4.5 Article

Decreasing expression of glucose-regulated protein GRP78/BiP as a significant prognostic predictor in patients with advanced laryngeal squamous cell carcinoma

出版社

WILEY-BLACKWELL
DOI: 10.1002/hed.24471

关键词

endoplasmic reticulum stress; glucose-regulated protein 78 (GRP78); immunoglobulin heavy chain binding protein (BiP); laryngeal cancer; squamous cell carcinoma; immunohistochemistry

资金

  1. Ministry of Education, Culture, Sports, Science, and Technology, Japan [23591750, 23592523]
  2. National Hospital Organization Policy Based Medical Services
  3. Grants-in-Aid for Scientific Research [23591750, 15K10798, 23592523] Funding Source: KAKEN

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Background. The immunoglobulin heavy chain binding protein (BiP)/glucose-regulated protein 78 (GRP78) is important in the endoplasmic reticulum stress, and is highly expressed in various human cancers. The clinical and pathological features of GRP78/BiP are unclear in patients with advanced laryngeal squamous cell carcinoma (SCC). The purpose of this study was to investigate the clinicopathological significance of GRP78/BiP as a prognostic marker for laryngeal SCC. Methods. A total of 59 patients with advanced laryngeal SCC (stage III/IV) were analyzed, and tumor specimens were stained by immunohistochemistry for GRP78/BiP and Ki-67. Microvessel density was determined by immunohistochemical staining for CD34 and p53. Results. Expression of GRP78/BiP was confirmed in 87% of cases. Decreased expression of GRP78/BiP was highly associated with positive expression of p53. Decreased GRP78/BiP expression was identified on multivariate analysis as an independent factor of decreased progression-free survival (PFS). Conclusion. GRP78/BiP was found to be commonly expressed in laryngeal SCC, whereas its downregulation was found to serve a significant prognostic role for predicting poor survival in patients with laryngeal SCC with advanced disease. GRP78/BiP may be a potentially attractive target for the treatment of various human neoplasms. (C) 2016 Wiley Periodicals, Inc.

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