4.3 Article

The role of S100A14 in epithelial ovarian tumors

期刊

ONCOTARGET
卷 5, 期 11, 页码 3482-3496

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.1947

关键词

Epithelial ovarian cancer; tumor marker; S100A14; shRNA

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education, Science and Technology [2010-0011153, 2011-0010286, 2011-0007146]
  2. Korea Healthcare Technology R&D Project, Ministry for Health & Welfare Affairs, Republic of Korea [A121387]
  3. Yonsei University College of Medicine [6-2013-0106]
  4. National Research Foundation of Korea [2011-0007146, 2010-0011153, 2011-0010286] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

S100A14 is an EF-hand calcium-binding protein that has been reported to be involved in the progression of many malignancies. However, its role in ovarian cancer has not yet been clarified. In this study, we investigated the significance of S100A14 expression in epithelial ovarian cancers (EOCs) as well as it's mechanism of action. On both RNA and protein levels, S100A14 was overexpressed in transformed cells. Immunohistochemical staining demonstrated that S100A14 expression was associated with advanced stage (P < 0.001) and poor tumor grade (P < 0.001). Moreover, S100A14 overexpression was an independent prognostic factor for overall survival (HR = 4.53, P = 0.029). We also investigated S100A14's functional role by employing lentiviral-mediated overexpression and knockdown in EOC cells. S100A14 overexpression promoted cell proliferation, tumorigenesis, migration, and invasion, whereas S100A14 knockdown inhibited these properties. TOV112D cells that overexpressed S100A14 also exhibited greater tumor growth potential in xenografted mice. S100A14 promoted such a malignant phenotype in EOC cells through the PI3K/Akt pathway. Taken together, our data indicate that S100A14 has a crucial role in EOC progression, and its overexpression is associated with poor prognosis. Further study of S100A14's molecular mechanisms may lead to the development of a novel therapeutic target for ovarian cancer.

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