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Year : 2019  |  Volume : 32  |  Issue : 1  |  Page : 1-7

Platelet-derived growth factor in patients with liver fibrosis

1 Clinical Pathology Department, Faculty of Medicine, Menoufia University, Shebeen El-Kom, Egypt
2 Clinical Pathology Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt

Date of Submission02-Jul-2017
Date of Acceptance01-Aug-2017
Date of Web Publication17-Apr-2019

Correspondence Address:
Amira Z Badawy
Clinical Pathology Department, Faculty of Medicine, Menoufia University, Shebeen El-Kom, Menoufia Governorate
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/mmj.mmj_468_17

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To asses the changes in platelet-derived growth factor (PDGF) in liver fibrosis.
Data sources
The data were sourced from the PubMed database from the start of the database to 2017 and from all materials available in the Internet.
Study selection
The initial search presented 423 articles of which 39 met the inclusion criteria. The articles studied the relation between PDGF and liver fibrosis.
Data extraction
If the studies did not fulfill the inclusion criteria, they were excluded. Study quality assessment included when ethical approval was obtained, eligibility criteria defined, sufficient information, convenient controls, and known assessment measures.
Data synthesis
Comparisons were made through structured review with the results tabulated.
In total, 39 potentially relevant publications were included. The studies indicate an association between PDGF and liver fibrosis as PDGF increases in patients with hepatic fibrosis and correlates well with the grade of fibrosis. The majority of studies were performed on the effect of PDGF antagonists on liver fibrosis and they found that interference of PDGF pathway leads to reduction of liver fibrosis.
We found that PDGF levels increase in patients with liver fibrosis and its level correlates well with the stage of fibrosis; thus, PDGF can be used as a potential noninvasive marker for liver fibrosis either alone or in association with other fibrosis markers. Further, antagonizing the pathway of PDGF may offer a promising strategy for the treatment of liver fibrosis.

Keywords: fibrosis markers, growth factors, hepatitis, liver fibrosis, platelet-derived growth factor

How to cite this article:
Essa ES, Eskander FG, Badawy AZ. Platelet-derived growth factor in patients with liver fibrosis. Menoufia Med J 2019;32:1-7

How to cite this URL:
Essa ES, Eskander FG, Badawy AZ. Platelet-derived growth factor in patients with liver fibrosis. Menoufia Med J [serial online] 2019 [cited 2020 Jun 2];32:1-7. Available from: http://www.mmj.eg.net/text.asp?2019/32/1/1/256117

  Introduction Top

Fibrosis and cirrhosis of the liver are important causes of morbidity and mortality globally and are related to increasing economic and social impact [1]. Liver fibrosis is an outcome of almost all chronic liver diseases, which is either because of chronic viral infection through hepatotropic viruses (especially hepatitis-B and hepatitis-C viruses) or autoimmune injury, in addition to metabolic and toxin-induced injury [2]. Hepatic fibrosis is the final event of chronic liver injury; it is characterized by excessive extracellular matrix deposition that distorts the hepatic architecture by forming fibrotic scars, and the subsequent development of nodules of regenerating hepatocytes leading to liver cirrhosis [3].

To date, percutaneous liver biopsy assessed using histological analysis is still the primary technique for evaluating the severity of liver injury. However, clinically, using this diagnostic technique is limited because of the invasiveness of the process and its associated hazards such as pain, bleeding, and sampling errors. In recent years, there has been growing interest in identifying and describing liver fibrosis using molecular serum markers [4]. For example, the aspartate aminotransferase-to-platelet ratio (APRI) and fibrosis index based on a total of four factors (FIB-4) have been the most commonly used scoring systems; these were initially used to asses patients with persistent hepatitis-C virus infection but a number of research studies have found that APRI and FIB-4 are also suitable markers for detecting liver fibrosis in patients with chronic hepatitis-B (CHB) infection [5]. It has been established that cytokines, growth factors, and other mediators produced locally control the progression from chronic liver injury to fibrosis, cirrhosis, and, lately, tumor formation. Platelet-derived growth factor (PDGF) belongs to a family of growth factors that were previously recognized as key mediators of vascular pathologies [6].

Several studies have been performed over the last two decades to assess the relation between PDGF and liver fibrosis [Table 1] and [Table 2]. They have indicated that PDGF, one of the most potent recognized mitogens, promotes liver fibrosis through activation of hepatic stellate cells (HSCs). Moreover, PDGF is overexpressed in liver tissue during fibrogenesis [15]. Besides, a substantial number of studies on the effect of PDGF antagonists on liver fibrosis have been published [Table 3]. These studies found that usage of PDGF antagonists inhibit liver fibrosis, whereas only one study has found that PDGF expression decreases with advancement of fibrosis [14]. Thus, this review aims to assess the potential changes of PDGF levels in liver fibrosis and evaluate their relation to the grade of fibrosis.
Table 1: Relation between hepatic platelet-derived growth factor and liver fibrosis according to evidence-based medicine

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Table 2: Relation between serum and platelet platelet-derived growth factor and liver fibrosis according to evidence-based medicine

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Table 3: Effects of platelet-derived growth factor antagonists on liver fibrosis according to evidence-based medicine

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  Patients and Methods Top

Search strategy

We reviewed papers on the relation between PDGF and liver fibrosis from the PubMed database. We used PDGF and liver fibrosis as search terms. The search was performed in the electronic database from the start of the database to 2017.

Study selection

Each study was independently assessed for the following inclusion criteria:

  • Posted in peer-reviewed journals
  • Published in English language
  • Targeted on PDGF in liver fibrosis.

We used the latest publication when a study had several publications on certain aspects.

Data extraction

If the studies did not fulfill the above criteria, they were excluded, such as studies on other growth factors, studies about liver fibrosis without assessment of level of PDGF, report without peer-review, studies not within the national research program, letters/comments/editorials/news, and studies not focused on PDGF in liver fibrosis.

The assessed studies were evaluated according to evidence-based medicine (EBM) criteria using the classification of the US Preventive Services Task Force and UK National Health Service protocol for EBM in addition to the Evidence Pyramid [Figure 1].
Figure 1: The pyramid of evidence-based medicine.

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US Preventive Services Task Force:

Level I: evidence taken from at least one well-designed randomized controlled trial

Level II-1: evidence came from properly designed controlled trials but without randomization

Level II-2: evidence that was obtained from properly designed cohort or case–control studies, especially, from more than one center or research group

Level II-3: evidence that came from multiple time series with or without an intervention. Dramatic results in uncontrolled trials might also be regarded as this type of evidence

Level III: opinions of expert committees, based on clinical experience, descriptive studies, or reports of respected authorities.

Quality assessment

The quality of all the studies was evaluated. Important factors included, design of the study, possessing ethical approval, evidence of a power calculation, specified eligibility criteria, appropriate controls, sufficient information, and specified assessment measures. It was expected that confounding factors would be reported and controlled for and that appropriate data analysis was carried out in addition to an explanation of any missing data.

Data synthesis

A structured systematic review was performed with the results tabulated.

  Results Top

Study selection and characteristics

In total, 423 potentially relevant publications were identified, and 384 articles were excluded as they did not meet our inclusion criteria [Figure 2]. A total of 39 studies were included in the review as they were deemed eligible by fulfilling the inclusion criteria. The majority of the studies assessed the changes of PDGF in liver fibrosis.
Figure 2: Flow chart of study selection.

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The relation between platelet-derived growth factor and liver fibrosis was investigated in eight studies

Out of eight studies four of which measured PDGF level in hepatic tissue [Table 1] and four measured it in serum and one study measured it in platelets [Table 2].

Changes in hepatic PDGF according to evidence-based medicine [Table 1].

There are four studies that measured the PDGF level in hepatic tissue, one of which was animal study and three were human studies.

The animal study [Table 1] [12] (which comes in the base of the Evidence Pyramid and provides the least strength of evidence) investigating PDGF in liver fibrosis induced in experimental animals found that PDGF and its receptors are overexpressed in liver fibrosis and they help the progression of fibrosis.

Regarding the three human studies [Table 1], there were two case–control studies with level II-2 or (level B) EBM [8],[10], which reported that hepatitis B virus particles may stimulate HSC proliferation by acting on PDGF-B/platelet-derived growth factor receptor (PDGFR)-β signaling pathway that plays a key role in liver fibrosis and that mRNA expression of PDGF in platelets was remarkably lower in late fibrosis than in early-stage fibrosis, respectively. There was also one purposive nonrandomized study with level II-1 EBM [9], which concluded that PDGF and its receptor mediate the progression of liver fibrosis and highly correlate with the stage of liver fibrosis.

Changes in serum platelet-derived growth factor according to evidence-based medicine [Table 2].

In all, four studies had measured PDGF level in serum, two of which were cohort studies with level II-2 EBM [11],[14], which reported that serum levels of PDGF-BB can predict degree of liver damage and stage of liver fibrosis in CHB and that serum PDGF-BB reduced significantly with advancement of fibrosis in patients with CHB, respectively.

There was also one case–control study with level II-2 EBM [12], which reported that there was significant positive correlation between serum levels of PDGF and degree of liver fibrosis.

There was also one case report [13], which comes in level II-3 EBM, which reported that the PDGF pathway may play a central role in the fibrogenesis of multiple organs in patients with transient myeloproliferative disorder.

Changes in platelet platelet-derived growth factor according to evidence-based medicine [Table 2].

Only one case–control study with level II-2 or (level B) EBM [10] exists, which assessed PDGF in platelets and found that mRNA expression of PDGF in platelets was remarkably lower in late fibrosis than in early-stage fibrosis and that PDGF level is lower in platelets than in hepatic tissue.

The effect of platelet-derived growth factor antagonists on liver fibrosis was investigated in five studies

Out of eight studies four of which were animal studies [16],[17],[18],[19] (which comes in the base of the Evidence Pyramid and provides the least strength of evidence). They all reported that interfering with the PDGF pathway by PDGF antagonists leads to inhibition of liver fibrosis and this provides a promising treatment for liver fibrosis. Of five studies, there was only a mini review [15] (which comes in the second level regarding the pyramid of EBM) which reported that several PDGF antagonists inhibit fibrogenic activation in culture and in some animal models of liver fibrosis and suppression of PDGFR-β signaling with tyrosine kinase inhibitors proved effective in the early stage than in the advanced stage of fibrosis [Table 3].

  Discussion Top

Liver fibrosis is the unusual accumulation of extracellular matrix (ECM) proteins like collagen, which occurs in the majority of chronic liver diseases. Advanced liver fibrosis leads to cirrhosis, liver-cell failure, and portal hypertension and usually requires liver transplantation [20].

The underlying cellular mechanisms involved in hepatic fibrogenesis basically include the activation of HSCs, which is the principal fibrogenic cell type in the liver. After injury by any of the causes of hepatic fibrosis, HSCs go through a reaction called 'activation', in which quiescent cells transition into proliferative myofibroblasts that have the ability to produce ECM proteins. Hepatocytes and Kupffer cells are involved in the initiation and perpetuation of HSC activation through release of several compounds that cause paracrine stimulation of HSCs, including reactive oxygen species, cytokines, and growth factors [Figure 3]. Activated HSCs respond to these paracrine signals through proliferation, chemotaxis, contractility, release of cytokines and chemokines, deposition of ECM molecules, and loss of retinoids [21]. PDGF plays a central role in most of these responses, especially, in HSC proliferation and chemotaxis.
Figure 3: Proinflammatory cytokines and growth factors involved in hepatic fibrogenesis.

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Liver biopsy is considered the gold-standard technique for investigating liver fibrosis [4]. Histological examination is useful in recognizing the underlying cause of liver illness and in evaluating the necroinflammatory stage and the degree of fibrosis. Fibrosis stage is assessed using scales such as Metavir (stages I–IV) and Ishak score (stages I–V). Liver biopsy is an invasive process, associated with pain occurring in 40% of patients and major complications in 0.5% of patients [22] in addition to sampling error, especially when the biopsies are too small to be analyzed. Histological examination is vulnerable to intraobserver and interobserver variation and does no longer predict disease progression [23]. Consequently, there is a need for dependable, easy, and noninvasive methods for assessing liver fibrosis. Scores that involve routine laboratory tests, such as platelet count, prothrombin time, aminotransferase levels, and serum levels of acute-phase proteins, have been proposed [24]. Serum levels of proteins that directly associate with hepatic fibrogenesis are also used as alternative markers of liver fibrosis [25], including N-terminal propeptide of type-III collagen, hyaluronic acid, tissue inhibitor of metalloproteinase type-1, and YKL-40. PDGF is one of these proteins that is closely related to liver fibrogenesis and several studies have been carried out to asses its efficacy as a potential marker for liver fibrosis [11].

PDGF is a stimulant and an important regulator for the proliferation, migration, and survival of mesenchymatous cell lineages. According to the distribution of its receptors, it is capable of inducing stimulation or inhibition of the development of these cells. It is also a potent mitogen for fibroblasts and smooth muscle cells [26].

The PDGF family of growth factors includes four different polypeptide chains encoded using the classical PDGF-A and PDGF-B chains, and by the lately discovered PDGF-C and PDGF-D chains. The four PDGF chains assemble into dimers through homodimerization or heterodimerization and five different resultant dimeric isoforms have been observed so far: PDGF-AA PDGF-AB, PDGF-BB, PDGF-CC, and PDGF-DD [27].

PDGF was first discovered and purified from human blood platelets in 1979. It is synthesized and secreted from a wide variety of cells including macrophages, tumor cells, smooth muscle cells, vascular endothelial cells, and fibroblasts [28].

PDGF comprises a series of secretory growth factors that play critical roles in the pathogenesis of liver fibrosis. PDGF activates HSCs and stimulates portal fibroblast proliferation. Besides, it regulates chemotaxis, cell migration, and cell survival [15]. Inside the liver, PDGF levels have been shown to correlate with the incidence of liver fibrosis attributable to different causes [9]. During fibrogenesis, PDGF is secreted by variable cell types as a response to injury, and numerous proinflammatory cytokines control their mitogenic effects through the autocrine release of PDGF. The effect of PDGF is determined through the relative expression of PDGFR-α and PDGFR-β on myofibroblasts. These receptors are stimulated during fibrogenesis, therefore, amplifying biological responses to PDGF isoforms. The effect of PDGF is also mediated by extracellular binding proteins and matrix molecules [29].

Reviewing recent studies about the relation between PDGF and liver fibrosis, we found that serum and hepatic PDGF levels increase in patients with liver fibrosis [Table 1] and [Table 2]. Although the platelet level of PDGF was measured in only one study (case–control study) [10] and it was lower in platelets than in hepatic tissue, the author explains this lower level of PDGF as being consumed by TGFB1 activation.

There was a strong positive correlation between PDGF and fibrosis grade in almost all studies except in one cohort study [14] that had inconsistent results, as it reported that serum PDGF-BB decreased remarkably as fibrosis progressed in patients with CHB. There could be a potential bias in study methodology or in the selection of patients.

Studies in our review that investigated the effect of PDGF antagonists on liver fibrosis [Table 3] had found that inhibition of PDGF pathway leads to reduction of liver fibrosis.

It is recommended that future studies should be carried out to identify the source of PDGF that is elevated during liver fibrosis, and whether it is secreted from hepatic cells, blood platelets, or from platelet pools in the liver.

  Conclusion Top

This review concluded that PDGF levels increase in patients with liver fibrosis and its level correlates well with fibrosis stage; therefore, PDGF could be used as a potential noninvasive marker for liver fibrosis. Further, antagonizing the pathway of PDGF may offer a promising strategy for the treatment of liver fibrosis.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

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  [Figure 1], [Figure 2], [Figure 3]

  [Table 1], [Table 2], [Table 3]


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