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Proteomic signature corresponding to the response to gefitinib (Iressa, ZD1839), an epidermal growth factor receptor tyrosine kinase inhibitor in lung adenocarcinoma.

作者信息

Okano Tetsuya, Kondo Tadashi, Fujii Kiyonaga, Nishimura Toshihide, Takano Toshimi, Ohe Yuichiro, Tsuta Koji, Matsuno Yoshihiro, Gemma Akihiko, Kato Harbumi, Kudoh Shoji, Hirohashi Setsuo

机构信息

Proteome Bioinformatics Project, National Cancer Center Research Institute, Department of Surgery, Tokyo Medical University, and Clinical Laboratory Division, National Cancer Center Hospital, Japan.

出版信息

Clin Cancer Res. 2007 Feb 1;13(3):799-805. doi: 10.1158/1078-0432.CCR-06-1654.

Abstract

PURPOSE

We aimed to identify candidate proteins for tumor markers to predict the response to gefitinib treatment.

EXPERIMENTAL DESIGN

We did two-dimensional difference gel electrophoresis to create the protein expression profile of lung adenocarcinoma tissues from patients who showed a different response to gefitinib treatment. We used a support vector machine algorithm to select the proteins that best distinguished 31 responders from 16 nonresponders. The prediction performance of the selected spots was validated by an external sample set, including six responders and eight nonresponders. The results were validated using specific antibodies.

RESULTS

We selected nine proteins that distinguish responders from nonresponders. The predictive performance of the nine proteins was validated examining an additional six responders and eight nonresponders, resulting in positive and negative predictive values of 100% (six of six) and 87.5% (seven of eight), respectively. The differential expression of one of the nine proteins, heart-type fatty acid-binding protein, was successfully validated by ELISA. We also identified 12 proteins as a signature to distinguish tumors based on their epidermal growth factor receptor gene mutation status.

CONCLUSIONS

Study of these proteins may contribute to the development of personalized therapy for lung cancer patients.

摘要

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