Trastuzumab has anti-metastatic and anti-angiogenic activity in a spontaneous metastasis xenograft model of esophageal adenocarcinoma.

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Trastuzumab has anti-metastatic and anti-angiogenic activity in a spontaneous metastasis xenograft model of esophageal adenocarcinoma. / Lange, Tobias; Nentwich, Michael; Lueth, Manuel; Yekebas, Emre F.; Schumacher, Udo.

In: CANCER LETT, Vol. 308, No. 1, 1, 2011, p. 54-61.

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@article{f2ee95651956405f803783cc94cc7444,
title = "Trastuzumab has anti-metastatic and anti-angiogenic activity in a spontaneous metastasis xenograft model of esophageal adenocarcinoma.",
abstract = "HER-2/neu over-expression occurs in 10-40% of patients with esophageal adenocarcinoma. Therefore, inhibitory effects of trastuzumab on proliferation, neoangiogenesis and metastatic spread of the esophageal adenocarcinoma cell line PT1590 were investigated (subcutaneous xenograft model). PT1590 revealed an amplified copy number of c-erbB2 and HER-2/neu over-expression occured in xenograft tumors and spontaneous lung metastases. PT1590 proliferation was significantly inhibited by trastuzumab in vitro. In vivo, tumor weight, volume, microvessel density and number of lung metastases decreased significantly after three weeks of treatment. These data suggest the importance of HER-2/neu for metastatic spread in esophageal adenocarcinoma and encourages clinical trials.",
keywords = "Animals, Humans, Female, Immunohistochemistry, Mice, Cell Line, Tumor, Neoplasm Metastasis, Gene Amplification, Dose-Response Relationship, Drug, Cell Growth Processes/drug effects, Mice, SCID, Xenograft Model Antitumor Assays, Adenocarcinoma/*drug therapy/genetics/pathology, Angiogenesis Inhibitors/pharmacology, Antibodies, Monoclonal/*pharmacology, Antibodies, Monoclonal, Humanized, Antineoplastic Agents/pharmacology, Esophageal Neoplasms/blood supply/*drug therapy/genetics/pathology, Genes, erbB-2, Lung Neoplasms/drug therapy/secondary, Receptor, erbB-2/antagonists & inhibitors/biosynthesis/genetics, Animals, Humans, Female, Immunohistochemistry, Mice, Cell Line, Tumor, Neoplasm Metastasis, Gene Amplification, Dose-Response Relationship, Drug, Cell Growth Processes/drug effects, Mice, SCID, Xenograft Model Antitumor Assays, Adenocarcinoma/*drug therapy/genetics/pathology, Angiogenesis Inhibitors/pharmacology, Antibodies, Monoclonal/*pharmacology, Antibodies, Monoclonal, Humanized, Antineoplastic Agents/pharmacology, Esophageal Neoplasms/blood supply/*drug therapy/genetics/pathology, Genes, erbB-2, Lung Neoplasms/drug therapy/secondary, Receptor, erbB-2/antagonists & inhibitors/biosynthesis/genetics",
author = "Tobias Lange and Michael Nentwich and Manuel Lueth and Yekebas, {Emre F.} and Udo Schumacher",
year = "2011",
language = "English",
volume = "308",
pages = "54--61",
journal = "CANCER LETT",
issn = "0304-3835",
publisher = "Elsevier Ireland Ltd",
number = "1",

}

RIS

TY - JOUR

T1 - Trastuzumab has anti-metastatic and anti-angiogenic activity in a spontaneous metastasis xenograft model of esophageal adenocarcinoma.

AU - Lange, Tobias

AU - Nentwich, Michael

AU - Lueth, Manuel

AU - Yekebas, Emre F.

AU - Schumacher, Udo

PY - 2011

Y1 - 2011

N2 - HER-2/neu over-expression occurs in 10-40% of patients with esophageal adenocarcinoma. Therefore, inhibitory effects of trastuzumab on proliferation, neoangiogenesis and metastatic spread of the esophageal adenocarcinoma cell line PT1590 were investigated (subcutaneous xenograft model). PT1590 revealed an amplified copy number of c-erbB2 and HER-2/neu over-expression occured in xenograft tumors and spontaneous lung metastases. PT1590 proliferation was significantly inhibited by trastuzumab in vitro. In vivo, tumor weight, volume, microvessel density and number of lung metastases decreased significantly after three weeks of treatment. These data suggest the importance of HER-2/neu for metastatic spread in esophageal adenocarcinoma and encourages clinical trials.

AB - HER-2/neu over-expression occurs in 10-40% of patients with esophageal adenocarcinoma. Therefore, inhibitory effects of trastuzumab on proliferation, neoangiogenesis and metastatic spread of the esophageal adenocarcinoma cell line PT1590 were investigated (subcutaneous xenograft model). PT1590 revealed an amplified copy number of c-erbB2 and HER-2/neu over-expression occured in xenograft tumors and spontaneous lung metastases. PT1590 proliferation was significantly inhibited by trastuzumab in vitro. In vivo, tumor weight, volume, microvessel density and number of lung metastases decreased significantly after three weeks of treatment. These data suggest the importance of HER-2/neu for metastatic spread in esophageal adenocarcinoma and encourages clinical trials.

KW - Animals

KW - Humans

KW - Female

KW - Immunohistochemistry

KW - Mice

KW - Cell Line, Tumor

KW - Neoplasm Metastasis

KW - Gene Amplification

KW - Dose-Response Relationship, Drug

KW - Cell Growth Processes/drug effects

KW - Mice, SCID

KW - Xenograft Model Antitumor Assays

KW - Adenocarcinoma/drug therapy/genetics/pathology

KW - Angiogenesis Inhibitors/pharmacology

KW - Antibodies, Monoclonal/pharmacology

KW - Antibodies, Monoclonal, Humanized

KW - Antineoplastic Agents/pharmacology

KW - Esophageal Neoplasms/blood supply/drug therapy/genetics/pathology

KW - Genes, erbB-2

KW - Lung Neoplasms/drug therapy/secondary

KW - Receptor, erbB-2/antagonists & inhibitors/biosynthesis/genetics

KW - Animals

KW - Humans

KW - Female

KW - Immunohistochemistry

KW - Mice

KW - Cell Line, Tumor

KW - Neoplasm Metastasis

KW - Gene Amplification

KW - Dose-Response Relationship, Drug

KW - Cell Growth Processes/drug effects

KW - Mice, SCID

KW - Xenograft Model Antitumor Assays

KW - Adenocarcinoma/drug therapy/genetics/pathology

KW - Angiogenesis Inhibitors/pharmacology

KW - Antibodies, Monoclonal/pharmacology

KW - Antibodies, Monoclonal, Humanized

KW - Antineoplastic Agents/pharmacology

KW - Esophageal Neoplasms/blood supply/drug therapy/genetics/pathology

KW - Genes, erbB-2

KW - Lung Neoplasms/drug therapy/secondary

KW - Receptor, erbB-2/antagonists & inhibitors/biosynthesis/genetics

M3 - SCORING: Journal article

VL - 308

SP - 54

EP - 61

JO - CANCER LETT

JF - CANCER LETT

SN - 0304-3835

IS - 1

M1 - 1

ER -