Circulating miR-21-5p level has limited prognostic value in patients with hepatocellular carcinoma and is influenced by renal function

Abstract

BACKGROUND

MicroRNAs (miRNAs) have been suggested as biomarkers for malignant diseases including hepatocellular carcinoma (HCC). Specifically, hsa-miR-21-5p (miR-21) is among the most frequently deregulated miRNA in cancer. The diagnostic and prognostic value of miR-21 has been demonstrated in HCC tissue, mostly in the Asian population. Although the impact of various factors has been recently reported for circulating hsa-miR-122-5p (miR-122), at present only limited knowledge is available for miR-21.

AIM

To evaluate the value of miR-21 for the assessment of prognosis in HCC patients and to delineate the influence of clinical and preanalytical factors on miR-21 level in sera.

METHODS

Patients with confirmed HCC from our European cohort with predominantly alcohol-associated liver damage were included in the study. All subjects were characterized according to their clinical and laboratory work-up and overall survival data were obtained. Quantitative real-time polymerase chain reaction was performed for miR-21 and spiked-in cel-miR-39-3p. The results were compared to previously reported miR-122 data.

RESULTS

Survival of HCC patients was comparable between patients with low and high serum miR-21 concentration. No association was observed between miR-21 level in sera and Child-Pugh score, Barcelona Clinic Liver Cancer staging system, or etiology of HCC/liver disease. Age, gender, or pretreatment had no association with miR-21 level. A positive correlation was observed between miR-21 and aspartate aminotransferase (r = 0.2854, P = 0.0061), serum miR-122 (r = 0.2624, P = 0.0120), and the International Normalized Ratio (r = 0.2065, P = 0.0496). Negative correlation of miR-21 with serum creatinine (r = -0.2215, P = 0.0348) suggests renal function as a potential influencing factor in miR-21 biogenesis in blood.

CONCLUSION

The results from this work do not support clinically relevant prognostic value of circulating miR-21 in HCC patients in real-life settings. Following systematic evaluation, we identified renal function and aspartate aminotransferase as potential factors that may affect miR-21 concentration in blood. This knowledge should be considered in future miRNA-based biomarker studies not only for HCC but also for other diseases.

Key Words: Hepatocellular cancer, Hepatocellular carcinoma, MicroRNA, Prognosis, miR-21-5p, Renal function

Core Tip: In our previous work, we identified renal function, hemoglobin, and liver injury as potential factors that may impact circulating microRNA expression. miR-21-5p is the most frequently deregulated miRNA in various types of cancer. Several reports have proposed miR-21-5p as a prognostic biomarker in hepatocellular carcinoma. In this study, serum miR-21-5p values were not associated with prognosis of hepatocellular carcinoma in a European cohort of patients with predominantly alcohol-related liver injury. In a similar fashion as previously reported for miR-122-5p, changes in circulating miR-21-5p level correlated with renal function and liver injury. This observation shows that caution should be taken in interpreting circulating miR-21-5p level and its biomarker potential.

INTRODUCTION

There is a substantial effort to identify disease-specific biomarkers. Increasing evidence from intense research in the past several years strongly suggests that microRNAs (miRNAs) may become a valuable tool for the early identification and assessment of disease prognosis or treatment prediction. However, prior potential implementation of novel biomarkers including miRNAs in clinical settings, there is a great need for studies that deal with possible influencing factors[1]. At present, only limited knowledge is available regarding the translational utility of miRNAs as biomarkers in the real-life setting.

Hepatocellular carcinoma (HCC) is one of the most common cancers, even though the factors responsible for disease development are very heterogeneous[2,3]. Prognosis of patients with HCC is dependent on multiple factors including tumor biology, but is also strongly related to residual liver and kidney function. Therefore, HCC is probably the disease that may be best suited for evaluation of various influencing factors in biomarker research. There are several prognostic assessment models and staging systems for liver diseases and/or HCC available including Child-Pugh score[4,5], Model of End-Stage Liver Disease score[6], the Cancer of the Liver Italian Program score[7], Okuda staging system[8], and the Barcelona Clinic Liver Cancer (BCLC) staging system[9] and many of those include multiple variables related to liver and/or renal function.

There is a great need for novel diagnostic, prognostic, and predictive biomarkers for HCC patients that would help to refine the forecast and subsequently individualize treatment decisions. MiRNA analyses of different solid cancers suggest the extensive involvement of miRNAs in cancer pathogenesis[10]. Multiple miRNAs have been examined in HCC previously, but substantial heterogeneity of data has hampered its utility[11]. We recently re-evaluated the prognostic value of hsa-miR-122-5p (miR-122) in a European cohort of well-characterized patients[1]. According to our data, circulating miR-122 was associated with the overall survival (OS) of HCC patients only in a subgroup of patients. We and others have identified multiple co-existing factors that may influence circulating miR-122 levels such as liver injury, hemoglobin concentration, or kidney function, but knowledge of other miRNAs in HCC is limited.

Undoubtedly, hsa-miR-21-5p (miR-21) is among the most frequently deregulated miRNA in human cancers[10-12]. In-depth evidence gathered over the past several years clearly demonstrates the pro-oncogenic function of miR-21 in carcinogenesis[13,14]. For instance, an in vivo study used an miR-21-overexpression mouse model where miR-21 overexpression led to a pre-B malignant lymphoid-like phenotype, indicating that miR-21 is an oncogenic miRNA[15].

In HCC, miR-21 promotes lipid accumulation in the liver and carcinogenesis through the Hbp1-p53-Srebp1c pathway, and therefore represents a potential link between non-alcoholic fatty liver disease and HCC[16]. It may play a role in mediating sorafenib resistance of HCC[17]. In a mouse model, treatment with a miR-21 inhibitor led to inhibition of tumor growth implicating miR-21 as potential therapeutic target in HCC[18]. Overexpression of miR-21 in HCC tumors was uniformly described[19-21] and is associated with poor OS and disease-free survival of HCC patients[19,20].

Higher miR-21 blood level was described in patients with HCC compared to healthy donors[22-24], but the opposite observation has also been reported[25]. Several studies have reported discordant results on circulating miR-21, particularly in patients with chronic hepatitis B virus (HBV) infection and HCC[22,26,27]. Diagnostic value of miR-21 in HCC has mostly been evaluated in HBV-dominant cohorts[22,23,27]. However, a recently published meta-analysis suggested that high ubiquitous miR-21 expression may be a limiting factor in the diagnostic performance of circulating miR-21[28].

In this study, we evaluated the value of serum miR-21 as a prognostic marker in a European cohort with mainly alcohol-induced HCC. Furthermore, we identified and explored the potential clinical conditions and laboratory co-factors that may influence performance of miR-21 as a biomarker in HCC and potentially in other conditions.

MATERIALS AND METHODS

Study cohort

In total, the sera of 91 patients with HCC were available for analysis. The samples were collected between January 2009 and April 2011 as previously described[1]. Diagnosis of HCC was confirmed either histologically or via non-invasive criteria based on typical imaging using computer tomography and magnetic resonance imaging. The study was performed according to the World Medical Association “Declaration of Helsinki–Ethical Principles for medical research involving human subjects,” and was approved by the local Institutional Review Board of Otto-von-Guericke University Magdeburg (No. 99/10). Written informed consent was obtained from patients prior inclusion in the primary study. All patients were well characterized according to laboratory parameters, concomitant liver disease, and HCC including Child-Pugh score and BCLC staging as previously reported[1].

Extraction of RNA and miRNA expression analysis

Following centrifugation, all serum samples were stored at -80 °C prior to further use. We performed extraction of RNA (including miRNA) according to a previously described and established protocol using the miRNeasy Mini Kit (QIAGEN, Hilden, Germany)[29]. Briefly, 700 µL QIAzol Lysis Reagent were initially mixed with 100 µL serum. During this step, we added 5 μL of a 5 nM cel-miR-39 solution for internal normalization. The quality of RNA was examined using spectrophotometry. Following washing steps, RNA was finally eluted in 30 µL RNase-free water and stored at -80 °C until further use. Quantification of cel-miR-39-3p (assay ID: 000200) and hsa-miR-122-5p (assay ID: 002245) expression were assessed using the TaqMan miRNA assay and TaqMan Universal Master Mix II (Applied Biosystems, Foster City, CA, United States). Hsa-miR-21-5p was assessed with internally validated SYBR green method as previously described[30]. RNA (20 ng) was transcribed and used for the quantitative PCR (qPCR). The analyses were performed on the BioRad CFX Cycler System (BioRad, Hercules, CA, United States) in duplicate and the Ct or threshold cycle value was used for normalization and subsequent relative quantification.

Statistical analysis

For statistical analysis, we used GraphPad Prism Version 7.0 (GraphPad Software, San Diego, CA, United States). Two-sided P values ≤ 0.05 were defined as significant. Based on the normality of distribution of miRNA values (2-deltaCt [miR-21/cel-miR-39]), we used nonparametric tests such as Spearman’s rank correlation coefficient, Mann-Whitney test, Kruskal-Wallis test, and Dunn’s post-hoc test. Chi-square (χ²) test and Fisher’s exact test were used for contingency testing accordingly. Additionally, the unpaired t-test was used for analysis of laboratory parameters as appropriate. The data are presented as boxplots with whiskers for minimum and maximum. The survival time was defined as the time between inclusion in our study (date of blood withdrawal) and death or last documented contact. Kaplan-Meier survival curves and nonparametric log-rank test were used to evaluate survival differences. Median (50% percentile) was used to define the groups with high and low serum miR-21 expression, miR-122, alpha-fetoprotein (AFP) expression.

RESULTS

The analysis of miR-21 in serum showed high variability between samples (mean Ct value: 29.61 ± 0.78, [min: 27.38, max: 31.22, range: 3.84]). First, we divided the cohort in two groups with miR-21-high and miR-21-low serum levels based on the median as shown in Table 1. Most parameters showed no statistically significant difference between the groups including gender, age, etiology of HCC, BCLC stage, or treatment status.

Table 1 Clinical and laboratory characteristics of hepatocellular carcinoma patients and hsa-miR-21-5p expression.

		All patients	miR-21 low1	miR-21 high2	P value
Patient number:		91	47	44
Gender (n, %):	Women	17 (18.7%)	7 (14.9%)	10 (22.7%)	0.4231
	Men	74 (81.3%)	40 (85.1%)	34 (77.3%)
Age in yr	mean ± SD	67.91 ± 8.98	69.11 ± 8.84	66.64 ± 9.05	0.1912
Etiology (n, %):	Alcohol abuse	41 (45.1%)	22 (46.8%)	19 (43.2%)	0.7560
	Viral hepatitis	12 (13.2%)	5 (10.6%)	7 (15.9%)
	NASH	13 (14.3%)	8 (17.0%)	5 (11.4%)
	Rare or other cause3	25 (27.5%)	12 (25.5%)	13 (29.5%)
BCLC stage (n, %):	A	16 (17.6%)	7 (14.9%)	9 (20.5%)	0.7787
	B	37 (40.7%)	20 (42.6%)	17 (38.6%)
	C + D	38 (41.8%)	20 (42.6%)	18 (40.9%)
Child-Pugh score (n, %):	No liver cirrhosis	16 (17.6%)	8 (17.0%)	8 (18.2%)	0.7443
	A	45 (49.5%)	25 (53.2%)	20 (45.5%)
	B + C	30 (33.0%)	14 (29.8%)	16 (36.4%)
Treatment (n, %)4:	Therapy naïve	26 (28.6%)	11 (23.4%)	15 (34.1%)	0.3535
	Pretreated	65 (71.4%)	36 (76.6%)	29 (65.9%)
Ascites (n, %):	No ascites	58 (63.7%)	30 (63.8%)	28 (63.6%)	0.9999
	Ascites present	33 (36.3%)	17 (36.2%)	16 (36.4%)
Bilirubin (µmol/L):	mean ± SD	23.38 ± 31.73	24.27 ± 40.47	22.43 ± 18.78	0.7833
AFP (ng/mL):	mean ± SD	4593 ± 20162	540 ± 1533	8922 ± 28481	0.0469
INR5:	mean ± SD	1.076 ± 0.2127	1.034 ± 0.1450	1.122 ± 0.2611	0.0486
Platelets (Gpt/L):	mean ± SD	195.6 ± 118.7	182.7 ± 80.5	209.3 ± 149.0	0.2870
ALAT (μmol/Ls):	mean ± SD	0.7457 ± 0.4460	0.6955 ± 0.3425	0.7993 ± 0.5340	0.2697
ASAT (μmol/Ls):	mean ± SD	1.267 ± 1.041	1.040 ± 0.597	1.510 ± 1.330	0.0307
Hemoglobin (mmol/L):	mean ± SD	7.811 ± 1.254	7.655 ± 1.122	7.977 ± 1.375	0.2230
Creatinine (µmol/L):	mean ± SD	92.92 ± 67.95	102.3 ± 88.46	82.91 ± 33.08	0.1751
Albumin (g/L):	mean ± SD	36.29 ± 6.539	36.47 ± 5.668	36.10 ± 7.420	0.7938

¹miR-21 50% percentile.

²miR-21 > 50% percentile.

³Including hemochromatosis.

⁴Patients with different kind of pretreatments (for example hepatic resection, transarterial chemoembolization, selective internal radiation therapy and sorafenib) were included.

⁵For 30 patients we obtained no exact laboratory value of the International Normalized Ratio (only < 1.5). For these patients, we calculated the International Normalized Ratio based on the Quick. P values were calculated with unpaired t-test, Fisher’s exact test, and χ² test as appropriate. AFP: Alpha-fetoprotein; ALAT: Alanine aminotransferase; ASAT: Aspartate aminotransferase; BCLC: Barcelona Clinic Liver Cancer; INR: International Normalized Ratio; NASH: Non-alcoholic steatohepatitis; SD: Standard deviation.

Circulating miR-21 in relation to staging and etiology of liver disease

To evaluate the role of disease stage or etiology of the concomitant liver disease, we performed subgroup testing. Circulating miR-21 in patients with HCC were similar between patients with different Child-Pugh scores (P = 0.7991; Figure 1A), BCLC stages (P = 0.3947; Figure 1B) or was interdependent of etiologies of underlying liver disease (P = 0.6331; Figure 1C) suggesting that other factors than HCC or liver disease may contribute to miR-21 variation.

Figure 1 Serum hsa-miR-21-5p level in correlation to Child-Pugh score, Barcelona Clinic Liver Cancer stage, and underlying etiology. A: Serum hsa-miR-21-5p (miR-21) level and Child-Pugh score: No liver cirrhosis (n = 16), Child-Pugh A (n = 45), Child-Pugh B (n = 27), Child-Pugh C (n = 3), P = 0.7991; B: Serum miR-21 and Barcelona Clinic Liver Cancer (BCLC) staging system: Stage A (n = 16), stage B (n = 37), stage C (n = 32), stage D (n = 6), P = 0.3947; and C: Serum miR-21 and underlying etiology of the hepatocellular carcinoma: Alcohol abuse (n = 41), viral hepatitis (n = 12), non-alcoholic steatohepatitis (NASH) (n = 13), hemochromatosis (n = 6), rare or other (n = 19), P = 0.6331. Kruskal-Wallis test and post-hoc Dunn’s test were used for statistical analysis. MiR-21: Hsa-miR-21-5p.

Circulating miR-21 and parameters of liver and kidney injury

To evaluate if concomitant conditions including liver injury, liver function or kidney injury may affect miR-21 level, we performed comparison of various laboratory parameters and serum miR-21. As shown in Figure 2A, there was a non-significant trend for a positive correlation between miR-21 and alanine aminotransferase (ALAT) (r = 0.1709, P = 0.1053). In much stronger fashion, we observed a statistically significant positive correlation between miR-21 and aspartate aminotransferase (ASAT) (r = 0.2854, P = 0.0061; Figure 2B). Correspondingly, patients with higher miR-21 had also significantly higher ASAT levels (P = 0.0307; Table 1). Even though, miR-21 showed no correlation with AFP (r = 0.1025, P = 0.3337; Figure 2C), the miR-21-high group was associated with higher AFP levels (P = 0.0469; Table 1). MiR-21 levels were furthermore associated with the International Normalized Ratio (r = 0.2065, P = 0.0496; Figure 2D) and patients with high miR-21 had higher International Normalized Ratio accordingly (P = 0.0486; Table 1). Subsequent analysis of other parameters of the liver function such as bilirubin or albumin revealed not association with miR-21 (Tables 1 and 2). Most importantly from the clinical perspective, we observed a negative correlation between miR-21 level and creatinine level (r = -0.2215, P = 0.0348; Figure 2E), suggesting that renal function may impact miR-21 level in blood. Tables 1 and 2 provide a detailed overview on other factors that have been evaluated in the study with no significant difference.

Figure 2 Correlation analysis of serum hsa-miR-21-5p and common laboratory parameters. Correlation between serum hsa-miR-21-5p and A: Alanine aminotransferase (ALAT); B: Aspartate aminotransferase (ASAT); C: Alpha-fetoprotein (AFP); D: International Normalized Ratio (INR); and E: Creatinine. For 30 patients only laboratory quick value was available and reverse calculation of International Normalized Ratio for values below < 1.5 were performed. Spearman’s correlation coefficient was used for statistical analysis. MiR-21: Hsa-miR-21-5p.

Table 2 Correlation analyses of hsa-miR-21-5p and clinical or laboratory parameters.

Parameter	2-ΔCt miR-21 / cel-miR-39
	Spearman r	Confidence interval	P value
Age in yr	-0.1147	-0.3188 to 0.09956	0.2789
Creatinine (µmol/L)	-0.2215	-0.4139 to -0.01013	0.0348
Bilirubin (µmol/L)	0.1484	-0.06547 to 0.3493	0.1603
ALAT (µmol/Ls)	0.1709	-0.0425 to 0.3694	0.1053
ASAT (µmol/Ls)	0.2854	0.07828 to 0.4689	0.0061
Albumin (g/L)	-0.01562	-0.2267 to 0.1969	0.8832
AFP (ng/mL)	0.1025	-0.1118 to 0.3077	0.3337
Hemoglobin (mmol/L)	0.1377	-0.07638 to 0.3396	0.1931
INR1	0.2065	-0.005615 to 0.4008	0.0496
Platelets (Gpt/L)	0.09185	-0.1224 to 0.2979	0.3865
2-ΔCt miR-122 / cel-miR-39	0.2624	0.05357 to 0.4493	0.0120

¹For 30 patients, we obtained no exact laboratory value of the International Normalized Ratio (only < 1.5). For these patients, we calculated the International Normalized Ratio based on the Quick. ALAT: Alanine aminotransferase; ASAT: Aspartate aminotransferase; AFP: Alpha-fetoprotein; INR: International Normalized Ratio; miR-21: Hsa-miR-21-5p.

Circulating miR-21 and survival analysis

The survival data of our cohort have been previously validated and reported[1]. To evaluate the prognostic value of miR-21, we divided our study population based on the 50^th percentile of miR-21 into patients with high and low level. We did not find any significant difference in survival between these groups (P = 0.2697; Figure 3A). Furthermore, no survival difference was found between the groups if the cohort was divided into three groups according to the 25^th, 33^th, and 75^th percentile (data not shown). Taking into account the differences in tumor biology, we performed subgroup analysis for different BCLC stages. Neither separate analysis for combined BCLC A and B (P = 0.1428; Figure 3B) nor BCLC C and D (P = 0.4955; Figure 3C) were associated with survival differences. Having shown an association to creatinine, we further explored the prognostic value in subjects with normal and impaired renal function, but no prognostic difference was observed based on miR-21 level in patients with normal or pathological creatinine (P = 0.2564, Figure 4A and P = 0.8378, Figure 4B, respectively). Higher miR-21 levels were not associated with a worse prognosis in patients with normal ALAT (P = 0.8094, Figure 4C), while a slight trend for worse OS was observed in patients with pathological ALAT (P = 0.0800, Figure 4D). In a similar way, we found no significant difference in OS in patients with normal ASAT but a non-significant trend in patients with pathological ASAT (P = 0.8423, Figure 4E, P = 0.1170, Figure 4F, respectively).

Figure 3 Overall survival analysis in relation to hsa-miR-21-5p level. A: All patients were divided into two groups: (1) Low: < 50^th percentile (n = 47) and (2) High: > 50^th percentile (n = 44), two patients exhibit exactly the median expression of serum hsa-miR-21-5p, that is why, the group division is not exactly symmetric; B: Overall survival analysis in patients with Barcelona Clinic Liver Cancer staging system A + B (divided into two groups: (1) Low: < 50^th percentile [n = 27] and (2) High: > 50^th percentile [n = 26]); C: Survival analysis in patients with Barcelona Clinic Liver Cancer staging system C + D (divided into two groups: (1) Low: < 50^th percentile [n = 20] and (2) High: > 50^th percentile [n = 18]). Nonparametric log-rank test was used for statistical analysis. MiR-21: Hsa-miR-21-5p.

Figure 4 Overall survival analysis in subgroups of patients in relation to hsa-miR-21-5p level. A: Survival analysis in patients with normal creatinine (divided into two groups: (1) Low: < 50^th percentile (n = 33) and (2) High: > 50^th percentile [n = 33]); B: Survival analysis in patients with pathological creatinine (hsa-miR-21-5p [miR-21] low n = 13; miR-21 high n = 12); C: Survival analysis in patients with normal alanine aminotransferase (miR-21 low n = 29; miR-21 high n = 29); D: Survival analysis in patients with pathological alanine aminotransferase (ALAT) (miR-21 low n = 17, miR-21 high n = 16); E: Survival analysis in patients with normal aspartate aminotransferase (ASAT) (miR-21 low n = 15; miR-21 high n = 15); and F: Survival analysis in patients with pathological ASAT (miR-21 low n = 31; miR-21 high n = 30). Nonparametric log-rank test was used for statistical analysis. MiR-21: Hsa-miR-21-5p.

Circulating miR-21, miR-122 and AFP

Next, we evaluated the link between serum miR-21 and serum miR-122 levels. There was a positive correlation between miR-21 and miR-122 (r = 0.2624, P = 0.0120; Figure 5A), which suggests that circulating miRNAs may behave in a similar manner dependent on certain conditions like liver disease or renal function. We investigated if the combination of serum miR-21 and miR-122 may improve prognostic value in patients with HCC. After dividing our study group according to the median of miR-21 and miR-122 level, we formed three groups (patients with low miR-21 and low miR-122, patients with either low miR-21 or low miR-122, patients with high miR-21 and high miR-122); however, no significant difference in OS was observed (P = 0.3377; Figure 5B).

Figure 5 Overall survival analysis in hepatocellular carcinoma patients in relation to serum hsa-miR-21-5p, hsa-miR-122-5p, and alpha-fetoprotein levels. A: Correlation between serum hsa-miR-21-5p (miR-21) and serum hsa-miR-122-5p (miR-122); B: All patients were divided into three groups: Both miR-21 and miR-122 low (50^th percentile, n = 28); one of miR-21 or miR-122 low (50^th percentile, n = 37); both miR-21 and miR-122 high (> 50^th percentile, n = 26); C: Analysis of overall survival of alpha-fetoprotein (AFP) low (n = 24) vs AFP high (n = 23) in patients with low miR-21 levels; and D: Analysis of overall survival of AFP low (n = 22) vs AFP high (n = 22) in patients with high miR-21 levels. Spearman correlation and nonparametric log-rank test were used for statistical analysis. MiR-21: Hsa-miR-21-5p; MiR-122: Hsa-miR-122-5p.

In a similar fashion, we investigated the association of serum miR-21 in correlation with AFP on OS. In HCC patients, higher AFP levels were associated with shorter OS in subjects with miR-21 Low (P = 0.0237; Figure 5C) but only with a trend for shorter OS in miR-21 high group (P = 0.0917; Figure 5D). In subgroup analysis, AFP was indeed associated with a worse prognosis, but the impact was independent of miR-21 level (data not shown).

DISCUSSION

Data on translational value of serum miR-21 in HCC in real-life settings are heterogeneous and only limited evidence is available for the European population. In this work, we systematically analyzed the prognostic value of serum miR-21 in our well-characterized European cohort of HCC patients, and evaluated the potential influence of various factors on its level in serum. The results of our study do not support the prognostic role of miR-21 in HCC. MiR-21 was neither associated with worse OS nor with etiology or tumor stage. Most interestingly, circulating miR-21 levels correlated significantly with ASAT, as surrogate for liver injury, and with creatinine, as a surrogate for renal function.

The prognostic value of circulating miR-21 has been studied in several studies. The overview of the studies is provided in Table 3. Among those, four studies reported that high miR-21 was associated with a worse prognosis[18,24,31,32], while one study[25], in concordance with our data, did not support prognostic role of miR-21. Another study demonstrated significantly better liver transplantation-free survival in HCC patients with higher plasma miR-21 levels[33]. As mentioned above, the available data are mostly based on the evidence from Asian populations and mainly include HBV/hepatitis C virus-induced HCC, while our work is among the first to evaluate the survival in patients from European origin. One may speculate if etiology of HCC may be responsible for the differences in the study outcome; however, our subgroup analysis did not reveal any difference in this regards. From another point of view, differences in tumor stage may also influence miR-21 level. Our cohort involved a large proportion of patients with intermediate or advanced HCC (BCLC B and C). Nevertheless, the samples size in our work may be too low to precisely delineate the interaction and larger studies with possibility to perform multivariate adjustments for liver and renal injury in view of tumor stage and etiology of the disease will be needed.

Table 3 Comparison of studies with a statement about the prognostic value of blood hsa-miR-21-5p in patients with hepatocellular carcinoma.

Characteristics	Qi et al[25]	Tomimaru et al[24]	Liu et al[32]	Wang et al[31]	Cho et al[33]	Zhang et al[18]	Current data
High miR-21 and prognosis	↔	Trend for worse prognosis	Worse prognosis	Worse prognosis	Better liver transplant-free survival	Worse prognosis	↔
Group allocation: Cut-off-value	NA	Cut-off based on ROC analyzes	50th percentile	50th percentile	50th percentile	NA	50th percentile
Origin of the cohort	Asia	Asia	Asia	Asia	Asia	Asia	Europe
Predominant etiology	HBV	HCV/HBV	HBV	HBV	HBV	NA	Mainly alcohol abuse
TNM reported	Yes	Yes		Yes	Yes	Yes
BCLC reported		Yes	Yes				Yes
Child-Pugh score reported	Yes	Yes	Yes		Yes		Yes
Sampling	Before surgery	Before surgery	Before TACE	No exact information, surgical resection	Before surgery or RFA	Pre- and postoperative serum samples	Therapy naïve and pretreated
Patients	70	126	136	97	120	46	91
Specimen	Serum	Plasma	Serum	Serum	Plasma	Serum	Serum
qPCR method	TaqMan®	TaqMan®	SYBRGreen	SYBR Green	TaqMan®	Unknown	TaqMan® SYBRGreen
Normalization	miR-16	miR-16	Quanto EC1, Quanto EC2	cel-miR-39	MiR-16	RNU6b	cel-miR-39
Publishing year	2011	2012	2014	2015	2017	2019	2020

BCLC: Barcelona Clinic Liver Cancer; HBV: Hepatitis B virus; HCC: Hepatocellular carcinoma; HCV: Hepatitis C virus; NA: Non-available; NASH: Non-alcoholic steatohepatitis; qPCR: Quantitative PCR; RFA: Radiofrequency ablation; ROC: Receiver operating characteristic; TACE: Transarterial chemoembolization; TNM: Tumor-Node-Metastasis Classification of Malignant Tumors.

AFP is among the most valuable prognostic markers in HCC. Wang et al[19] reported a positive correlation between miR-21 in tissues and serum AFP[19]. Tomimaru et al[24] and Liu et al[32] reported a similar correlation between circulating miR-21 in the blood and AFP[24,32]. In concordance with the data form Zhang et al[18], although our study demonstrated higher AFP values in patients with high serum miR-21 levels, it still did not reveal any correlation among the parameters.

An open question remains regarding the source of circulating miR-21 in HCC patients. Since miR-21 is present at a relatively high level in serum, it is hard to consider it a specific surrogate for the HCC tumor load. Nevertheless, several reports have suggested that circulating miR-21 may originate from tumor tissue. Studies have shown a reduction of miR-21 in blood after surgery[18,22,24,26]. Furthermore, concordant data have been reported for serum miR-21 and associated tissue levels[18,22,24], hypothesizing HCC tumor tissue as a potential source of miR-21 in HCC patients. At the same time, another hypothesis suggests that elevated circulating miR-21 may be triggered by non-specific liver damage. Based on our observation, miR-21 correlated with ASAT, which at least indirectly supports the hypothesis of liver injury. Additionally, miR-21 correlated significantly with serum miR-122 as highly abundant liver-specific miRNA[34,35]. Non-specific release of miR-122 from liver tissue has also been previously discussed[36,37]. Another study explored the influence of necroinflammation in patients with hepatitis C virus with and without HCC[38]. The authors demonstrated similar values of serum miR-21 between patients with and without HCC, suggesting that higher miR-21 level may be caused by non-specific liver injury rather than tumor-induced miR-21 release. Although our results do not link miR-21 with liver cirrhosis or liver function, Karakatsanis et al[20] showed that miR-21 was associated with cirrhosis[20], and Wang et al[39] correlated exosomal miR-21 with presence of liver cirrhosis[39].

Renal function seems to be a crucial confounding factor for miRNA analysis in blood not only for miR-122[1] as previously reported, but also for miR-21. On one hand, upregulation of miR-21 in kidney plays a role in acute kidney injury as a defense mechanism to reduce cell death. On the other hand, overexpression of miR-21, caused by massive cell death, leads to renal inflammation and fibrosis[40]. Renal injury in animal studies is associated with increased miR-21 expression in tissue and lower levels in blood[41]. In human, miR-21 was lower in subjects with cardiac surgery-associated acute kidney injury[42]. Our data strongly support the suggestion that renal function may affect circulating miRNAs as both miR-21 and miR-122 have shown a clear correlation with creatinine values. Taking into account the fact that miR-21 has been suggested as a potential biomarker for a large number of diseases including cancer[11,43] it will be necessary in the future to consider those variations in ongoing studies. In particular, miR-21 has been suggested as a diagnostic marker for malignant diseases including gastric, colorectal cancer, and HCC. Because of the miR-21 variation in our cohort, we speculate that the diagnostic value of miR-21 may be also affected by the renal and liver function. In-depth systematic data including miRNA-profiling are encouraged to address this topic in detail.

CONCLUSION

In summary, the results of this study do not support the role of circulating miR-21 as prognostic biomarker for patients with HCC in our European cohort. A positive correlation between miR-21 and ASAT and negative correlation with creatinine strongly emphasizes that non-specific liver injury and renal function may influence the sensitivity and specificity of miRNAs as biomarkers, and that those factors need to be carefully assessed in future studies.

ARTICLE HIGHLIGHTS

Research background

MiR-21-5p (miR-21) is one of the most frequently deregulated microRNAs (miRNAs) in tissue and in body fluids in different diseases and most importantly in cancer. Overexpression and prognostic value of tissue miR-21 in hepatocellular carcinoma (HCC) has been previously suggested, but the data are heterogeneous. Greatest evidence in support of miR-21 as a biomarker originate from Asian population, highlighting the need for additional scientific effort and search for potential confounding factors including etiological background of HCC.

Research motivation

Data on prognostic value of serum miR-21 in patients with mainly alcohol abuse-induced HCC as well as the knowledge of potential influencing factors and underlying mechanism are still limited.

Research objectives

We evaluated the prognostic value of serum miR-21 in a European cohort of HCC patients with mainly alcohol-associated liver disease in real-life settings. We also explored the potential confounding clinical or laboratory influencing factors on the serum miR-21 levels.

Research methods

Circulating miR-21 level were analyzed in 91 sera samples from well-characterized patients with HCC. Clinical and laboratory parameters (including alpha-fetoprotein), miR-122 as well as the overall survival (OS) were examined.

Research results

We observed no association between serum miR-21 and OS, Child-Pugh scores, or BCLC staging data. Significant correlation between serum miR-21 and aspartate aminotransferase, International Normalized Ratio, creatinine, and hsa-miR-122 suggested the potential influence of liver and renal function on circulating miR-21 levels.

Research conclusions

Our data do not support prognostic role of miR-21 in HCC patients. An association of miR-21 with surrogate markers of liver injury and renal function strongly support the need for better understanding of influencing factors in miRNA biogenesis.

Research perspectives

Systematic profiling studies that provide overall data assessment of miRNAs in view of potential influencing factors in blood are needed prior clinical implementation of miRNAs as clinical biomarkers.

ACKNOWLEDGEMENTS

The authors would like to thank Ursula Stolz (from the GI Research Laboratory of the Department of Gastroenterology, Hepatology and Infectious Diseases) for technical support.