Global Health & Medicine
Online ISSN : 2434-9194
Print ISSN : 2434-9186
Original Article
A newly established monoclonal antibody against ERCC1 detects major isoforms of ERCC1 in gastric cancer
Takayuki OishiYuka SasakiYing TongLichao ChenTakae OnoderaSatoru IwasaEmiko UdoBungo FurusatoHiroaki FujimoriShoji ImamichiTakuya HondaTadayoshi BesshoJunya FukuokaKazuto AshizawaKazuyoshi YanagiharaKazuhiko NakaoYasuhide YamadaNobuyoshi HiraokaMitsuko Masutani
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2021 Volume 3 Issue 4 Pages 226-235


Identifying patients resistant to cisplatin treatment is expected to improve cisplatin-based chemotherapy for various types of cancers. Excision repair cross-complementing group 1 (ERCC1) is involved in several repair processes of cisplatin-induced DNA crosslinks. ERCC1 overexpression is reported as a candidate prognostic factor and considered to cause cisplatin resistance in major solid cancers. However, anti-ERCC1 antibodies capable of evaluating expression levels of ERCC1 in clinical specimens were not fully optimized. A mouse monoclonal antibody against human ERCC1 was generated in this study. The developed antibody 9D11 specifically detected isoforms of 201, 202, 203 but not 204, which lacks the exon 3 coding region. To evaluate the diagnostic usefulness of this antibody, we have focused on gastric cancer because it is one of the major cancers in Japan. When ERCC1 expression was analyzed in seventeen kinds of human gastric cancer cell lines, all the cell lines were found to express either 201, 202, and/or 203 as major isoforms of ERCC1, but not 204 by Western blotting analysis. Immunohistochemical staining showed that ERCC1 protein was exclusively detected in nuclei of the cells and a moderate level of constant positivity was observed in nuclei of vascular endothelial cells. It showed a clear staining pattern in clinical specimens of gastric cancers. Antibody 9D11 may thus be useful for estimating expression levels of ERCC1 in clinical specimens.

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© 2021 National Center for Global Health and Medicine
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