Insulin-like growth factor-1 receptor as a novel prognostic marker and its implication as a cotarget in the treatment of human adenocarcinoma of the esophagus.

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Insulin-like growth factor-1 receptor as a novel prognostic marker and its implication as a cotarget in the treatment of human adenocarcinoma of the esophagus. / Kalinina, Tatiana; Bockhorn, Maximilian; Kaifi, Jussuf; Thieltges, Sabrina; Güngör, Cenap; Harms-Effenberger, Katharina; Strelow, Andrea; Reichelt, Uta; Sauter, Guido; Pantel, Klaus; Izbicki, Jakob R.; Yekebas, Emre F.

In: INT J CANCER, Vol. 127, No. 8, 8, 2010, p. 1931-1940.

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

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@article{e7f29fb9f5b6473e81d6796c121923ca,
title = "Insulin-like growth factor-1 receptor as a novel prognostic marker and its implication as a cotarget in the treatment of human adenocarcinoma of the esophagus.",
abstract = "Insulin-like growth factor-1 receptor (IGF-1R) and HER2 receptor expression has been found to be a key regulator of tumorigenesis. The purpose of our study was to establish the prognostic significance of IGF-1R in esophageal cancer, and to determine the effect of IGF-1R and HER2 targeting with alpha-IR3 and Herceptin antibodies on the proliferation of esophageal cancer cells in vitro.IGF-1R expression and clinico-pathological correlations were analyzed with a tissue micro array containing 234 esophageal cancer specimens (131 adeno-, 101 squamous cell carcinomas). Proliferation changes associated with Herceptin and alpha-IR3 blockage were evaluated with the unique human esophageal cancer cell lines Pt1590 and LN1590. IGF-1R and HER2 expression levels, activation and phosphorylation status of downstream signalling proteins involved in the activation pathways were analyzed by Western blotting.IGF-1R overexpression was detected in 121 (52%) of the 234 esophageal tumors examined. In the subgroup of 87 HER2-positive tumors, 93.1% showed concordant overexpression for IGF-1R. IGF-1R was identified as a variable associated with reduced overall survival for adenocarcinoma (P=0.05), but not for squamous cell carcinoma. The combination of Herceptin and alpha-IR3 was more effective in inhibiting in vitro proliferation than treatment with either agent alone (P",
author = "Tatiana Kalinina and Maximilian Bockhorn and Jussuf Kaifi and Sabrina Thieltges and Cenap G{\"u}ng{\"o}r and Katharina Harms-Effenberger and Andrea Strelow and Uta Reichelt and Guido Sauter and Klaus Pantel and Izbicki, {Jakob R.} and Yekebas, {Emre F.}",
year = "2010",
language = "Deutsch",
volume = "127",
pages = "1931--1940",
journal = "INT J CANCER",
issn = "0020-7136",
publisher = "Wiley-Liss Inc.",
number = "8",

}

RIS

TY - JOUR

T1 - Insulin-like growth factor-1 receptor as a novel prognostic marker and its implication as a cotarget in the treatment of human adenocarcinoma of the esophagus.

AU - Kalinina, Tatiana

AU - Bockhorn, Maximilian

AU - Kaifi, Jussuf

AU - Thieltges, Sabrina

AU - Güngör, Cenap

AU - Harms-Effenberger, Katharina

AU - Strelow, Andrea

AU - Reichelt, Uta

AU - Sauter, Guido

AU - Pantel, Klaus

AU - Izbicki, Jakob R.

AU - Yekebas, Emre F.

PY - 2010

Y1 - 2010

N2 - Insulin-like growth factor-1 receptor (IGF-1R) and HER2 receptor expression has been found to be a key regulator of tumorigenesis. The purpose of our study was to establish the prognostic significance of IGF-1R in esophageal cancer, and to determine the effect of IGF-1R and HER2 targeting with alpha-IR3 and Herceptin antibodies on the proliferation of esophageal cancer cells in vitro.IGF-1R expression and clinico-pathological correlations were analyzed with a tissue micro array containing 234 esophageal cancer specimens (131 adeno-, 101 squamous cell carcinomas). Proliferation changes associated with Herceptin and alpha-IR3 blockage were evaluated with the unique human esophageal cancer cell lines Pt1590 and LN1590. IGF-1R and HER2 expression levels, activation and phosphorylation status of downstream signalling proteins involved in the activation pathways were analyzed by Western blotting.IGF-1R overexpression was detected in 121 (52%) of the 234 esophageal tumors examined. In the subgroup of 87 HER2-positive tumors, 93.1% showed concordant overexpression for IGF-1R. IGF-1R was identified as a variable associated with reduced overall survival for adenocarcinoma (P=0.05), but not for squamous cell carcinoma. The combination of Herceptin and alpha-IR3 was more effective in inhibiting in vitro proliferation than treatment with either agent alone (P

AB - Insulin-like growth factor-1 receptor (IGF-1R) and HER2 receptor expression has been found to be a key regulator of tumorigenesis. The purpose of our study was to establish the prognostic significance of IGF-1R in esophageal cancer, and to determine the effect of IGF-1R and HER2 targeting with alpha-IR3 and Herceptin antibodies on the proliferation of esophageal cancer cells in vitro.IGF-1R expression and clinico-pathological correlations were analyzed with a tissue micro array containing 234 esophageal cancer specimens (131 adeno-, 101 squamous cell carcinomas). Proliferation changes associated with Herceptin and alpha-IR3 blockage were evaluated with the unique human esophageal cancer cell lines Pt1590 and LN1590. IGF-1R and HER2 expression levels, activation and phosphorylation status of downstream signalling proteins involved in the activation pathways were analyzed by Western blotting.IGF-1R overexpression was detected in 121 (52%) of the 234 esophageal tumors examined. In the subgroup of 87 HER2-positive tumors, 93.1% showed concordant overexpression for IGF-1R. IGF-1R was identified as a variable associated with reduced overall survival for adenocarcinoma (P=0.05), but not for squamous cell carcinoma. The combination of Herceptin and alpha-IR3 was more effective in inhibiting in vitro proliferation than treatment with either agent alone (P

M3 - SCORING: Zeitschriftenaufsatz

VL - 127

SP - 1931

EP - 1940

JO - INT J CANCER

JF - INT J CANCER

SN - 0020-7136

IS - 8

M1 - 8

ER -