Literature DB >> 7516264

Detection of hepatocellular carcinoma-specific alpha-fetoprotein by isoelectric focusing.

L J Burditt1, M M Johnson, P J Johnson, R Williams.   

Abstract

BACKGROUND: Serum alpha-fetoprotein (AFP) is elevated in up to 80% of patients with hepatocellular carcinoma (HCC). Modestly raised AFP levels (10-400 ng/ml) are also found in patients with nonmalignant liver diseases. In the present study, isoelectric focusing of AFP was used to differentiate the AFP found in patients with HCC.
METHODS: To establish the assay conditions, isoelectric focusing was performed on sera from 14 patients with HCC and 13 with nonmalignant liver diseases. Sera was also analyzed under coded conditions from 16 patients with HCC, 14 with chronic active hepatitis (CAH), and 6 with cirrhosis to determine the specificity and sensitivity of the assay in the diagnosis of HCC.
RESULTS: Isoelectric focusing of sera from patients with HCC and various non malignant liver diseases identified AFP variants (AFP I-IV). All 14 patients with HCC had AFP variants I and III, and 7 of the 14 also had variant IV. When analyzed in the coded study 13 of the 16 cases of HCC were predicted correctly by the presence of AFP variants III or III and IV. AFP bands III and IV were not discernible in 12 of the 14 patients with CAH and 4 of the 6 with cirrhosis.
CONCLUSION: Isoelectric focusing of sera from patients with HCC and nonmalignant liver disease identified two AFP variants apparently specific for HCC. In the setting of borderline elevation of AFP, this technique has a sensitivity of 81% and specificity of 85% for detecting the presence of bands III or IV and may prove suitable for use in a routine laboratory as a screening assay.

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Year:  1994        PMID: 7516264     DOI: 10.1002/1097-0142(19940701)74:1<25::aid-cncr2820740106>3.0.co;2-u

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  6 in total

1.  'Hepatoma-specific' alphafetoprotein may permit preclinical diagnosis of malignant change in patients with chronic liver disease.

Authors:  P J Johnson; N Leung; P Cheng; C Welby; W T Leung; W Y Lau; S Yu; S Ho
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

2.  Diagnosis of hepatocellular carcinoma.

Authors:  Eldad S Bialecki; Adrian M Di Bisceglie
Journal:  HPB (Oxford)       Date:  2005       Impact factor: 3.647

3.  Isoelectric focusing of alphafetoprotein in patients with hepatocellular carcinoma--frequency of specific banding patterns at non-diagnostic serum levels.

Authors:  S Ho; P Cheng; J Yuen; A Chan; N Leung; W Yeo; T Leung; W Y Lau; A K Li; P J Johnson
Journal:  Br J Cancer       Date:  1996-04       Impact factor: 7.640

4.  Structures of disease-specific serum alpha-fetoprotein isoforms.

Authors:  P J Johnson; T C Poon; N M Hjelm; C S Ho; C Blake; S K Ho
Journal:  Br J Cancer       Date:  2000-11       Impact factor: 7.640

5.  Glycan composition of serum alpha-fetoprotein in patients with hepatocellular carcinoma and non-seminomatous germ cell tumour.

Authors:  P J Johnson; T C Poon; N M Hjelm; C S Ho; S K Ho; C Welby; D Stevenson; T Patel; R Parekh; R R Townsend
Journal:  Br J Cancer       Date:  1999-12       Impact factor: 7.640

6.  Simultaneous Detection of α-Fetoprotein and Carcinoembryonic Antigen Based on Si Nanowire Field-Effect Transistors.

Authors:  Kuiyu Zhu; Ye Zhang; Zengyao Li; Fan Zhou; Kang Feng; Huiqiang Dou; Tong Wang
Journal:  Sensors (Basel)       Date:  2015-08-05       Impact factor: 3.576

  6 in total

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