| Literature DB >> 29090499 |
Koji Okudela1, Hideaki Mitsui1, Mai Matsumura1, Hiromasa Arai2,3, Kimihisa Shino3, Akimasa Sekine4, Tetsukan Woo2, Takehisa Suzuki1, Yoshihiro Ishikawa2, Shigeaki Umeda1, Michihiko Tajiri3, Munetaka Masuda2, Kenichi Ohashi1.
Abstract
We herein analyzed the relationships among the immunohistochemical expression of alpha-enolase (ENO1) and clinicopathological factors in order to define the significance of ENO1 in lung adenocarcinomas (ADCs). ENO1 expression was detected in most of the ADCs examined (95.8%), but not in bronchial and alveolar epithelia. ENO1 expression was typically observed in the cytoplasm among most ADCs (95.8%), but was also detected in the nucleus (56.3%). The levels were significantly higher in terminal respiratory unit (TRU) cytological subtype ADCs. Neither cytoplasmic nor nuclear expression was associated with any other clinicopathological factors including post-operative survival and growth activity. These results suggest that ENO1 is a crucial factor promoting neoplastic transformation exclusively in TRU subtype ADCs. We also investigated the potential utility of the immunohistochemical expression of ENO1 to differentiate TRU-type ADC cells from the reactive hyperplasia of pneumocytes and bronchiolar epithelial cells because difficulties are associated with discriminating these lesions in small biopsy specimens. The sensitivity and specificity of ENO1 (cytoplasmic/nuclear) were 87.5%/37.5% and 88.9%/100%, respectively, which are superior to those of p53 (18.8% and 100%). ENO1 has potential as a biomarker to assist in the histopathological detection of TRU subtype ADC cells.Entities:
Keywords: ENO1; biomarker; lung adenocarcinomas
Mesh:
Substances:
Year: 2017 PMID: 29090499 DOI: 10.1111/pin.12607
Source DB: PubMed Journal: Pathol Int ISSN: 1320-5463 Impact factor: 2.534