Abstract
Background
Associations between polymorphisms in vitamin D receptor (VDR)/vascular endothelial growth factor (VEGF)/interleukin-18 (IL-18)/mannose-binding lectin (MBL) and susceptibility to hepatocellular carcinoma (HCC) were already explored by many studies, yet the results of these studies were inconsistent. The aim of this meta-analysis was to better clarify associations between polymorphisms in VDR/VEGF/IL-18/MBL and HCC by combing the results of all relevant studies.
Methods
Eligible publications were searched from PubMed, Embase, WOS, and CNKI. We used Review Manager to combine the results of individual studies.
Results
Thirty studies were included in this study. Combined results revealed that VDR rs7975232, VDR rs2228570, VEGF rs699947, VEGF rs3025039, IL-18 rs1946518, and MBL rs7096206 polymorphisms were all significantly associated with HCC in the overall pooled population. We also obtained similar significant associations for VDR rs7975232, VDR rs2228570, IL-18 rs1946518, and MBL rs7096206 polymorphisms in Asians.
Conclusions
Collectively, this meta-analysis proved that VDR rs7975232, VDR rs2228570, VEGF rs699947, VEGF rs3025039, IL-18 rs1946518, and MBL rs7096206 polymorphisms may confer susceptibility to HCC in certain populations.
Keywords: Vitamin D receptor (VDR), Vascular endothelial growth factor (VEGF), Mannose-binding lectin (MBL), Interleukin-18 (IL-18), Hepatocellular carcinoma (HCC), Meta-analysis
Background
Hepatocellular carcinoma (HCC) is one of the leading causes of death all over the world [1, 2]. Although we still did not reveal the exact mechanism of its pathogenesis, it was evident that genetic components were essential in the development of HCC. Firstly, the incidences of HCC in different populations were quite different [3, 4], and genetic background was probably one of the reasons behind differences in disease prevalence across different populations. Secondly, numerous susceptible genetic loci of HCC were also identified and validated by existing genetic association studies [5, 6].
Mannose-binding lectin (MBL) and interleukin-18 (IL-18) are crucial modulators of immunological reactions, whereas vitamin D receptor (VDR) and vascular endothelial growth factor (VEGF) are vital for both immune-regulation and angiogenesis [7–10]. So, if a genetic polymorphism could alter the transcription activity of VDR/VEGF/IL-18/MBL or the protein structure of VDR/VEGF/IL-18/MBL, there is a possibility that this polymorphism may lead to the development of chronic inflammatory cellular injuries and also confer susceptibility to many types of malignancy including HCC.
In the past 20 years, many studies explored associations between polymorphisms in VDR/VEGF/IL-18/MBL and HCC, yet the conclusions of these studies were somehow inconsistent [11–40]. To better clarify associations between polymorphisms in VDR/VEGF/IL-18/MBL and HCC, we designed this study to get a more credible conclusion by combing the results of all relevant studies.
Methods
We wrote this meta-analysis in accordance with the requirements of the PRISMA guideline [41].
Literature search and inclusion criteria
To retrieve eligible articles, we searched PubMed, WOS, Embase, and CNKI with keywords listed below: (“vitamin D receptor” or “VDR” or “vascular endothelial growth factor” or “VEGF” or “interleukin 18” or “IL 18” or “mannose-binding lectin” or “Mannose-binding protein” or “MBL” or “MBP”) and (“polymorphism” or “variant” or “variation” or “mutation” or “SNP” or “genome-wide association study” or “genetic association study” or “genotype” or “allele”) and (“hepatocellular carcinoma” or “HCC”). The references of retrieved articles were also screened by us to identify other potentially relevant articles.
To be included in this meta-analysis, some criteria must be met: (I) about associations between polymorphisms in VDR/VEGF/IL-18/MBL and HCC in humans; (II) Offer genotypic distribution of VDR/VEGF/IL-18/MBL polymorphisms in patients with HCC and controls; (III) full manuscript in English or Chinese is retrievable. Publications were deemed to be ineligible for inclusion if (I) not about polymorphisms in VDR/VEGF/IL-18/MBL and HCC; (II) narrative reviews, systematic reviews, or comments; (III) studies only involved HCC patients. We only included the most up to date study for analyses if duplicate publications were found during the literature search.
Data extraction and quality assessment
Two authors extracted the following essential information from eligible studies: (I) name of the leading author; (II) published year; (III) country of the leading author; (IV) ethnicity of involved participants; (V) number of patients with HCC and controls in each study; (VI) genotype distributions of polymorphisms in VDR/VEGF/IL-18/MBL among patients with HCC and controls. P values of Hardy-Weinberg equilibrium (HWE) were also calculated.
The authors used the Newcastle-Ottawa scale (NOS) to assess the quality of eligible publications [42]. The score range of NOS is between 0 and 9, when a study got a score of 7 or more, we considered that the methodology quality of this study was good
Two authors extracted data and assessed the quality of eligible studies. The authors wrote to the leadings authors for additional information if essential information was found to be incomplete.
Statistical analyses
We used Review Manager to combine the results of individual studies. Z test was employed to assess associations between polymorphisms in VDR/VEGF/IL-18/MBL and susceptibility to HCC. The statistical significance threshold of P value was set at 0.05. We used I2 statistics to assess between-study heterogeneities. We used Random-effect models (DerSimonian-Laird method) to combine the results if I2 is larger than 50%. Otherwise, fixed-effect models (Mantel-Haenszel method) were used to combine the results [43, 44]. We further carried out subgroup analyses by ethnicity to get ethnic-specific results. We examined the stability of combined results by deleting one study each time and combining the results of the remaining studies. We used funnel plots to estimate whether our combined results may be influenced by publication biases.
Results
Characteristics of included studies
We found 168 articles during literature searching. Forty-five articles were assessed for eligibility after excluding unrelated or duplicate articles. We further excluded eight reviews and six case series, and another one publication was excluded because of missing crucial data. Totally, 30 articles were ultimately found to be eligible for inclusion (Fig. 1). Extracted data of eligible articles were summarized in Table 1.
Table 1.
First author, year | Country | Ethnicity | Type of disease | Medical history of patients | Sample size Case/control |
Genotype distribution (wtwt/wtmt/mtmt) |
P value for HWE | NOS score | |
---|---|---|---|---|---|---|---|---|---|
Cases controls | |||||||||
VDR rs7975232 | |||||||||
Barooah 2019 [11] | India | South Asian | HCC | NA | 60/102 | 49/11/0 | 59/35/8 | 0.391 | 8 |
Falleti 2010 [12] | Italy | Caucasian | HCC | Viral hepatitis 87% | 80/160 | 27/38/15 | 53/85/22 | 0.189 | 8 |
Hung 2014 [13] | Taiwan | East Asian | HCC | NA | 92/100 | 65/24/3 | 55/40/5 | 0.505 | 8 |
Yao 2013 [16] | China | East Asian | HCC | HBV 100%, alcohol intake 34.9% | 436/532 | 112/216/108 | 114/275/143 | 0.395 | 8 |
VDR rs1544410 | |||||||||
Barooah 2019 [11] | India | South Asian | HCC | NA | 60/102 | 52/8/0 | 80/16/6 | < 0.001 | 8 |
Falleti 2010 [12] | Italy | Caucasian | HCC | Viral hepatitis 87% | 80/160 | 33/35/12 | 45/87/28 | 0.206 | 8 |
Hung 2014 [13] | Taiwan | East Asian | HCC | NA | 92/100 | 85/7/0 | 89/11/0 | 0.560 | 8 |
Yao 2013 [16] | China | East Asian | HCC | HBV 100%, alcohol intake 34.9% | 436/532 | 112/217/107 | 142/259/131 | 0.550 | 8 |
VDR rs2228570 | |||||||||
Falleti 2010 [12] | Italy | Caucasian | HCC | Viral hepatitis 87% | 80/160 | 36/36/8 | 69/73/18 | 0.843 | 8 |
Liu 2015 [14] | China | East Asian | HCC | NA | 105/100 | 41/44/20 | 23/48/29 | 0.715 | 8 |
Peng 2014 [15] | China | East Asian | HCC | HBV 100%, alcohol intake 90.2% | 184/296 | 54/90/40 | 77/152/67 | 0.628 | 8 |
Yao 2013 [16] | China | East Asian | HCC | HBV 100%, alcohol intake 34.9% | 436/532 | 131/198/107 | 102/241/189 | 0.111 | 8 |
VDR rs731236 | |||||||||
Barooah 2019 [11] | India | South Asian | HCC | NA | 60/102 | 48/8/4 | 71/21/10 | <0.001 | 8 |
Falleti 2010 [12] | Italy | Caucasian | HCC | Viral hepatitis 87% | 80/160 | 32/38/10 | 44/88/28 | 0.160 | 8 |
Hung 2014 [13] | Taiwan | East Asian | HCC | NA | 92/100 | 86/6/0 | 86/14/0 | 0.452 | 8 |
Yao 2013 [16] | China | East Asian | HCC | HBV 100%, alcohol intake 34.9% | 436/532 | 115/212/109 | 137/252/143 | 0.226 | 8 |
VEGF rs699947 | |||||||||
Liu 2017 [19] | China | East Asian | HCC | HBV 60.2%, alcohol intake 60.8% | 476/526 | 301/157/18 | 290/202/34 | 0.882 | 8 |
Machado 2014 [20] | Portugal | Caucasian | HCC | Alcohol intake 100% | 26/101 | 7/14/5 | 19/49/33 | 0.914 | 7 |
Ratnasari 2017 [22] | Indonesia | East Asian | HCC | HBV58%, HCV 11% | 44/59 | 18/21/5 | 23/30/6 | 0.402 | 7 |
Wu 2009 [23] | China | East Asian | HCC | NA | 92/90 | 48/40/4 | 58/28/4 | 0.792 | 8 |
Wu 2013 [24] | China | East Asian | HCC | HBV48.5% | 101/110 | 79/21/1 | 91/17/2 | 0.271 | 8 |
VEGF rs1570360 | |||||||||
Baitello 2016 [17] | Canada | Mixed | HCC | HBV 50%, HCV 21%, alcohol intake 56% | 102/127 | 61/35/6 | 73/47/7 | 0.875 | 8 |
Wu 2009 [23] | China | East Asian | HCC | NA | 90/99 | 66/24/0 | 72/27/0 | 0.116 | 8 |
Wu 2013 [24] | China | East Asian | HCC | HBV48.5% | 101/110 | 83/17/1 | 75/31/4 | 0.723 | 8 |
VEGF rs2010963 | |||||||||
Liu 2017 [19] | China | East Asian | HCC | HBV 60.2%, alcohol intake 60.8% | 476/526 | 162/232/82 | 200/248/78 | 0.937 | 8 |
Ratnasari 2016 [21] | Indonesia | East Asian | HCC | HBV56.5%, HCV 10.8% | 46/136 | 16/29/1 | 26/105/5 | <0.001 | 7 |
Wu 2009 [23] | China | East Asian | HCC | NA | 92/99 | 34/40/18 | 34/52/13 | 0.320 | 8 |
Wu 2013 [24] | China | East Asian | HCC | HBV48.5% | 101/110 | 28/52/21 | 35/51/24 | 0.506 | 8 |
VEGF rs3025039 | |||||||||
Baitello 2016 [17] | Canada | Mixed | HCC | HBV 50%, HCV 21%, alcohol intake 56% | 102/127 | 72/30/0 | 90/37/0 | 0.055 | 8 |
Giacalone 2011 [18] | Italy | Caucasian | HCC | NA | 96/162 | 81/14/1 | 120/38/4 | 0.636 | 8 |
Liu 2017 [19] | China | East Asian | HCC | HBV 60.2%, alcohol intake 60.8% | 476/526 | 359/112/5 | 370/140/16 | 0.536 | 8 |
Wu 2009 [23] | China | East Asian | HCC | NA | 92/99 | 63/26/3 | 68/30/1 | 0.239 | 8 |
Yvamoto 2015 [25] | Brazil | Mixed | HCC | Alcohol intake 47.1% | 228/56 | 164/64/0 | 43/13/0 | 0.326 | 7 |
IL-18 rs187238 | |||||||||
Bakr 2018 [26] | Egypt | South Asian | HCC | HCV 100% | 90/90 | 66/22/2 | 33/65/1 | <0.001 | 8 |
Bao 2015 [27] | China | East Asian | HCC | HBV 100% | 153/165 | 122/28/3 | 106/54/5 | 0.548 | 8 |
Chen 2012 [28] | China | East Asian | HCC | NA | 228/300 | 159/59/10 | 173/115/12 | 0.183 | 7 |
Dai 2017 [29] | China | East Asian | HCC | HBV 100%, alcohol intake 42% | 245/250 | 187/49/9 | 183/65/2 | 0.142 | 8 |
Karra 2015 [30] | India | South Asian | HCC | HBV 100% | 271/280 | 123/134/14 | 159/108/13 | 0.320 | 7 |
Kim 2009 [31] | Korea | East Asian | HCC | HBV 100% | 56/558 | 37/17/2 | 434/122/2 | 0.031 | 7 |
Lau 2016 [32] | Taiwan | East Asian | HCC | Alcohol intake 63.5% | 342/559 | 266/73/3 | 476/78/5 | 0.370 | 8 |
Migita 2009 [33] | Japan | East Asian | HCC | HBV 100% | 47/63 | 43/3/1 | 52/10/1 | 0.531 | 7 |
Teixeira 2009 [34] | Brazil | Mixed | HCC | Viral hepatitis 67.8%, alcohol intake 63.4% | 112/202 | 57/48/7 | 100/84/18 | 0.952 | 7 |
Zhang 2016 [35] | China | East Asian | HCC | HBV 100% | 109/127 | 82/25/2 | 99/24/4 | 0.110 | 8 |
IL18 rs1946518 | |||||||||
Bakr 2018 [26] | Egypt | South Asian | HCC | HCV 100% | 90/99 | 13/34/43 | 17/45/37 | 0.603 | 8 |
Bao 2015 [27] | China | East Asian | HCC | HBV 100% | 153/165 | 37/73/43 | 41/76/48 | 0.322 | 8 |
Chen 2012 [28] | China | East Asian | HCC | NA | 228/300 | 47/126/55 | 83/156/61 | 0.429 | 7 |
Dai 2017 [29] | China | East Asian | HCC | HBV 100%, alcohol intake 42% | 247/250 | 62/118/67 | 64/124/62 | 0.900 | 8 |
Karra 2015 [30] | India | South Asian | HCC | HBV 100% | 271/280 | 70/152/49 | 102/144/34 | 0.119 | 7 |
Lau 2016 [32] | Taiwan | East Asian | HCC | Alcohol intake 63.5% | 342/559 | 88/167/87 | 148/276/135 | 0.777 | 8 |
Migita 2009 [33] | Japan | East Asian | HCC | HBV 100% | 47/63 | 13/26/8 | 20/30/13 | 0.777 | 7 |
Teixeira 2009 [34] | Brazil | Mixed | HCC | Viral hepatitis 67.8%, alcohol intake 63.4% | 112/202 | 38/56/18 | 85/105/12 | 0.202 | 7 |
Zhang 2016 [35] | China | East Asian | HCC | HBV 100% | 109/127 | 22/55/32 | 38/66/23 | 0.127 | 8 |
MBL rs7096206 | |||||||||
Eurich 2011 [36] | Germany | Caucasian | HCC | NA | 62/115 | 27/34/1 | 76/37/2 | 0.292 | 7 |
Gu 2016 [37] | China | East Asian | HCC | NA | 334/171 | 232/95/7 | 131/33/7 | 0.015 | 8 |
Lin 2015 [38] | China | East Asian | HCC | Alcohol intake 77.7% | 220/220 | 125/86/9 | 153/65/2 | 0.082 | 8 |
Su 2016 [40] | China | East Asian | HCC | HBV 70.2% | 315/315 | 207/91/17 | 239/72/4 | 0.583 | 8 |
MBL rs1800450 | NA | ||||||||
Gu 2016 [37] | China | East Asian | HCC | NA | 334/171 | 234/89/11 | 104/59/8 | 0.920 | 8 |
Segat 2008 [39] | Italy | Caucasian | HCC | NA | 215/164 | 127/78/10 | 102/49/13 | 0.050 | 7 |
Su 2016 [40] | China | East Asian | HCC | HBV 70.2% | 308/315 | 208/88/20 | 239/69/7 | 0.450 | 8 |
Abbreviations: HWE Hardy-Weinberg equilibrium, NOS Newcastle-Ottawa scale, NA not available, HBV hepatitis B virus infection, HCV hepatitis C virus infection
Meta-analyses results for polymorphisms in VDR and HCC
Six studies were eligible for estimation of associations between polymorphisms in VDR and HCC. VDR rs7975232 (dominant comparison OR = 1.58, 95% CI 1.04–2.39; over-dominant comparison OR = 0.80, 95% CI 0.65–0.98) and rs2228570 (dominant comparison OR = 1.54, 95% CI 1.25–1.89; recessive comparison OR = 0.67, 95 % CI 0.54–0.84; allele comparison OR = 1.34, 95% CI 1.06–1.68) polymorphisms were found to be significantly associated with HCC in overall combined analyses. Subgroup analyses showed similar positive findings for rs7975232 (dominant comparison) and rs2228570 (dominant, recessive, and allele comparisons) polymorphisms in East Asians (see Table 2 and Additional file 1: Supplementary Figure S1).
Table 2.
Variables | Sample size | Dominant comparison | Recessive comparison | Over-dominant comparison | Allele comparison | ||||
---|---|---|---|---|---|---|---|---|---|
P value OR (95%CI) I2 statistic | P value | OR (95%CI) I2 statistic | P value OR (95% CI) I2 statistic | P value | OR (95%CI) I2 statistic | ||||
VDR rs7975232 | |||||||||
Overall | 668/894 |
0.03 60% |
1.58 (1.04–2.39) |
0.42 31% |
0.90 (0.69–1.17) |
0.03 44% |
0.80 (0.65–0.98) |
0.09 76% |
1.41 (0.94–2.12) |
East Asian | 528/632 |
0.02 40% |
1.39 (1.06–1.81) |
0.40 0% |
0.88 (0.67–1.17) |
0.28 62% |
0.75 (0.45–1.26) |
0.17 55% |
1.30 (0.89–1.89) |
VDR rs1544410 | |||||||||
Overall | 668/894 |
0.26 44% |
1.15 (0.90–1.45) |
0.62 8% |
0.93 (0.71–1.22) |
0.54 0% |
0.93 (0.75–1.16) |
0.30 50% |
1.09 (0.93–1.27) |
East Asian | 528/632 |
0.98 0% |
1.00 (0.74–1.34) |
0.91 0% |
0.98 (0.75–1.30) |
0.90 0% |
1.02 (0.79–1.30) |
0.96 0% |
1.00 (0.83–1.19) |
VDR rs2228570 | |||||||||
Overall | 805/1088 |
< 0.0001 46% |
1.54 (1.25–1.89) |
0.0004 19% |
0.67 (0.54–0.84) |
0.58 0% |
0.95 (0.79–1.14) |
0.01 59% |
1.34 (1.06–1.68) |
East Asian | 725/928 |
< 0.0001 45% |
1.63 (1.31–2.04) |
0.0003 40% |
0.66 (0.53–0.83) |
0.58 0% |
0.95 (0.78–1.15) |
0.01 65% |
1.40 (1.08–1.82) |
VDR rs731236 | |||||||||
Overall | 668/894 |
0.06 43% |
1.25 (0.99–1.58) |
0.26 0% |
0.86 (0.66–1.12) |
0.42 38% |
0.92 (0.74–1.14) |
0.06 42% |
1.16 (0.99–1.36) |
East Asian | 528/632 |
0.44 57% |
1.34 (0.64–2.82) |
0.51 0% |
0.91 (0.68–1.21) |
0.54 66% |
0.77 (0.33–1.78) |
0.39 55% |
1.08 (0.91–1.29) |
VEGF rs699947 | |||||||||
Overall | 739/886 |
0.92 54% |
1.02 (0.69–1.52) |
0.04 0% |
0.63 (0.41–0.98) |
0.61 45% |
0.95 (0.77–1.17) |
0.61 51% |
1.08 (0.80–1.46) |
East Asian | 713/785 |
0.84 64% |
1.05 (0.66–1.66) |
0.10 0% |
0.67 (0.41–1.08) |
0.70 56% |
1.08 (0.72–1.65) |
0.99 59% |
1.00 (0.70–1.42) |
VEGF rs1570360 | |||||||||
Overall | 293/336 |
0.12 37% |
1.31 (0.93–1.85) |
0.57 19% |
0.75 (0.29–1.98) |
0.17 7% |
0.78 (0.55–1.11) |
0.13 49% |
1.26 (0.94–1.70) |
East Asian | 191/209 |
0.28 60% |
1.49 (0.72–3.06) |
0.24 0% |
0.27 (0.03–2.41) |
0.15 44% |
0.71 (0.45–1.13) |
0.28 64% |
1.46 (0.73–2.91) |
VEGF rs2010963 | |||||||||
Overall | 715/871 |
0.79 55% |
1.05 (0.72–1.54) |
0.26 0% |
1.17 (0.89–1.55) |
0.80 48% |
0.97 (0.80–1.19) |
0.32 13% |
0.93 (0.81–1.07) |
East Asian | 715/871 |
0.79 55% |
1.05 (0.72–1.54) |
0.26 0% |
1.17 (0.89–1.55) |
0.80 48% |
0.97 (0.80–1.19) |
0.32 13% |
0.93 (0.81–1.07) |
VEGF rs3025039 | |||||||||
Overall | 994/970 |
0.08 12% |
1.20 (0.98–1.48) |
0.08 38% |
0.50 (0.23–1.09) |
0.21 0% |
0.87 (0.71–1.08) |
0.05 28% |
1.21 (1.00–1.46) |
East Asian | 568/625 |
0.10 0% |
1.24 (0.96–1.59) |
0.87 69% |
0.83 (0.09–7.41) |
0.25 0% |
0.86 (0.66–1.11) |
0.06 34% |
1.24 (0.99–1.56) |
IL-18 rs187238 | |||||||||
Overall | 1653/2594 |
0.38 85% |
1.19 (0.81–1.77) |
0.50 16% |
1.14 (0.78–1.66) |
0.26 88% |
0.77 (0.49–1.21) |
0.56 78% |
1.09 (0.82–1.43) |
East Asian | 1180/2022 |
0.62 81% |
1.11 (0.73–1.70) |
0.27 33% |
1.33 (0.80–2.22) |
0.49 81% |
0.86 (0.55–1.34) |
0.76 78% |
1.06 (0.74–1.50) |
South Asian | 361/370 |
0.60 97% |
1.70 (0.24–12.29) |
0.65 0% |
1.19 (0.57–2.47) |
0.53 98% |
0.45 (0.04–5.35) |
0.69 92% |
1.25 (0.42–3.66) |
HBV | 881/1443 |
0.90 78% |
1.03 (0.65–1.63) |
0.23 43% |
1.38 (0.81–2.33) |
0.73 78% |
0.92 (0.57–1.48) |
0.96 74% |
1.01 (0.70–1.46) |
IL18 rs1946518 | |||||||||
Overall | 1599/2045 |
0.002 0% |
0.79 (0.68–0.92) |
0.004 30% |
1.26 (1.08–1.48) |
0.75 0% |
1.02 (0.90–1.17) |
0.002 59% |
0.78 (0.67–0.91) |
East Asian | 1126/1464 |
0.09 0% |
0.86 (0.71–1.02) |
0.15 0% |
1.14 (0.95–1.37) |
0.79 0% |
1.02 (0.87–1.19) |
0.04 68% |
0.80 (0.65–0.99) |
South Asian | 589/679 |
0.001 0% |
0.66 (0.51–0.85) |
0.02 0% |
1.57 (1.09–2.27) |
0.98 54% |
0.99 (0.61–1.61) |
0.002 0% |
0.72 (0.59–0.89) |
HBV | 827/885 |
0.01 9% |
0.77 (0.62–0.95 |
0.06 21% |
1.25 (0.99–1.57) |
0.52 0% |
1.06 (0.88–1.29) |
0.03 73% |
0.73 (0.55–0.96) |
MBL rs7096206 | |||||||||
Overall | 931/821 | < 0.0001 0.59 (0.48–0.73) 0% |
0.37 70% |
1.81 (0.50–6.59) |
< 0.0001 0% |
1.59 (1.28–1.97) | < 0.0001 0% | 0.63 (0.53–0.76) | |
East Asian | 869/706 |
< 0.0001 0% |
0.62 (0.50–0.78) |
0.35 79% |
2.08 (0.44–9.80) |
0.0005 0% |
1.50 (1.19–1.88) | < 0.0001 4% | 0.65 (0.53–0.79) |
MBL rs1800450 | |||||||||
Overall | 857/650 |
0.85 79% |
0.95 (0.58–1.55) |
0.91 77% |
1.06 (0.37–3.06) |
0.70 75% |
1.10 (0.69–1.74) |
0.95 80% |
0.99 (0.65–1.50) |
East Asian | 642/486 |
0.99 90% |
0.99 (0.44–2.23) |
0.61 81% |
1.47 (0.34–6.30) |
0.99 86% |
1.00 (0.49–2.03) |
0.95 90% |
0.98 (0.48–1.99) |
Abbreviations: OR odds ratio, CI confidence interval, NA not available, HBV hepatitis B virus infection
The values in italics represent that there is statistically significant differences between cases and controls
Meta-analyses results for polymorphisms in VEGF and HCC
Nine studies were eligible for the estimation of associations between polymorphisms in VEGF and HCC. VEGF rs699947 (recessive comparison OR = 0.63, 95% CI 0.41–0.98) and rs3025039 (allele comparison OR = 1.21, 95% CI 1.00–1.46) polymorphisms were found to be significantly associated with HCC in overall combined analyses. Nevertheless, we did not observe any positive associations in subgroup analyses (see Table 2 and Additional file 1: Supplementary Figure S1).
Meta-analyses results for polymorphisms in IL-18 and HCC
Ten studies were eligible for the estimation of associations between polymorphisms in IL-18 and HCC. IL-18 rs1946518 (dominant comparison OR = 0.79, 95% CI 0.68–0.92; recessive comparison OR = 1.26, 95 % CI 1.08–1.48; allele comparison OR = 0.78, 95% CI 0.67–0.91) polymorphism was found to be significantly associated with HCC in overall combined analyses. Subgroup analyses showed similar positive findings for rs1946518 polymorphism in East Asians (allele comparison), South Asians (dominant, recessive, and allele comparisons), and those with hepatitis B virus (HBV) infection (dominant and allele comparisons) (see Table 2 and Additional file 1: Supplementary Figure S1).
Meta-analyses results for polymorphisms in MBL and HCC
Five studies were eligible for the estimation of associations between polymorphisms in MBL and HCC. MBL rs7096206 (dominant comparison OR = 0.59, 95% CI 0.48–0.73; over-dominant comparison OR = 1.59, 95% CI 1.28–1.97; allele comparison: OR = 0.63, 95% CI 00.53–0.76) polymorphism was found to be significantly associated with HCC in overall combined analyses. Subgroup analyses showed similar positive findings for rs7096206 polymorphism in East Asians (dominant, over-dominant, and allele comparisons) (see Table 2 and Additional file 1: Supplementary Figure S1).
Sensitivity analyses
We examined the stability of combined results by deleting one study each time and combining the results of the remaining studies. The trends of associations remained consistent in sensitivity analyses, which indicated that the combined results were statistically stable.
Publication biases
Funnels plots were employed to estimate whether our combined results may be influenced by publication biases. Funnel plots of every comparison were symmetrical, which indicated that the combined results were unlikely to be seriously impacted by overt publication biases.
Discussion
The combined results of this meta-analysis revealed that VDR rs7975232, VDR rs2228570, VEGF rs699947, VEGF rs3025039, IL-18 rs1946518, and MBL rs7096206 polymorphisms were significantly associated with susceptibility to HCC in certain populations. The trends of associations remained consistent in sensitivity analyses, which indicated that the combined results were statistically stable.
To better understand the combined results of this meta-analysis, some points should be considered. First, past basic studies revealed that all investigated polymorphisms were either correlated with altered transcription activity or protein structure [45–48]. So, these variations may influence the biological function of VDR/VEGF/IL-18/MBL, result in immune dysfunction, cause chronic inflammatory hepatocellular injury, and ultimately confer susceptibility to HCC. Thus, our meta-analysis may be statistically insufficient to observe the real underlying associations between polymorphisms in VDR/VEGF/IL-18/MBL and HCC in certain subgroups. Therefore, future studies still need to confirm our findings. Second, we noticed that most eligible studies were from Asian countries, whereas studies in other countries were highly scarce, so scholars from European and African countries should also try to examine associations between polymorphisms in VDR/VEGF/IL-18/MBL and HCC. Besides, considering the functional importance of VDR/VEGF/IL-18/MBL in regulating inflammatory reactions and angiogenesis, future studies also need to test the relationship between polymorphisms in VDR/VEGF/IL-18/MBL and other types of malignancies. Third, the etiology of HCC is very complicated, so we highly recommend further genetic association studies to explore the effects of haplotypes and gene-gene interactions on disease susceptibility [49]. Fourth, we aimed to investigate associations between all polymorphisms in VDR/VEGF/IL-18/MBL and HCC in the very beginning. However, we did not find any study on other VDR/VEGF/IL-18/MBL polymorphisms, so we only focused on 12 polymorphisms in this meta-analysis. Fifth, it is worth noting that Zhu et al. [50] also performed a meta-analysis about IL-18 polymorphisms and HCC in 2016. Based on combined analyses of eight eligible studies with 3572 subjects, they did not find any positive results regarding IL-18 polymorphisms and HCC in general or subgroup analyses. Since our pooled analyses about IL-18 polymorphisms were based on more eligible studies and larger sample sizes, our results should be more statistically robust. Nevertheless, studies with larger sample sizes are still warranted to test the genetic associations between IL-18 polymorphisms and HCC in the future.
Some limitations of this meta-analysis should also be mentioned. Firstly, the results regarding associations between polymorphisms in VDR/VEGF/IL-18/MBL and HCC were based on combining unadjusted findings of eligible studies due to the lack of raw data [51]. Secondly, the relationship between polymorphisms in VDR/VEGF/IL-18/MBL and HCC may also be affected by environmental factors. Unfortunately, the majority of eligible studies only focused on associations between polymorphisms in VDR/VEGF/IL-18/MBL and HCC, so we could not explore genetic-environmental interactions in this meta-analysis [52]. Thirdly, grey literatures were not searched. So although funnel plots of every comparison were symmetrical, it is still possible that the combined results may be affected by publication biases [53].
Conclusion
In summary, this meta-analysis proved that VDR rs7975232, VDR rs2228570, VEGF rs699947, VEGF rs3025039, IL-18 rs1946518, and MBL rs7096206 polymorphisms may confer susceptibility to HCC in certain populations. These results also indicated that VDR, VEGF, IL-18, and MBL may involve in the development of HCC. However, the combined results of this meta-analysis should still be verified by studies with larger sample sizes.
Supplementary information
Acknowledgements
None.
Ethical approval and consent to participate
Not applicable.
Informed consent
For this type of study formal consent is not required.
Abbreviations
- VDR
Vitamin D receptor
- VEGF
Vascular endothelial growth factor
- MBL
Mannose-binding lectin
- IL-18
Interleukin-18
- HCC
Hepatocellular carcinoma
- HWE
Hardy-Weinberg equilibrium
- NOS
Newcastle-Ottawa scale
- OR
Odds ratios
- CI
Confidence intervals
Authors’ contributions
YQ and YH conceived and designed the study. YQ and JY conducted the literature review. TQ analyzed the data. YQ and YH drafted the manuscript. All authors have read and approved the final manuscript.
Funding
This article was funded by the Research Project of Guangxi Autonomous Region Ministry of Education (2019KY0536). Fund Project: Department of education of Guangxi Autonomous Region project, No.: 2019ky0536.
Availability of data and materials
The current study was based on the results of relevant published studies.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Contributor Information
Yi Quan, Email: quanyizai@163.com.
Jun Yang, Email: junyangs121@126.com.
Tao Qin, Email: qin158tao@163.com.
Yufang Hu, Email: huyfangh@163.com.
Supplementary information
Supplementary information accompanies this paper at 10.1186/s12957-019-1748-8.
References
- 1.Siegel RL, Miller KD, Jemal A. Cancer statistics, 2017. CA Cancer J Clin. 2017;67:7–30. doi: 10.3322/caac.21387. [DOI] [PubMed] [Google Scholar]
- 2.Marcellin P, Kutala BK. Liver diseases: A major, neglected global public health problem requiring urgent actions and large-scale screening. Liver Int. 2018;38(Suppl 1):2–6. doi: 10.1111/liv.13682. [DOI] [PubMed] [Google Scholar]
- 3.Asrani SK, Devarbhavi H, Eaton J, Kamath PS. Burden of liver diseases in the world. J Hepatol. 2019;70:151–171. doi: 10.1016/j.jhep.2018.09.014. [DOI] [PubMed] [Google Scholar]
- 4.Ghouri YA, Mian I, Rowe JH. Review of hepatocellular carcinoma: Epidemiology, etiology, and carcinogenesis. J Carcinog. 2017;16:1. doi: 10.4103/jcar.JCar_9_16. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Zucman-Rossi J, Villanueva A, Nault JC, Llovet JM. Genetic landscape and biomarkers of hepatocellular carcinoma. Gastroenterology. 2015;149:1226–1239. doi: 10.1053/j.gastro.2015.05.061. [DOI] [PubMed] [Google Scholar]
- 6.Niu ZS, Niu XJ, Wang WH. Genetic alterations in hepatocellular carcinoma: An update. World J Gastroenterol. 2016;22:9069–9095. doi: 10.3748/wjg.v22.i41.9069. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Swierzko AS, Kilpatrick DC, Cedzynski M. Mannan-binding lectin in malignancy. Mol Immunol. 2013;55:16–21. doi: 10.1016/j.molimm.2012.09.005. [DOI] [PubMed] [Google Scholar]
- 8.Esmailbeig M, Ghaderi A. Interleukin-18: a regulator of cancer and autoimmune diseases. Eur Cytokine Netw. 2017;28:127–140. doi: 10.1684/ecn.2018.0401. [DOI] [PubMed] [Google Scholar]
- 9.Campbell MJ, Trump DL. Vitamin D Receptor Signaling and Cancer. Endocrinol Metab Clin North Am. 2017;46:1009–1038. doi: 10.1016/j.ecl.2017.07.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Carmeliet P. VEGF as a key mediator of angiogenesis in cancer. Oncology. 2005;69(Suppl 3):4–10. doi: 10.1159/000088478. [DOI] [PubMed] [Google Scholar]
- 11.Barooah P, Saikia S, Bharadwaj R, Sarmah P, Bhattacharyya M, Goswami B, Medhi S. Role of VDR, GC, and CYP2R1 Polymorphisms in the development of hepatocellular carcinoma in hepatitis C virus-infected patients. Genet Test Mol Biomarkers. 2019;23:325–331. doi: 10.1089/gtmb.2018.0170. [DOI] [PubMed] [Google Scholar]
- 12.Falleti E, Bitetto D, Fabris C, Cussigh A, Fontanini E, Fornasiere E, Fumolo E, Bignulin S, Cmet S, Minisini R, Pirisi M, Toniutto P. Vitamin D receptor gene polymorphisms and hepatocellular carcinoma in alcoholic cirrhosis. World J Gastroenterol. 2010;16:3016–3024. doi: 10.3748/wjg.v16.i24.3016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Hung CH, Chiu YC, Hu TH, Chen CH, Lu SN, Huang CM, Wang JH, Lee CM. Significance of vitamin d receptor gene polymorphisms for risk the carcinoma in chronic hepatitis C. Transl Oncol. 2014;7:503–507. doi: 10.1016/j.tranon.2014.05.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Liu Q, Pan G, Zhen M. Study on correlation between Fok I polymorphism of VDR gene and susceptibility to hepatocellular carcinoma. J Chengdu Med College. 2015; 28: 369-371. [Article in Chinese]
- 15.Peng Q, Yang S, Lao X, Li R, Chen Z, Wang J, Qin X, Li S. Association of single nucleotide polymorphisms in VDR and DBP genes with HBV-related hepatocellular carcinoma risk in a Chinese population. PLoS One. 2014;9:e116026. doi: 10.1371/journal.pone.0116026. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Yao X, Zeng H, Zhang G, Zhou W, Yan Q, Dai L, Wang X. The associated ion between the VDR gene polymorphisms and susceptibility to hepatocellular carcinoma and the clinicopathological features in subjects infected with HBV. Biomed Res Int. 2013;2013:953974. doi: 10.1155/2013/953974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Baitello ME, Tenani GD, Ferreira RF, Nogueira V, Pinhel MA, da Silva RC, da Silva RF, Fucuta PD, de Godoy MF, Souza DR. VEGF polymorphisms related to higher serum levels of protein identify patients with hepatocellular carcinoma. Can J Gastroenterol Hepatol. 2016;2016:9607054. doi: 10.1155/2016/9607054. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Giacalone A, Montalto G, Giannitrapani L, Balasus D, Terranova A, Cervello M, Soresi M, Marasà L. Association between single nucleotide polymorphisms in the cyclooxygenase-2, tumor necrosis factor-α, and vascular endothelial growth factor-A genes, and susceptibility to hepatocellular carcinoma. OMICS. 2011;15:193–196. doi: 10.1089/omi.2010.0095. [DOI] [PubMed] [Google Scholar]
- 19.Liu F, Luo L, Wei Y, Wang W, Wen T, Yang J, Xu M, Li B. Association of VEGFA polymorphisms with susceptibility and clinical outcome of hepatocellular carcinoma in a Chinese Han population. Oncotarget. 2017;8:16488–16497. doi: 10.18632/oncotarget.14870. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Machado MV, Janeiro A, Miltenberger-Miltenyi G, Cortez-Pinto H. Genetic polymorphisms of proangiogenic factors seem to favor hepatocellular carcinoma development in alcoholic cirrhosis. Eur J Gastroenterol Hepatol. 2014;26:438–443. doi: 10.1097/MEG.0000000000000044. [DOI] [PubMed] [Google Scholar]
- 21.Ratnasari N, Nurdjanah S, Sadewa AH, Hakimi M. The role of vascular endothelial growth factor -634 G/C and its soluble receptor on chronic liver disease and hepatocellular carcinoma. Arab J Gastroenterol. 2016;17:61–66. doi: 10.1016/j.ajg.2016.06.005. [DOI] [PubMed] [Google Scholar]
- 22.Ratnasari N, Nurdjanah S, Sadewa AH, Hakimi M, Yano Y. Difference of polymorphism VEGF-gene rs699947 in Indonesian chronic liverdisease population. PLoS One. 2017;12:e0183503. doi: 10.1371/journal.pone.0183503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Wu LM, Xie HY, Zhou L, Yang Z, Zhang F, Zheng SS. A single nucleotide polymorphism in the vascular endothelial growth factor gene is associated with recurrence of hepatocellular carcinoma after transplantation. Arch Med Res. 2009;40:565–570. doi: 10.1016/j.arcmed.2009.07.011. [DOI] [PubMed] [Google Scholar]
- 24.Wu X, Xin Z, Zhang W, Wu J, Chen K, Wang H, Zhu X, Pan L, Li Z, Li H, Liu Y. Polymorphisms in the VEGFA promoter are associated with susceptibility to hepatocellular carcinoma by altering promoter activity. Int J Cancer. 2013;133:1085–1093. doi: 10.1002/ijc.28109. [DOI] [PubMed] [Google Scholar]
- 25.Yvamoto EY, Ferreira RF, Nogueira V, Pinhe MA, Tenani GD, Andrade JG, Baitello ME, Gregório ML, Fucuta PS, Silva RF, Souza DR, Silva RC. Influence of vascular endothelial growth factor and alpha-feto protein on hepatocellular carcinoma. Genet Mol Res. 2015;14:17453–17462. doi: 10.4238/2015.December.21.16. [DOI] [PubMed] [Google Scholar]
- 26.Bakr NM. Awad A, A Moustafa E. Association of genetic variants in the interleukin-18 gene promoter with risk of hepatocellular carcinoma and metastasis in patients with hepatitis C virus infection. IUBMB Life. 2018;70:165–174. doi: 10.1002/iub.1714. [DOI] [PubMed] [Google Scholar]
- 27.Bao J, Lu Y, Deng Y, Rong C, Liu Y, Huang X, Song L, Li S, Qin X. Association between IL-18 polymorphisms, serum levels, and HBV-related hepatocellular carcinoma in a Chinese population: a retrospective case-control study. Cancer Cell Int. 2015;15:72. doi: 10.1186/s12935-015-0223-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Chen Q. The correlation between single nucleotide polymorphism of interleukin-18 gene promoter and genetic susceptibility to hepatocellular carcinoma. Immunol J. 2012; 28: 1051-1055. [Article in Chinese]
- 29.Dai ZJ, Liu XH, Wang M, Guo Y, Zhu W, Li X, Lin S, Tian T, Liu K, Zheng Y, Xu P, Jin T, Li X. IL-18 polymorphisms contribute to hepatitis B virus-related cirrhosis and hepatocellular carcinoma susceptibility in Chinese population: a case-control study. Oncotarget. 2017;8:81350–81360. doi: 10.18632/oncotarget.18531. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Karra VK, Gumma PK, Chowdhury SJ, Ruttala R, Polipalli SK, Chakravarti A, Kar P. IL-18 polymorphisms in hepatitis B virus related liver disease. Cytokine. 2015;73:277–282. doi: 10.1016/j.cyto.2015.02.015. [DOI] [PubMed] [Google Scholar]
- 31.Kim YS, Cheong JY, Cho SW, Lee KM, Hwang JC, Oh B, Kimm K, Lee JA, Park BL, Cheong HS, Shin HD, Kim JH. A functional SNP of the Interleukin-18 gene is associated with the presence of hepatocellular carcinoma in hepatitis B virus-infected patients. Dig Dis Sci. 2009;54:2722–2778. doi: 10.1007/s10620-009-0970-6. [DOI] [PubMed] [Google Scholar]
- 32.Lau HK, Hsieh MJ, Yang SF, Wang HL, Kuo WH, Lee HL, Yeh CB. Association between Interleukin-18 Polymorphisms and Hepatocellular Carcinoma Occurrence and Clinical Progression. Int J Med Sci. 2016;13:556–561. doi: 10.7150/ijms.15853. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Migita K, Sawakami-Kobayashi K, Maeda Y, Nakao K, Kondoh S, Sugiura M, Kawasumi R, Segawa O, Tajima H, Machida M, Nakamura M, Yano K, Abiru S, Kawasaki E, Yatsuhashi H, Eguchi K, Ishibashi H. Interleukin-18 promoter polymorphisms and the disease progression of Hepatitis B virus-related liver disease. Transl Res. 2009;153:91–96. doi: 10.1016/j.trsl.2008.11.008. [DOI] [PubMed] [Google Scholar]
- 34.Teixeira AC, Mendes CT, Jr, Marano LA, Deghaide NH, Secaf M, Elias J, Jr, Muglia V, Donadi EA, Martinelli AL. Alleles and genotypes of polymorphisms of IL-18, TNF-α and IFN-γ are associated with a higher risk and severity of hepatocellular carcinoma (HCC) in Brazil. Hum Immunol. 2013;74:1024–1029. doi: 10.1016/j.humimm.2013.04.029. [DOI] [PubMed] [Google Scholar]
- 35.Zhang QX, Yao YQ, Li SL, Long Q. Association between interleukin-18 gene polymorphisms and hepatocellular carcinoma caused by hepatitis B virus. Chin J Hepatol. 2016; 24: 352. [Article in Chinese] [DOI] [PubMed]
- 36.Eurich D, Boas-Knoop S, Morawietz L, Neuhaus R, Somasundaram R, Ruehl M, Neumann UP, Neuhaus P, Bahra M, Seehofer D. Association of mannose-binding lectin-2 gene polymorphism with the development of hepatitis C-induced hepatocellular carcinoma. Liver Int. 2011;31:1006–1012. doi: 10.1111/j.1478-3231.2011.02522.x. [DOI] [PubMed] [Google Scholar]
- 37.Gu X, Ji Q, Wang H, Jiang M, Yang J, Fang M, Wang M, Gao C. Genetic variants of mannose-binding lectin 2 gene influence progression and prognosis of patients with hepatitis B virus infection in China. Clin Res Hepatol Gastroenterol. 2016;40:614–621. doi: 10.1016/j.clinre.2015.12.015. [DOI] [PubMed] [Google Scholar]
- 38.Lin Y, Su C, Niu J, Guo Z, Cai L. Impact of mannose-binding lectin 2 polymorphism on the risk of hepatocellular carcinoma: a case-control study in Chinese Han population. J Epidemiol. 2015;25:387–391. doi: 10.2188/jea.JE20140194. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Segat L, Fabris A, Padovan L, Milanese M, Pirulli D, Lupo F, Salizzoni M, Amoroso A, Crovella S. MBL2 and MASP2 gene polymorphisms in patients with hepatocellular carcinoma. J Viral Hepat. 2008;15:387–391. doi: 10.1111/j.1365-2893.2008.00965.x. [DOI] [PubMed] [Google Scholar]
- 40.Su C, Lin Y, Cai L, Mao Q, Niu J. Association between mannose-binding lectin variants, haplotypes and risk of hepatocellular carcinoma: A case-control study. Sci Rep. 2016;6:32147. doi: 10.1038/srep32147. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA group Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151:264–269. doi: 10.7326/0003-4819-151-4-200908180-00135. [DOI] [PubMed] [Google Scholar]
- 42.Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol. 2010;25:603–605. doi: 10.1007/s10654-010-9491-z. [DOI] [PubMed] [Google Scholar]
- 43.Rai V. Methylenetetrahydrofolate reductase (MTHFR) C677T Polymorphism and Alzheimer disease risk: a meta-analysis. Mol Neurobiol. 2017;54:1173–1186. doi: 10.1007/s12035-016-9722-8. [DOI] [PubMed] [Google Scholar]
- 44.Mostafa T, Taymour M. TNF-α -308 polymorphisms and male infertility risk: a meta-analysis and systematic review. J Adv Res. 2016;7:185–192. doi: 10.1016/j.jare.2015.07.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Thompson SR, Humphries SE. Interleukin-18 genetics and inflammatory disease susceptibility. Genes Immun. 2007;8:91–99. doi: 10.1038/sj.gene.6364366. [DOI] [PubMed] [Google Scholar]
- 46.Luo J, Xu F, Lu GJ, Lin HC, Feng ZC. Low mannose-binding lectin (MBL) levels and MBL genetic polymorphisms associated with the risk of neonatal sepsis: an updated meta-analysis. Early Hum Dev. 2014;90:557–564. doi: 10.1016/j.earlhumdev.2014.07.007. [DOI] [PubMed] [Google Scholar]
- 47.Uitterlinden AG, Fang Y, Van Meurs JB, Pols HA, Van Leeuwen JP. Genetics and biology of vitamin D receptor polymorphisms. Gene. 2004;338:143–156. doi: 10.1016/j.gene.2004.05.014. [DOI] [PubMed] [Google Scholar]
- 48.Koukourakis MI, Papazoglou D, Giatromanolaki A, Bougioukas G, Maltezos E, Sivridis E. VEGF gene sequence variation defines VEGF gene expression status and angiogenic activity in non-small cell lung cancer. Lung Cancer. 2004;46:293–298. doi: 10.1016/j.lungcan.2004.04.037. [DOI] [PubMed] [Google Scholar]
- 49.Nishi A, Milner DA, Jr, Giovannucci EL, Nishihara R, Tan AS, Kawachi I, Ogino S. Integration of molecular pathology, epidemiology and social science for global precision medicine. Expert Rev Mol Diagn. 2016;16:11–23. doi: 10.1586/14737159.2016.1115346. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Zhu SL, Zhao Y, Hu XY, Luo T, Chen ZS, Zhang Y, Yang SH, Zhou L, Li LQ. Genetic polymorphisms -137 (rs187238) and -607 (rs1946518) in the interleukin-18 promoter may not be associated with development of hepatocellular carcinoma. Sci Rep. 2016;6:39404. doi: 10.1038/srep39404. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Liu L, Guo W, Zhang J. Association of HLA-DRB1 gene polymorphisms with hepatocellular carcinoma risk: a meta-analysis. Minerva Med. 2017;108:176–184. doi: 10.23736/S0026-4806.16.04571-7. [DOI] [PubMed] [Google Scholar]
- 52.Dondeti MF, El-Maadawy EA, Talaat RM. Hepatitis-related hepatocellular carcinoma: Insights into cytokine gene polymorphisms. World J Gastroenterol. 2016;22:6800–6816. doi: 10.3748/wjg.v22.i30.6800. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Lu SC, Zhong JH, Tan JT, Tang HL, Liu XG, Xiang BD, Li LQ, Peng T. Association between COX-2 gene polymorphisms and risk of hepatocellular carcinoma development: a meta-analysis. BMJ Open. 2015;5:e008263. doi: 10.1136/bmjopen-2015-008263. [DOI] [PMC free article] [PubMed] [Google Scholar]
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Data Availability Statement
The current study was based on the results of relevant published studies.