascular density, vessel diameter, and vessel distribution were quantified over 14 days. Tumor growth and microcirculation could be quantified at a high spatial resolution. Tumor progression was associated with a rapid remodeling process of the microcirculation within the tumor and the surrounding tissue. Although the total functional vascular density remained unaltered, we found a significant loss in small vessels and a concomitant increase in vascular diameter. The presented study demonstrates for the first time dynamics of morphological microcirculatory alterations of tumor growth in bone. The observed changes in tumor vascularization exhibit strong similarities to soft tissue tumors; however, the dynamics of vascular alterations are more rapid in the bone microenvironment.",
author = "Ina Fuhrhop and Malte Schr{\"o}der and Rafnsd{\'o}ttir, {Svanheidur Loa} and Lennart Viezens and Wolfgang R{\"u}ther and Nils Hansen-Algenstaedt and Christian Sch{\"a}fer",
year = "2010",
language = "Deutsch",
volume = "28",
pages = "27--31",
journal = "J ORTHOP RES",
issn = "0736-0266",
publisher = "John Wiley and Sons Inc.",
number = "1",

}

RIS

TY - JOUR

T1 - Dynamics of microvascular remodelling during tumor growth in bone.

AU - Fuhrhop, Ina

AU - Schröder, Malte

AU - Rafnsdóttir, Svanheidur Loa

AU - Viezens, Lennart

AU - Rüther, Wolfgang

AU - Hansen-Algenstaedt, Nils

AU - Schäfer, Christian

PY - 2010

Y1 - 2010

N2 - Microcirculatory properties of tumors have been shown to play a pivotal role in tumor progression and inefficacy of therapies. Although the influence of the microenvironment on angiogenesis has been intensively investigated in soft tissue tumors, little is known about the microvascular properties in bone metastasis. To determine the impact of the bone microenvironment on tumor growth and microcirculation we performed intravital microscopy using the "femur window" after implantation of red-fluorescent-protein-transduced breast cancer cells into the femura of severe-combined-immunodeficient mice. Tumor size, functional vascular density, vessel diameter, and vessel distribution were quantified over 14 days. Tumor growth and microcirculation could be quantified at a high spatial resolution. Tumor progression was associated with a rapid remodeling process of the microcirculation within the tumor and the surrounding tissue. Although the total functional vascular density remained unaltered, we found a significant loss in small vessels and a concomitant increase in vascular diameter. The presented study demonstrates for the first time dynamics of morphological microcirculatory alterations of tumor growth in bone. The observed changes in tumor vascularization exhibit strong similarities to soft tissue tumors; however, the dynamics of vascular alterations are more rapid in the bone microenvironment.

AB - Microcirculatory properties of tumors have been shown to play a pivotal role in tumor progression and inefficacy of therapies. Although the influence of the microenvironment on angiogenesis has been intensively investigated in soft tissue tumors, little is known about the microvascular properties in bone metastasis. To determine the impact of the bone microenvironment on tumor growth and microcirculation we performed intravital microscopy using the "femur window" after implantation of red-fluorescent-protein-transduced breast cancer cells into the femura of severe-combined-immunodeficient mice. Tumor size, functional vascular density, vessel diameter, and vessel distribution were quantified over 14 days. Tumor growth and microcirculation could be quantified at a high spatial resolution. Tumor progression was associated with a rapid remodeling process of the microcirculation within the tumor and the surrounding tissue. Although the total functional vascular density remained unaltered, we found a significant loss in small vessels and a concomitant increase in vascular diameter. The presented study demonstrates for the first time dynamics of morphological microcirculatory alterations of tumor growth in bone. The observed changes in tumor vascularization exhibit strong similarities to soft tissue tumors; however, the dynamics of vascular alterations are more rapid in the bone microenvironment.

M3 - SCORING: Zeitschriftenaufsatz

VL - 28

SP - 27

EP - 31

JO - J ORTHOP RES

JF - J ORTHOP RES

SN - 0736-0266

IS - 1

M1 - 1

ER -