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AFP, PIVKAII, GP3, SCCA-1 and follisatin as surveillance biomarkers for hepatocellular cancer in non-alcoholic and alcoholic fatty liver disease
- Gary Beale†1,
- Dipankar Chattopadhyay†1,
- Joe Gray2,
- Stephen Stewart3,
- Mark Hudson3,
- Christopher Day3, 4,
- Paolo Trerotoli5,
- Gianluigi Giannelli6,
- Derek Manas3 and
- Helen Reeves1, 3, 4Email author
© Beale et al; licensee BioMed Central Ltd. 2008
Received: 09 April 2008
Accepted: 18 July 2008
Published: 18 July 2008
The incidence and mortality of hepatocellular cancer (HCC) complicating alcoholic and non-alcoholic fatty liver diseases (ALD and NAFLD) is rising in western societies. Despite knowing the at risk populations for HCC development, the lack of sensitive and specific means of surveillance hampers disease detection at curable stages. The most widely used serum HCC marker is alpha-fetoprotein (AFP), while PIVKA-II, glypican-3 (GP3) and Squamous Cell Carcinoma Antigen -1 (SCCA-1) have been proposed as new biomarkers. Assessment of these HCC biomarkers has largely been performed in patients with viral hepatitis. We conducted a cross sectional study assessing the value of these serum proteins, as well a novel candidate biomarker -follistatin – in patients with HCC arising on a background of ALD or NAFLD.
Pre-treatment serum samples from 50 patients with HCC arising on a background of ALD (n = 31) or NAFLD (n = 19) were assessed by specific ELISA assay for PIVKAII, Glypican-3, SCCA-1 and Follistatin. Results were compared and contrasted with a control patient group with biopsy proven steatohepatitis-related cirrhosis (n = 41). The diagnostic accuracy of each of the candidate biomarkers was evaluated using receiver operating characteristic (ROC) curve analysis, reporting the area under the curve (AUC) and its 95% confidence interval (CI). Performance was compared to that of the established biomarker, AFP.
Serum levels of all proteins were assessed by specific ELISA assays. GP3, SCCA-1 and follistatin had no HCC surveillance benefit in these patients. AFP and PIVKAII were superior to the other markers, particularly in combination.
We conclude that while novel means of surveillance are urgently required, the combination of AFP and PIVKAII for HCC is an improvement on AFP alone in ALD/NAFLD patients. Furthermore, our data in this homogenous subset of patients- particularly that confirming no role for SCCA-1 – suggests that the choice of optimal biomarkers for HCC surveillance may be determined by the aetiology of underlying chronic liver disease.
Hepatocellular carcinoma (HCC) is a major health problem worldwide, with more than 500,000 cases diagnosed annually . While the incidence of HCC has reportedly risen over the last 5–8 years, the survival of those affected has not changed significantly in the last two decades [1–3]. This is related to both its late detection the lack of effective therapies for advanced stage disease . Up to 80% of HCCs develop against a background of cirrhosis of the liver and while we believe that surveillance of the at risk cirrhotic population could aid earlier detection of the disease and decrease the cancer related mortality rate, our present success is limited by the lack of sensitive biomarkers. Currently, standard surveillance includes a combination of 6 monthly abdominal ultrasound scan (USS) and serum alphafetoprotein (AFP) measurement, but this strategy does not reliably detect early disease. The diagnostic performance of AFP is inadequate as it is only elevated in 40–60% of cases, while abdominal USS is difficult in cirrhotic nodular livers and notoriously user dependent. Alternative serum biomarkers are being actively sought and proposed candidates include Prothrombin Induced by Vitamin K Absence (PIVKA-II), glypican-3 (GP3), and more recently, Squamous Cell Carcinoma Antigen -1 (SCCA-1).
PIVKA-II is an abnormal prothrombin identified as an HCC biomarker in 1984  and since reported elevated most notably in advanced cases with portal vein invasion [8, 9]. It is proposed that PIVKA-II may be useful primarily as a prognostic biomarker, predicting rapid tumour progression and a poorer prognosis . The oncofetal antigen glypican3 (GP3) is a heparan sulfate proteoglycan that is expressed in more than 70% of HCC. When combined with AFP it has a sensitivity of up to 82% for HCC detection on a background of viral hepatitis . SCCA-1 is a member of the high molecular weight serine protease family called serpins  initially reported elevated in epithelial tumours such as the cancer of the head  and more recently in the serum of individuals with HCC and cirrhosis. 
On a global scale, viral causes of chronic liver disease are the commonest predecessors of HCC and these proposed biomarkers  have largely been studied in this disease group. Our own HCC patients have tumours arising predominantly on a background of alcoholic (ALD) and non-alcoholic fatty liver diseases (NAFLD). Here we present the data on a cross-sectional study comparing the efficacy of these markers, as well as a novel candidate biomarker, Follistatin, for the diagnosis of HCC arising on a background of steatohepatitis related cirrhosis. Follistatin is a secreted monomeric protein overexpressed in rat and human liver tumours and reportedly contributing to hepatocarcinogenesis by the inhibition of activins . Follistatin mRNA was markedly overexpressed in HCC cell line microarray studies performed in our own laboratory (unpublished data).
Our data indicate differences in biomarker performance in NAFLD and ALD patients compared to performances reported in viral hepatitis. Neither PIVKAII, GP3, SCCA-1, nor the novel candidate Follistatin, has a role independent of AFP in HCC surveillance in steatohepatitis related cirrhosis. We show that the combination of AFP and PIVKAII is more valuable than AFP alone and suggest this approach be adopted as standard surveillance in this disease group.
Patient serum samples
All patient serum and clinical information were collected with patient consent after approval by The Newcastle and North Tyneside Ethics Committee approved this study. Patients were diagnosed as having HCC as per guidelines proposed by the European Association for the Study of the Liver . Pre-treatment samples from 50 patients with HCC, all of whom had an underlying cirrhosis, were selected for study. Of these, 31 patients had alcoholic liver disease (ALD) and 19 patients had NAFLD. The serum was immediately separated by centrifugation and frozen at -80°C. These serum samples were compared to an independent group of 41 patients with biopsy proven ALD or NAFLD cirrhosis. The diagnosis of NAFLD cirrhosis was made in patients who had clinical features and liver biopsies compatible with NAFLD. Females and males consuming greater than 14 or 21 units of alcohol per week respectively were excluded from this category, as were any individuals with viral or autoimmune liver diseases. The presence of steatosis was necessary for the diagnosis to be made, as was stage 4 fibrosis defined by modified Brunt criteria
The biochemical serum tests, including serum AFP, were measured using routine automated methods in the Biochemistry Laboratory at the Freeman Hospital, Newcastle upon Tyne. No patient positive for either HBsAg or HCV were included in this study.
Western blotting and serum ELISA assays
PIVKA-II was measured using a commercially available ELISA kit (Asserachrom PIVKAII kit, Stago, France), according to the manufacturer's instructions. The detection limit is 01 ng/ml. The cut-off value was set as 20 ng/ml for differentiation between HCC and cirrhosis based on the findings in this study. Glypican-3 was measured using commercially available ELISA kit (Biomosaics limited) following the manufacturer's protocol. Serum SCCA-1 was measured as previously described an ELISA kit purchased from Xeptagen (Xeptagen, Naples, Italy) and following the manufacturer's instructions. 
Follistatin was selected for study based on its marked expression in HCC cell lines on microarray analysis and literature review identifying it as a secretory protein with a previously suspected role in hepatocarcinogenesis. Ten samples each from patients with NAFLD, NAFLD and cirrhosis, or NAFLD with cirrhosis and HCC were immunedepleted by multiple affinity removal (MARS HPLC column;Agilent technologies) and desalted using 5 K molecular weight cut off spin filters (Agilent technologies). Subsequently, 50 μg of protein was separated by SDS-PAGE and transferred to PVDF membrane (250 mA for 90 min). The membrane was then probed with mouse anti-follistatin antibody (R&D Systems) at 1:500 dilution at room temperature overnight. After washing in Tris Buffered Saline (0.1% Tween), the membranes were incubated with secondary peroxidase conjugated rabbit anit-mouse immunoglobulin and developed using ECL (Amersham). Subsequently, a direct ELISA assay for quantitative analysis, was developed using different concentrations of serum (raw; 1:10; 1:50; 1:100: 1:1000) with serial dilution of primary antibody. Optimal conditions were using a raw serum dilution of 1:10 and an antibody dilution of 1:250.
Quantitative variables were expressed as mean and standard deviation. Comparison between groups was by Pearson Chi-square, Wilcoxon or Student's t-test, as appropriate. Qualitative variables were expressed as count and percentage and comparisons between independent groups was by Pearson Chi-square. The diagnostic accuracy of each of the candidate biomarkers was evaluated using receiver operating characteristic (ROC) curve analysis, reporting the area under the curve (AUC) and its 95% confidence interval (CI). The diagnostic cut-off and the related sensitivity and specificity were determined. Statistical analysis was performed with SAS V8.2 software for PC, MedCalc version 18.104.22.168, as well as SPPS version 14.
Clinical characteristics of the patients with cirrhosis and cirrhosis plus HCC
54.3 ± 9.62
67.5 ± 12.02
Portal vein invasion
≥ 3 nodules
Serum AFP and PIVKAII as biomarkers of HCC in steatohepatitis related cirrhosis
Levels of candidate biomarkers (ng/ml) as detected by specific ELISA assays
Cirrhosis + HCC
Mean ± S.D.
Mean ± S.D.
5.96 ± 2.65
5934.66 ± 13025.02
23.47 ± 59.69
135.17 ± 168.96
125.41 ± 281.05
161.41 ± 422.33
72.41 ± 76.16
87.33 ± 131.31
Performance of combinations of candidate biomarkers
sensitivity (HCC = 50)
specificity (LC = 41)
Serum GP3 and SCCA-1 have no role in HCC surveillance in steatohepatitis-related cirrhosis
The data for GP3 and SCCA-1 in this group of ALD/NAFLD patients with and without HCC is also presented in Figures 1 and 2 and Table 2 and 3. These data demonstrate that neither had any value in HCC detection in this group of patients. While their expression was elevated in the serum of patients with chronically diseased livers and HCC, there was no significant difference between the levels detected in cirrhotic patients with and without a cancer.
Follistatin is raised in the serum of individuals with cirrhosis and HCC, but its specificity for HCC is poor
The increasing incidence of HCC, compounded by the fact that the majority of these tumours are diagnosed at a late stage when curative treatments are not possible, has prompted the international community into performing regular surveillance of high risk individuals. Unfortunately, surveillance programmes are hindered by the poor performance of the commonly used serum marker, namely AFP, even in combination with abdominal USS. A tremendous amount of effort has been and continues to be applied to the search for improved HCC biomarkers. As yet, none has proved superior to AFP in performance, but in combination some may have complimentary roles in HCC arising on a background of viral hepatitis . Our own particular concern relates to the marked increase in the prevalence of ALD and NAFLD related HCC on our own unit.
In our study, serum AFP performs moderately well as a biomarker of HCC in ALD/NAFLD patients, with a sensitivity of 58% (15 ng/ml) in combination with a specificity of 100%. The AASLD recommended cut off level for diagnosis of HCC is 200 ng/ml , although lower levels, particularly if rising, should be deemed suspicious and followed very carefully. In ALD/NAFLD patients, where a mild to moderately elevated but stable AFP level similar to that occasionally observed in individuals with viral hepatitis is rare, it may be possible to attach a more sinister connotation to much lower levels of expression. While this data is encouraging, the sensitivity of AFP is not good enough for it to be used in isolation, as over a third of cancers will be missed.
Both the sensitivity and specificity for PIVKAII as an HCC biomarker were in the order of 80% at a level of 20 ng/ml. The addition of PIVKAII serum analysis to that of AFP increases the combined sensitivity to 94%. While this is at the modest expense of the specificity (reduced to 80.5%), the combination of both AFP and PIVKAII analyses may well be justified in our patients. It should be noted, however, that the added benefit is only in the detection of more advanced disease – as indicated in previous viral hepatitis studies and confirmed in our own NAFLD/ALD patients -the encouraging performance of PIVKA-II is predominantly a result of detection of larger, more advanced cancers.
Assessment of the other candidate biomarkers was disappointing. Both the sensitivity and specificity of GP3 were poor in our patient set, indicating that it has no role at all in the surveillance of HCC in individuals with steatohepatitis related cirrhosis. Follistatin is an expressed transcript in fetal liver and has previously been identified by microarray as an up-regulated gene in HCC relative to dysplastic nodules . Although we had high hopes for this activin antagonising protein,  based on both our preliminary microarray data and a pilot study in immune depleted sera, the ELISA data assessing its discriminatory function between cirrhotic individuals with and without HCC was poor. The discrepancy between the western and ELISA data is most likely a result simply of assessing a greater number of patients using the latter method, but it is also that follistatin, or an isoform of it, was enriched during the column preparation phase of the serum of HCC patients assessed by western blotting. Perhaps the most surprising of results, however, in this homogenous group of patients with steatohepatitis related HCC, was the disappointing performance of SCCA-1. SCCA-1 has previously shown promise, particularly as an AFP complementary biomarker, in viral hepatitis related HCC [24, 25]. In our study in NAFLD/ALD, however, there was no significant difference between levels in patients with and without HCC and while the combination with AFP does modestly improve its sensitivity (78% from 56%), this is at an unacceptable cost to specificity (73% from 100%). Why this serum protein should be significantly elevated in the serum of HCV related HCC patients relative to HCV cirrhosis alone, and not similarly elevated in steatohepatitis related HCC patients relative to steatohepatitis cirrhosis alone is unclear. It is possible that the study of these novel candidate biomarkers complexed to immunoglobulins, rather than the study of their free forms, may yet improve their performance, as has been shown for other biomarkers . Whether or not there is room for improvement, however, our SCCA-1 data clearly indicate that as we come to consider further candidate biomarkers it is important to assess HCC arising in different disease backgrounds independently when performing validation studies.
In summary, while we propose the combination of AFP and PIVKAII for HCC surveillance in NAFLD/ALD patients, the search for novel biomarkers of early HCC disease should continue.
We thank the individuals agreeing to study participation, the Newcastle NHS Combined Trust for acting as study sponsor, The LiverNorth patient support group for financial support and encouragement, and the Hepatologists and Hepatobiliary Surgeons who have contributed to patient recruitment to the study.
Funding: LiverNorth patient support group award to HR. LiverNorth have provided the funds for sample collection and sample analysis. The SCCA-1 assays and statistical analysis were supported by grant number 202200GNN08 from the Regione Puglia, awarded to GG.
Ethics: The Newcastle and North Tyneside Ethics Committee approved this study.
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