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Daisuke Uchida,
Hitoshi Kawamata, Fumie Omotehara, Yoshihiro Miwa, Satoshi Hino, Nasima-Mila
Begum, Hideo Yoshida, and Mitsunobu Sato
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Second
Department of Oral and Maxillofacial Surgery (DU, HK, FO, SH, NMB, HY, MS)
and Department of Biochemistry (YM), Tokushima University School of Dentistry,
Tokushima, Japan
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SUMMARY:
We have recently isolated TSC-22 (transforming growth factor-b-stimulated
clone-22) cDNA as an anticancer, drug-inducible (with vesnarinone) gene
in a human salivary gland cancer cell line, TYS. We have also reported
that TSC-22 negatively regulates the growth of TYS cells and that down-regulation
of TSC-22 in TYS cells plays a major role in salivary gland tumorigenesis
(Nakashiro et al, 1998). In this study, we transfected TYS cells with
an expression vector encoding the TSC-22-GFP (green fluorescent protein)
fusion protein, and we established TSC-22-GFP-expressing TYS cell clones.
Next, we examined (a) the subcellular localization of the fusion protein,
(b) the sensitivity of the transfectants to several anticancer drugs (5-fluorouracil,
cis-diaminedichloroplatinum, peplomycin), and (c) induction of apoptotic
cell death in the transfectants by 5-fluorouracil treatment. The TSC-22-GFP
fusion protein was clearly localized to the cytoplasm, but not to the
nucleus. Over-expression of the TSC-22-GFP fusion protein did not affect
cell growth, but significantly increased the sensitivity of the cells
to the anticancer drugs (p< 0.01; one-way ANOVA). Furthermore, over-expression
of the TSC-22-GFP fusion protein markedly enhanced 5-fluorouracil-induced
apoptosis. These findings suggest that over-expression of TSC-22-GFP protein
in TYS cells enhances the chemo-sensitivity of the cells via induction
of apoptosis.
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