Oncotarget

Research Papers:

Indoleamine 2,3-dioxygenase mediates immune-independent human tumor cell resistance to olaparib, gamma radiation, and cisplatin

Saman Maleki Vareki, Mateusz Rytelewski, Rene Figueredo, Di Chen, Peter J. Ferguson, Mark Vincent, Weiping Min, Xiufen Zheng, James Koropatnick _

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Abstract

Saman Maleki Vareki1,5, Mateusz Rytelewski1,5, Rene Figueredo5, Di Chen2, Peter J. Ferguson3,5, Mark Vincent3,5, Weiping Min2, Xiufen Zheng2, and James Koropatnick1,2,3,4,5

1 Department of Microbiology and Immunology, Western University, London, Ontario, Canada

2 Department of Pathology, Western University, London, Ontario, Canada

3 Department of Oncology, Western University, London, Ontario, Canada

4 Department of Physiology and Pharmacology, Western University, London, Ontario, Canada

5 Cancer Research Laboratory Program, Lawson Health Research Institute, London, Ontario, Canada

Correspondence:

James Koropatnick, email:

Keywords: IDO- PARP- OLAPARIB- RADIATION- CISPLATIN- BRCA2

Received: March 11, 2014 Accepted: April 16, 2014 Published: April 18, 2014

Abstract

Indoleamine 2,3-dioxygenase-1 (IDO) is an immunosuppressive molecule expressed by most human tumors. IDO levels correlate with poor prognosis in cancer patients and IDO inhibitors are under investigation to enhance endogenous anticancer immunosurveillance. Little is known of immune-independent functions of IDO relevant to cancer therapy. We show, for the first time, that IDO mediates human tumor cell resistance to a PARP inhibitor (olaparib), gamma radiation, cisplatin, and combined treatment with olaparib and radiation, in the absence of immune cells. Antisense-mediated reduction of IDO, alone and (in a synthetic lethal approach) in combination with antisense to the DNA repair protein BRCA2 sensitizes human lung cancer cells to olaparib and cisplatin. Antisense reduction of IDO decreased NAD+ in human tumor cells. NAD+ is essential for PARP activity and these data suggest that IDO mediates treatment resistance independent of immunity and at least partially due to a previously unrecognized role for IDO in DNA repair. Furthermore, IDO levels correlated with accumulation of tumor cells in G1 and depletion of cells in G2/M of the cell cycle, suggesting that IDO effects on cell cycle may also modulate sensitivity to radiation and chemotherapeutic agents. IDO is a potentially valuable therapeutic target in cancer treatment, independent of immune function and in combination with other therapies.

Author Information

Saman Maleki Vareki

Mateusz Rytelewski

Rene Figueredo

Di Chen

Peter J. Ferguson

Mark Vincent

Weiping Min

Xiufen Zheng

James Koropatnick
Primary Contact  _


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