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Transcription factor NF‑YA promotes a malignant phenotype by upregulating fatty acid synthase expression

  • Authors:
    • Jing Guo
    • Ling Min Kong
    • Ai Fen Peng
    • Xin Hua Long
    • Yang Zhou
    • Yong Shu
  • View Affiliations / Copyright

    Affiliations: Department of Oral and Maxillofacial Surgery, The Affiliated Stomatological Hospital of Nanchang University, Nanchang, Jiangxi 330006, P.R. China, Department of Orthopedics, The Central People's Hospital of Ji'an City, Ji'an, Jiangxi 343000, P.R. China, Jiangxi University of Traditional Chinese Medicine, Nanchang, Jiangxi 330004, P.R. China, Department of Orthopedics, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330006, P.R. China
    Copyright: © Guo et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 5007-5014
    |
    Published online on: October 27, 2016
       https://doi.org/10.3892/mmr.2016.5897
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Abstract

Recent studies have revealed that increased expression of the alpha subunit of nuclear transcription factor Y (NF‑YA) is associated with the malignant phenotype of various tumors. However, whether elevated expression of NF‑YA promotes a malignant phenotype in osteosarcoma (OS), and the molecular mechanisms underlying this predicted effect is currently unknown. In the present study, small hairpin RNA (shRNA)‑mediated knockdown of endogenous NF‑YA significantly inhibited the migration and invasion capabilities of OS cells in vitro, whereas ectopic expression of NF‑YA increased the migration and invasion capabilities of these cells. In addition, the induction of upregulated NF‑YA expression on the malignant phenotype of OS cells was attenuated by silencing fatty acid synthase (FASN) expression. Furthermore, the expression level of FASN was increased by upregulating NF‑YA, while decreased FASN expression was observed following NF‑YA silencing in OS cells. The results of the present study suggest that NF‑YA may promote a malignant phenotype in OS cells, in part, by activating the FASN signaling pathway, which may represent a promising target for the management of OS.
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Copy and paste a formatted citation
Spandidos Publications style
Guo J, Kong LM, Peng AF, Long XH, Zhou Y and Shu Y: Transcription factor NF‑YA promotes a malignant phenotype by upregulating fatty acid synthase expression. Mol Med Rep 14: 5007-5014, 2016.
APA
Guo, J., Kong, L.M., Peng, A.F., Long, X.H., Zhou, Y., & Shu, Y. (2016). Transcription factor NF‑YA promotes a malignant phenotype by upregulating fatty acid synthase expression. Molecular Medicine Reports, 14, 5007-5014. https://doi.org/10.3892/mmr.2016.5897
MLA
Guo, J., Kong, L. M., Peng, A. F., Long, X. H., Zhou, Y., Shu, Y."Transcription factor NF‑YA promotes a malignant phenotype by upregulating fatty acid synthase expression". Molecular Medicine Reports 14.6 (2016): 5007-5014.
Chicago
Guo, J., Kong, L. M., Peng, A. F., Long, X. H., Zhou, Y., Shu, Y."Transcription factor NF‑YA promotes a malignant phenotype by upregulating fatty acid synthase expression". Molecular Medicine Reports 14, no. 6 (2016): 5007-5014. https://doi.org/10.3892/mmr.2016.5897
Copy and paste a formatted citation
x
Spandidos Publications style
Guo J, Kong LM, Peng AF, Long XH, Zhou Y and Shu Y: Transcription factor NF‑YA promotes a malignant phenotype by upregulating fatty acid synthase expression. Mol Med Rep 14: 5007-5014, 2016.
APA
Guo, J., Kong, L.M., Peng, A.F., Long, X.H., Zhou, Y., & Shu, Y. (2016). Transcription factor NF‑YA promotes a malignant phenotype by upregulating fatty acid synthase expression. Molecular Medicine Reports, 14, 5007-5014. https://doi.org/10.3892/mmr.2016.5897
MLA
Guo, J., Kong, L. M., Peng, A. F., Long, X. H., Zhou, Y., Shu, Y."Transcription factor NF‑YA promotes a malignant phenotype by upregulating fatty acid synthase expression". Molecular Medicine Reports 14.6 (2016): 5007-5014.
Chicago
Guo, J., Kong, L. M., Peng, A. F., Long, X. H., Zhou, Y., Shu, Y."Transcription factor NF‑YA promotes a malignant phenotype by upregulating fatty acid synthase expression". Molecular Medicine Reports 14, no. 6 (2016): 5007-5014. https://doi.org/10.3892/mmr.2016.5897
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