Expression of MAGE-1 and -3 genes and gene products in human hepatocellular carcinoma

Kazuya Kariyama(Okayama University), Toshihiro Higashi(Okayama University), Yoshihisa Kobayashi(Okayama University), Kazuhiro Nouso(Okayama University), H Nakatsukasa(Okayama University), Taketoshi Yamano(Okayama University), Masahiko Ishizaki(Okayama University), Toshihiko Kaneyoshi(Okayama University), Nobuyuki Toshikuni(Okayama University), Teppei Ohnishi(Okayama University), Keishi Fujiwara(Okayama University), Eiichi Nakayama(Okayama University), Luigi Terracciano(University of Basel), Giulio C. Spagnoli(University Hospital of Basel), Tetsuya Tsuji(Okayama University)
British Journal of Cancer
October 29, 1999
Cited by 42Open Access
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Abstract

MAGE gene family encodes peptides recognized by autologous cytotoxic T lymphocytes in a major histocompatibility complex (MHC) class-I restricted fashion. In the present study, we have performed reverse-transcription polymerase chain reaction (RT-PCR) for the genes, as well as immunohistochemical analysis and Western blotting of MAGE-1 and -3 proteins in 33 surgically resected hepatocellular carcinomas (HCCs). MAGE-1 and -3 mRNAs were constitutively expressed exclusively in 78 and 42% of HCCs respectively. On immunohistochemistry with monoclonal antibodies, 77B for MAGE-1 and 57B for MAGE-3, MAGE-1 and -3 proteins were recognized in cytoplasm of only six among 33 (18%) and two of 29 HCCs (7%) respectively. The distribution pattern was mostly focal in HCC nodules. By contrast, the Western blot analysis revealed that the MAGE-1 (46 kDa) and -3 proteins (48 kDa) were expressed in 80 and 60% of 15 HCCs examined respectively. The proteins of MAGE-1 and -3 were also expressed exclusively in HCCs regardless of the histological grading and clinical staging. Our results indicate that the detection of the genes by RT-PCR or the proteins by Western blotting is useful for differentiating early HCCs from non-cancerous lesions, and that the peptides derived from MAGE-1 and -3 proteins might be suitable targets for immunotherapy of human HCC.


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