Volume 4, Issue 4 pp. 422-432
Original Article

Increased EHD1 in non-small cell lung cancer predicts poor survival

Hailing Lu

Hailing Lu

The Forth Department of Medical Oncology, The Tumor Hospital of Harbin Medical University, Harbin, China

These authors contributed equally to this work.Search for more papers by this author
Qingwei Meng

Qingwei Meng

The Forth Department of Medical Oncology, The Tumor Hospital of Harbin Medical University, Harbin, China

These authors contributed equally to this work.Search for more papers by this author
Yuan Wen

Yuan Wen

The Forth Department of Medical Oncology, The Tumor Hospital of Harbin Medical University, Harbin, China

These authors contributed equally to this work.Search for more papers by this author
Jing Hu

Jing Hu

The Forth Department of Medical Oncology, The Tumor Hospital of Harbin Medical University, Harbin, China

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Yanbin Zhao

Yanbin Zhao

The Forth Department of Medical Oncology, The Tumor Hospital of Harbin Medical University, Harbin, China

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Li Cai

Corresponding Author

Li Cai

The Forth Department of Medical Oncology, The Tumor Hospital of Harbin Medical University, Harbin, China

Correspondence

Li Cai, The Forth Department of Medical Oncology, The Tumor Hospital of Harbin Medical University, 150 Haping Road, Harbin, Heilongjiang 150040, China.

Tel: +86 451 86298283

Fax: +86 451 86298735

Email: [email protected], [email protected]

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First published: 03 April 2013
Citations: 7

Abstract

Background

One of the main challenges of lung cancer research is identifying patients at high risk for recurrence after surgical resection. We evaluated the prognostic power of four proteins in the endocytic pathway in 114 non-small cell lung cancer patients (NSCLC).

Methods

We tested the four proteins (epidermal growth factor receptor [EGFR], RAB11FIP3, EHD1, and caveolin-1), critical nodes in the endocytosis/recycling pathway, by immunohistochemistry in paraffin sections from 114 non-small cell lung cancer patients. We analyzed the correlation between our target proteins and clinical variables. Within these variables, an overall survival (OS) prediction model was constructed using Cox proportional hazard regression.

Results

EHD1 expression correlated with gender (P = 0.001), histology type (P < 0.001), and EGFR expression (P = 0.008), but not with any of the other clinical parameters. Statistical correlation analysis showed that the expression of EHD1 positively correlated with high level of EGFR (P < 0.001) and RAB11FIP3 (P < 0.001), and the expression of caveolin-1 positively correlated with high level of EGFR (P < 0.001) in the NSCLC samples. EHD1 expression was an OS prognostic factor for all of the patients (P = 0.009), for the group of adjuvant chemotherapy-treated patients (P = 0.006), and for the EGFR positive patients (P = 0.034).

Conclusions

We identified EHD1 as a strong prognostic predictive factor in NSCLC. The expression level of EHD1 would potentially be useful in developing customized strategies for managing lung cancer, such as the selection of patients eligible for chemotherapy.

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