5FU resistance caused by reduced fluoro-deoxyuridine monophosphate and its reversal using deoxyuridine

The mechanism of 5-fluorouracil (5FU) resistance was investigated, focusing on the level of thymidylate synthase (TS) ternary complex formed with fluoro-deoxyuridine monophosphate (FdUMP). MKN45 and 5FU-resistant MKN45/F2R cells were treated with 5FU and fluoro-deoxyuridine (FdU) in combination with...

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Bibliographic Details
Published in:Oncology letters 2017-09, Vol.14 (3), p.3162-3168
Main Authors: Mori, Ryutaro, Futamura, Manabu, Tanahashi, Toshiyuki, Tanaka, Yoshihiro, Matsuhashi, Nobuhisha, Yamaguchi, Kazuya, Yoshida, Kazuhiro
Format: Article
Language:English
Subjects:
5FU
Cancer therapies
Cytotoxicity
Deoxyribonucleic acid
DNA
Drug resistance
Drug therapy
fluorodeoxyuridylate
Fluorouracil
Gastric cancer
Genetic aspects
Health aspects
Immunoglobulins
Investigations
Oncology
Patient outcomes
Phosphatase
Proteins
stomach neoplasms
Transferases
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Summary:The mechanism of 5-fluorouracil (5FU) resistance was investigated, focusing on the level of thymidylate synthase (TS) ternary complex formed with fluoro-deoxyuridine monophosphate (FdUMP). MKN45 and 5FU-resistant MKN45/F2R cells were treated with 5FU and fluoro-deoxyuridine (FdU) in combination with deoxyuridine (dU) and thymidine (dT). Subsequently, the levels of ternary complex were determined by western blotting and the cell viability was calculated using an MTT assay. MKN45/F2R cells exhibited 5FU resistance (56.2-fold relative to MKN45 cells), and demonstrated decreased orotate phosphoribosyltransferase (OPRT) and increased TS levels, requiring a higher concentration of 5FU to induce ternary complex formation than MKN45 cells. Following transfection of small interfering RNA against OPRT, MKN45 exhibited increased resistance to 5FU and decreased ternary complex formation subsequent to treatment with 5FU, indicating that decreased OPRT led to increased 5FU resistance. However, MKN45/F2R also exhibited resistance to FdU, which can be converted to FdUMP without OPRT, and there was decreased ternary complex formation after treatment with FdU, indicating that the 5FU-resistant cells had the ability to decrease intracellular FdUMP. The addition of dU and thymidine dT to 5FU promoted the formation of ternary complexes and reversed 5FU resistance in MKN45/F2R cells, although dT inhibited the efficacy of raltitrexed (another TS inhibitor). These results suggested that 5FU-resistant cells had the ability to reduce intracellular FdUMP irrespective of decreased OPRT, which led to resistance to 5FU. This resistance was then inhibited by treatment with dT or dU.
ISSN:1792-1074
1792-1082
DOI:10.3892/ol.2017.6512