論文

査読有り
2014年1月

Lipase member H is a novel secreted protein selectively upregulated in human lung adenocarcinomas and bronchioloalveolar carcinomas

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
  • Yasuhiro Seki
  • Yukihiro Yoshida
  • Hisako Ishimine
  • Aya Shinozaki-Ushiku
  • Yoshimasa Ito
  • Kenya Sumitomo
  • Jun Nakajima
  • Masashi Fukayama
  • Tatsuo Michiue
  • Makoto Asashima
  • Akira Kurisaki
  • 全て表示

443
4
開始ページ
1141
終了ページ
1147
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.bbrc.2013.12.106
出版者・発行元
ACADEMIC PRESS INC ELSEVIER SCIENCE

Lung cancer is one of the most frequent causes of cancer-related death worldwide. However, molecular markers for lung cancer have not been well established. To identify novel genes related to lung cancer development, we surveyed publicly available DNA microarray data on lung cancer tissues. We identified lipase member H (LIPH, also known as mPA-PLA1) as one of the significantly upregulated genes in lung adenocarcinoma. LIPH was expressed in several adenocarcinoma cell lines when they were analyzed by quantitative real-time polymerase chain reaction (qPCR), western blotting, and sandwich enzyme-linked immunosorbent assay (ELISA). Immunohistochemical analysis detected LIPH expression in most of the adenocarcinomas and bronchioloalveolar carcinomas tissue sections obtained from lung cancer patients. LIPH expression was also observed less frequently in the squamous lung cancer tissue samples. Furthermore, LIPH protein was upregulated in the serum of early- and late-phase lung cancer patients when they were analyzed by ELISA. Interestingly, high serum level of LIPH was correlated with better survival in early phase lung cancer patients after surgery. Thus, LIPH may be a novel molecular biomarker for lung cancer, especially for adenocarcinoma and bronchioloalveolar carcinoma. (C) 2013 Elsevier Inc. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.bbrc.2013.12.106
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/24380866
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000331921500003&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.bbrc.2013.12.106
  • ISSN : 0006-291X
  • eISSN : 1090-2104
  • PubMed ID : 24380866
  • Web of Science ID : WOS:000331921500003

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