Oncotarget

Research Papers:

Overcoming resistance of targeted EGFR monotherapy by inhibition of STAT3 escape pathway in soft tissue sarcoma

Xiaochun Wang, David Goldstein, Philip J. Crowe, Mark Yang, Kerryn Garrett, Nikolajs Zeps and Jia-Lin Yang _

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Oncotarget. 2016; 7:21496-21509. https://doi.org/10.18632/oncotarget.7452

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Abstract

Xiaochun Wang1,3, David Goldstein2, Philip J. Crowe1,3, Mark Yang3, Kerryn Garrett4,5, Nikolajs Zeps4,5 and Jia-Lin Yang1,3

1 Department of Surgery, Adult Cancer Program, Lowy Cancer Research Centre, Clinical School of Prince of Wales Hospital, Faculty of Medicine, University of New South Wales, Sydney, Australia

2 Department of Medical Oncology, Adult Cancer Program, Lowy Cancer Research Centre, Clinical School of Prince of Wales Hospital, Faculty of Medicine, University of New South Wales, Sydney, Australia

3 Sarcoma and Nanooncology Group, Adult Cancer Program, Lowy Cancer Research Centre, Clinical School of Prince of Wales Hospital, Faculty of Medicine, University of New South Wales, Sydney, Australia

4 Bendat Family Comprehensive Cancer Centre, St John of God HealthCare, Perth, Australia

5 School of Surgery, The University of Western Australia, Perth, Australia

Correspondence to:

Jia-Lin Yang, email:

Keywords: STAT3, EGFR, sarcoma, resistance, targeted therapy

Received: August 25, 2015 Accepted: February 05, 2016 Published: February 17, 2016

Abstract

Although epidermal growth factor receptor (EGFR) is often over-expressed in soft tissue sarcoma (STS), a phase II trial using an EGFR inhibitor gefitinib showed a low response rate. This study identified a new secondary resistance mechanism of gefitinib in STS, and developed new strategies to improve the effectiveness of EGFR inhibition particularly by blocking the STAT3 pathway.

We demonstrated that seven STS cell lines of diverse histological origin showed resistance to gefitinib despite blockade of phosphorylated EGFR (pEGFR) and downstream signal transducers (pAKT and pERK) in PI3K/AKT and RAS/ERK pathways. Gefitinib exposure was not associated with decrease in the ratio of pSTAT3/pSTAT1. The relative STAT3 abundance and activation may be responsible for the drug resistance. We therefore hypothesized that the addition of a STAT3 inhibitor could overcome the STAT3 escape pathway.

We found that the addition of STAT3 inhibitor S3I-201 to gefitinib achieved synergistic anti-proliferative and pro-apoptotic effects in all three STS cell lines examined. This was confirmed in a fibrosarcoma xenografted mouse model, where the tumours from the combination group (418mm3) were significantly smaller than those from untreated (1032mm3) or single drug (912 and 798mm3) groups.

Our findings may have clinical implications for optimising EGFR-targeted therapy in STS.


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