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Table of Contents   
ORIGINAL ARTICLE  
Year : 2016  |  Volume : 22  |  Issue : 5  |  Page : 375-379
Pigment epithelium-derived factor and matrix metalloproteinase-9 in liver cirrhosis


Department of Infectious and Tropical Diseases and Hepatology, Medical University of Warsaw, Warsaw, Poland

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Date of Submission18-Feb-2016
Date of Acceptance12-Aug-2016
Date of Web Publication27-Sep-2016
 

   Abstract 

Background/Aim: The aim of this study was to assess the role of serum pigment epithelium-derived factor (PEDF) and matrix metalloproteinase-9 (MMP-9) in progression of liver cirrhosis and development of hepatocellular carcinoma (HCC). Patients and Methods: Serum levels of PEDF and MMP-9 were tested in 212 patients with liver cirrhosis and in a control group of 30 healthy volunteers. HCC was diagnosed in 45 of the 212 patients studied (21%). Results: Serum PEDF and MMP-9 were higher in the study group than that in the control group (P < 0.001). In patients with alcoholic or mixed (alcoholic and viral hepatitis-related) cirrhosis, serum PEDF was higher than that in other patients (13970.2 ± 13406.9 ng/ml vs. 8563.5 ± 9602.7 ng/ml, P = 0.008). In patients with viral hepatitis-related cirrhosis, significantly higher PEDF levels were recorded in those with HCC (13429.1 ± 12045.8) than that in patients without HCC (6660.1 ± 7927.1; P = 0.04). There was a trend for higher serum MMP-9 in patients with HCC (5778.7 ± 12426.6 vs. 1389.8 ± 1944.7 in those without HCC; P = 0.07). Significant negative correlation between serum MMP-9 and serum alpha-fetoprotein in patients with HCC was observed (r = −0.54; P = 0.04). Conclusion: Serum PEDF and MMP-9 could be auxiliary markers in diagnosis of HCC, especially in patients with low alpha-fetoprotein level. Alcohol consumption can affect serum PEDF.

Keywords: Fibrosis markers, hepatocellular carcinoma, liver cirrhosis

How to cite this article:
Kozlowska J, Mikula T, Suchacz M, Jabnonska J, Stanczak W, Cianciara J, Wiercinska-Drapalo A. Pigment epithelium-derived factor and matrix metalloproteinase-9 in liver cirrhosis. Saudi J Gastroenterol 2016;22:375-9

How to cite this URL:
Kozlowska J, Mikula T, Suchacz M, Jabnonska J, Stanczak W, Cianciara J, Wiercinska-Drapalo A. Pigment epithelium-derived factor and matrix metalloproteinase-9 in liver cirrhosis. Saudi J Gastroenterol [serial online] 2016 [cited 2019 Aug 23];22:375-9. Available from: http://www.saudijgastro.com/text.asp?2016/22/5/375/191143


The pathogenesis of hepatocellular carcinoma (HCC) is a multifactorial process which has not been fully explained so far. Early diagnosis is still difficult; this neoplasm is frequently diagnosed in the advanced phase. Serum α-fetoprotein (AFP) and ultrasound imaging (US) for many years have been the gold standard of HCC screening. However, sensitivity and specificity of serum AFP in HCC diagnosis are relatively low, [1],[2] therefore, it was excluded from the American Association for the Study of Liver Diseases (AASLD) guidelines for HCC screening in 2010 [3] and from European Association for the Study of the Liver (EASL) guidelines in 2012, [4] whereas others still recommend testing AFP in addition to US. [5],[6],[7]] There is a need for new, more sensitive, and reliable diagnostic tests. There are several molecular markers of HCC currently under investigation including cellular markers, cellular cycle regulators, markers of apoptosis, telomerase activity, adhesive molecules, markers of extracellular matrix degradation, markers of angiogenesis, growth factors and their receptors, oncofetal and glycoprotein antigens, enzymes and isoenzymes, and genetic markers. [8]

Pigment epithelium-derived factor (PEDF) is an endogenously produced glycoprotein with a molecular weight of 50 kD, occurring commonly in various organs and exhibiting diverse biological activity. It belongs to the superfamily of serine protease inhibitors. PEDF reaches high concentrations in serum, which can be used for diagnostic purposes. [9] Repeatedly confirmed effect of this molecule is inhibition of angiogenesis. [10] It is believed that PEDF has neuroprotective properties, [11] acts as an antioxidant and anti-inflammatory agent, [12] inhibits cellular proliferation and supports cell differentiation, and protects against tumor metastasis. [13] Liver is the major site of PEDF synthesis. [14] PEDF is an important factor in many liver diseases. [15] The mechanism of its action remains largely unclear. Antifibrogenic activity of intrahepatic PEDF has been demonstrated. [16] PEDF is secreted by fat cells as well, playing a role in the development of insulin resistance, metabolic syndrome, and liver steatosis. [17],[18],[19],[20],[21],[22]

Matrix metalloproteinase-9 (MMP-9) is a zinc-dependent enzyme also called gelatinase B, with a molecular weight of 92 kD. It degrades extracellular matrix proteins, particularly collagen IV, which is a component of basement membrane. This enzyme plays an important role in inflammation, tissue remodeling process, as well as promotes tumor cell migration and metastasis. [23],[24] The main sources of matrix metalloproteinases in the damaged liver are stellate cells with endothelium and inflammatory cells. [25] It was found that serum or plasma MMP-9 may be a useful marker of the processes that occur in the tissues. [26] Elevated MMP-9 levels were observed in colorectal cancer and breast cancer, [27] stomach cancer, [28] bladder cancer, acute leukemia, rheumatoid arthritis, melanoma, and HCC. [29] The activity of MMP-9 is checked on several levels: transcription - control of cytokines, activation of the proenzyme - enzyme cascade, including serine proteases and other metalloproteinases, finally - regulation by specific tissue inhibitors of metalloproteinases (TIMP). The data on the serum MMP-9 as a marker of fibrosis are controversial. [30]

In this study, we investigated the usefulness of serum PEDF and MMP-9 in evaluating the progression of liver cirrhosis and development of HCC.


   Patients and Methods Top


The study group consisted of 212 patients with cirrhosis from the database e-Hepar; 127 men and 85 women, aged from 28 to 86 years, with a mean age of 54.6 years. The study also included a control group of 30 healthy volunteers; 12 men and 18 women, aged from 28 to 52 years, with a mean age 38.3 years. Informed consent was obtained from each patient included in the study. Serum PEDF and MMP-9 were determined by ELISA Kits (PEDF - ChemiKine, Chemicon International; MMP-9 - Platinum ELISA, eBioscience). Standard biochemical serum tests were carried out, including aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alpha-fetoprotein (AFP). The severity of liver cirrhosis was assessed using the Child-Pugh score. Statistical analysis was performed using Statistica; Spearman's rank correlation test and the Mann-Whitney U test were used. P value of < 0.05 was considered to be statistically significant.

Analyzing the etiology of liver cirrhosis in the study group, pure viral hepatitis-related cirrhosis was identified in 124 patients, pure alcoholic cirrhosis in 27 patients, cirrhosis of mixed etiology (viral hepatitis-related and alcoholic) in 43 patients, and cirrhosis of other or unknown etiology in 18 patients. From 167 patients infected with hepatotropic viruses, 126 patients were infected with hepatitis C virus (HCV), 33 with hepatitis B virus (HBV), and 8 patients were co-infected with HBV and HCV.

HCC was diagnosed in 45 of the 212 patients studied (21%). These were patients with viral hepatitis-related liver cirrhosis (36 patients) and cirrhosis of mixed etiology (8 patients). None of the patients with alcoholic liver disease were diagnosed with HCC. Among patients with HCC, 40 were infected with HCV, 4 patients were diagnosed with HBV, and 1 patient was infected with both viruses.


   Results Top


The concentration of both PEDF and MMP-9 was significantly higher in patients with cirrhosis than in the control group (for PEDF, respectively, 11000.7 ± 11367.7 ng/ml vs. 417.3 ± 266.5 ng/ml, P < 0.001; for MMP-9 1863.5 ± 4692.8 ng/ml vs. 94.9 ± 21.6 ng/ml, P < 0.001). There were no significant differences in levels of PEDF or MMP-9 between the groups A, B, and C according to the Child-Pugh classification [Figure 1] and [Figure 2]. There were significant differences in the levels of PEDF, depending on the etiology of cirrhosis. In patients with alcoholic or mixed (alcoholic and viral hepatitis-related) cirrhosis, serum PEDF was higher than in other patients (13970.2 ± 13406.9 ng/ml vs. 8563.5 ± 9602.7 ng/ml, P = 0.008) [Figure 3].
Figure 1: Serum PEDF in groups A, B, and C according to the Child-Pugh; P = NS

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Figure 2: Serum MMP-9 in groups A, B, and C according to the Child-Pugh; P = NS

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Figure 3: Serum PEDF depending on the alcoholic etiology of cirrhosis; P = 0.008. AC, alcoholic cirrhosis; non-AC, non-alcoholic cirrhosis.

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In further analysis of the group of patients with viral hepatitis-related cirrhosis, there were significantly higher PEDF levels recorded in patients with HCC (13429.1 ± 12045.8) than that in patients without HCC (6660.1 ± 7927.1; P = 0.04) [Figure 4].
Figure 4: Serum PEDF in patients with viral hepatitis-related cirrhosis, depending on the presence of HCC; P = 0.04

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Similarly, there was also a trend for higher serum MMP-9 in patients with HCC (5778.7 ± 12426.6 vs. 1389.8 ± 1944.7 in those without HCC; P = 0.07). The analysis was performed in all patients, regardless of the etiology of cirrhosis [Figure 5].
Figure 5: Serum MMP-9 in patients with cirrhosis, depending on the presence of HCC; P = 0.07

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By examining correlations of various factors associated with the disease to the value of serum PEDF, a negative correlation between serum PEDF and ALT level (r = −0.18, P = 0.06) was found. This correlation was particularly visible and statistically significant in patients without HCC (r = −0.27; P = 0.03). Significant negative correlation between serum MMP-9 and serum AFP in patients with HCC was observed (r = −0.54; P = 0.04).


   Discussion Top


In this study, serum PEDF and MMP-9 were determined in patients with cirrhosis of different etiologies, and their value in the diagnosis of HCC was assessed. PEDF, which has antiangiogenic and antiproliferative activity, is considered to be a protective factor, reducing the risk of HCC development. [31] In contrast, MMP-9 is an enzyme whose activity promotes tumor growth and invasion. [32] In our study, we have shown that both of these markers are elevated in patients with cirrhosis, especially in patients with HCC. There are few reports describing changes in serum levels of PEDF in patients with cirrhosis; decreased level of PEDF in liver tissue was reported in these patients. [16],[33] Elevated serum PEDF was described in patients with liver steatosis. [18],[20] As MMP-9 is the enzyme involved in the degradation of PEDF in the liver, it is postulated that there is a relationship of these two markers in certain liver diseases. [33],[34] There was a decrease of PEDF in liver tissue of humans and animals with alcoholic liver disease with concomitant increase of MMP-9. [33] There is a hypothesis that PEDF inhibits the development of cirrhosis by direct inactivation of the stellate cells and the induction of apoptosis [16] and by stimulating apoptosis in the HCC cells. [35],[36]

Some studies have confirmed elevated levels of MMP-9 in patients with chronic liver disease. [29],[37] Studies have also shown a correlation of serum MMP-9 with the progression of liver fibrosis, [37] as well as transaminase levels, [37],[38] which was not confirmed in our study. Other authors, in contrast to us, found reduction in serum MMP-9 in patients with chronic hepatitis C and cirrhosis. [39] Many studies have demonstrated higher MMP-9 levels in plasma [22] and in liver tissue [40],[41] in patients with HCC. In tumor tissue, higher expression of this enzyme was detected than in adjacent liver tissue. [40],[41],[42] Hayasaka et al. [29] determined the sensitivity (53%) and specificity (89%) of plasma MMP-9 for the detection of HCC. It was also found that MMP-9 correlated with the progression of cancer: Vascular invasion, [28],[29],[42] a low tumor cell differentiation, [42] capsule infiltration, [40] the incidence of metastasis, [28] overall stage of HCC, and with poor prognosis. [42],[43] The value of simultaneous determination of MMPs and tissue inhibitors of MMP (TIMPs) is emphasized. The ratios of MMP: TIMP and MMP-9:MMP-2 are important in the diagnosis and prognosis of HCC. [44],[45]

In our study, we found that serum MMP-9 correlates negatively with serum AFP. Other studies do not confirm these results. [29],[46] Our results can be partially explained by a possible diversity of histopathological forms of HCC in the study group. Carcinoma with low cell differentiation may not produce AFP. In this case, the determination of MMP-9 would increase the likelihood of the diagnosis of HCC.

In the study group, we found significantly higher level of serum PEDF in patients who abuse alcohol (alcoholic or mixed cirrhosis) than that in patients with viral hepatitis-related cirrhosis. Sogawa et al. [47] also confirmed that PEDF levels may be an independent exponent of excessive alcohol consumption. A negative correlation of PEDF and ALT level in our study suggests that PEDF is not a marker of inflammation in the liver.

These are only preliminary studies regarding the potential role of serum PEDF and MMP-9 as adjunctive diagnostic biochemical markers in HCC. The limitations of these tests is that their cut-offs are not defined. Further studies are needed to better characterize the suitability of these tests in clinical practice.

In conclusion, serum PEDF and MMP-9 may aid in the diagnosis of HCC, especially in patients with low AFP, where the diagnosis is questionable. Alcohol consumption can affect the level of serum PEDF. Serum PEDF and MMP-9 are higher in cirrhosis, however, their level does not differentiate the stages of cirrhosis.

Acknowledgement

Grant number 12710 from The National Centre for Research and Development, Ministry of Science and Higher Education, Poland.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
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Correspondence Address:
Joanna Kozlowska
Department of Infectious and Tropical Diseases and Hepatology, Medical University of Warsaw, 01 201 Warsaw, Wolska 37
Poland
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1319-3767.191143

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