Significance of vascular stabilization for tumor growth and metastasis.

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Significance of vascular stabilization for tumor growth and metastasis. / Ergun, Suleyman; Tilki, Derya; Oliveira-Ferrer, Leticia; Schuch, Gunter; Kilic, Nerbil.

In: CANCER LETT, Vol. 238, No. 2, 2, 2006, p. 180-187.

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@article{487ac975f3cb4a64b43eddf8ab83bf85,
title = "Significance of vascular stabilization for tumor growth and metastasis.",
abstract = "This mini review highlights the role of vascular stabilization which is apparently mediated by factors belonging to both the pro- and anti-angiogenic group. Knowingly angiopoietin-1 has pro-angiogenic properties while endostatin acts anti-angiogenic. But both factors suppress tumor growth in experimental tumor models. The crossing points of mechanisms of their action are the parameters vascular stabilization and vascular permeability, which are of high importance not only for tumor vascularization, but also for tissue vascularization in general. Both angiopoietin-1 and endostatin reduce the vascular permeability, but promote vascular stabilization. Vascular stabilization is significantly increased under experimental treatment of tumors with angiogenesis inhibitors such as endostatin. It inhibits tumor growth and probably tumor metastasis. The understanding of temporal and spatial sequences of vascular stabilization is an important challenge for scientists working on tumor vascularization and anti-angiogenic tumor therapy.",
author = "Suleyman Ergun and Derya Tilki and Leticia Oliveira-Ferrer and Gunter Schuch and Nerbil Kilic",
year = "2006",
language = "Deutsch",
volume = "238",
pages = "180--187",
journal = "CANCER LETT",
issn = "0304-3835",
publisher = "Elsevier Ireland Ltd",
number = "2",

}

RIS

TY - JOUR

T1 - Significance of vascular stabilization for tumor growth and metastasis.

AU - Ergun, Suleyman

AU - Tilki, Derya

AU - Oliveira-Ferrer, Leticia

AU - Schuch, Gunter

AU - Kilic, Nerbil

PY - 2006

Y1 - 2006

N2 - This mini review highlights the role of vascular stabilization which is apparently mediated by factors belonging to both the pro- and anti-angiogenic group. Knowingly angiopoietin-1 has pro-angiogenic properties while endostatin acts anti-angiogenic. But both factors suppress tumor growth in experimental tumor models. The crossing points of mechanisms of their action are the parameters vascular stabilization and vascular permeability, which are of high importance not only for tumor vascularization, but also for tissue vascularization in general. Both angiopoietin-1 and endostatin reduce the vascular permeability, but promote vascular stabilization. Vascular stabilization is significantly increased under experimental treatment of tumors with angiogenesis inhibitors such as endostatin. It inhibits tumor growth and probably tumor metastasis. The understanding of temporal and spatial sequences of vascular stabilization is an important challenge for scientists working on tumor vascularization and anti-angiogenic tumor therapy.

AB - This mini review highlights the role of vascular stabilization which is apparently mediated by factors belonging to both the pro- and anti-angiogenic group. Knowingly angiopoietin-1 has pro-angiogenic properties while endostatin acts anti-angiogenic. But both factors suppress tumor growth in experimental tumor models. The crossing points of mechanisms of their action are the parameters vascular stabilization and vascular permeability, which are of high importance not only for tumor vascularization, but also for tissue vascularization in general. Both angiopoietin-1 and endostatin reduce the vascular permeability, but promote vascular stabilization. Vascular stabilization is significantly increased under experimental treatment of tumors with angiogenesis inhibitors such as endostatin. It inhibits tumor growth and probably tumor metastasis. The understanding of temporal and spatial sequences of vascular stabilization is an important challenge for scientists working on tumor vascularization and anti-angiogenic tumor therapy.

M3 - SCORING: Zeitschriftenaufsatz

VL - 238

SP - 180

EP - 187

JO - CANCER LETT

JF - CANCER LETT

SN - 0304-3835

IS - 2

M1 - 2

ER -