Lysyl oxidase expression is an independent marker of prognosis and a predictor of lymph node metastasis in oral and oropharyngeal squamous cell carcinoma (OSCC)

被引:69
作者
Albinger-Hegyi, Andrea [2 ]
Stoeckli, Sandro J. [3 ]
Schmid, Stephan [4 ]
Storz, Martina [5 ]
Iotzova, Guergana [2 ,6 ]
Probst-Hensch, Nicole M. [5 ,7 ]
Rehrauer, Hubert [8 ]
Tinguely, Marianne [5 ]
Moch, Holger [5 ]
Hegyi, Ivan [1 ,9 ]
机构
[1] Univ Hosp, Inselspital Bern, Dept Dermatol, CH-3010 Bern, Switzerland
[2] Univ Zurich Hosp, Dept Otorhinolaryngol Head & Neck Surg, CH-8091 Zurich, Switzerland
[3] Kantonsspital St Gallen, Clin Otorhinolaryngol Head & Neck Surg, St Gallen, Switzerland
[4] Clin Bethanien, Zurich, Switzerland
[5] Univ Zurich Hosp, Inst Surg Pathol, Dept Pathol, CH-8091 Zurich, Switzerland
[6] Univ Zurich Hosp, Dept Dermatol, CH-8091 Zurich, Switzerland
[7] Univ Zurich, Natl Inst Canc Epidemiol & Registrat, CH-8006 Zurich, Switzerland
[8] Funct Genom Ctr Zurich, Zurich, Switzerland
[9] Univ Bern, CH-3010 Bern, Switzerland
关键词
Oral and oropharyngeal squamous cell carcinoma; dysplastic oral mucosa; lysyl oxidase; tumour biomarker; tissue microarray; cDNA microarray; DATA-BASE REPORT; MESSENGER-RNA; BREAST-CANCER; GENE-EXPRESSION; UP-REGULATION; H-RAS; HEAD; NECK; HYPOXIA; LOX;
D O I
10.1002/ijc.24948
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Proteins of the lysyl oxidase (LOX) family are important modulators of the extracellular matrix. However, they have an important role in the tumour development as well as in tumour progression. To evaluate the diagnostic and prognostic value of the LOX protein in oral and oropharyngeal squamous cell carcinoma (OSCC) we performed QRT-PCR and immunohistochemical analysis on two tissue microarrays (622 tissue samples in total). Significantly higher LOX expression was detected in high grade dysplastic oral mucosa as well as in OSCC when compared to normal oral mucosa (P < 0.001). High LOX expression was correlated with clinical TNM stage (P = 0.020), lymph node metastases for the entire cohort (P < 0.001), as well as in the subgroup of small primary tumours (T1/12, P < 0.001). Moreover, high LOX expression was correlated with poor overall survival (P = 0.004) and disease specific survival (P = 0.037). In a multivariate analysis, high LOX expression was an independent prognostic factor, predicting unfavourable overall survival. In summary, LOX expression is an independent prognostic biomarker and a predictor of lymph node metastasis in OSCC. Moreover, LOX overexpression may be an early phenomenon in the pathogenesis of OSCC and thus an attractive novel target for chemopreventive and therapeutic strategies.
引用
收藏
页码:2653 / 2662
页数:10
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