Real‐time monitoring of circulating tumor cell release during tumor manipulation using in vivo photoacoustic and fluorescent flow cytometry

Author:

Juratli Mazen A.12,Sarimollaoglu Mustafa1,Siegel Eric R.3,Nedosekin Dmitry A.1,Galanzha Ekaterina I.14,Suen James Y.4,Zharov Vladimir P.14

Affiliation:

1. Phillips Classic Laser and Nanomedicine Laboratories at the Arkansas Nanomedicine Center University of Arkansas for Medical Sciences Little Rock Arkansas

2. Department of Otolaryngology – Head and Neck Surgery Philipps University of Marburg Marburg Germany

3. Department of Biostatistics University of Arkansas for Medical Sciences Little Rock Arkansas

4. Department of Otolaryngology – Head and Neck Surgery University of Arkansas for Medical Sciences Little Rock Arkansas

Abstract

AbstractBackgroundCirculating tumor cells (CTCs) form metastases in distant organs. The purpose of this research was to determine if tumor manipulation could enhance cancer cell release from the primary tumor into the circulatory system.MethodsNude mice were inoculated with melanoma or breast cancer cells. The implanted tumor underwent compression, biopsy, complete resection, or laser treatment. CTCs were monitored in the bloodstream using in vivo photoacoustic and fluorescence flow cytometry.ResultsWe discovered that pressure, biopsy, and laser treatment can dramatically increase CTC counts (up to 60‐fold), whereas proper tumor resection significantly decrease CTC counts.ConclusionStandard medical procedures could trigger CTC release that may increase the risk of metastases. This finding suggests the guidance of cancer treatment and likely diagnosis by real‐time monitoring of CTC dynamics followed by well‐timed treatment to reduce CTCs in the blood. In vivo detection of intervention‐amplified CTCs could be used for early diagnosis of a small tumor, which is undetectable with conventional methods. © 2013 Wiley Periodicals, Inc. Head Neck 36: 1207–1215, 2014

Publisher

Wiley

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