Literature DB >> 9369941

Detection of MAGE-4 protein in the sera of patients with hepatitis-C virus-associated hepatocellular carcinoma and liver cirrhosis.

S Tsuzurahara1, M Sata, O Iwamoto, S Shichijo, M Kojiro, K Tanikawa, K Itoh.   

Abstract

The aim of this study was to determine whether MAGE-4 protein is detectable in sera of patients with hepatocellular carcinoma and other liver diseases. An enzyme-linked immunosorbent assay was employed for detection of MAGE-4 protein in sera of liver disease patients, healthy men and women (control I) and those undergoing prostatic cancer screening (control II). MAGE-4 protein levels in sera of patients with hepatitis C virus-associated HCC (HCC-C) (n = 45, mean = 2.160 ng/ml) and HCV-associated cirrhosis (LC-C) (n = 55, 1.072 ng/ml) were significantly higher (P < 0.0001) than those of control I (0.327 ng/ml) or control II (0.394 ng/ml). MAGE-4 protein was positive in 21/45 (46.7%) HCC-C patients and 18/55 (32.7%) LC-C patients (cut-off, mean plus 2 SD in healthy controls) but in 0/12 (0%) hepatitis B virus-associated HCC (HCC-B) patients, 3/49 (6.1%) hepatitis B virus-associated LC (LC-B) patients, 4/47 (8.5%) alcoholic liver disease patients, and 1/49 (2.0%) controls. Serum MAGE-4 protein level may be useful as a marker for identification of LC-C patients suffering from HCC that is undetectable by presently available methods.

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Year:  1997        PMID: 9369941      PMCID: PMC5921520          DOI: 10.1111/j.1349-7006.1997.tb00469.x

Source DB:  PubMed          Journal:  Jpn J Cancer Res        ISSN: 0910-5050


alcoholic liver disease chronic hepatitis liver cirrhosis hepatocellular carcinoma hepatitis B virus hepatitis C virus HCV‐associated HBV‐associated enzyme‐linked immunosorbent assay reverse transcription‐nested polymerase chain reaction branched DNA signal amplification assay hepatitis B surface antigen hepatitis B core antibody enzyme‐immuno assay fetal bovine serum monoclonal antibody tris‐buffered saline phosphate‐buffered saline
  15 in total

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Authors:  O Iwamoto; Y Nagao; S Shichijo; M Eura; T Kameyama; K Itoh
Journal:  Int J Cancer       Date:  1997-01-27       Impact factor: 7.396

2.  Risk factors for hepatocellular carcinoma among patients with chronic liver disease.

Authors:  H Tsukuma; T Hiyama; S Tanaka; M Nakao; T Yabuuchi; T Kitamura; K Nakanishi; I Fujimoto; A Inoue; H Yamazaki
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3.  A peptide encoded by human gene MAGE-3 and presented by HLA-A2 induces cytolytic T lymphocytes that recognize tumor cells expressing MAGE-3.

Authors:  P van der Bruggen; J Bastin; T Gajewski; P G Coulie; P Boël; C De Smet; C Traversari; A Townsend; T Boon
Journal:  Eur J Immunol       Date:  1994-12       Impact factor: 5.532

4.  A gene encoding an antigen recognized by cytolytic T lymphocytes on a human melanoma.

Authors:  P van der Bruggen; C Traversari; P Chomez; C Lurquin; E De Plaen; B Van den Eynde; A Knuth; T Boon
Journal:  Science       Date:  1991-12-13       Impact factor: 47.728

5.  A high prevalence of antibody to the hepatitis C virus in patients with hepatocellular carcinoma in Japan.

Authors:  K Nishioka; J Watanabe; S Furuta; E Tanaka; S Iino; H Suzuki; T Tsuji; M Yano; G Kuo; Q L Choo
Journal:  Cancer       Date:  1991-01-15       Impact factor: 6.860

6.  Expression of MAGE-1, MAGE-2, MAGE-3/-6 and MAGE-4a/-4b genes in ovarian tumors.

Authors:  A Yamada; A Kataoka; S Shichijo; T Kamura; Y Imai; T Nishida; K Itoh
Journal:  Int J Cancer       Date:  1995-12-20       Impact factor: 7.396

7.  HLA A2601-restricted CTLs recognize a peptide antigen expressed on squamous cell carcinoma.

Authors:  M Nakao; H Yamana; Y Imai; Y Toh; U Toh; A Kimura; S Yanoma; T Kakegawa; K Itoh
Journal:  Cancer Res       Date:  1995-10-01       Impact factor: 12.701

8.  Establishment of an enzyme-linked immunosorbent assay (ELISA) for measuring cellular MAGE-4 protein on human cancers.

Authors:  S Shichijo; R Tsunosue; K Kubo; T Kuramoto; Y Tanaka; A Hayashi; K Itoh
Journal:  J Immunol Methods       Date:  1995-10-12       Impact factor: 2.303

9.  Identification of MAGE-1 and MAGE-4 proteins in spermatogonia and primary spermatocytes of testis.

Authors:  K Takahashi; S Shichijo; M Noguchi; M Hirohata; K Itoh
Journal:  Cancer Res       Date:  1995-08-15       Impact factor: 12.701

10.  Autologous cytolytic T lymphocytes recognize a MAGE-1 nonapeptide on melanomas expressing HLA-Cw*1601.

Authors:  P van der Bruggen; J P Szikora; P Boël; C Wildmann; M Somville; M Sensi; T Boon
Journal:  Eur J Immunol       Date:  1994-09       Impact factor: 5.532

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  3 in total

1.  MAGE-3 and MAGE-4 genes as possible markers for early detection of metastases in hepatitis C virus Egyptian patients complicated by hepatocellular carcinoma.

Authors:  Yousri M Hussein; Amal F Ghareib; Randa H Mohamed; Mohamed I Radwan; Wael H Elsawy
Journal:  Med Oncol       Date:  2011-03-31       Impact factor: 3.064

2.  Proteomic profiling of triple-negative breast carcinomas in combination with a three-tier orthogonal technology approach identifies Mage-A4 as potential therapeutic target in estrogen receptor negative breast cancer.

Authors:  Teresa Cabezón; Irina Gromova; Pavel Gromov; Reza Serizawa; Vera Timmermans Wielenga; Niels Kroman; Julio E Celis; José M A Moreira
Journal:  Mol Cell Proteomics       Date:  2012-11-20       Impact factor: 5.911

3.  Elevation of serum MAGE-4 protein levels and prediction of hepatocellular carcinogenesis in patients with liver cirrhosis.

Authors:  Shigeru Yutani; Masatoshi Tanaka; Hajime Mutsumoto; Nobue Imai; Michio Sata; Shigeki Shichijo; Mamoru Harada; Kyogo Itoh
Journal:  Jpn J Cancer Res       Date:  2002-04
  3 in total

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