| Literature DB >> 10576668 |
K Kariyama1, T Higashi, Y Kobayashi, K Nouso, H Nakatsukasa, T Yamano, M Ishizaki, T Kaneyoshi, N Toshikuni, T Ohnishi, K Fujiwara, E Nakayama, L Terracciano, G C Spagnoli, T Tsuji.
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.Entities:
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Year: 1999 PMID: 10576668 PMCID: PMC2362936 DOI: 10.1038/sj.bjc.6690810
Source DB: PubMed Journal: Br J Cancer ISSN: 0007-0920 Impact factor: 7.640