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Targeting CDK9: A novel biomarker in the treatment of endometrial cancer

Endometrial cancer is one of the three major malignant tumors of the female reproductive system. Although cyclin-dependent kinase 9 (CDK9) has a definitive pathogenic role in various types of cancer, little is known concerning its function in endometrial cancer. Our study was conducted to evaluate t...

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Autores principales: He, Shasha, Fang, Xiaoling, Xia, Xiaomeng, Hou, Tao, Zhang, Tingting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7551504/
https://www.ncbi.nlm.nih.gov/pubmed/32901849
http://dx.doi.org/10.3892/or.2020.7746
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author He, Shasha
Fang, Xiaoling
Xia, Xiaomeng
Hou, Tao
Zhang, Tingting
author_facet He, Shasha
Fang, Xiaoling
Xia, Xiaomeng
Hou, Tao
Zhang, Tingting
author_sort He, Shasha
collection PubMed
description Endometrial cancer is one of the three major malignant tumors of the female reproductive system. Although cyclin-dependent kinase 9 (CDK9) has a definitive pathogenic role in various types of cancer, little is known concerning its function in endometrial cancer. Our study was conducted to evaluate the expression and therapeutic potential of CDK9 in endometrial cancer. CDK9 expression was determined by immunohistochemistry in endometrial cancer tissues constructed with paired primary, metastatic, and recurrent tumor tissues from 32 endometrial cancer patients. Small interfering RNA (siRNA) and inhibitors of CDK9 were used to evaluate the effect of CDK9 inhibition on the anti-apoptotic activity and proliferation in endometrial cancer cells. Colony formation assay and wound-healing assays were adopted to assess clonal formation and migratory capacity. The results of the immunohistochemistry demonstrated that CDK9 was highly expressed in the human endometrial cancer cell lines; moreover, it was elevated in metastatic and recurrent endometrial tumor tissue compared when compared with that in patient-matched primary endometrial tumor tissue. Knockdown of CDK9 with siRNA and inhibition of CDK9 activity with the inhibitor suppressed cell proliferation and promoted apoptosis in endometrial cancer. In conclusion, our results provide evidence that CDK9 may be a potential prognostic biomarker and a promising therapeutic target for the treatment of endometrial cancer in the future.
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spelling pubmed-75515042020-10-14 Targeting CDK9: A novel biomarker in the treatment of endometrial cancer He, Shasha Fang, Xiaoling Xia, Xiaomeng Hou, Tao Zhang, Tingting Oncol Rep Articles Endometrial cancer is one of the three major malignant tumors of the female reproductive system. Although cyclin-dependent kinase 9 (CDK9) has a definitive pathogenic role in various types of cancer, little is known concerning its function in endometrial cancer. Our study was conducted to evaluate the expression and therapeutic potential of CDK9 in endometrial cancer. CDK9 expression was determined by immunohistochemistry in endometrial cancer tissues constructed with paired primary, metastatic, and recurrent tumor tissues from 32 endometrial cancer patients. Small interfering RNA (siRNA) and inhibitors of CDK9 were used to evaluate the effect of CDK9 inhibition on the anti-apoptotic activity and proliferation in endometrial cancer cells. Colony formation assay and wound-healing assays were adopted to assess clonal formation and migratory capacity. The results of the immunohistochemistry demonstrated that CDK9 was highly expressed in the human endometrial cancer cell lines; moreover, it was elevated in metastatic and recurrent endometrial tumor tissue compared when compared with that in patient-matched primary endometrial tumor tissue. Knockdown of CDK9 with siRNA and inhibition of CDK9 activity with the inhibitor suppressed cell proliferation and promoted apoptosis in endometrial cancer. In conclusion, our results provide evidence that CDK9 may be a potential prognostic biomarker and a promising therapeutic target for the treatment of endometrial cancer in the future. D.A. Spandidos 2020-11 2020-09-01 /pmc/articles/PMC7551504/ /pubmed/32901849 http://dx.doi.org/10.3892/or.2020.7746 Text en Copyright: © He et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
He, Shasha
Fang, Xiaoling
Xia, Xiaomeng
Hou, Tao
Zhang, Tingting
Targeting CDK9: A novel biomarker in the treatment of endometrial cancer
title Targeting CDK9: A novel biomarker in the treatment of endometrial cancer
title_full Targeting CDK9: A novel biomarker in the treatment of endometrial cancer
title_fullStr Targeting CDK9: A novel biomarker in the treatment of endometrial cancer
title_full_unstemmed Targeting CDK9: A novel biomarker in the treatment of endometrial cancer
title_short Targeting CDK9: A novel biomarker in the treatment of endometrial cancer
title_sort targeting cdk9: a novel biomarker in the treatment of endometrial cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7551504/
https://www.ncbi.nlm.nih.gov/pubmed/32901849
http://dx.doi.org/10.3892/or.2020.7746
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