Abstract |
We have isolated transforming growth factor-beta-stimulated clone-22 (TSC-22) cDNA as an anti- cancer drug-inducible gene in a human salivary gland cancer cell line, TYS. We have previously reported that TSC-22 negatively regulates the growth of TYS cells, and that overexpression of TSC-22 protein in TYS cells enhanced the in vitro chemosensitivity of the cells. In this study, we examined the in vivo chemosensitivity of TSC-22-expressing TYS cells. TSC-22-expressing TYS cells formed tumors in nude mice, but tumors formed by TSC-22-expressing TYS cells were significantly smaller than tumors formed by control cells (p<0.001, one way ANOVA). Furthermore, intraperitoneal injection of 5-fluorouracil (5-FU) markedly inhibited the growth of the TSC-22-expressing TYS tumors, but did not affect the growth of control tumors. It was found by TUNEL assay that TSC-22-expressing TYS tumors were induced to undergo apoptosis by 5-FU treatment. These findings suggest that overexpression of TSC-22 protein in TYS cells enhances the in vivo chemosensitivity of the cells to 5-FU via induction of apoptosis.
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Authors | F Omotehara, D Uchida, S Hino, N M Begum, H Yoshida, M Sato, H Kawamata |
Journal | Oncology reports
(Oncol Rep)
2000 Jul-Aug
Vol. 7
Issue 4
Pg. 737-40
ISSN: 1021-335X [Print] Greece |
PMID | 10854535
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Recombinant Fusion Proteins
- Recombinant Proteins
- Repressor Proteins
- TSC22D1 protein, human
- Tgfb1i4 protein, mouse
- Fluorouracil
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Topics |
- Analysis of Variance
- Animals
- Antineoplastic Agents
(therapeutic use, toxicity)
- Apoptosis
(drug effects)
- Cell Survival
(drug effects)
- Clone Cells
- Fluorouracil
(therapeutic use, toxicity)
- Humans
- Mice
- Mice, Nude
- Recombinant Fusion Proteins
(analysis)
- Recombinant Proteins
(biosynthesis)
- Repressor Proteins
(genetics, physiology)
- Salivary Gland Neoplasms
(drug therapy, pathology)
- Transfection
- Transplantation, Heterologous
- Tumor Cells, Cultured
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