Efficacy of irreversible electroporation in human pancreatic adenocarcinoma: advanced murine model

Irreversible electroporation (IRE) is a promising cell membrane ablative modality for pancreatic cancer. There have been recent concerns regarding local recurrence and the potential use of IRE as a debulking (partial ablation) modality. We hypothesize that incomplete ablation leads to early recurren...

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Main Authors: Prejesh Philips, Yan Li, Suping Li, Charles R St Hill, Robert CG Martin
Format: Article
Language:English
Published: Elsevier 2015-01-01
Series:Molecular Therapy: Methods & Clinical Development
Online Access:http://www.sciencedirect.com/science/article/pii/S2329050116300134
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spelling doaj-5d8538aea2b84034b5aeff79d2e761d62020-11-25T01:23:28ZengElsevierMolecular Therapy: Methods & Clinical Development2329-05012015-01-012Efficacy of irreversible electroporation in human pancreatic adenocarcinoma: advanced murine modelPrejesh Philips0Yan Li1Suping Li2Charles R St Hill3Robert CG Martin4Division of Surgical Oncology, Department of Surgery, University of Louisville, Louisville, Kentucky, USADivision of Surgical Oncology, Department of Surgery, University of Louisville, Louisville, Kentucky, USADivision of Surgical Oncology, Department of Surgery, University of Louisville, Louisville, Kentucky, USADivision of Surgical Oncology, Department of Surgery, University of Louisville, Louisville, Kentucky, USADivision of Surgical Oncology, Department of Surgery, University of Louisville, Louisville, Kentucky, USAIrreversible electroporation (IRE) is a promising cell membrane ablative modality for pancreatic cancer. There have been recent concerns regarding local recurrence and the potential use of IRE as a debulking (partial ablation) modality. We hypothesize that incomplete ablation leads to early recurrence and a more aggressive biology. We created the first ever heterotopic murine model by inoculating BALB/c nude mice in the hindlimb with a subcutaneous injection of Panc-1 cells, an immortalized human pancreatic adenocarcinoma cell line. Tumors were allowed to grow from 0.75 to 1.5 cm and then treated with the goal of complete ablation or partial ablation using standard IRE settings. Animals were recovered and survived for 2 days (n = 6), 7 (n = 6), 14 (n = 6), 21 (n = 6), 30 (n = 8), and 60 (n = 8) days. All 40 animals/tumors underwent successful IRE under general anesthesia with muscle paralysis. The mean tumor volume of the animals undergoing ablation was 1,447.6 mm3 ± 884). Histologically, in the 14-, 21-, 30-, and 60-day survival groups the entire tumor was nonviable, with a persistent tumor nodule completely replaced fibrosis. In the group treated with partial ablation, incomplete electroporation/recurrences (N = 10 animals) were seen, of which 66% had confluent tumors and this was a significant predictor of recurrence (P < 0.001). Recurrent tumors were also significantly larger (mean 4,578 mm3 ± SD 877 versus completed electroporated tumors 925.8 ± 277, P < 0.001). Recurrent tumors had a steeper growth curve (slope = 0.73) compared with primary tumors (0.60, P = 0.02). Recurrent tumors also had a significantly higher percentage of EpCAM expression, suggestive of stem cell activation. Tumors that recur after incomplete electroporation demonstrate a biologically aggressive tumor that could be more resistant to standard of care chemotherapy. Clinical correlation of this data is limited, but should be considered when IRE of pancreatic cancer is being considered.http://www.sciencedirect.com/science/article/pii/S2329050116300134
collection DOAJ
language English
format Article
sources DOAJ
author Prejesh Philips
Yan Li
Suping Li
Charles R St Hill
Robert CG Martin
spellingShingle Prejesh Philips
Yan Li
Suping Li
Charles R St Hill
Robert CG Martin
Efficacy of irreversible electroporation in human pancreatic adenocarcinoma: advanced murine model
Molecular Therapy: Methods & Clinical Development
author_facet Prejesh Philips
Yan Li
Suping Li
Charles R St Hill
Robert CG Martin
author_sort Prejesh Philips
title Efficacy of irreversible electroporation in human pancreatic adenocarcinoma: advanced murine model
title_short Efficacy of irreversible electroporation in human pancreatic adenocarcinoma: advanced murine model
title_full Efficacy of irreversible electroporation in human pancreatic adenocarcinoma: advanced murine model
title_fullStr Efficacy of irreversible electroporation in human pancreatic adenocarcinoma: advanced murine model
title_full_unstemmed Efficacy of irreversible electroporation in human pancreatic adenocarcinoma: advanced murine model
title_sort efficacy of irreversible electroporation in human pancreatic adenocarcinoma: advanced murine model
publisher Elsevier
series Molecular Therapy: Methods & Clinical Development
issn 2329-0501
publishDate 2015-01-01
description Irreversible electroporation (IRE) is a promising cell membrane ablative modality for pancreatic cancer. There have been recent concerns regarding local recurrence and the potential use of IRE as a debulking (partial ablation) modality. We hypothesize that incomplete ablation leads to early recurrence and a more aggressive biology. We created the first ever heterotopic murine model by inoculating BALB/c nude mice in the hindlimb with a subcutaneous injection of Panc-1 cells, an immortalized human pancreatic adenocarcinoma cell line. Tumors were allowed to grow from 0.75 to 1.5 cm and then treated with the goal of complete ablation or partial ablation using standard IRE settings. Animals were recovered and survived for 2 days (n = 6), 7 (n = 6), 14 (n = 6), 21 (n = 6), 30 (n = 8), and 60 (n = 8) days. All 40 animals/tumors underwent successful IRE under general anesthesia with muscle paralysis. The mean tumor volume of the animals undergoing ablation was 1,447.6 mm3 ± 884). Histologically, in the 14-, 21-, 30-, and 60-day survival groups the entire tumor was nonviable, with a persistent tumor nodule completely replaced fibrosis. In the group treated with partial ablation, incomplete electroporation/recurrences (N = 10 animals) were seen, of which 66% had confluent tumors and this was a significant predictor of recurrence (P < 0.001). Recurrent tumors were also significantly larger (mean 4,578 mm3 ± SD 877 versus completed electroporated tumors 925.8 ± 277, P < 0.001). Recurrent tumors had a steeper growth curve (slope = 0.73) compared with primary tumors (0.60, P = 0.02). Recurrent tumors also had a significantly higher percentage of EpCAM expression, suggestive of stem cell activation. Tumors that recur after incomplete electroporation demonstrate a biologically aggressive tumor that could be more resistant to standard of care chemotherapy. Clinical correlation of this data is limited, but should be considered when IRE of pancreatic cancer is being considered.
url http://www.sciencedirect.com/science/article/pii/S2329050116300134
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