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Differential activation of cell death and autophagy results in an increased cytotoxic potential for trifluorothymidine compared to 5‐fluorouracil in colon cancer cells
Author(s) -
Bijnsdorp Irene V.,
Peters Godefridus J.,
Temmink Olaf H.,
Fukushima Masakazu,
Kruyt Frank A.
Publication year - 2010
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.24943
Subject(s) - programmed cell death , clonogenic assay , autophagy , apoptosis , caspase , cancer research , biology , microbiology and biotechnology , cell culture , caspase 3 , chemistry , biochemistry , genetics
Abstract Trifluorothymidine (TFT) is part of the oral drug formulation TAS‐102. Both 5‐fluorouracil (5‐FU) and TFT can inhibit thymidylate synthase and be incorporated into DNA. TFT shows only moderate cross‐resistance to 5‐FU. Therefore, we examined whether mechanistic differences in cell death could underlie their different modes of action in colorectal cancer cell lines (WiDR, Lovo92 and Colo320). Drug cytotoxicity was determined by SRB‐ and clonogenic assays, cell death by flow cytometry (PI and annexin V), caspase cleavage by Western blotting and activity assays and in vivo activity in the hollow fiber assay. The IC 50 values of TFT were 1‐6 fold lower than for 5‐FU, and clonogenic survival was less than 0.9% at 3 μM TFT, while 2–20% of the cells still survived after 20 μM 5‐FU. In general, TFT was a more potent inducer of apoptosis than 5‐FU, although the contribution of caspases varied between the used cell lines and necrosis‐like cell death was detected. Accordingly, both drugs induced caspase (Z‐VAD) independent cell death and lysosomal cathepsin B was involved. Activation of autophagy recovery mechanisms was only triggered by 5‐FU, but not by TFT as determined by LC3B expression and cleavage. Inhibition of autophagy by 3‐MA in 5‐FU exposed cells reduced cell survival. Also, in vivo TFT (as TAS‐102) caused more cell death than a 5‐FU formulation. We conclude that TFT and 5‐FU induce cell death via both caspase‐dependent and independent mechanisms. The TFT was more potent than 5‐FU, because it induces higher levels of cell death and does not elicit an autophagic survival response in the cancer cell lines. This provides a strong molecular basis for further application of TFT in cancer therapy.