Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

High YBX1 expression indicates poor prognosis and promotes cell migration and invasion in nasopharyngeal carcinoma

Journal Article · · Experimental Cell Research
 [1];  [2]; ; ;  [1]; ;  [3];  [4];  [2];  [1]
  1. Department of Oncology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, Jiangsu (China)
  2. Nanjing Medical University Affliated Cancer Hospital, Department of Clinical Cancer Research Center, Jiangsu Cancer Hospital, Jiangsu Institute of Cancer Research, Nanjing, Jiangsu (China)
  3. Department of Pathology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, Jiangsu (China)
  4. Department of Otolaryngology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, Jiangsu (China)
Highlights: • YBX1 overexpressed in cytoplasmic of nasopharyngeal carcinoma cells. • YBX1 expression associated with the EMT process in nasopharyngeal carcinoma. • TGF-β1 induced YBX1 expression in NPC cell lines. • TGF-β1/YBX1 signaling mediated the EMT process in NPC cell lines. Y-box binding protein-1 (YBX1) is a multifunctional protein and often acts as an indicator of poor prognosis in cancers. Increasing evidence has shown that the levels of YBX1 protein were closely associated with multidrug resistance, relapse, metastasis and poor prognosis in cancers. However, its role in nasopharyngeal carcinoma (NPC) metastasis remains unknown. In our study, we discovered that the expression of YBX1 was increased in nasopharyngeal carcinoma tissues. YBX1 protein levels positively correlated with T stage and metastasis of NPC patients. Moreover, expression of YBX1 was negatively correlated with membrane E-cadherin levels and positively correlated with Vimentin expression. In vitro, the expression of YBX1 was closely related to the invasive and migratory ability of nasopharyngeal carcinoma cells. Knockdown of YBX1 inhibited migration and invasion in 5–8 F cells, and over-expression of YBX1 promoted CNE1 cells migration and invasion. Transforming growth factor-β1 (TGF-β1) treatment led to epithelial-to-mesenchymal transition (EMT) in CNE1 cells accompanied by elevated YBX1 expression. On the contrary, knockdown of YBX1 partially inhibited the TGF-β1-induced CNE1 cell migration, together with changes of EMT-associated markers. Our study revealed that TGF-β1/YBX1 signaling might be one of novel mechanisms mediating EMT in NPC, providing a new target for the treatment of nasopharyngeal carcinoma.
OSTI ID:
22901315
Journal Information:
Experimental Cell Research, Journal Name: Experimental Cell Research Journal Issue: 1 Vol. 361; ISSN 0014-4827; ISSN ECREAL
Country of Publication:
United States
Language:
English

Similar Records

FPPS mediates TGF-β1-induced non-small cell lung cancer cell invasion and the EMT process via the RhoA/Rock1 pathway
Journal Article · Wed Feb 14 23:00:00 EST 2018 · Biochemical and Biophysical Research Communications · OSTI ID:23127405

Celastrol inhibits TGF-β1-induced epithelial–mesenchymal transition by inhibiting Snail and regulating E-cadherin expression
Journal Article · Fri Aug 09 00:00:00 EDT 2013 · Biochemical and Biophysical Research Communications · OSTI ID:22239693

Curcumin inhibits metastasis in human papillary thyroid carcinoma BCPAP cells via down-regulation of the TGF-β/Smad2/3 signaling pathway
Journal Article · Sun Feb 14 23:00:00 EST 2016 · Experimental Cell Research · OSTI ID:22746413