TY - JOUR
T1 - Method for the validation of immunohistochemical staining using SCID mouse xenografts
T2 - Expression of CD40 and CD154 in human non-small cell lung cancer
AU - Ishikawa, Keidai
AU - Miyamoto, Masaki
AU - Yoshioka, Tatsuya
AU - Kadoya, Masatoshi
AU - Li, Li
AU - Mishra, Roshan
AU - Ichinokawa, Kazuomi
AU - Shoji, Yasuhito
AU - Matsumura, Yoshiyuki
AU - Hida, Yasuhiro
AU - Kaga, Kichizo
AU - Kato, Tatsuya
AU - Kaji, Mitsuhito
AU - Ohbuchi, Toshiro
AU - Itoh, Tomoo
AU - Dosaka-Akita, Hirotoshi
AU - Matsui, Yoshiro
AU - Hirano, Satoshi
PY - 2013/4
Y1 - 2013/4
N2 - This report proposes a concept for the standardization of immunohistochemical evaluation. Immunohistochemical staining has several problems associated with the sensitivity of the technical process and standardization of the assessment of potent staining. We provided data focusing on this concept through immunostaining for CD154 in non-small cell lung cancer (NSCLC). We used two types of anti-CD154 antibody as primary antibodies in immunohistochemical staining, as previously reported. Western blot analysis confirmed strong CD154 expression in the cultured cell line PC10, but not in LK2. We also assessed CD154 expression in SCID mouse xenografts of these cell lines. SCID xenograft data on western blot analysis were consistent with those of cultured cell lines. These xenografts could thus be used as positive or negative tissue controls for CD154 immunostaining. Primary antibodies should therefore be confirmed as recognizing target lesions, while control tissue specimens should be objectively confirmed as having target products using another experimental method. Our method would allow results to be unified at more than one laboratory and could act as an objective control assessment method in immunohistochemistry.
AB - This report proposes a concept for the standardization of immunohistochemical evaluation. Immunohistochemical staining has several problems associated with the sensitivity of the technical process and standardization of the assessment of potent staining. We provided data focusing on this concept through immunostaining for CD154 in non-small cell lung cancer (NSCLC). We used two types of anti-CD154 antibody as primary antibodies in immunohistochemical staining, as previously reported. Western blot analysis confirmed strong CD154 expression in the cultured cell line PC10, but not in LK2. We also assessed CD154 expression in SCID mouse xenografts of these cell lines. SCID xenograft data on western blot analysis were consistent with those of cultured cell lines. These xenografts could thus be used as positive or negative tissue controls for CD154 immunostaining. Primary antibodies should therefore be confirmed as recognizing target lesions, while control tissue specimens should be objectively confirmed as having target products using another experimental method. Our method would allow results to be unified at more than one laboratory and could act as an objective control assessment method in immunohistochemistry.
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U2 - 10.3892/or.2013.2275
DO - 10.3892/or.2013.2275
M3 - Article
C2 - 23404288
AN - SCOPUS:84874719867
SN - 1021-335X
VL - 29
SP - 1315
EP - 1321
JO - Oncology reports
JF - Oncology reports
IS - 4
ER -