PMID- 23364922 OWN - NLM STAT- MEDLINE DCOM- 20130725 LR - 20201209 IS - 1097-0215 (Electronic) IS - 0020-7136 (Linking) VI - 133 IP - 3 DP - 2013 Aug 1 TI - Increased expression of metadherin protein predicts worse disease-free and overall survival in laryngeal squamous cell carcinoma. PG - 671-9 LID - 10.1002/ijc.28071 [doi] AB - Metadherin (MTDH) is involved in tumourigenesis and cancer progression in multiple human malignancies. However, the MTDH protein has rarely been reported in laryngeal squamous cell carcinoma (LSCC). The expression pattern of the MTDH protein in 176 primary archival LSCC and 27 corresponding adjacent noncarcinoma specimens was detected by immunohistochemistry and further correlated with clinicopathological parameters. The results demonstrated that 161 (91.48%) primary LSCC samples stained positive for MTDH; however, staining was barely detectable in all adjacent noncarcinoma samples. Moreover, the expression of the MTDH protein was significantly associated with the primary tumour site (p = 0.021), T classification (p = 0.002), clinical stage (I + II/III + IV; p < 0.001), lymph node metastasis (p < 0.001) and postoperational recurrence (p < 0.001). Kaplan-Meier analysis revealed that MTDH expression was significantly associated with worse disease-free survival (DFS) and overall survival (OS) rates in patients with LSCC (both p < 0.001). When lymph node metastasis and MTDH expression were considered together, patients with lymph node metastasis and high MTDH expression had both poorer DFS and OS rates than others (both p < 0.001). Finally, multivariate analysis demonstrated that MTDH expression was an independent prognostic factor for both DFS and OS rates in patients with LSCC. Strong MTDH expression was negatively correlated with a canonical epithelial-mesenchymal transition molecule E-cadherin (p < 0.001) and positively associated with proangiogenic protein vascular endothelial growth factor (p < 0.001). MTDH overexpression was tightly associated with more aggressive tumour behaviour and a poor prognosis, indicating that MTDH is a valuable molecular biomarker for LSCC progression. CI - Copyright (c) 2013 UICC. FAU - Liu, Yong AU - Liu Y AD - Department of Otolaryngology Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China. FAU - Su, Zhongwu AU - Su Z FAU - Li, Guo AU - Li G FAU - Yu, Changyun AU - Yu C FAU - Ren, Shuling AU - Ren S FAU - Huang, Donghai AU - Huang D FAU - Fan, Songqing AU - Fan S FAU - Tian, Yongquan AU - Tian Y FAU - Zhang, Xin AU - Zhang X FAU - Qiu, Yuanzheng AU - Qiu Y LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130307 PL - United States TA - Int J Cancer JT - International journal of cancer JID - 0042124 RN - 0 (Biomarkers, Tumor) RN - 0 (Cadherins) RN - 0 (Cell Adhesion Molecules) RN - 0 (MTDH protein, human) RN - 0 (Membrane Proteins) RN - 0 (RNA-Binding Proteins) RN - 0 (Vascular Endothelial Growth Factor A) SB - IM MH - Biomarkers, Tumor MH - Cadherins/metabolism MH - Carcinoma, Squamous Cell/*metabolism/*mortality MH - Cell Adhesion Molecules/biosynthesis/*metabolism MH - Disease Progression MH - Disease-Free Survival MH - Epithelial-Mesenchymal Transition MH - Female MH - Humans MH - Kaplan-Meier Estimate MH - Laryngeal Neoplasms/*metabolism/*mortality MH - Lymphatic Metastasis MH - Male MH - Membrane Proteins MH - Middle Aged MH - Neoplasm Recurrence, Local MH - Neoplasm Staging MH - RNA-Binding Proteins MH - Survival MH - Vascular Endothelial Growth Factor A/metabolism EDAT- 2013/02/01 06:00 MHDA- 2013/07/26 06:00 CRDT- 2013/02/01 06:00 PHST- 2012/08/11 00:00 [received] PHST- 2012/12/09 00:00 [revised] PHST- 2013/01/09 00:00 [accepted] PHST- 2013/02/01 06:00 [entrez] PHST- 2013/02/01 06:00 [pubmed] PHST- 2013/07/26 06:00 [medline] AID - 10.1002/ijc.28071 [doi] PST - ppublish SO - Int J Cancer. 2013 Aug 1;133(3):671-9. doi: 10.1002/ijc.28071. Epub 2013 Mar 7.