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Rapid in-vitro testing for chemotherapy sensitivity in leukaemia patients

Anderson, Elizabeth; Salisbury, Vyv

Authors

Vyv Salisbury



Contributors

T Scheper
Editor

A Belkin
Editor

PM Doran
Editor

I Endo
Editor

MB Gu
Editor

WS Hu
Editor

B Mattiasson
Editor

J Nielsen
Editor

GN Stephanopoulos
Editor

R Ulber
Editor

A-P Zeng
Editor

J-J Zhong
Editor

W Zhou
Editor

S Harald
Editor

Abstract

© Springer-Verlag Berlin Heidelberg 2014. Bioluminescent bacterial biosensors can be used in a rapid in vitro assay to predict sensitivity to commonly used chemotherapy drugs in acute myeloid leukemia (AML). The nucleoside analog cytarabine (ara-C) is the key agent for treating AML; however, up to 30% of patients fail to respond to treatment. Screening of patient blood samples to determine drug response before commencement of treatment is needed. To achieve this aim, a self-bioluminescent reporter strain of Escherichia coli has been constructed and evaluated for use as an ara-C biosensor and an in vitro assay has been designed to predict ara-C response in clinical samples. Transposition mutagenesis was used to create a cytidine deaminase (cdd)-deficient mutant of E. coli MG1655 that responded to ara-C. The strain was transformed with the luxCDABE operon and used as a whole-cell biosensor for development an 8-h assay to determine ara-C uptake and phosphorylation by leukemic cells. Intracellular concentrations of 0.025 lmol/L phosphorylated ara-C were detected by significantly increased light output (P\0.05) from the bacterial biosensor. Results using AML cell lines with known response to ara-C showed close correlation between the 8-h assay and a 3-day cytotoxicity test for ara-C cell killing. In retrospective tests with 24 clinical samples of bone marrow or peripheral blood, the biosensor-based assay predicted leukemic cell response to ara-C within 8 h. The biosensor-based assay may offer a predictor for evaluating the sensitivity of leukemic cells to ara-C before patients undergo chemotherapy and allow customized treatment of drug-sensitive patients with reduced ara-C dose levels. The 8-h assay monitors intracellular ara-CTP (cytosine arabinoside triphosphate) levels and, if fully validated, may be suitable for use in clinical settings.

Citation

Anderson, E., & Salisbury, V. (2014). Rapid in-vitro testing for chemotherapy sensitivity in leukaemia patients. Advances in Biochemical Engineering Biotechnology, 145, 189-214. https://doi.org/10.1007/978-3-662-43619-6_6

Journal Article Type Article
Publication Date Jan 1, 2014
Journal Advances in Biochemical Engineering/Biotechnology
Print ISSN 0724-6145
Publisher Springer Verlag
Peer Reviewed Not Peer Reviewed
Volume 145
Pages 189-214
Series Title Advances in Biochemical Engineering/Biotechnology
Book Title Bioluminescence: Fundamentals and Applications in Biotechnology - Volume 2
ISBN 0724-6145
DOI https://doi.org/10.1007/978-3-662-43619-6_6
Keywords in-vitro testing, chemotherapy, leukaemia
Public URL https://uwe-repository.worktribe.com/output/822778
Publisher URL http://dx.doi.org/10.1007/978-3-662-43619-6_6
Related Public URLs http://link.springer.com/book/10.1007/978-3-662-43619-6