@article{bdb0780ab72b46d89485d960bd8a9652,
title = "Biglycan, tumor endothelial cell secreting proteoglycan, as possible biomarker for lung cancer",
abstract = "Objectives: In lung cancer, surgery remains the most curative treatment and limited resection is beneficial for patients with low cardiopulmonary function and low malignancy tumors. However, there are no biomarkers of low malignancy to select candidates for limited resection without compromising the outcome of treatments. Recently we identified biglycan (BGN) as a tumor endothelial cell (TEC) marker that is associated with tumor progression in various cancers. In this study, we analyzed the association between BGN expression in TECs in lung cancer and cancer progression in patients. Materials and Methods: First, we performed immunohistochemistry of BGN with resected lung tumor tissues of 155 patients who had undergone thoracic surgery and analyzed the correlation between BGN-positive vessel density in primary lung tumors and clinicopathological factors. Second, we measured the BGN levels in preoperative serum of other 46 patients with lung cancer by ELISA, and analyzed the correlation between BGN expression in tumor tissues and blood BGN levels. Results: High BGN expression in the TECs was significantly associated with T factor, and was a significant negative predictor. BGN levels in preoperative serum of 46 patients with lung cancer was significantly correlated with BGN expression in the TECs. Preoperative serum BGN level was significantly lower in healthy volunteers and less invasive adenocarcinoma than in invasive adenocarcinoma and other lung carcinomas. These results suggest that low BGN level in preoperative serum in patients with lung cancer might indicate low malignancy. Conclusions: BGN can be a potential biomarker for lung cancer.",
keywords = "angiogenesis, biglycan, endothelial cell, lung cancer, tumor progression",
author = "Hirofumi Morimoto and Yasuhiro Hida and Nako Maishi and Hiroshi Nishihara and Yutaka Hatanaka and Cong Li and Yoshihiro Matsuno and Toru Nakamura and Satoshi Hirano and Kyoko Hida",
note = "Funding Information: We would like to thank Ms. M. Sasaki and Ms. Y. Suzuki for their technical assistance with the experiments. This research was supported by the Japan Society for the Promotion of Science Grants‐in‐Aid for Scientific Research to N.M. (JP18K09715) and Y.H. (JP18H02891), and Grants from the Japan Agency for Medical Research and Development (AMED) to N.M. (JP18ck0106198h0003) and K.H. (JP19ck0106406h0002). Funding Information: We would like to thank Ms. M. Sasaki and Ms. Y. Suzuki for their technical assistance with the experiments. This research was supported by the Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research to N.M. (JP18K09715) and Y.H. (JP18H02891), and Grants from the Japan Agency for Medical Research and Development (AMED) to N.M. (JP18ck0106198h0003) and K.H. (JP19ck0106406h0002). Funding Information: Grants from Japan Agency for Medical Research and Development, Grant/Award Numbers: JP18ck0106198h0003, JP19ck0106406h0002; JSPS Grants‐in‐Aid for Scientific Research, Grant/Award Numbers: JP18H02891, JP18K09715; Japan Society for the Promotion of Science Funding information Publisher Copyright: {\textcopyright} 2021 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.",
year = "2021",
month = may,
doi = "10.1111/1759-7714.13907",
language = "English",
volume = "12",
pages = "1347--1357",
journal = "Thoracic Cancer",
issn = "1759-7706",
publisher = "Blackwell Publishing Asia Pty Ltd",
number = "9",
}