alexa Cytotoxicity of Hypo-osmolar Lavage Fluid on Ovarian Cancer Cells In vitro | OMICS International
ISSN: 2472-4971

Journal of Medical & Surgical Pathology
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Research Article

Cytotoxicity of Hypo-osmolar Lavage Fluid on Ovarian Cancer Cells In vitro

Elena M Paulus1, Joseph T Santoso2, Michelle M Sims3, Jashmin K Patel4 and Lawrence M Pfeffer3*

1Department of Surgery, The University of Tennessee Health Science Center, USA

2Division of Gynecologic Oncology, The West Clinic, The University of nTennessee Health Science Center, USA

3Center for Cancer Research, Department of Pathology, The University of Tennessee Health Science Center, USA

4Department of Hematology and Oncology, The West Clinic, The University of Tennessee Health Science Center, USA

*Corresponding Author:
Lawrence M Pfeffer
Department of Pathology and Laboratory Medicine
University of Tennessee Health Science Center, USA
Tel: 901-448-7855
E-mail: [email protected]

Received Date: November 20, 2015; Accepted Date: January 22, 2016; Published Date: January 26, 2016

Citation: Paulus EM, Santoso JT, Sims MM, Patel JK, Pfeffer LM (2016) Cytotoxicity of Hypo-osmolar Lavage Fluid on Ovarian Cancer Cells In vitro. J Med Surg Pathol 1:105.doi: 10.4172/jmsp.1000105

Copyright: © 2016 Paulus EM, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Objective: Ovarian cancer is difficult to diagnose early and many patients present with advanced disease. The presence of exfoliated ovarian cancer cells in the peritoneal cavity after debulking surgery is a poor prognostic indicator. Sterilization of the peritoneum during surgery may have clinical benefit in reducing tumor burden. Several studies have evaluated osmotic cytotoxicity in gastrointestinal and genitourinary cancers with varied results. We studied the cytotoxic effect of lavage fluids of differing osmolarities against multiple ovarian cancer cell lines (SKOV3, OV90, and OVCAR3) in vitro. Methods: Cells were treated for either 10 minutes or 30 minutes with water, or 5 mOsm, 10 mOsm, 50 mOsm, 100 mOsm, 200 mOsm, 280 mOsm NaCl (dilutions in water), and PBS. After 24 hours, surviving cells were enumerated in a Coulter Counter. Results: All 3 ovarian cancer cell lines were lysed progressively as lavage osmolarity was reduced (p<0.01). For the OVCAR3 ovarian cancer cells, lavage for 30 min resulted in greater cell cytotoxicity for lavage with the water, 5, 10, 50, and 200 mOsm saline when compared to lavage for 10 min. For the OV90 cancer cell line, lavage for 30 min resulted in greater cell cytotoxicity for the water, 5, and 10 mOsm saline lavages. In the SKOV3 ovarian cancer cell line, only lavage for the 30 min water had cytotoxicity. Conclusions: Since ovarian cancer uniquely resides in the peritoneal cavity, this anatomic feature allows concentrated washing to directly target these cancer cells residing in the peritoneal cavity. Hypo-osmolar treatment was found to be most effective in lysing ovarian cancer cell lines in vitro.

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