Abstract

Cancer cell lines are important tools for anticancer drug research and assessment. Impedance measurements can provide valuable information about cell viability in real time. This work presents the proof-of-concept development of a bioelectrical, impedance-based analysis technique applied to four adherent mammalian cancer cells lines immobilized in a three-dimensional (3D) calcium alginate hydrogel matrix, thus mimicking in vivo tissue conditions. Cells were treated with cytostatic agent5-fluoruracil (5-FU). The cell lines used in this study were SK-N-SH, HEK293, HeLa, and MCF-7. For each cell culture, three cell population densities were chosen (50,000, 100,000, and 200,000 cells/100 μL). The aim of this study was the extraction of mean impedance values at various frequencies for the assessment of the different behavior of various cancer cells when 5-FU was applied. For comparison purposes, impedance measurements were implemented on untreated immobilized cell lines. The results demonstrated not only the dependence of each cell line impedance value on the frequency, but also the relation of the impedance level to the cell population density for every individual cell line. By establishing a cell line-specific bioelectrical behavior, it is possible to obtain a unique fingerprint for each cancer cell line reaction to a selected anticancer agent.

Highlights

  • Cancer is the main cause of death in many countries, as it appears in different types, most commonly affecting women [1,2]

  • In wewe evaluated the applicability of impedance measurements for the bioelectric profiling

  • The development of cancer diagnostics was primarily controlled by direct tumor tissue biopsies for either pathologic and/or histologic analyses

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Summary

Introduction

Cancer is the main cause of death in many countries, as it appears in different types, most commonly affecting women (e.g., cervical, breast, and lung adenocarcinoma cancers) [1,2]. Doctors take steps to anticipate the development of the disease (primary prophylaxis) or to minimize its further development (secondary prophylaxis) [3]. Considering secondary prophylaxis measures, sophisticated processes are required to detect possible cellular disorders at the very earliest stages of the disease’s incubation period, taking into account the dependence of the timeliness with which the disease is detected [4]. Due to the fact that many cancer diagnostic methods combined with radiological, surgical biopsy, and pathological assessments of tissue samples based on immunohistochemical and morphological characteristics [5] are time-consuming, invasive, and complicated, and require rigorous laboratory conditions, new cancer detection methods are being developed which are minimally invasive, more reliable, cheaper, and easier to use [6].

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