Oncotarget

Clinical Research Papers:

Drag reducing polymers decrease hepatic injury and metastases after liver ischemia-reperfusion

Samer Tohme _, Marina V. Kameneva, Hamza O. Yazdani, Vikas Sud, Julie Goswami, Patricia Loughran, Hai Huang, Richard L. Simmons and Allan Tsung

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Oncotarget. 2017; 8:59854-59866. https://doi.org/10.18632/oncotarget.18322

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Abstract

Samer Tohme1,*, Marina V. Kameneva1,2,3,*, Hamza O. Yazdani1, Vikas Sud1, Julie Goswami1, Patricia Loughran1,4, Hai Huang1, Richard L. Simmons1 and Allan Tsung1

1 Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, USA

2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA, USA

3 Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA

4 Center for Biologic Imaging, Department of Cell Biology, University of Pittsburgh, PA, USA

* These authors have contributed equally to this work

Correspondence to:

Samer Tohme, email:

Keywords: liver, Ischemia reperfusion injury, drag reducing polymers, liver metastasis, metastatic colorectal cancer

Received: January 09, 2017 Accepted: March 10, 2017 Published: May 31, 2017

Abstract

Introduction: Surgery, a crucial therapeutic modality in the treatment of solid tumors, can induce sterile inflammatory processes which can result in metastatic progression. Liver ischemia and reperfusion (I/R) injury, an inevitable consequence of hepatic resection of metastases, has been shown to foster hepatic capture of circulating cancer cells and accelerate metastatic growth. Efforts to reduce these negative consequences have not been thoroughly investigated. Drag reducing polymers (DRPs) are blood-soluble macromolecules that can, in nanomolar concentrations, increase tissue perfusion, decrease vascular resistance and decrease near-wall microvascular concentration of neutrophils and platelets thereby possibly reducing the inflammatory microenvironment. We hypothesize that DRP can potentially be used to ameliorate metastatic capture of tumor cells and tumor growth within the I/R liver.

Methods: Experiments were performed utilizing a segmental ischemia model of mice livers. Five days prior or immediately prior to ischemia, murine colon adenocarcinoma cells (MC38) were injected into the spleen. DRP (polyethylene oxide) or a control of low-molecular-weight polyethylene glycol without drag reducing properties were administered intraperitoneally at the onset of reperfusion.

Results: After three weeks from I/R, we observed that liver I/R resulted in an increased ability to capture and foster growth of circulating tumor cells; in addition, the growth of pre-existing micrometastases was accelerated three weeks later. These effects were significantly curtailed when mice were treated with DRPs at the time of I/R. Mechanistic investigations in vivo indicated that DRPs protected the livers from I/R injury as evidenced by significant decreases in hepatocellular damage, neutrophil recruitment into the liver, formation of neutrophil extracellular traps, deposition of platelets, formation of microthrombi within the liver sinusoids and release of inflammatory cytokines.

Conclusions: DRPs significantly attenuated metastatic tumor development and growth. DRPs warrant further investigation as a potential treatment for liver I/R injury in the clinical setting to improve cancer-specific outcomes.


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