Abstract | BACKGROUND: METHODS: PFTK1 expression was initially examined by expression microarray in 77 ESCC patients. Using independent samples of 223 patients, PFTK1 expression was evaluated immunohistochemically to assess the relationship between expression and various clinicopathological parameters. The association between PFTK1 and the response to chemotherapy was also investigated in pretreatment samples of 85 patients who received chemotherapy as first treatment. RESULTS: Significant upregulation of PFTK1 expression was noted in ESCC compared with normal epithelium. PFTK1 expression was positive in 51.6% (115 out of 223) of the tumours, but did not correlate with any clinicopathological parameter. The 5-year overall survival rate was poorer in patients positive for PFTK1 (43.6%) than those with negative expression (66.2%, P<0.001). Uni- and multivariate analyses identified PFTK1 as an independent marker of prognosis (RR=2.428, 95% CI=1.615-3.711, P<0.001). Out of 85 biopsy samples, 40 (47.1%) tumours showed PFTK1-positive expression, and the response rate to chemotherapy was significantly lower than PFTK1-negative tumours (27.9% vs 72.1%, P<0.001). CONCLUSION: PFTK1 is not only useful as a prognostic marker, but also as a predictor of the response to chemotherapy.
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Authors | H Miyagaki, M Yamasaki, H Miyata, T Takahashi, Y Kurokawa, K Nakajima, S Takiguchi, Y Fujiwara, H Ishii, F Tanaka, M Mori, Y Doki |
Journal | British journal of cancer
(Br J Cancer)
Vol. 106
Issue 5
Pg. 947-54
(Feb 28 2012)
ISSN: 1532-1827 [Electronic] England |
PMID | 22333595
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Biomarkers, Tumor
- CDK14 protein, human
- Cyclin-Dependent Kinases
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Biomarkers, Tumor
(metabolism)
- Carcinoma, Squamous Cell
(drug therapy, metabolism, mortality, pathology)
- Cyclin-Dependent Kinases
(genetics, metabolism)
- Esophageal Neoplasms
(drug therapy, metabolism, mortality, pathology)
- Female
- Follow-Up Studies
- Gene Expression Regulation, Neoplastic
- Humans
- Male
- Middle Aged
- Survival Rate
- Treatment Outcome
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