Correlation of TNFAIP8 overexpression with the proliferation, metastasis, and disease-free survival in endometrial cancer

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• 作者：Tianbo Liu (1)
  Hongyu Gao (2)
  Meng Yang (1)
  Tingting Zhao (3)
  Yunduo Liu (1)
  Ge Lou (1)
  
• 关键词：Tumor necrosis factor alpha ; induced protein 8 ; Endometrial cancer ; Disease ; free survival ; Proliferation ; Metastasis
• 刊名：Tumor Biology
• 出版年：2014
• 出版时间：June 2014
• 年：2014
• 卷：35
• 期：6
• 页码：5805-5814
• 全文大小：
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• 作者单位：Tianbo Liu (1)
  Hongyu Gao (2)
  Meng Yang (1)
  Tingting Zhao (3)
  Yunduo Liu (1)
  Ge Lou (1)
  
  1. Department of Gynecology, The Third Affiliated Hospital, Harbin Medical University, 6 Baojian Road, Harbin, 150040, China
  2. Gastroenterologic Surgery, The Third Affiliated Hospital, Harbin Medical University, Harbin, China
  3. Department of Obstetrics and Gynecology, The First Affiliated Hospital, Changjiang University, Jingzhou, China
  
• ISSN：1423-0380

文摘

Tumor necrosis factor alpha-induced protein 8 (TNFAIP8) is an apoptosis regulator proven to have an important function in the proliferation, invasion, metastasis, and progression of malignancies. In this study, we investigated the clinical role of TNFAIP8 overexpression in endometrial cancer (EC) and determined the relationship of TNFAIP8 with the proliferative antigen Ki-67 and metastasis-related gene matrix metallopeptidase 9 (MMP9) in 225 tumor specimens by immunohistochemistry and western blot, in order to elucidate more information on the role of TNFAIP8 protein with regard to the pathogenesis of EC. An association was observed between TNFAIP8 overexpression and clinicopathologic factors, such as advanced International Federation of Gynecology and Obstetrics stage (P-lt;-.001), higher histologic grade (P--.017), deep myometrial invasion (P--.030), lymphovascular space invasion (P--.011), lymph node metastasis (P-lt;-.001), and recurrence. Furthermore, TNFAIP8 overexpression was strongly correlated with MMP9 and Ki-67 expression in the progression of ECs. Patients with high expression of TNFAIP8 (P-lt;-.001 for both) and Ki-67 (P--.007 and P--.008) had poor overall survival and disease-free survival (DFS) rates. MMP9 overexpression did not affect survival outcomes (P-gt;-.05). Multivariate Cox regression analysis revealed that TNFAIP8 (P--.029) and lymph node metastasis (P--.022) were independent factors of DFS in patients with EC. These findings suggested that TNFAIP8 may be used as a prognostic marker for the recurrence of EC, and its promotion of the proliferation and metastasis in EC may be due to its mediation of Ki-67 and MMP9.