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Prognostic importance of CDK4/6-specific activity as a predictive marker for recurrence in patients with endometrial cancer, with or without adjuvant chemotherapy
BACKGROUND: Pathologically low-risk endometrial cancer patients do not receive postoperative treatment; however, 10–15% of these patients show recurrence with poor prognosis. We evaluated the clinical importance of cyclin-dependent kinase 4/6 (CDK4/6) activity, and its significance as a novel biomar...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815892/ https://www.ncbi.nlm.nih.gov/pubmed/26554657 http://dx.doi.org/10.1038/bjc.2015.369 |
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author | Ikeda, Yuji Oda, Katsutoshi Ishihara, Hideki Wada-Hiraike, Osamu Miyasaka, Aki Kashiyama, Tomoko Inaba, Kanako Fukuda, Tomohiko Sone, Kenbun Matsumoto, Yoko Arimoto, Takahide Maeda, Daichi Ikemura, Masako Fukayama, Masahi Kawana, Kei Yano, Tetsu Aoki, Daisuke Osuga, Yutaka Fujii, Tomoyuki |
author_facet | Ikeda, Yuji Oda, Katsutoshi Ishihara, Hideki Wada-Hiraike, Osamu Miyasaka, Aki Kashiyama, Tomoko Inaba, Kanako Fukuda, Tomohiko Sone, Kenbun Matsumoto, Yoko Arimoto, Takahide Maeda, Daichi Ikemura, Masako Fukayama, Masahi Kawana, Kei Yano, Tetsu Aoki, Daisuke Osuga, Yutaka Fujii, Tomoyuki |
author_sort | Ikeda, Yuji |
collection | PubMed |
description | BACKGROUND: Pathologically low-risk endometrial cancer patients do not receive postoperative treatment; however, 10–15% of these patients show recurrence with poor prognosis. We evaluated the clinical importance of cyclin-dependent kinase 4/6 (CDK4/6) activity, and its significance as a novel biomarker for the prognosis and chemo-sensitivity of endometrioid endometrial carcinoma (EEC). METHODS: Cyclin-dependent kinase 4/6 expression and enzyme activity in 109 tumour samples from patients with EEC were examined with a cell-cycle profiling (C2P) assay. CDK4/6-specific activity (CDK4/6SA) was determined, and its relationship with clinicopathological factors and expression of Ki-67 was analysed. RESULTS: CDK4/6-specific activity was significantly correlated with Ki-67 (P=0.035), but not with any other clinicopathological characteristics. CDK4/6SA was significantly higher (P=0.002) in pathologically low-risk patients (not receiving adjuvant chemotherapy, n=74) than in intermediate- or high-risk patients (receiving adjuvant chemotherapy, n=35). In addition, patients with high CDK4/6SA (>3.0) showed significantly (P=0.024) shorter progression-free survival (PFS) than those with low CDK4/6SA (<3.0). Although Ki-67 expression itself was not a marker for prognosis, the combination of high CDK4/6SA and high Ki-67 expression (>15%) was robustly associated with shorter PFS (P=0.015), and this combination was an independent poor prognostic factor in the low-risk group. Inversely, in the intermediate-/high-risk group, patients with high CDK4/6SA had a tendency of a more favourable prognosis compared with patients with low CDK4/6SA (P=0.063). CONCLUSIONS: CDK4/6-specific activity can be used as a biomarker to predict prognosis and, possibly, chemo-sensitivity. The combination of Ki-67 expression might strengthen the clinical usefulness of CDK4/6SA as a biomarker. |
format | Online Article Text |
id | pubmed-4815892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48158922016-11-17 Prognostic importance of CDK4/6-specific activity as a predictive marker for recurrence in patients with endometrial cancer, with or without adjuvant chemotherapy Ikeda, Yuji Oda, Katsutoshi Ishihara, Hideki Wada-Hiraike, Osamu Miyasaka, Aki Kashiyama, Tomoko Inaba, Kanako Fukuda, Tomohiko Sone, Kenbun Matsumoto, Yoko Arimoto, Takahide Maeda, Daichi Ikemura, Masako Fukayama, Masahi Kawana, Kei Yano, Tetsu Aoki, Daisuke Osuga, Yutaka Fujii, Tomoyuki Br J Cancer Molecular Diagnostics BACKGROUND: Pathologically low-risk endometrial cancer patients do not receive postoperative treatment; however, 10–15% of these patients show recurrence with poor prognosis. We evaluated the clinical importance of cyclin-dependent kinase 4/6 (CDK4/6) activity, and its significance as a novel biomarker for the prognosis and chemo-sensitivity of endometrioid endometrial carcinoma (EEC). METHODS: Cyclin-dependent kinase 4/6 expression and enzyme activity in 109 tumour samples from patients with EEC were examined with a cell-cycle profiling (C2P) assay. CDK4/6-specific activity (CDK4/6SA) was determined, and its relationship with clinicopathological factors and expression of Ki-67 was analysed. RESULTS: CDK4/6-specific activity was significantly correlated with Ki-67 (P=0.035), but not with any other clinicopathological characteristics. CDK4/6SA was significantly higher (P=0.002) in pathologically low-risk patients (not receiving adjuvant chemotherapy, n=74) than in intermediate- or high-risk patients (receiving adjuvant chemotherapy, n=35). In addition, patients with high CDK4/6SA (>3.0) showed significantly (P=0.024) shorter progression-free survival (PFS) than those with low CDK4/6SA (<3.0). Although Ki-67 expression itself was not a marker for prognosis, the combination of high CDK4/6SA and high Ki-67 expression (>15%) was robustly associated with shorter PFS (P=0.015), and this combination was an independent poor prognostic factor in the low-risk group. Inversely, in the intermediate-/high-risk group, patients with high CDK4/6SA had a tendency of a more favourable prognosis compared with patients with low CDK4/6SA (P=0.063). CONCLUSIONS: CDK4/6-specific activity can be used as a biomarker to predict prognosis and, possibly, chemo-sensitivity. The combination of Ki-67 expression might strengthen the clinical usefulness of CDK4/6SA as a biomarker. Nature Publishing Group 2015-11-17 2015-11-10 /pmc/articles/PMC4815892/ /pubmed/26554657 http://dx.doi.org/10.1038/bjc.2015.369 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Molecular Diagnostics Ikeda, Yuji Oda, Katsutoshi Ishihara, Hideki Wada-Hiraike, Osamu Miyasaka, Aki Kashiyama, Tomoko Inaba, Kanako Fukuda, Tomohiko Sone, Kenbun Matsumoto, Yoko Arimoto, Takahide Maeda, Daichi Ikemura, Masako Fukayama, Masahi Kawana, Kei Yano, Tetsu Aoki, Daisuke Osuga, Yutaka Fujii, Tomoyuki Prognostic importance of CDK4/6-specific activity as a predictive marker for recurrence in patients with endometrial cancer, with or without adjuvant chemotherapy |
title | Prognostic importance of CDK4/6-specific activity as a predictive marker for recurrence in patients with endometrial cancer, with or without adjuvant chemotherapy |
title_full | Prognostic importance of CDK4/6-specific activity as a predictive marker for recurrence in patients with endometrial cancer, with or without adjuvant chemotherapy |
title_fullStr | Prognostic importance of CDK4/6-specific activity as a predictive marker for recurrence in patients with endometrial cancer, with or without adjuvant chemotherapy |
title_full_unstemmed | Prognostic importance of CDK4/6-specific activity as a predictive marker for recurrence in patients with endometrial cancer, with or without adjuvant chemotherapy |
title_short | Prognostic importance of CDK4/6-specific activity as a predictive marker for recurrence in patients with endometrial cancer, with or without adjuvant chemotherapy |
title_sort | prognostic importance of cdk4/6-specific activity as a predictive marker for recurrence in patients with endometrial cancer, with or without adjuvant chemotherapy |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815892/ https://www.ncbi.nlm.nih.gov/pubmed/26554657 http://dx.doi.org/10.1038/bjc.2015.369 |
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