# Plasma Levels of Matrix Metalloproteinase (MMP)-2, MMP-9 and Tumor Necrosis Factor-α in Chronic Hepatitis C Virus Patients

**Authors:** Mohamed S Abdel-Latif

PMC · DOI: 10.2174/1874285801509010136 · The Open Microbiology Journal · 2015-08-31

## TL;DR

This study examines how certain proteins in the blood relate to liver disease caused by hepatitis C virus.

## Contribution

The study identifies plasma levels of MMP-2, MMP-9, and TNF-α as potential markers for liver fibrosis in chronic HCV patients.

## Key findings

- MMP-2, MMP-9, and TNF-α levels were significantly higher in chronic HCV patients compared to controls.
- These proteins did not differentiate between fibrotic and cirrhotic liver cases.
- MMP-2, MMP-9, and TNF-α could serve as markers for liver fibrosis but not for disease progression.

## Abstract

In chronic HCV infection, pathological accumulation of the extracellular matrix is the main feature of liver fibrosis; that indicates the imbalanced rate of increased matrix synthesis to decreased breakdown of connective tissue proteins. Matrix metalloproteinases (MMPs) play a crucial role in remodeling of extracellular matrix. It is known that expression of MMPs is regulated by Tumor necrosis factor (TNF)-α. Also, levels of TNF-α in liver and serum are increased in chronic HCV patient. Accordingly, this study aimed to correlate the plasma levels of MMP-2, MMP-9 and TNF-α in chronic HCV patients with the pathogenesis of the liver.

The current study was conducted on 15 ﬁbrotic liver cases with detectable HCV RNA, 10 HCV cirrhotic liver cases, and 15 control subjects of matched age and sex. Plasma MMP-2, MMP-9 and TNF-α were measured by ELISA.

Data revealed that the MMP2, MMP9 and TNF-α levels showed a significant elevation in chronic HCV patients compared to control group (p= 0.001). But, no significant correlation was observed in levels of MMP-2, MMP-9, and TNF-α between fibrotic and cirrhotic cases.

MMP-2, MMP-9 and TNF-α showed high reproducibility to differentiate chronic HCV patients from control group. On the contrary, MMP-2, MMP-9 and TNF-α were not able to differentiate fibrotic from cirrhotic liver cases. Thus, MMP-2, MMP-9 and TNF-α could not be correlated with the progression of liver disease. Rather they could be used as prognostic markers of liver fibrosis.

## Linked entities

- **Proteins:** MMP2 (matrix metallopeptidase 2), MMP9 (matrix metallopeptidase 9), TNF (tumor necrosis factor)
- **Diseases:** cirrhosis (MONDO:0005155)

## Full-text entities

- **Genes:** MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313] {aka CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** HBV infection (MESH:D006509), HCC (MESH:D006528), steatosis (MESH:D005234), cirrhotic (MESH:D000094724), CLD (MESH:D008107), cirrhosis (MESH:D005355), chronic hepatitis (MESH:D006521), diabetes mellitus (MESH:D003920), cirrhotic liver (MESH:D008103), hepatic inflammation (MESH:D007249), Chronic HCV (MESH:D006526), fibrotic liver (MESH:D017093), schistosomiasis (MESH:D012552), carcinogenesis (MESH:D063646), Chronic Hepatitis C Virus (MESH:D019698)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4598372/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC4598372/full.md

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Source: https://tomesphere.com/paper/PMC4598372