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Main insights of genome wide association studies into HCV-related HCC

Egyptian Liver Journal volume 10, Article number: 4 (2020) Cite this article

Abstract

Background

Hepatocellular carcinoma (HCC) is one of the most common causes of cancer-mortality globally. Hepatocarcinogenesis is a complex multifactorial process. Host genetic background appeared to play a crucial role in the progression of HCC among chronic hepatitis C patients, especially in the era of Genome Wide Association Studies (GWAS) which allowed us to study the association of millions of single nucleotide polymorphisms (SNPs) with different complex diseases. This article aimed to review the discovered SNPs associated with the risk of HCV-related HCC development which was reported in the published GWA studies and subsequent validation studies and also try to explain the possible functional pathways.

Main text

We reviewed the recent GWA studies which reported several new loci associated with the risk of HCV-related HCC, such as (SNPs) in MHC class I polypeptide-related sequence A (MICA), DEP domain-containing 5 (DEPDC5), Tolloid-like protein 1 (TLL1), and human leukocyte antigen (HLA) genes. We also explained the possible underlying biological mechanisms that affect the host immune response pathways. Additionally, we discussed the controversial results reported by the subsequent validation studies of different ethnicities.

Conclusions

Although GWA studies reported strong evidence of the association between the identified SNPs and the risk of HCV-related HCC development, more functional experiments are necessary to confirm the defined roles of these genetic mutations for the future clinical application in different populations.

Background

Hepatocellular carcinoma is the fifth most common cancer worldwide and the third leading cause of cancer-related death, with a 5-year survival rate of 6.9%. The incidence of HCC is increasing dramatically in the last few years, the annual estimated number of HCC new cases is about 782,000 and causing 600,000 deaths annually worldwide [1].

Hepatocellular carcinoma is a multifactorial disease; host and environmental risk factors can influence its development. About 80% of HCC cases are caused by HBV and HCV [2].

About 7.8% of new HCC cases were attributed to HCV [3]. Recognizing patients who are more susceptible to HCC risk and following them with continuing surveillance for early detection and treatment will help to decrease HCC burden.

Recently, host genetics appeared to play a crucial role. Identifying host genetics would enhance the accuracy of risk prediction models, increasing the efficacy of surveillance programs, and allowing personalized assessment of disease management.

Current progress in sequencing technologies has allowed us for the identification of 500,000 or more single-nucleotide polymorphism (SNP) DNA markers selected to capture the full human genome, using genome-wide association studies (GWAS) [4].

In this review, we discussed the four main genome-wide association studies which investigate the association of single nucleotide polymorphisms (SNPs) with the risk of HCC development among chronic hepatitis C patients, the subsequent validation studies among different ethnicities and the possible underlying biological functional pathways in HCC carcinogenesis.

MICA (rs2596542) and HCC

The first GWA study of HCV-related HCC was conducted by Kumar [5], and his colleagues in the Japanese population (Table 1), which was a multi-stage study. In the discovery phase, they genotyped for 432,703 SNPs in 721 HCC patients and 2890 healthy HCV-negative controls, and they identified eight possible loci for the possible association. In the replication stage, independent 673 HCC and 2596 HCV-negative controls were genotyped at these 8 loci, One SNP rs2596542 showed positive association in the 5′ flanking region of MICA on the chromosome (6p21.33), which located within the class I of the major histocompatibility complex (MHC) region (Fig. 1) [9]. Risk allele A was statistically significantly higher in HCC cases than controls (P = 8.62 × 10−9, odds ratio (OR) = 1.44, 95% confidence interval (CI) = 1.27–1.63). The result remained significant after adjusting for age, gender, and alcohol consumption. They further analyzed for rs2596542 in 1730 chronic hepatitis C without cirrhosis compared with HCC cases and found it was significantly associated with progression from CHC to HCC (P = 3.13 × 10−8, OR = 1.36).

Table 1 Brief summary of four main GWAS in HCV-related HCC
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Fig. 1
figure 1

The MICA gene locus on the short arm of human chromosome 6 [9]

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They also reported another locus rs9275572 located between HLA-DQA and HLA-DQB which showed a significant association with HCV-induced HCC (P = 9.38 × 10−9, OR = 1.30), moderate association with chronic hepatitis C susceptibility (P = 0.03, OR = 1.09), and increased the risk of progression from CHC to HCC (P = 2.58 × 10−5, OR = 1.29).

MHC class I polypeptide-related sequence A (MICA) is a membrane protein, completely absent or present only at low levels on the surface of normal cells, but they are overexpressed by infected, transformed, senescent, and stressed cells, which play a role as a ligand for natural killer (NK) group 2D (NKG2D), that triggers natural killer cells and CD8+ T cells to attack the target cells. Soluble MICA (sMICA) is secreted into the serum by alternative splicing, proteolytic shedding, and cause blocking the anti-tumor action of natural killer cells and CD8+ T cells.

Kumar and his team [5] identified that the rs2596542 risk genotype AA was significantly associated with low levels of sMICA. As the levels of sMICA were shown to be correlated to the level of membrane-bound MICA which is needed for NK cell activation, they suggested that persons with rs2596542 A risk allele would show low levels of membrane-bound MICA in response to HCV infection, which thus leads to poor natural killer cell cytotoxicity. That can make them more susceptible to HCC progression.

Validation studies for MICA and HCC (Table 2)

The same research group conducted a replication study [10]. However, they genotyped SNP rs2596542 in 407 HBV-HCC cases, 699 CHB subjects, and 5657 non-HBV controls. SNP rs2596542 showed also a statistically significant association with HCC development in chronic hepatitis B patients. The rs2596542 G allele was more prevalent in HBV-induced HCC cases than the A allele (P = 0.029, OR = 1.19, 95% CI 1.02–1.4) compared to controls. The risk allele was opposite to their previous study [5] as the A allele was associated with increased risk of HCV-related HCC.

Table 2 Validation studies for association of MICA with the risk of HCC development among chronic hepatitis patients
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Similar results to Kumar GWA study [5] reported in different ethnicities, Chang and his team conducted a replication study in the Chinese population and reported a statistically significant difference in the distribution of SNP rs2596542 A allele between 120 HCC patients and 124 healthy controls (OR = 1.57, 95% CI = 1.07–2.31) [13]. An Egyptian team also reported that the rs2596542 T allele was significantly higher in HCC versus control and liver cirrhosis (LC) versus control, suggesting that the rs2596542 T allele may be a risk factor for developing HCC and liver cirrhosis [16]. A subsequent study was conducted by Huang and his colleagues, MICA rs2596542 genotype and serum MICA (sMICA) levels were evaluated in 705 chronic hepatitis C patients who received antiviral therapy and were followed up for HCC diagnosis. They reported that MICA risk alleles and high sMICA levels > 175 ng/mL were independently associated with HCC development in cirrhotic patients non-SVR, suggesting that combining the MICA gene polymorphism and sMICA will give the best accuracy in predicting HCC [15].

Interestingly, when replicating these studies on the Caucasian population, opposite rs2596542 A minor allele association with HCV-HCC was observed. In the study of Lange and his colleagues [12], they genotyped rs2596542 in 1860 HCV patients and 68 HCV-related HCC patients from the European population, rs2596542 allele A was protective for HCC development which represented an opposite to the results of Kumar [5]. They suggested another novel susceptibility locus for HCV-related HCC development rs2244546 in HCP5 which located between MICA and HLA-DQA/HLA-DQB. This was in agreement with another report from the Italian population found that homozygous AA was significantly lower frequent in HCC patients than in healthy controls, OR = 0.599 (95% CI = 0.371–0.968) [18].

However, Bruza and his colleagues reported in their study on population from Italy, Switzerland, and Germany that SNP s2596542 polymorphism had no statistical association with the progression of HCC in cirrhotic patients [14]. Also, Lo [11] reported after genotyping SNP rs2596542 in different groups of patients: 1043 chronic hepatitis C, 586 liver cirrhosis without HCC, and 1394 HCV-induce HCC that it was significantly associated with disease progression from CHC to LC (OR = 1.17, P value = 0.048) but was not associated with progression of HCC from liver cirrhosis.

DEPDC5 (rs1012068) and HCC

Another GWAS conducted in the Japanese population identified a new SNP associated with the increased risk of HCV-related HCC. The SNP rs1012068 located in the DEP domain-containing 5 genes (DEPDC5) on chromosome 22 (Fig. 2) [19]. They identified it after analyzing 467,538 SNPs in 212 chronic HCV-HCC and 765 individuals with chronic HCV without HCC, followed by independent replication case-control study (710 cases and 1625 controls), (rs1012068 G, P combined = 1.27 × 10−13, odds ratio = 1.75) and the significance level of rs1012068 increased after adjusting for age, gender, and platelet count (P = 1.35 × 10−14, OR = 1.96) [6].

Fig. 2
figure 2

The DEP domain-containing 5 genes (DEPDC5) location on chromosome 22 [19]

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Further adjusting of other predictive factors of HCV-related HCC including alcohol consumption, diabetes mellitus, obesity, ethnicity, and co-infection with HBV was performed using multiple logistic regression analysis in only 994 subjects (480 cases and 514 controls) with fully available data for these factors and rs1012068 remained highly significant with OR = 1.87 (95% CI 1.39–2.52). Looking for the function of DEPDC5 polymorphism, they investigated the association between rs1012068 genotype and DEPDC5 mRNA expression in 43 HCV patients. DEPDC5 mRNA expression was significantly higher in tumor tissues than non-tumor tissues, but no significant difference in DEPDC5 mRNA expression concerning rs1012068 genotype [6]. They recommended further research on the effect of rs1012068 polymorphism and the role of the DEPDC5 gene in HCV-related hepatocarcinogenesis.

The function of the DEPDC5 has not been defined yet; however, the protein encoded by this gene is a component of the GATOR1 (GAP activity toward Rags) complex, which has been demonstrated to act as an inhibitor of the mammalian target of rapamycin (mTOR) pathway, a multi-functional protein involved in many cellular systems including inflammation, cell growth and tumorigenesis including hepatocarcinogenesis. Most pathogenic variants described in DEPDC5 are inactivating leading to decreased amounts of the encoded protein or no protein at all, which predicted to increase the activity of the mTORC1 signaling pathway [20].

Validation studies for DEPDC5 and HCC (Table 3)

In the few past years, several studies were conducted to identify the association of the DEPDC5 gene with HCC development. Al-Qahtani and his colleagues validated the susceptible association of DEPDC5 variants with the risk of developing HCC in chronic HCV-infected patients among the Saudi Arabian population [22]. They genotyped for DEPDC5 polymorphisms (rs1012068 and rs5998152) in 601 HCV patients and 592 healthy controls. They reported that subjects carrying G allele of rs1012068 or C allele of rs5998152 appeared to have a higher risk for HCV-related cirrhosis/HCC compared to T allele carriers of both SNPs (P = 0.038, OR = 1.353, 95 % CI = 1.017–1.800) (P = 0.043, OR = 1.342, 95 % CI = 1.010–1.784), respectively.

Table 3 Validation studies for association of DEPDC5 with the risk of HCC development among chronic hepatitis patients
Full size table

Similar results noticed in the Han Chinese population, two separate studies postulated that The DEPDC5-rs1012068 C allele was associated with increased susceptibility to HBV-related HCC [23, 24].

In contrast, a Japanese study tried to identify the association of MICA and DEPDC5 genetic polymorphisms with HCC recurrence following hepatectomy [21]. They genotyped for MICA (rs2596542) and DEPDC5 (rs1012068) and compared recurrence-free survival rates (RFS) for different genotypes in 96 HCC patients who underwent hepatectomy. They reported that neither MICA nor DEPDC5 genetic polymorphisms were associated with increased HCC recurrence risk after hepatectomy. This was consistent with another recent Japanese study that genotyped for MICA, DEPDC5, HCP5, and PNPLA3 SNPs in 717 patients with CHC (HCC = 142 and non-HCC = 575) [17]. These results were in line with the recent reports from Europe, which reported that the DEPDC5 variant was not associated with HCC but associated with increased fibrosis. The frequency of DEPDC5 rs1012068G was higher in cirrhotic patients (stage F4) than in those with no/mild fibrosis (stage F0-F1). The DEPDC5 rs1012068 G allele was associated with a 40% increased risk of cirrhosis, OR 95%CI (1.40:1.08–1.81; P = 0.011) [25]. Another European study genotyped for 7 SNPs (DEPDC5 rs1012068, GRIK1 rs455804, KIF1B rs17401966, STAT4 rs7574865, MICA rs2596542, DLC1 rs2275959, and DDX18 rs2551677) in 1020 HCC, 2021 chronic liver diseases (CLD) but without HCC and 2484 healthy subjects and found also no significant association of MICA or DEPDC5 with HCC development [26]. This is indicating that the role of the DEPDC5 gene in the HCC development needs further research and validation in different ethnicities.

TLL1 (rs17047200) and HCC

Matsuura and his colleagues were interested in identifying the genetic variants associated with HCC development in HCV patients who achieved SVR after IFN-based therapy by conducting a GWA study [7]. 457 DNA samples for the discovery stage and subsequent independent 486 DNA samples for the replication stage obtained from Japanese patients who successfully achieved SVR after IFN-based therapy. The patients were followed up, and the endpoint was the HCC diagnosis date in patients who develop HCC and the date for confirming the absence of HCC in the last follow-up. In the discovery stage, they genotyped 123 patients who developed HCC and 333 who did not develop HCC ≥ 5 years. The 70 SNPs which reached the GWAS level of significance further genotyped in the replication stage. Their results showed that the SNP rs17047200, located within the intron of the Tolloid-like 1 (TLL1) gene on chromosome 4 (Fig. 3) [19] had the strongest association (OR = 2.35; 95%CI = 1.48–3.75) with HCC development after the eradication of HCV by IFN-based therapy. By performing Cox proportional hazard analysis, they developed a multivariate predictive model for HCC occurrence including rs17047200 AT/TT as an independent risk factor [(HR) = 1.78; 95%CI = 1.17–2.70, P = 0.008], male gender, older age, presence of diabetes, advanced hepatic fibrosis stage, and higher post-treatment AFP level.

Fig. 3
figure 3

The Tolloid-like 1 (TLL1) gene location on chromosome 4 [19]

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For evaluating the biological role of the TLL1 gene in hepatocarcinogenesis, they assessed TLL1 mRNA expression which was higher in mice models of liver injury and fibrotic human liver tissues, compared with controls. Their results were consistent with previous literature that suggested that TLL1 may be involved in carcinogenesis through activating hepatic fibrogenesis pathways by upregulation of TGF-β signaling and subsequently activate human hepatic stellate cells (HSCs), causing excessive accumulation of the various extracellular matrix proteins in the liver [27, 28].

Cirrhosis is thought to cause initiation and promotion of neoplastic clones in regenerative nodules by facilitating genetic aberrations and cellular transformation, resulting in HCC development [29].

Another probable explanation, suggesting that the TLL1 gene has an independent pro-oncogenic role by activating insulin-like growth factors (IGFs) through cleavage of their binding proteins and IGF signaling pathway [30]. Moreover, activation of NF-κB and ERK by activated HSC promoting HCC development [31].

HLA-DQB1 (rs2856723)

Another recent GWAS [8] genotyped 502 HCV-related HCC cases and 749 HCV non-HCC controls, 8 SNPs showed a significant statistical association with the risk of HCC. The SNPs clustered in the human leukocyte antigen region HLA-DQB1 on chromosome 6. In the replication stage, 7 SNPs remained significantly associated with HCC, when they compared 16000 healthy controls with 669 HCC cases, and 429 HCV patients with 669 HCC cases. The SNP with the highest odds ratio was rs2856723, OR (95% CI) = 2.68 (2.32–3.09), P = 2.58 × 10-43.

Because the HLA region is highly polymorphic, they performed a cohort study genotyping the DQB1 locus in 994 HCV patients and measuring the HCC cumulative risk among different HLA-DQB1 variants. They reported that HLA-DQB1*03:01 and DQB1*06:02 (P < 0.05) were statistically associated with HCC occurrence, and the adjusted HRs were 0.45 (0.30–0.68) and 2.11 (1.34–3.34) for DQB1*03: 01 and DQB1*06: 02, respectively.

To identify the reported association in different HCV genotypes, they performed a stratified analysis by HCV genotypes, DQB1*03: 01 showed protective effects on HCC development with HCV genotype-1 patients; meanwhile, DQB1*06:02 increased risk of HCC only with HCV non-1 genotype patients.

The role of HLA genotypes in HCC development is not fully identified. HLA genes located on the short arm of chromosome 6 (Fig. 4) [32]; these genes encode proteins that are present on the surface of almost all cells, and their role is binding to peptides and presenting them to the immune system to be recognized as foreign to initiate a cascade of immune responses. Many studies were conducted to identify the role of HLA variants in liver disease progression, but most of them have used limited numbers of patients with a cross-sectional design and have reported inconsistent results with different ethnicities [33, 34]. This reflects the importance of providing insights into a more detailed understanding of the association of HLA polymorphism with HCC development and its functional pathway.

Fig. 4
figure 4

Gene map of the human leukocyte antigen (HLA) region [32]

Full size image

Conclusions

Undoubtedly, host genetic variants influence the clinical progression of HCV infection. In the present review, we summarized the four published genome-wide association studies of HCV-related HCC in the Asian population. Their subsequent validation studies were recruited to discuss GWAS efficiency. Most of the discovered SNPs were approved to be involved in the pathway of immune reactions. However, the identified polymorphisms need further functional analysis for their molecular role in carcinogenesis. Further GWA studies and replication studies of HCV-related HCC in different ethnicities are necessary for the future as all previous published GWA studies were conducted on the Asian population. The identified polymorphisms may serve as the potential markers for screening the patients at high risk of HCC and help in modeling preventive or therapeutic strategies based on inter-individual susceptibilities, which present a great step toward personalized medicine.

Availability of data and materials

Data materials are available under reasonable request.

Abbreviations

AFP:

Alpha-fetoprotein

CHC:

Chronic liver cirrhosis

DAA:

Direct-acting antiviral

DEPDC5:

DEP domain-containing 5

GWAS:

Genome-wide association study

HBV:

Hepatitis B virus

HCC:

Hepatocellular carcinoma

HCV:

Hepatitis C virus

HLA:

Human leukocyte antigen

IFN:

Interferon

IGFs:

Insulin-like growth factors

LC:

Liver cirrhosis

MICA:

MHC class I polypeptide-related sequence A

NKG2D:

Natural Killer (NK) Group 2D

sMICA:

Serum MICA

SNP:

Single nucleotide polymorphism

SVR:

Sustained virological response

TGF-β:

Transforming growth factor beta 1

TLL1:

Tolloid-like protein 1

References

  1. Ozakyol A (2017) Global epidemiology of hepatocellular carcinoma (HCC epidemiology). J Gastrointest Cancer. 48(3):238–240. https://doi.org/10.1007/s12029-017-9959-0

    Article  PubMed  Google Scholar 

  2. Fung J, Lai C-L, Yuen M-F (2009) Hepatitis B and C virus-related carcinogenesis. Clin Microbiol Infect. 15(11):964–970. https://doi.org/10.1111/j.1469-0691.2009.03035.x

    CAS  Article  PubMed  Google Scholar 

  3. Plummer M, de Martel C, Vignat J, Ferlay J, Bray F, Franceschi S (2016) Global burden of cancers attributable to infections in 2012: a synthetic analysis. Lancet Glob Heal. 4(9):e609–e616. https://doi.org/10.1016/S2214-109X(16)30143-7

    Article  Google Scholar 

  4. O’Brien TR, Yang HI, Groover S, Jeng WJ (2019) Genetic factors that affect spontaneous clearance of hepatitis C or B virus, response to treatment, and disease progression. Gastroenterology. 156(2):400–417. https://doi.org/10.1053/j.gastro.2018.09.052

    Article  PubMed  Google Scholar 

  5. Kumar V, Kato N, Urabe Y et al (2011) Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma. Nat Genet. 43(5):455–458. https://doi.org/10.1038/ng.809

    CAS  Article  PubMed  Google Scholar 

  6. Miki D, Ochi H, Hayes CN et al (2011) Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers. Nat Genet. 43(8):797–800. https://doi.org/10.1038/ng.876

    CAS  Article  PubMed  Google Scholar 

  7. Matsuura K, Sawai H, Ikeo K et al (2017) Genome-wide association study identifies TLL1 variant associated with development of hepatocellular carcinoma after eradication of hepatitis C virus infection. Gastroenterology. 152(6):1383–1394. https://doi.org/10.1053/j.gastro.2017.01.041

    CAS  Article  PubMed  Google Scholar 

  8. Lee M-H, Huang Y-H, Chen H-Y et al (2018) Human leukocyte antigen variants and risk of hepatocellular carcinoma modified by hepatitis C virus genotypes: a genome-wide association study. Hepatology. 67(2):651–661. https://doi.org/10.1002/hep.29531

    CAS  Article  PubMed  Google Scholar 

  9. Mizuki N, Ando H, Kimura M et al (1997) Nucleotide sequence analysis of the HLA class I region spanning the 237-kb segment around the HLA-B and -C genes. Genomics. 42(1):55–66. https://doi.org/10.1006/geno.1997.4708

    CAS  Article  PubMed  Google Scholar 

  10. Kumar V, Matsuda K, Kato N et al (2012) Soluble MICA and a MICA Variation as Possible Prognostic Biomarkers for HBV-Induced Hepatocellular Carcinoma. PLoS One. 7(9):e44743. https://doi.org/10.1371/journal.pone.0044743

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  11. Lo PHY, Kumar V, Kubo M et al (2013) Identification of a functional variant in the MICA promoter which regulates MICA expression and increases HCV-related hepatocellular carcinoma risk. PLoS One. 8(4):e61279. https://doi.org/10.1371/journal.pone.0061279

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  12. Lange CM, Bibert S, Dufour JF et al (2013) Comparative genetic analyses point to HCP5 as susceptibility locus for HCV-associated hepatocellular carcinoma. J Hepatol. 59(3):504–509. https://doi.org/10.1016/j.jhep.2013.04.032

    CAS  Article  PubMed  Google Scholar 

  13. Chang H, Zhou X, Zhu H, et al. Interaction between polymorphisms of IFN-γ and MICA correlated with hepatocellular carcinoma. Med Sciefile///C/Users/user/Documents/review/CH2/2018_Book_GeneticEpidemiology.pdfnce Monit. 2016;22:549-553. doi: https://doi.org/10.12659/msm.895101

    CAS  Article  Google Scholar 

  14. Burza MA, Motta BM, Mancina RM et al (2016) DEPDC5 variants increase fibrosis progression in Europeans with chronic hepatitis C virus infection. Hepatology. 63(2):418–427. https://doi.org/10.1002/hep.28322

    CAS  Article  PubMed  Google Scholar 

  15. Huang C, Huang C, Yeh M et al (2017) EBioMedicine genetics variants and serum levels of MHC class I chain-related A in predicting hepatocellular carcinoma development in chronic hepatitis C patients post antiviral treatment. EBIOM. 15:81–89. https://doi.org/10.1016/j.ebiom.2016.11.031

    Article  Google Scholar 

  16. Mohamed AA, Elsaid OM, Amer EA et al (2017) Clinical significance of SNP (rs2596542) in histocompatibility complex class I-related gene A promoter region among hepatitis C virus related hepatocellular carcinoma cases. J Adv Res. 8(4):343–349. https://doi.org/10.1016/j.jare.2017.03.004

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  17. Hai H, Tamori A, Thuy LTT et al (2017) Polymorphisms in MICA, but not in DEPDC5, HCP5 or PNPLA3, are associated with chronic hepatitis C-related hepatocellular carcinoma. Sci Rep. 7(1):11912. https://doi.org/10.1038/s41598-017-10363-5

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  18. Augello G, Cervello M, Balasus D et al (2018) Association between MICA gene variants and the risk of hepatitis C virus-induced hepatocellular cancer in a Sicilian Population Sample. Omi A J Integr Biol. 22(4):274–282. https://doi.org/10.1089/omi.2017.0215

    CAS  Article  Google Scholar 

  19. Zerbino DR, Achuthan P, Akanni W et al (2018) Ensembl 2018. Nucleic Acids Res. 46(D1):D754–D761. https://doi.org/10.1093/nar/gkx1098

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  20. Bar-Peled L, Chantranupong L, Cherniack AD et al (2013) A tumor suppressor complex with GAP activity for the Rag GTPases that signal amino acid sufficiency to mTORC1. Science (80- ) 340(6136):1100–1106. https://doi.org/10.1126/science.1232044

    CAS  Article  Google Scholar 

  21. Motomura T, Ono Y, Shirabe K et al (2012) Neither MICA Nor DEPDC5 Genetic polymorphisms correlate with hepatocellular carcinoma recurrence following hepatectomy. HPB Surg 2012:1–6. https://doi.org/10.1155/2012/185496

    Article  Google Scholar 

  22. Al-Qahtani AA, Al-Anazi MR, Matou-Nasri S et al (2014) Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia. BMC Infect Dis. 14(1):632. https://doi.org/10.1186/s12879-014-0632-y

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  23. Ma N, Zhang X, Yu F et al (2014) Role of IFN-λs, IFN-λs related genes and the DEPDC5 gene in hepatitis B virus-related liver disease. J Viral Hepat. 21(7):e29–e38. https://doi.org/10.1111/jvh.12235

    CAS  Article  PubMed  Google Scholar 

  24. Liu W, Ma N, Zhao D et al (2019) Correlation between the DEPDC5 rs1012068 polymorphism and the risk of HBV-related hepatocellular carcinoma. Clin Res Hepatol Gastroenterol. https://doi.org/10.1016/j.clinre.2018.12.005

    CAS  Article  Google Scholar 

  25. Mancina RM, Fargion S, Stickel F et al (2015) DEPDC5 variants increase fibrosis progression in Europeans with chronic hepatitis C virus infection. Hepatology. 63(2):418–427. https://doi.org/10.1002/hep.28322

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  26. Yang J, Trépo E, Nahon P et al (2019) PNPLA3 and TM6SF2 variants as risk factors of hepatocellular carcinoma across various etiologies and severity of underlying liver diseases. Int J Cancer. 144(3):533–544. https://doi.org/10.1002/ijc.31910

    CAS  Article  PubMed  Google Scholar 

  27. Ge G, Greenspan DS (2006) BMP1 controls TGFβ1 activation via cleavage of latent TGFβ-binding protein. J Cell Biol. 175(1):111–120. https://doi.org/10.1083/jcb.200606058

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  28. BENYON RC (2000) Is liver fibrosis reversible? Gut. 46(4):443–446. https://doi.org/10.1136/gut.46.4.443

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  29. Aihara T, Noguchi S, Sasaki Y, Nakano H, Imaoka S (1994) Clonal analysis of regenerative nodules in hepatitis C virus-induced liver cirrhosis. Gastroenterology. 107(6):1805–1811 http://www.ncbi.nlm.nih.gov/pubmed/7958695

    CAS  Article  Google Scholar 

  30. Nalesnik MA, Michalopoulos GK (2012) Growth factor pathways in development and progression of hepatocellular carcinoma. Front Biosci (Schol Ed) 4:1487–1515 http://www.ncbi.nlm.nih.gov/pubmed/22652888

    Article  Google Scholar 

  31. Amann T, Bataille F, Spruss T et al (2009) Activated hepatic stellate cells promote tumorigenicity of hepatocellular carcinoma. Cancer Sci. 100(4):646–653. https://doi.org/10.1111/j.1349-7006.2009.01087.x

    CAS  Article  PubMed  Google Scholar 

  32. Berlingerio M, Bonchi F, Curcio M, Giannotti F, Turini F. Mining clinical, immunological, and genetic data of solid organ transplantation. In: ; 2009:211-236. doi: https://doi.org/10.1007/978-3-642-02193-0_9

    Chapter  Google Scholar 

  33. Duggal P, Thio CL, Wojcik GL et al (2013) Genome-wide association study of spontaneous resolution of hepatitis C virus infection: data from multiple cohorts. Ann Intern Med. 158(4):235. https://doi.org/10.7326/0003-4819-158-4-201302190-00003

    Article  PubMed  PubMed Central  Google Scholar 

  34. López-Vázquez A, Rodrigo L, Miña-Blanco A et al (2004) Extended human leukocyte antigen haplotype EH18.1 influences progression to hepatocellular carcinoma in patients with hepatitis C virus infection. J Infect Dis. 189(6):957–963. https://doi.org/10.1086/382189

    Article  PubMed  Google Scholar 

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  1. Epidemiology and Preventive Medicine Department, National Liver Institute, Menoufia University, Gamal Abdel Nasser Street, Shebein El–Kom, Menoufia, Egypt

    Inas Maged Moaz, Ayat Rushdy Abdallah, Marwa Fekry Yousef & Sameera Ezzat

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IM collected, critically interprited the study data, and contributed in the manuscript writing. AA and MF contributed in the manuscript writing. SE was a major contributor to the manuscript writing and revising. All authors read and approved the final manuscript.

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Correspondence to Sameera Ezzat.

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Moaz, I.M., Abdallah, A.R., Yousef, M.F. et al. Main insights of genome wide association studies into HCV-related HCC. Egypt Liver Journal 10, 4 (2020). https://doi.org/10.1186/s43066-019-0013-8

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  • DOI: https://doi.org/10.1186/s43066-019-0013-8

Keywords

  • HCV
  • HCC
  • GWAS