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MicroRNA-22 Suppresses Breast Cancer Cell Growth and Increases Paclitaxel Sensitivity by Targeting NRAS.
Song, Ying-Kui; Wang, Yang; Wen, Yi-Yang; Zhao, Pei; Bian, Zhi-Jie.
Affiliation
  • Song YK; 1 Intensive Care Unit, Jining No. 1 People's Hospital, Jining, Shandong Province, People's Republic of China.
  • Wang Y; 2 Department of Breast and Thyroid, Jining No. 1 People's Hospital, Jining, Shandong Province, People's Republic of China.
  • Wen YY; 3 Department of Pathology, Jining No. 1 People's Hospital, Jining, Shandong Province, People's Republic of China.
  • Zhao P; 2 Department of Breast and Thyroid, Jining No. 1 People's Hospital, Jining, Shandong Province, People's Republic of China.
  • Bian ZJ; 2 Department of Breast and Thyroid, Jining No. 1 People's Hospital, Jining, Shandong Province, People's Republic of China.
Technol Cancer Res Treat ; 17: 1533033818809997, 2018 01 01.
Article in En | MEDLINE | ID: mdl-30384806
ABSTRACT
In recent study, microRNAs have various important functions in diverse biological processes and progression of cancer. In human breast cancer, microRNA-22 has been reported to be downregulated. However, molecular mechanism of microRNA-22 in breast cancer progression and chemosensitivity has not been well studied. In our study, these results demonstrated that microRNA-22 expression levels were significantly reduced in 40 pairs of human breast cancer tissues when compared to normal tissues. Enforced expression of microRNA-22 inhibited activity of cell proliferation and cell migration in breast cancer cells. Furthermore, microRNA-22 targeted NRAS proto-oncogene, GTPase (NRAS) in breast cancer cells. The expression levels of NRAS in human clinical specimens were higher in breast cancer tissues when compared to normal tissues. Moreover, microRNA-22 sensitized breast cancer cells to paclitaxel by regulation of NRAS. Our results then demonstrated that microRNA-22 functioned as a tumor suppressor microRNA and indicated potential application for the diagnosis and treatment of cancer in the future.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Paclitaxel / MicroRNAs / Cell Proliferation / GTP Phosphohydrolases / Membrane Proteins Type of study: Diagnostic_studies Limits: Female / Humans Language: En Journal: Technol Cancer Res Treat Journal subject: NEOPLASIAS / TERAPEUTICA Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Paclitaxel / MicroRNAs / Cell Proliferation / GTP Phosphohydrolases / Membrane Proteins Type of study: Diagnostic_studies Limits: Female / Humans Language: En Journal: Technol Cancer Res Treat Journal subject: NEOPLASIAS / TERAPEUTICA Year: 2018 Document type: Article
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