Oncotarget

Research Papers:

High cytidine deaminase expression in the liver provides sanctuary for cancer cells from decitabine treatment effects

Quteba Ebrahem, Reda Z Mahfouz, Kwok Peng Ng and Yogen Saunthararajah _

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Oncotarget. 2012; 3:1137-1145. https://doi.org/10.18632/oncotarget.597

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Abstract

Quteba Ebrahem1, Reda Z Mahfouz1, Kwok Peng Ng1, Yogen Saunthararajah1

1 Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH

Correspondence:

Yogen Saunthararajah, email:

Keywords: cytidine analogues, decitabine, cytidine deaminase, chemotherapy resistance, sanctuary

Received: August 08, 2012, Accepted: September 25, 2012, Published: September 27, 2012

Abstract

We document for the first time that sanctuary in an organ which expresses high levels of the enzyme cytidine deaminase (CDA) is a mechanism of cancer cell resistance to cytidine analogues. This mechanism could explain why historically, cytidine analogues have not been successful chemotherapeutics against hepatotropic cancers, despite efficacy in vitro. Importantly, this mechanism of resistance can be readily reversed, without increasing toxicity to sensitive organs, by combining a cytidine analogue with an inhibitor of cytidine deaminase (tetrahydrouridine). Specifically, CDA rapidly metabolizes cytidine analogues into inactive uridine counterparts. Hence, to determine if sheltering/protection of cancer cells in organs which express high levels of CDA (e.g., liver) is a mechanism of resistance, we utilized a murine xenotransplant model of myeloid cancer that is sensitive to epigenetic therapeutic effects of the cytidine analogue decitabine in vitro and hepato-tropic in vivo. Treatment of tumor-bearing mice with decitabine (subcutaneous 0.2mg/kg 2X/week) doubled median survival and significantly decreased extra-hepatic tumor burden, but hepatic tumor burden remained substantial, to which the animals eventually succumbed. Combining a clinically-relevant inhibitor of CDA (tetrahydrouridine) with a lower dose of decitabine (subcutaneous 0.1mg/kg 2X/week) markedly decreased liver tumor burden without blood count or bone marrow evidence of myelotoxicity, and with further improvement in survival. In conclusion, sanctuary in a CDA-rich organ is a mechanism by which otherwise susceptible cancer cells can resist the effects of decitabine epigenetic therapy. This protection can be reversed without increasing myelotoxicity by combining tetrahydrouridine with a lower dose of decitabine.


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