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ORIGINAL RESEARCH article

Front. Med., 27 October 2021
Sec. Gastroenterology
This article is part of the Research Topic Women in Science - Gastroenterology 2021 View all 12 articles

Role of Galectins in the Liver Diseases: A Systematic Review and Meta-Analysis

\nYang An,&#x;Yang An1,2Shixue Xu&#x;Shixue Xu1Yiting Liu,&#x;Yiting Liu1,3Xiangbo Xu,&#x;Xiangbo Xu1,2Cyriac Abby Philips&#x;Cyriac Abby Philips4Jiang ChenJiang Chen1Nahum Mndez-SnchezNahum Méndez-Sánchez5Xiaozhong GuoXiaozhong Guo1Xingshun Qi
Xingshun Qi1*
  • 1Meta-Analysis Study Group, Department of Gastroenterology, General Hospital of Northern Theater Command, Shenyang, China
  • 2Postgraduate College, Shenyang Pharmaceutical University, Shenyang, China
  • 3Department of Physical Examination Center, The First Affiliated Hospital, China Medical University, Shenyang, China
  • 4The Liver Unit and Monarch Liver Laboratory, Cochin Gastroenterology Group, Ernakulam Medical Center, Kochi, India
  • 5Liver Research Unit Medica Sur Clinic and Foundation and Faculty of Medicine, National Autonomous University of Mexico, Mexico City, Mexico

Background: Galectins, a family of β-galactoside-binding proteins, are related to the development and progression of various human diseases such as cancer, heart failure, and chronic kidney disease. However, its role in liver diseases is unclear.

Methods: The PubMed, Embase, and Cochrane Library databases were searched. Hazard ratios (HRs), odds ratios (ORs), and mean differences (MDs) with 95% CIs were pooled to evaluate the association of the galectins with the outcomes and risk of liver diseases by a random effects model.

Results: Thirty three studies involving 43 cohorts and 4,168 patients with liver diseases were included. In the patients with hepatocellular carcinoma (HCC), high expression of galectin-1 and -3 in the tissues was significantly associated with worse overall survival (galectin-1: HR = 1.94, 95% CI = 1.61–2.34, p < 0.001; galectin-3: HR = 3.29, 95% CI = 1.62–6.68, p < 0.001) and positive vascular invasion (galectin-1: OR = 1.74, 95% CI = 1.18–2.58, p = 0.005; galectin-3: OR = 2.98, 95% CI = 1.58–5.60, p = 0.001); but, high expression of galectin-4 and −9 in the tissues was significantly associated with better overall survival (galectin-4: HR = 0.53, 95% CI = 0.36–0.79, p = 0.002; galectin-9: HR = 0.56, 95% CI = 0.44–0.71, p < 0.001) and negative vascular invasion (galectin-4: OR = 0.36, 95% CI = 0.19–0.72, p = 0.003; galectin-9: OR = 0.60, 95% CI = 0.37–0.97, p = 0.037). Serum galectin-3 level was significantly higher in HCC (MD = 3.06, 95% CI = 1.79–4.32, p < 0.001), liver failure (MD = 0.44, 95% CI = 0.23–0.66, p < 0.001), liver cirrhosis (MD = 1.83, 95% CI = 1.15–2.51, p < 0.001), and chronic active hepatitis B (MD = 18.95, 95% CI = 10.91–27.00, p < 0.001); serum galectin-9 level was significantly higher in HCC (MD = 3.74, 95% CI = 2.57–4.91, p < 0.001) and autoimmune hepatitis (MD = 8.80, 95% CI = 7.61–9.99, p < 0.001).

Conclusion: High galectin-1 and -3 and low galectin-4 and -9 expression indicate worse outcomes of patients with HCC. Serum galectin-3 and -9 levels are positively associated with the risk of chronic liver diseases.

Introduction

Liver diseases, including chronic hepatitis, liver fibrosis or cirrhosis, acute liver injury or liver failure, and hepatocellular carcinoma (HCC), are a major global health burden. They are often subtle, but potentially lethal (1). According to the report of the Global Burden of Disease Study 2019, there are 79,200 deaths from acute hepatitis (2), 1,470,000 deaths from liver cirrhosis and other chronic liver diseases (3), and 485,000 deaths from HCC (4) in the world. Early assessment and identification of liver diseases by molecular biomarkers are clinically important.

Galectins are a family of lectins composed of one or two carbohydrate recognition domains (CRDs) that bind to the β-galactoside-containing glycans (5). Galectins are classified into three groups according to their molecular-structural characteristics: “prototype” galectins with a single CRD (i.e., galectin-1,-2,-5,-7,-10,-11,-13,-14,-15, and -16); “chimeric-type” galectins (i.e., galectin-3) with the tandem repeats of proline- and glycine-rich short stretches fused onto the CRD; and “tandem repeat”-type galectins with two distinct CRDs (i.e., galectin-4,-6,-8,-9, and -12) (6). Galectins are responsible for the regulation of premessenger RNA (mRNA) splicing, cell cycle, cell growth, and cell apoptosis (7), and the development and/or progression of many human diseases, including cancer, heart failure, and chronic kidney disease (8).

Galectins play a regulatory role in liver diseases by binding their CRDs to the glycoconjugates expressed in the hepatocytes (9). Abnormal expression of the galectins may be related to the development of hepatitis and liver fibrosis/cirrhosis and the progression of HCC (10). In this study, we conducted a systematic review and meta-analysis to evaluate the role of galectins in various liver diseases.

Methods

This meta-analysis was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement (11).

Registration

The registration number was CRD42020210038 in the PROSPERO.

Literature Search

The literature was searched via the PubMed, Embase, and Cochrane Library databases from the earliest available publication until September 18, 2020. Search items were as follows: “(galectin)” and “(liver)” or “(hepatic)” or “(hepatitis)” or “(hepatocellular)” or “(fibrosis)” or “(failure).” There was no language restriction.

Selection Criteria

The inclusion criteria were as follows: (1) study population should be the patients diagnosed with liver diseases and (2) galectin expression or level was detected in patients with liver diseases. The exclusion criteria were as follows: (1) duplicate papers; (2) reviews, meta-analyses, or case reports; (3) notes, conferences, corrections, editorials, comments, or letters; (4) experimental or animal studies; and (5) studies which were lacking of detailed data regarding galectin expression or level.

Data Extraction

We extracted the following data from each study, including first author, publication year, country, study design, enrollment period, sample size, subtypes of the galectins, and methods to detect the galectins. As for the studies regarding the clinicopathological features and the outcomes of HCC, we specifically extracted the data as follows: galectin expression and its grouping; clinicopathological features including tumor size, tumor-node-metastasis (TNM) stage, differentiation grade, and vascular invasion; and outcomes, which include overall survival (OS), disease-free survival (DFS), and relapse-free survival (RFS). As for the studies regarding the risk of liver diseases, we specifically extracted the data regarding the type of liver diseases, the Child–Pugh class, and the level of serum galectins.

As for the survival data, we directly extracted or indirectly estimated the hazard ratio (HR) and 95% CI. If a study did not give the HR and 95% CI, but only reported the Kaplan–Meier curves, we would employ the Engauge Digitizer 4.1 software (Linux, Mac OSX, and Windows Slashdot Media, CA, USA) to extract the survival rate at the different time points from the Kaplan–Meier curves and then utilize Tierney's table (12) to estimate its correlative HR with 95% CI.

Study Quality Assessment

Quality of the case–control and cohort studies were evaluated by the Newcastle–Ottawa Scale (NOS), which included the three parts (i.e., selection, comparability, and outcomes) and eight questions (13). The highest NOS score was nine points. High quality was considered if the NOS score was more than six points.

Statistical Analysis

The Stata version 12.0 (Stata Corporation, College Station, Texas, USA) was employed for the statistical analysis. Only a random effects model was implemented. HRs, odds ratios (ORs), and mean differences (MDs) with 95% CIs were pooled. A two-sided p < 0.05 was considered as statistically significant. If the data were expressed as median with range, mean with SD would be estimated (14). Heterogeneity was evaluated by the I2 statistics and the Cochran's Q test. I2 > 50% or p < 0.1 was considered as a statistically significant heterogeneity. Sensitivity analysis was performed after omitting one study at a time in order to check the consistency to estimate the overall effect. Publication bias was assessed by Egger's test (15) and p < 0.1 was considered to imply a significant publication bias.

Results

Study Selection and Characteristics

Among the 4,005 papers initially retrieved, 33 papers were eligible (Figure 1). They were published from 2008 to 2020 (1648). Members of the galectins evaluated included galectin-1,-3,-4, and -9. The sample size ranged from 10 to 386; 25 studies came from Asia (1620, 22, 2539, 42, 44, 46, 47), six studies came from Europe (21, 40, 41, 43, 45, 48), and two studies came from Oceania (23, 24); five studies were published as the abstracts (27, 28, 35, 37, 42) and 28 studies were published as the full texts (1626, 2934, 36, 3841, 4348); and 29 studies were of high quality (1626, 29, 30, 3239, 4148), but four studies were of low quality (27, 28, 31, 40).

FIGURE 1
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Figure 1. Flow diagram for the selection of the papers.

Meta-Analyses Regarding the Galectins With Prognosis and Clinicopathological Features of the Hepatocellular Carcinoma

Seventeen studies involving 19 cohorts and 3,120 patients focused on the relationship of the galectins expressed in the tissues with prognosis and clinicopathological features of HCC (1632) (Table 1). Among them, five study cohorts focused on galectin-1 (1721), seven study cohorts focused on galectin-3 (22, 2529, 31), one study cohort focused on galectin-4 (32), and six study cohorts focused on galectin-9 (16, 23, 24, 26, 30). Results of the meta-analyses are shown in Table 2.

TABLE 1
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Table 1. Characteristics of the included studies regarding the galectins with the prognosis and clinicopathological features of HCC in the tissues.

TABLE 2
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Table 2. Galectins with the prognosis and clinicopathological features of HCC: results of the meta-analyses.

Overall Survival

The relationship between the galectins and OS was explored in 17 study cohorts (1620, 2230, 32).

High galectin-1 expression was significantly correlated with worse OS in the patients with HCC (HR = 1.94, 95% CI = 1.61–2.34, p < 0.001) without significant heterogeneity (I2 = 0.0%, p = 0.739).

High galectin-3 expression was significantly correlated with worse OS in the patients with HCC (HR = 3.29, 95% CI = 1.62–6.68, p = 0.001) with a significant heterogeneity (I2 = 90.00%, p = 0.008). Sensitivity analysis illustrated that the study by Song et al. (22) displayed an apparent influence on the overall result of the meta-analysis (Supplementary Figure 1). After the exclusion of this study, the pooled HR was similar (HR = 2.51, 95% CI = 1.51–4.16, p < 0.001), but with a mild reduction in heterogeneity (I2 = 71.10%, p = 0.008).

High galectin-4 expression was significantly correlated with better OS in the patients with HCC (HR = 0.53, 95% CI = 0.36–0.79, p = 0.002).

High galectin-9 expression was significantly correlated with better OS in the patients with HCC (HR = 0.56, 95% CI = 0.44–0.71, p < 0.001) without significant heterogeneity (I2 = 3.7%, p = 0.393).

Relapse-Free Survival

The relationship between the galectins and RFS was explored in three study cohorts (20, 30, 32).

High galectin-1 expression was significantly correlated with worse RFS in the patients with HCC (HR = 1.62, 95% CI = 1.26–2.08, p < 0.001).

High galectin-4 (HR = 0.65, 95% CI = 0.47–0.89, p = 0.008) and galectin-9 (HR = 0.46, 95% CI = 0.26–0.82, p = 0.009) expression were significantly correlated with better RFS in the patients with HCC.

Tumor Size

The relationship between the galectins and tumor size was explored in 10 study cohorts (16, 18, 20, 22, 25, 26, 29, 30, 32).

High galectin-1 expression was not significantly associated with tumor size (OR = 1.59, 95% CI = 0.74–3.41, p = 0.238) with a significant heterogeneity (I2 = 75.8%, p = 0.042).

High galectin-3 expression was significantly associated with bigger tumor size (OR = 1.69, 95% CI = 1.01–2.84, p = 0.046) without significant heterogeneity (I2 = 48.8%, p = 0.119).

High galectin-4 expression was significantly associated with smaller tumor size (OR = 0.43, 95% CI = 0.2–0.91, p = 0.027); by contrary, high galectin-9 expression was not significantly associated with tumor size (OR = 0.98, 95% CI = 0.7–1.39, p = 0.924) without significant heterogeneity (I2 = 0.0%, p = 0.394).

Tumor-Node-Metastasis Stage

The relationship between the galectins and TNM stage was explored in eight study cohorts (18, 21, 22, 25, 26, 31, 32).

High galectin-1 expression was significantly associated with advanced TNM stage (OR = 2.53, 95% CI = 1.31–4.87, p = 0.006) without significant heterogeneity (I2 = 41.9%, p = 0.189).

High galectin-3 expression was not significantly associated with TNM stage (OR = 2.06, 95% CI = 0.82–5.16, p = 0.122) with a significant heterogeneity (I2 = 66.6%, p = 0.030). Sensitivity analysis illustrated that the study by Kong et al. (26) displayed an apparent influence on the overall result of the meta-analysis (Supplementary Figure 2). After the exclusion of this study, the pooled OR was similar (OR = 2.90, 95% CI = 1.84–4.56, p = 0.044), but the heterogeneity was statistically insignificant (I2 = 0.0%, p = 0.731).

High galectin-4 (OR = 0.49, 95% CI = 0.28–0.86, p = 0.013) and galectin-9 (OR = 0.44, 95% CI = 0.20–0.98, p = 0.044) expression were significantly associated with early TNM stage.

Differentiation Grade

The relationship between the galectins and tumor differentiation grade was explored in 11 study cohorts (16, 18, 2022, 26, 2932).

High galectin-1 expression was not significantly associated with differentiation grade (OR = 0.96, 95% CI = 0.7–1.32, p = 0.795) without significant heterogeneity (I2 = 0.0%, p = 0.830).

High galectin-3 expression was not significantly associated with differentiation grade (OR = 2.13, 95% CI = 0.97–4.69, p = 0.061) with a significant heterogeneity (I2 = 65.6%, p = 0.033). Sensitivity analysis demonstrated that the study by Fang et al. (31) displayed an apparent influence on the overall result of the meta-analysis (Supplementary Figure 3). After the exclusion of this study, the pooled OR was similar (OR = 1.65, 95% CI = 1.01–2.69, p = 0.044), but the heterogeneity was statistically insignificant (I2 = 18.5%, p = 0.293).

High galectin-4 expression was significantly associated with well-differentiation grade (OR = 0.35, 95% CI = 0.16–0.78, p = 0.010).

High galectin-9 expression was not significantly associated with tumor differentiation grade (OR = 0.70, 95% CI = 0.34–1.47, p = 0.348) with a significant heterogeneity (I2 = 70.2%, p = 0.035). Sensitivity analysis illustrated that the study by Gu et al. (30) displayed an apparent influence on the overall result of the meta-analysis (Supplementary Figure 4). After the exclusion of this study, the pooled OR was similar (OR = 0.51, 95% CI = 0.28–0.95, p = 0.034), but the heterogeneity was statistically insignificant (I2 = 35.0%, p = 0.215).

Vascular Invasion

The relationship between the galectins and vascular invasion was explored in seven study cohorts (16, 2022, 25, 30, 32).

High galectin-1 expression was significantly associated with positive vascular invasion (OR = 1.74, 95% CI = 1.18–2.58, p = 0.005) without significant heterogeneity (I2 = 0.0%, p = 0.679).

High galectin-3 expression was significantly associated with positive vascular invasion (OR = 2.98, 95% CI = 1.58–5.60, p = 0.001) without significant heterogeneity (I2 = 0.0%, p = 0.421).

High galectin-4 expression was significantly associated with negative vascular invasion (OR = 0.36, 95% CI = 0.19–0.72, p = 0.003).

High galectin-9 expression was significantly associated with negative vascular invasion (OR = 0.60, 95% CI = 0.37–0.97, p = 0.037) without significant heterogeneity (I2 = 2.8%, p = 0.311).

Meta-Analyses Regarding the Galectins With the Risk of Different Liver Diseases

About 18 studies involving 24 cohorts and 1,048 patients focused on the relationship between the serum galectin levels and the risk of different liver diseases (25, 30, 3348) (Table 3). Among them, 16 studies focused on galectin-3 (25, 3338, 4048), and two studies focused on galectin-9 (30, 39). Results of the meta-analyses are shown in Table 4.

TABLE 3
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Table 3. Characteristics of the included studies regarding the galectins with the risk of different liver diseases.

TABLE 4
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Table 4. Galectins with the risk of different liver diseases: results of the meta-analyses.

Hepatocellular Carcinoma

The relationship between the galectins and the risk of HCC was explored in six study cohorts (25, 30, 36, 4143). Among them, five study cohorts selected the healthy volunteers as the control subjects, and one study cohort selected the patients with chronic hepatitis as the control subjects.

Serum galectin-3 level was significantly higher in the patients with HCC compared to the healthy volunteers or the patients with chronic hepatitis (MD = 2.71, 95% CI = 1.56–3.85, p < 0.001) with a significant heterogeneity (I2 = 86.9%, p < 0.001). Sensitivity analysis illustrated that the study by Akyuz et al. (42) displayed an apparent influence on the overall result of the meta-analysis (Supplementary Figure 5). After the exclusion of this study, the pooled MD was similar (MD = 2.28, 95% CI = 2.07–2.50, p < 0.001), but the heterogeneity was statistically insignificant (I2 = 0.6%, p = 0.389).

Serum galectin-9 level was significantly higher in the patients with HCC compared to the healthy volunteers (MD = 3.74, 95% CI = 2.57–4.91, p < 0.001).

Liver Failure

The relationship between galectin-3 and the risk of liver failure was explored in two study cohorts, both of which selected the healthy volunteers as the control subjects (33, 35).

Serum galectin-3 level was significantly higher in the patients with liver failure compared to the healthy volunteers (MD = 0.44, 95% CI = 0.23–0.66, p < 0.001) with a significant heterogeneity (I2 = 97.8%, p < 0.001).

Liver Cirrhosis

The relationship between galectin-3 and the risk of liver cirrhosis was explored in six study cohorts, all of which selected healthy volunteers as the control subjects (25, 36, 38, 40, 48).

Serum galectin-3 level was significantly higher in the patients with liver cirrhosis compared to the healthy volunteers (MD = 1.83, 95% CI = 1.15–2.51, p < 0.001) with a significant heterogeneity (I2 = 98.3%, p < 0.001). Sensitivity analysis did not find any source of heterogeneity.

Other Chronic Liver Diseases

The relationship between the galectins and the risk of other chronic liver diseases, including inactive hepatitis B, chronic active hepatitis B, non-alcoholic steatohepatitis, hepatitis C, autoimmune hepatitis, non-alcoholic fatty liver disease, and biliary atresia, was explored in 10 study cohorts. All of them selected healthy volunteers as the control subjects (25, 34, 37, 39, 4447).

In comparison to the healthy volunteers, serum galectin-3 level was significantly higher in chronic active hepatitis B (MD = 18.95, 95% CI = 10.91–27.00, p < 0.001) and biliary atresia (MD = 1.30, 95% CI = 1.11–1.49, p < 0.001), but not inactive hepatitis B (MD = 1.29, 95% CI = 1.40–3.97, p = 0.347), non-alcoholic steatohepatitis (MD = 0.48, 95% CI = 0.77–1.73, p = 0.452), hepatitis (MD = 0.37, 95% CI = 0.65–1.39, p = 0.479), or non-alcoholic fatty liver disease (MD = 0.10, 95% CI = 0.30–0.50, p = 0.485); on the contrary, serum galectin-3 level was significantly lower in hepatitis C (MD = 0.27, 95% CI = 0.34–0.20, p < 0.001) (Figure 2).

FIGURE 2
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Figure 2. Forest plots showing the association between the risk of chronic liver diseases and galectin-3.

Serum galectin-9 level was significantly higher in the patients with autoimmune hepatitis compared to the healthy volunteers (MD = 8.80, 95% CI = 7.61–9.99, p < 0.001).

Publication Bias

Publication bias is reported in Supplementary Table 1.

Discussion

Until now, 11 subtypes of galectins family have been identified in humans, of which galectin-1,-3, and -9 are the most commonly studied in various diseases (49). According to the current systematic analyses, the role of galectin-1,-3,-4, and -9 was studied in patients with liver diseases.

Patients with HCC have a 5-year survival rate of <12% (50). Therefore, it is vital to identify the biomarkers to predict the prognosis of HCC (51). This study found that the higher serum galectin-3 and -9 levels were associated with an increased risk of HCC and high galectin-1 and -3 and low galectin-4 and -9 expression were significantly associated with worse OS and positive vascular invasion in HCC. Indeed, experimental studies have also suggested the potential mechanisms of galectin-1,-3, and -9 expression in the development and progression of HCC. First, galectin-1 can induce the epithelial–mesenchymal transition (EMT), which is a major process during the progression of cancer in the HCC cells of humans (52). Galectin-1 inhibitor combined with sorafenib can further decrease the tumor size (53). Second, galectin-3 can inhibit the tumor-reactive T cells and promote tumor growth in the mice receiving the tumor-reactive CD8+ T cells (54). Silencing of galectin-3 can significantly reduce the mRNA and protein levels of urokinase-type plasminogen activator receptor (uPAR) and downstream signaling transduction pathway of uPARs in the HCC cells by inhibiting the MEK/ERK signaling pathway, further influencing the proliferation, migration, and invasion of the HCC cells (55). Third, galectin-9 can inhibit the growth of the HCC cell lines by inducing cell apoptosis (56). Galectin-9 also increases the number of Tim-3+ dendritic cells and CD8+ T cells and enhances antitumor immunity through the interaction of galectin-9 with Tim-3 (57). By comparison, blockade of the Tim-3/galectin-9 signaling pathway importantly increases the functionality of tumor-infiltrating Tim-3+ T cells and is negatively associated with the survival of patients with HCC (58).

Another major finding of this study was that higher serum galectin-3 level was associated with an increased risk of liver failure, liver cirrhosis, and chronic active hepatitis B. Other evidence was also in favor of the importance of galectin-3 in these liver diseases. First, if the patients with acute-on-chronic liver failure related to hepatitis B had galectin-3 methylated promoter, they would have shorter survival time, higher 3-month mortality, and higher model for end-stage liver disease (MELD) score (59). Second, galectin-3 modulates the phagocytosis-induced hepatic stellate cell activation and liver fibrosis in vivo (60). Galectin-3 level is significantly higher in the Child–Pugh class C and positively correlates with the MELD score, suggesting the association of galectin-3 level with hepatic decompensation (61). By comparison, the galectin-3 inhibitor can reduce the hepatic venous pressure gradient in patients with esophageal varices (62). Third, galectin-3 deficiency can lead to a significant reduction in the incidence of concanavalin A-induced hepatitis in mice by inhibiting inflammation (63).

This study did not find any significant association of serum galectin-3 level with inactive hepatitis B, non-alcoholic steatohepatitis, or non-alcoholic fatty liver disease. This illustrated that the impact of galectin-3 level on chronic liver diseases might be dependent upon the severity and stage of liver damage (40). Indeed, the evidence regarding the role of galectin-3 in non-alcoholic fatty liver disease and non-alcoholic steatohepatitis is also controversial. Some studies have shown that galectin-3 deficiency in male mice can spontaneously develop non-alcoholic fatty liver disease and more severe hepatic injury (64, 65). In contrast, other studies have reported that galectin-3 ablation protected the mice from the diet-induced non-alcoholic steatohepatitis (66).

There were several limitations in this study. First, this meta-analysis contained a relatively small number of studies, which might lead to insufficient statistical power. Second, the cutoff values of high galectin expression were heterogeneous among the studies. Third, HR values were not directly reported in the six included studies, where their survival data were extracted from the Kaplan–Meier curves by the Engauge Digitizer 4.1 software. Fourth, most of the included studies were from Asia. Our findings are not a global representation.

In conclusion, based on this systematic review and meta-analysis, both high galectin-1 and -3 and low galectin-4 and -9 expression in the tissues were significantly related to worse prognosis and positive vascular invasion in patients with HCC and serum galectin-3 level was associated with the risk of HCC, liver failure, liver cirrhosis, and chronic active hepatitis B (Figure 3). Further studies are needed to explore the role of galectins as a potential therapeutic target and biomarker for liver diseases.

FIGURE 3
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Figure 3. A schematic drawing showing the major findings of this study. CKD, chronic kidney disease; OS, overall survival; RFS, relapse-free survival; HCC, hepatocellular carcinoma; TNM, tumor-node-metastasis.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.

Author Contributions

XQ contributed to the conceptualization, supervision, and project administration. YA, SX, YL, XX, and XQ contributed to the methodology, formal analysis, data curation, and writing the original draft. YA, SX, YL, XX, CP, JC, NM-S, XG, and XQ contributed to the validation, writing, review, and editing. All authors contributed to the article and approved the submitted version.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2021.744518/full#supplementary-material

Supplementary Figure 1. Sensitivity analysis of galectin-3 expression with overall survival (OS) in HCC.

Supplementary Figure 2. Sensitivity analysis of galectin-3 expression with TNM stage in HCC.

Supplementary Figure 3. Sensitivity analysis of galectin-3 expression with the differentiation grade in HCC.

Supplementary Figure 4. Sensitivity analysis of galectin-9 expression with the differentiation grade in HCC.

Supplementary Figure 5. Sensitivity analysis of serum galectin-3 level with the risk of HCC.

Supplementary Table 1. Publication bias.

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Keywords: galectins, hepatocellular carcinoma, cirrhosis, hepatitis, fibrosis

Citation: An Y, Xu S, Liu Y, Xu X, Philips CA, Chen J, Méndez-Sánchez N, Guo X and Qi X (2021) Role of Galectins in the Liver Diseases: A Systematic Review and Meta-Analysis. Front. Med. 8:744518. doi: 10.3389/fmed.2021.744518

Received: 20 July 2021; Accepted: 22 September 2021;
Published: 27 October 2021.

Edited by:

Carmen Peralta Uroz, Institut de Recerca Biomèdica August Pi i Sunyer (IDIBAPS), Spain

Reviewed by:

María Fernanda Troncoso, Universidad de Buenos Aires, Argentina
Debjyoti Kundu, Indiana University School of Medicine, United States

Copyright © 2021 An, Xu, Liu, Xu, Philips, Chen, Méndez-Sánchez, Guo and Qi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Xingshun Qi, xingshunqi@126.com

These authors share first authorship

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