BACKGROUND: The tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) death receptor, DR5, mediates proapoptotic signals and is implicated in the pathogenesis of many neoplasms including nonsmall-cell lung cancer (NSCLC). METHODS: In this study, immunohistochemical expression of DR5 was examined in 146 cases of stage I and II NSCLC as well as neoplastic precursor lesions and regional lymph node metastases using tissue microarrays. RESULTS: High DR5 expression was observed in 67.1% of primary NSCLC, 55.6% of bronchial squamous carcinoma in situ, 40% of squamous metaplasia, as well as 76.5% of lymph node metastases. In all of these lesions, DR5 expression was significantly higher than in normal bronchial epithelium. Increased expression of DR5 correlated with poorly differentiated tumors and was inversely correlated with bronchioloalveolar carcinomas. There was no correlation with other clinicopathologic variables. A significant association was found between high DR5 expression and reduced overall survival in univariate analysis. Among smokers, high DR5 and tumor stage were independent predictors of reduced disease-free survival in multivariate analysis, however, DR5 was not an independent prognostic marker among the entire cohort of NSCLC. CONCLUSIONS: These findings suggest that DR5 plays a role in the development of early-stage NSCLC and the high levels of DR5 expression suggest that these tumors may be susceptible to novel anticancer agents targeting the DR5 receptor and may improve patient survival, particularly for patients who are smokers. (Copyright) 2008 American Cancer Society.
BACKGROUND: The tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) death receptor, DR5, mediates proapoptotic signals and is implicated in the pathogenesis of many neoplasms including nonsmall-cell lung cancer (NSCLC). METHODS: In this study, immunohistochemical expression of DR5 was examined in 146 cases of stage I and II NSCLC as well as neoplastic precursor lesions and regional lymph node metastases using tissue microarrays. RESULTS: High DR5 expression was observed in 67.1% of primary NSCLC, 55.6% of bronchial squamous carcinoma in situ, 40% of squamous metaplasia, as well as 76.5% of lymph node metastases. In all of these lesions, DR5 expression was significantly higher than in normal bronchial epithelium. Increased expression of DR5 correlated with poorly differentiated tumors and was inversely correlated with bronchioloalveolar carcinomas. There was no correlation with other clinicopathologic variables. A significant association was found between high DR5 expression and reduced overall survival in univariate analysis. Among smokers, high DR5 and tumor stage were independent predictors of reduced disease-free survival in multivariate analysis, however, DR5 was not an independent prognostic marker among the entire cohort of NSCLC. CONCLUSIONS: These findings suggest that DR5 plays a role in the development of early-stage NSCLC and the high levels of DR5 expression suggest that these tumors may be susceptible to novel anticancer agents targeting the DR5 receptor and may improve patient survival, particularly for patients who are smokers. (Copyright) 2008 American Cancer Society.
Authors: Heath A Elrod; Songqing Fan; Susan Muller; Georgia Z Chen; Lin Pan; Mourad Tighiouart; Dong M Shin; Fadlo R Khuri; Shi-Yong Sun Journal: PLoS One Date: 2010-08-16 Impact factor: 3.240
Authors: Hendrik Fritsche; Thorsten Heilmann; Robert J Tower; Charlotte Hauser; Anja von Au; Doaa El-Sheikh; Graeme M Campbell; Göhkan Alp; Denis Schewe; Sebastian Hübner; Sanjay Tiwari; Daniel Kownatzki; Susann Boretius; Dieter Adam; Walter Jonat; Thomas Becker; Claus C Glüer; Margot Zöller; Holger Kalthoff; Christian Schem; Anna Trauzold Journal: Oncotarget Date: 2015-04-20
Authors: Jan-Paul Gundlach; Charlotte Hauser; Franka Maria Schlegel; Christine Böger; Christian Röder; Christoph Röcken; Thomas Becker; Jan-Hendrik Egberts; Holger Kalthoff; Anna Trauzold Journal: BMC Cancer Date: 2018-07-31 Impact factor: 4.430
Authors: Angeles Hernandez-Cueto; Daniel Hernandez-Cueto; Gabriela Antonio-Andres; Marisela Mendoza-Marin; Carlos Jimenez-Gutierrez; Ana Lilia Sandoval-Mejia; Rosario Mora-Campos; Cesar Gonzalez-Bonilla; Mario I Vega; Benjamin Bonavida; Sara Huerta-Yepez Journal: Mol Med Rep Date: 2014-08-21 Impact factor: 2.952