HOXC10 promotes gastric cancer cell invasion and migration via regulation of the NF-κB pathway
- Department of Gastroenterology and Hepatology, The First Affiliated Hospital, Sun Yat-sen University, 510080, 58 Zhongshan 2nd Road, Guangzhou (China)
- Department of Endoscopy, State Key Laboratory of Oncology in Southern China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, 510060, Guangzhou (China)
- Department of Hepatic Surgery, The First Affiliated Hospital, Sun Yat-sen University, 510080, 58 Zhongshan 2nd Road, Guangzhou (China)
- Department of Experimental Research, State Key Laboratory of Oncology in Southern China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, 510060 (China)
- Department of Pathology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, 58 Zhongshan 2nd Road (China)
- Department of Oncology, Karmanos Cancer Institute, Wayne State University, MI 48201, 4100 John R, Detroit (United States)
Homeobox gene C10 (HOXC10), known to regulate cell differentiation and proliferation, is upregulated in gastric cancer (GC). The mechanism underlying HOXC10 involvement in GC metastasis is unclear. Herein, we found that HOXC10 is overexpressed in GC relative to normal controls. In the 73 GC patients tissue microarrays (TMA) tested, HOXC10 expression was closely related with tumor-node-metastasis (TNM) stage, lymph node metastasis, and distant metastasis. HOXC10 overexpression tended to associate with low 5-year cumulative survival. Cox regression analysis identified HOXC10 as an independent prognostic factor for poor patient survival. HOXC10 promoted GC cell invasion and migration, regulated the expression of activated ATM and markers of NF-κB signaling. HOXC10 may promote invasion and migration of GC by regulating ATM/NF-κB signaling pathway. HOXC10 should be explored as a clinical marker of GC prognosis.
- OSTI ID:
- 23137017
- Journal Information:
- Biochemical and Biophysical Research Communications, Journal Name: Biochemical and Biophysical Research Communications Journal Issue: 3 Vol. 501; ISSN 0006-291X; ISSN BBRCA9
- Country of Publication:
- United States
- Language:
- English
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