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Cyclin-dependent kinase 15 upregulation is correlated with poor prognosis for patients with breast cancer
OBJECTIVE: To investigate the clinical significance of cyclin-dependent kinase (CDK) 15 in breast cancer. METHODS: This prospective observational study enrolled 154 patients with breast cancer. Tumor tissues and paired paracancerous normal tissues were collected. Additionally, 85 samples of benign b...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236788/ https://www.ncbi.nlm.nih.gov/pubmed/34162268 http://dx.doi.org/10.1177/0300060521999552 |
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author | Zhang, Xiquan Wang, Qin Luo, Yijun Song, Meijiao Zhou, Zhiyong Zeng, Lin Hu, Meng Yang, Chuyan |
author_facet | Zhang, Xiquan Wang, Qin Luo, Yijun Song, Meijiao Zhou, Zhiyong Zeng, Lin Hu, Meng Yang, Chuyan |
author_sort | Zhang, Xiquan |
collection | PubMed |
description | OBJECTIVE: To investigate the clinical significance of cyclin-dependent kinase (CDK) 15 in breast cancer. METHODS: This prospective observational study enrolled 154 patients with breast cancer. Tumor tissues and paired paracancerous normal tissues were collected. Additionally, 85 samples of benign breast lesions were obtained from patients with mammary gland hyperplasia. Patient characteristics were recorded, and CDK15, human epidermal growth factor receptor (HER)2, estrogen receptor, progesterone receptor, and Ki67 immunohistochemical expression were determined. RESULTS: The rate of strong CDK15 expression was 63.6% (98/154) in breast cancer tissues, which was remarkably higher than that in benign breast lesions (34.1%, 29/85). Similarly, the ratio of strong CDK15 expression was markedly higher in tumor tissues (63.6%, 98/15) than in paracancerous normal tissues (27.3%, 42/154). Pearson’s analysis showed that the CDK15 expression score was positively correlated with HER2 and Ki67. Patients with high CDK15 expression showed markedly higher ratios of TNM stage III to IV, lymph node metastasis, and increased tumor diameters but a significantly lower rate of ductal carcinoma in situ. The median survival time of these patients was significantly shorter. Kaplan–Meier curve analysis showed that low CDK15 expression predicted longer survival times. CONCLUSION: Upregulated CDK15 predicted poor clinical outcomes in breast cancer. |
format | Online Article Text |
id | pubmed-8236788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-82367882021-07-08 Cyclin-dependent kinase 15 upregulation is correlated with poor prognosis for patients with breast cancer Zhang, Xiquan Wang, Qin Luo, Yijun Song, Meijiao Zhou, Zhiyong Zeng, Lin Hu, Meng Yang, Chuyan J Int Med Res Prospective Clinical Research Report OBJECTIVE: To investigate the clinical significance of cyclin-dependent kinase (CDK) 15 in breast cancer. METHODS: This prospective observational study enrolled 154 patients with breast cancer. Tumor tissues and paired paracancerous normal tissues were collected. Additionally, 85 samples of benign breast lesions were obtained from patients with mammary gland hyperplasia. Patient characteristics were recorded, and CDK15, human epidermal growth factor receptor (HER)2, estrogen receptor, progesterone receptor, and Ki67 immunohistochemical expression were determined. RESULTS: The rate of strong CDK15 expression was 63.6% (98/154) in breast cancer tissues, which was remarkably higher than that in benign breast lesions (34.1%, 29/85). Similarly, the ratio of strong CDK15 expression was markedly higher in tumor tissues (63.6%, 98/15) than in paracancerous normal tissues (27.3%, 42/154). Pearson’s analysis showed that the CDK15 expression score was positively correlated with HER2 and Ki67. Patients with high CDK15 expression showed markedly higher ratios of TNM stage III to IV, lymph node metastasis, and increased tumor diameters but a significantly lower rate of ductal carcinoma in situ. The median survival time of these patients was significantly shorter. Kaplan–Meier curve analysis showed that low CDK15 expression predicted longer survival times. CONCLUSION: Upregulated CDK15 predicted poor clinical outcomes in breast cancer. SAGE Publications 2021-06-24 /pmc/articles/PMC8236788/ /pubmed/34162268 http://dx.doi.org/10.1177/0300060521999552 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Prospective Clinical Research Report Zhang, Xiquan Wang, Qin Luo, Yijun Song, Meijiao Zhou, Zhiyong Zeng, Lin Hu, Meng Yang, Chuyan Cyclin-dependent kinase 15 upregulation is correlated with poor prognosis for patients with breast cancer |
title | Cyclin-dependent kinase 15 upregulation is correlated with poor prognosis for patients with breast cancer |
title_full | Cyclin-dependent kinase 15 upregulation is correlated with poor prognosis for patients with breast cancer |
title_fullStr | Cyclin-dependent kinase 15 upregulation is correlated with poor prognosis for patients with breast cancer |
title_full_unstemmed | Cyclin-dependent kinase 15 upregulation is correlated with poor prognosis for patients with breast cancer |
title_short | Cyclin-dependent kinase 15 upregulation is correlated with poor prognosis for patients with breast cancer |
title_sort | cyclin-dependent kinase 15 upregulation is correlated with poor prognosis for patients with breast cancer |
topic | Prospective Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236788/ https://www.ncbi.nlm.nih.gov/pubmed/34162268 http://dx.doi.org/10.1177/0300060521999552 |
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