Premium
Fixation effect of SurePath preservative fluids using epidermal growth factor receptor mutation‐specific antibodies for immunocytochemistry
Author(s) -
Kawahara Akihiko,
Taira Tomoki,
Abe Hideyuki,
Watari Kosuke,
Murakami Yuichi,
Fukumitsu Chihiro,
Takase Yorihiko,
Yamaguchi Tomohiko,
Azuma Koichi,
Akiba Jun,
Ono Mayumi,
Kage Masayoshi
Publication year - 2014
Publication title -
cancer cytopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.29
H-Index - 57
eISSN - 1934-6638
pISSN - 1934-662X
DOI - 10.1002/cncy.21355
Subject(s) - microbiology and biotechnology , immunocytochemistry , lung cancer , epidermal growth factor receptor , pathology , antigen , antibody , adenocarcinoma , cancer research , cancer , medicine , biology , immunology
BACKGROUND Cytological diagnosis of respiratory disease has become important, not only for histological typing using immunocytochemistry (ICC) but also for molecular DNA analysis of cytological material. The aim of this study was to investigate the fixation effect of SurePath preservative fluids. METHODS Human lung cancer PC9 and 11‐18 cell lines, and lung adenocarcinoma cells in pleural effusion, were fixed in CytoRich Blue, CytoRich Red, 15% neutral‐buffered formalin, and 95% ethanol, respectively. PC9 and 11‐18 cell lines were examined by ICC with epidermal growth factor receptor (EGFR) mutation‐specific antibodies, the EGFR mutation DNA assay, and fluorescence in situ hybridization. The effect of antigenic storage time was investigated in lung adenocarcinoma cells in pleural effusion by ICC using the lung cancer detection markers. RESULTS PC9 and 11‐18 cell lines in formalin‐based fixatives showed strong staining of EGFR mutation‐specific antibodies and lung cancer detection markers by ICC as compared with ethanol‐based fixatives. DNA preservation with CytoRich Blue and CytoRich Red was superior to that achieved with 95% ethanol and 15% neutral‐buffered formalin fixatives, whereas EGFR mutations by DNA assay and EGFR gene amplification by fluorescence in situ hybridization were successfully identified in all fixative samples. Although cytoplasmic antigens maintained high expression levels, expression levels in nuclear antigens fell as storage time increased. CONCLUSIONS These results indicate that CytoRich Red is not only suitable for ICC with EGFR mutation‐specific antibodies, but also for DNA analysis of cytological material, and is useful in molecular testing of lung cancer, for which various types of analyses will be needed in future. Cancer (Cancer Cytopathol) 2014;122:145–52 . © 2013 American Cancer Society