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CXCR4/SDF-1α-mediated chemotaxis in an in vivo model of metastatic esophageal carcinoma.

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CXCR4/SDF-1α-mediated chemotaxis in an in vivo model of metastatic esophageal carcinoma. / Gros, Stephanie; Graeff, Hanna; Drenckhan, Astrid; Kurschat, Nina; Blessmann, Marco; Rawnaq, Tamina; Izbicki, Jakob R.

In: IN VIVO, Vol. 26, No. 4, 4, 2012, p. 711-718.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Gros, S, Graeff, H, Drenckhan, A, Kurschat, N, Blessmann, M, Rawnaq, T & Izbicki, JR 2012, 'CXCR4/SDF-1α-mediated chemotaxis in an in vivo model of metastatic esophageal carcinoma.', IN VIVO, vol. 26, no. 4, 4, pp. 711-718. <http://www.ncbi.nlm.nih.gov/pubmed/22773586?dopt=Citation>

APA

Gros, S., Graeff, H., Drenckhan, A., Kurschat, N., Blessmann, M., Rawnaq, T., & Izbicki, J. R. (2012). CXCR4/SDF-1α-mediated chemotaxis in an in vivo model of metastatic esophageal carcinoma. IN VIVO, 26(4), 711-718. [4]. http://www.ncbi.nlm.nih.gov/pubmed/22773586?dopt=Citation

Vancouver

Gros S, Graeff H, Drenckhan A, Kurschat N, Blessmann M, Rawnaq T et al. CXCR4/SDF-1α-mediated chemotaxis in an in vivo model of metastatic esophageal carcinoma. IN VIVO. 2012;26(4):711-718. 4.

Bibtex

@article{f03a3fee80d448ab862b84e5f7b7c270,
title = "CXCR4/SDF-1α-mediated chemotaxis in an in vivo model of metastatic esophageal carcinoma.",
abstract = "The chemokine receptor CXCR4 and its ligand (stromal cell-derived factor-1alpha; SDF-1?) play an important role in tumor cell chemotaxis and metastatic homing of esophageal carcinoma. Several methods are available to examine tumor cell migration in vitro. However, in vivo chemotaxis is subject to complex tumor-host interactions. The aim of this study was to establish an in vivo model of chemotaxis for esophageal carcinoma that allows the examination of tumor cell migration and metastatic homing in the complex microenvironment.",
keywords = "Animals, Mice, Neoplasm Metastasis, Chemokine CXCL12/*physiology, Chemotaxis/*physiology, Esophageal Neoplasms/*pathology, Receptors, CXCR4/*physiology, Animals, Mice, Neoplasm Metastasis, Chemokine CXCL12/*physiology, Chemotaxis/*physiology, Esophageal Neoplasms/*pathology, Receptors, CXCR4/*physiology",
author = "Stephanie Gros and Hanna Graeff and Astrid Drenckhan and Nina Kurschat and Marco Blessmann and Tamina Rawnaq and Izbicki, {Jakob R.}",
year = "2012",
language = "English",
volume = "26",
pages = "711--718",
journal = "IN VIVO",
issn = "0258-851X",
publisher = "International Institute of Anticancer Research",
number = "4",

}

RIS

TY - JOUR

T1 - CXCR4/SDF-1α-mediated chemotaxis in an in vivo model of metastatic esophageal carcinoma.

AU - Gros, Stephanie

AU - Graeff, Hanna

AU - Drenckhan, Astrid

AU - Kurschat, Nina

AU - Blessmann, Marco

AU - Rawnaq, Tamina

AU - Izbicki, Jakob R.

PY - 2012

Y1 - 2012

N2 - The chemokine receptor CXCR4 and its ligand (stromal cell-derived factor-1alpha; SDF-1?) play an important role in tumor cell chemotaxis and metastatic homing of esophageal carcinoma. Several methods are available to examine tumor cell migration in vitro. However, in vivo chemotaxis is subject to complex tumor-host interactions. The aim of this study was to establish an in vivo model of chemotaxis for esophageal carcinoma that allows the examination of tumor cell migration and metastatic homing in the complex microenvironment.

AB - The chemokine receptor CXCR4 and its ligand (stromal cell-derived factor-1alpha; SDF-1?) play an important role in tumor cell chemotaxis and metastatic homing of esophageal carcinoma. Several methods are available to examine tumor cell migration in vitro. However, in vivo chemotaxis is subject to complex tumor-host interactions. The aim of this study was to establish an in vivo model of chemotaxis for esophageal carcinoma that allows the examination of tumor cell migration and metastatic homing in the complex microenvironment.

KW - Animals

KW - Mice

KW - Neoplasm Metastasis

KW - Chemokine CXCL12/physiology

KW - Chemotaxis/physiology

KW - Esophageal Neoplasms/pathology

KW - Receptors, CXCR4/physiology

KW - Animals

KW - Mice

KW - Neoplasm Metastasis

KW - Chemokine CXCL12/physiology

KW - Chemotaxis/physiology

KW - Esophageal Neoplasms/pathology

KW - Receptors, CXCR4/physiology

M3 - SCORING: Journal article

VL - 26

SP - 711

EP - 718

JO - IN VIVO

JF - IN VIVO

SN - 0258-851X

IS - 4

M1 - 4

ER -