Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/20967
Title: Interference by anti-cancer chemotherapeutic agents in the MTT-tumor chemosensitivity assay
Authors: Wood, E.J.
Bursa Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyokimya Anabilim Dalı.
Ulukaya, Engin
Çolakoğulları, Mukaddes
K-5792-2018
Keywords: MTT assay
Tumor chemosensitivity assay
Anticancer drugs
Interference
Chronic lymphocytic-leukemia
Recurrent ovarian-cancer
Cell-lines
In-vitro
Luminescence assay
Tetrazolium assay
Invitro assay
Vivo
Cytotoxicity
Sensitivity
Oncology
Pharmacology & pharmacy
Issue Date: 2004
Publisher: Karger
Citation: Wood, E.J. vd. (2004). “Interference by anti-cancer chemotherapeutic agents in the MTT-tumor chemosensitivity assay”. Chemotherapy, 50(1), 43-50.
Abstract: Background: One of the major goals of oncology is to predict the response of patients with cancer to chemotherapeutic agents by employing laboratory methods variously called 'tumor chemosensitivity assays', 'drug response assays', or 'drug sensitivity assays', in vitro. The MTT assay is one of the methods used to predict the drug response in malignancies. However, it may suffer from interference by the anticancer drugs with the MTT assay. Methods: The MTT assay, a colorimetric viability assay, was checked in a cell-free system in terms of its possible chemical interactions with 22 different anticancer drugs. Results: It was found that epirubicine, paclitaxel, doxetaxel, and cisplatin caused a relatively significant increase in absorbance values, resulting in the MTT assay giving rise to false results (untrue increase in viability) although most of the drugs tested did not seem to cause any significant change. Conclusion: It was concluded that before employing the MTT assay, drugs (or any kind of substances) to be included in the assay should be checked first in terms of possible chemical interactions with MTT, otherwise it may be impossible to evaluate the MTT viability assay results correctly.
URI: https://doi.org/10.1159/000077285
https://www.karger.com/Article/Abstract/77285
http://hdl.handle.net/11452/20967
ISSN: 0009-3157
Appears in Collections:Web of Science

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