Issue 6, 2014

A microfluidic platform for chemoresistive testing of multicellular pleural cancer spheroids

Abstract

This study reports on a microfluidic platform on which single multicellular spheroids from malignant pleural mesothelioma (MPM), an aggressive tumor with poor prognosis, can be loaded, trapped and tested for chemotherapeutic drug response. A new method to detect the spheroid viability cultured on the microfluidic chip as a function of the drug concentration is presented. This approach is based on the evaluation of the caspase activity in the supernatant sampled from the chip and tested using a microplate reader. This simple and time-saving method does only require a minimum amount of manipulations and was established for very low numbers of cells. This feature is particularly important in view of personalised medicine applications for which the number of cells obtained from the patients is low. MPM spheroids were continuously perfused for 48 hours with cisplatin, one of the standard chemotherapeutic drugs used to treat MPM. The 50% growth inhibitory concentration of cisplatin in perfused MPM spheroids was found to be twice as high as in spheroids cultured under static conditions. This chemoresistance increase might be due to the continuous support of nutrients and oxygen to the perfused spheroids.

Graphical abstract: A microfluidic platform for chemoresistive testing of multicellular pleural cancer spheroids

Supplementary files

Article information

Article type
Paper
Submitted
25 Sep 2013
Accepted
25 Dec 2013
First published
06 Jan 2014
This article is Open Access
Creative Commons BY license

Lab Chip, 2014,14, 1198-1205

Author version available

A microfluidic platform for chemoresistive testing of multicellular pleural cancer spheroids

J. Ruppen, L. Cortes-Dericks, E. Marconi, G. Karoubi, R. A. Schmid, R. Peng, T. M. Marti and O. T. Guenat, Lab Chip, 2014, 14, 1198 DOI: 10.1039/C3LC51093J

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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