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Original Research

The clinicopathological and prognostic value of HSP27 in hepatocellular carcinoma: a systematic review and meta-analysis

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Pages 1293-1303 | Published online: 07 Mar 2018

Abstract

Background

In the recent past, there is increasing evidence demonstrating that HSP27 plays a key role in tumor progression. However, the relationship between HSP27 expression and the clinicopathological features of hepatocellular carcinoma (HCC), as well as its prognostic value in HCC patients remain controversial. Accordingly, we conducted a meta-analysis to assess the correlation between HSP27 expression and HCC, and determine the prognostic value of HSP27 in HCC.

Methods

The data included clinicopathological features and survival information extracted from the published literature in the databases PubMed, EMBASE, Cochrane Library, Web of Science, CNKI, and Wan Fang. The pooled odds ratios and hazard ratios with 95% CIs were calculated using Forest plot analysis.

Results

The meta-analysis results indicated that the positive HSP27 expression was significantly correlated with HCC incidence, tumor differentiation, and α-fetoprotein level in patients with HCC. However, the expression of HSP27 was not associated with metastasis, hepatitis B virus surface antigen, gender, tumor size, TNM stage, and vascular invasion. Additionally, HSP27 expression indicated a poor overall survival rate, but it was not related to disease-free survival rate.

Conclusion

This meta-analysis revealed that HSP27 may play a key role in the development of HCC and could be a reliable biomarker for the prognosis of patients with HCC. However, additional high-quality research is needed to support the results.

Introduction

Hepatocellular carcinoma (HCC) is one of the most common malignant tumors worldwide. The annual number of new cases is about 748,300, the number of deaths is 695,900, and nearly half of the new cases and deaths occur in China.Citation1 In recent years, with the development of surgical techniques, the prognosis of patients with HCC has improved. However, the clinical manifestations of HCC are not obvious; thus, its early diagnosis is difficult. Moreover, there is still a lack of specific markers for the diagnosis of HCC, and when HCC is diagnosed, it is frequently in late stage. Consequently, the rate of overall survival of patients with HCC is still poor.Citation2,Citation3 As a result, the search for reliable biomarkers to diagnose HCC and predict the survival rate of HCC patients has become a hot research topic in recent years.Citation4 Heat shock proteins (HSPs) are a family of conserved proteins produced by cells in response to stressful conditions. They play key roles in various cellular processes, such as maintaining cell homeostasis, apoptosis, invasion, cell signal transduction, and cellular response, and are closely related to the development of tumors.Citation5 In recent years, studies have found that the abnormal expression of HSPs is closely associated with the incidence and development of HCC, and can be used as one of the diagnosis and prognosis indicators.Citation6

HSP27 is an important member of the HSP family, which plays a key role in the occurrence and development of tumors.Citation7 HSP27 has been found to be overexpressed in various cancers, including esophageal cancer,Citation8 gastric cancer,Citation9 colon cancer,Citation10 prostate cancer,Citation11 breast cancer,Citation12 lung cancer,Citation13,Citation14 and HCC.Citation15,Citation16 In addition, some studies have shown that HSP27 expression was related to the clinicopathological features and prognosis of the tumors. However, the relationship between HSP27 expression and the clinicopathological features of HCC, as well as its prognostic value in patients with HCC remains controversial. King et alCitation17 determined that the expression of HSP27 was associated with tumor differentiation and poor prognosis, but they found no association with other clinicopathological features. Also, Harimoto et alCitation18 found that the expression of HSP27 was not correlated with vascular invasion, metastasis, tumor differentiation, and other clinical features, and in addition, HSP27 expression was not related to the overall survival and disease-free survival in hepatitis C virus-positive HCC patients. Moreover, Zhang et alCitation19 found that the expression of HSP27 predicted a poor overall survival and short disease-free survival time. Accordingly, we conducted a meta-analysis to determine the clinicopathological and prognostic value of HSP27 in patients with HCC.

Methods

Identification and eligibility of relevant studies

The PubMed, Cochrane Library, Web of Science, EMBASE, Chinese CNKI, and Wan Fang databases were searched to identify studies that evaluate the clinicopathological characteristics and prognostic value of HSP27 expression in HCC patients using immunohistochemistry (IHC) analysis. The search ended on September 1, 2017. Search words were “heat shock protein 27”, “HSP27” and “liver cancer”, “hepatic carcinoma”, “hepatocellular carcinoma”, “cancer of the liver”. The reference list of the included studies was also checked to find other qualified studies.

The studies should meet the following inclusion criteria: 1) patients in the study should be clearly diagnosed with HCC; 2) the study is published in Chinese or English, and the full text is available; 3) the expression of HSP27 was measured by IHC analysis; 4) the article should be a case–control study and assess the relationship between HSP27 expression and the HCC clinicopathological features or prognosis, and the study should include at least one primary outcome of interest; and 5) repeat publications were excluded.

Data extraction

Two reviewers (Chaojie Liang and Hua Ge) independently screened all the articles according to the inclusion criteria. The extracted data included the first author’s name, year of publication, sample size, country/region, antibody company, antibody concentration and clinicopathological parameters (HSP27 expression, gender, hepatitis B virus surface antigen [HbsAg], α-fetoprotein [AFP], tumor size, metastasis, vascular invasion, tumor differentiation, and TNM stage) and hazard ratios (HRs) with 95% CI for overall survival and disease-free survival. Disagreements were resolved by re-extraction or third-party adjudication.

Quality assessment

The quality of each of the included studies was assessed using the Newcastle–Ottawa Scale (NOS) criteria, and studies with NOS score of >6 were regarded as good quality, while <6 were considered as poor quality.

Statistical analysis

The STATA 14.2 software was used for statistical analyses. The association between HSP27 expression and the clinicopathological features (gender [male vs female], AFP [positive: negative ratio], HbsAg [yes vs no], tumor size [>5 cm vs ≤5 cm], metastasis [yes vs no], vascular invasion [yes vs no], tumor differentiation level [low vs high or moderate], and TNM stage [I/II vs III/IV] was evaluated by pooled odds ratios [ORs] with 95% CIs), and the differential expression of HSP27 between cancer tissues and control tissues was also evaluated. The software Engauge Digitizer 10.0 was used to extract the survival data from Kaplan–Meier curves in the articles. When the 95% CI did not overlap 1, it was considered to be statistically significant. The heterogeneity between the studies was evaluated by the I2 test. The fixed effects model was chosen when there was no significant heterogeneity (I2<50%, P-Het <0.1). When the heterogeneity was signifi-cant, the random effects model was used. Potential causes of statistical heterogeneity were analyzed by subgroup analysis. Publication bias was examined by the Begg’s funnel plot test and inverted funnel plots.

Results

Characteristics of studies

A total of 598 relevant articles were identified by searching the PubMed, Cochrane Library, Web of Science, EMBASE, Chinese CNKI, and Wan Fang databases, as illustrated in , which shows the details of the selection process. Ultimately, 11 eligible articles were included in this meta-analysis.Citation15Citation25 As shown in , these studies were published from 2000 to 2017, and included a total of 876 HCC patients. The sample size ranged from 34 to 194 patients, with 6 of studies including >60 patients and 5 including ≤60 patients. Eight of the studies evaluated patients from China, 2 from Japan, and 1 from Korea. All these studies scored ≥6 in methodological assessment, which implied that they were of high quality.

Table 1 Characteristics of studies included in the meta-analysis

Figure 1 Flowchart of study selection process.

Figure 1 Flowchart of study selection process.

The meta-analysis about the relationship between HSP27 expression and clinicopathological features in patients with HCC

The correlation between HSP27 expression and the clinicopathological features of HCC was assessed in this meta-analysis, and the results are shown in . Five studies, including a total of 237 patients were used to evaluate the differential expression of HSP27 in HCC and normal tissues. The results revealed that the expression of HSP27 in HCC was significantly higher than that in normal tissue (OR=7, 95% CI =2.35–20.79, P=0.000; ). The ORs for AFP were reported in 3 studies that included 167 cases. The results of our evaluation of these data indicated that HSP27 expression was associated with AFP expression (OR=3.86, 95% CI =1.11–13.39, P=0.034; ). Nine studies including 642 patients showed a significant relationship between HSP27 expression and tumor differentiation (OR=3.81, 95% CI =1.79–8.08, P=0.000; ). However, the expression of HSP27 was not significantly associated with any of the following parameters: gender (OR=1.13, 95% CI =0.72–1.77, P=0.606; ), HBsAg (OR=1.72, 95% CI =0.65–4.52, P=0.275; ), tumor size (OR=1.19, 95% CI =0.74–1.92, P=0.479; ), metastasis (OR=1.96, 95% CI =0.91–4.24, P=0.083; ), vascular invasion (OR=1.71, 95% CI =0.93–3.15, P=0.083; ), and TNM stage (OR=0.66, 95% CI =0.27–1.61, P=0.358; ).

Table 2 HSP27 clinicopathological features for HCC

Figure 2 Forest plot and funnel plots of studies evaluating the relationship between HSP27 expression and clinicopathological features.

Notes: (A) Expression; (B) gender; (C) AFP level. Weights are from random effects analysis.
Abbreviations: AFP, α-fetoprotein; OR, odds ratio.
Figure 2 Forest plot and funnel plots of studies evaluating the relationship between HSP27 expression and clinicopathological features.

Figure 3 Forest plot and funnel plots of studies evaluating the relationship between HSP27 expression and clinicopathological features.

Notes: (A) HBsAg; (B) tumor size; (C) metastasis. Weights are from random effects analysis.
Abbreviation: OR, odds ratio.
Figure 3 Forest plot and funnel plots of studies evaluating the relationship between HSP27 expression and clinicopathological features.

Figure 4 Forest plot and funnel plots of studies evaluating the relationship between HSP27 expression and clinicopathological features.

Notes: (A) Vascular invasion; (B) tumor differentiation; (C) TNM stage. Weights are from random effects analysis.
Abbreviation: OR, odds ratio.
Figure 4 Forest plot and funnel plots of studies evaluating the relationship between HSP27 expression and clinicopathological features.

The meta-analysis about the prognostic value of HSP27 in patients with HCC

The relationship between HSP27 expression and the prognosis of patients with HCC was also assessed in this meta-analysis. The HRs for the overall survival rate were examined in 4 studies (Harimoto et al had 2 sets of data), which included 203 and 162 HCC patients with and without HSP27 expression, respectively. Our evaluation of the data revealed that HSP27 expression was associated with poor overall survival (positive: negative: HR =1.13, 95% CI =1.39–2.53, P=0.000; ). Additionally, we examined the HRs for disease-free survival rate in 3 studies (Harimoto et al had 2 sets of data), which included 135 and 150 HCC patients with and without HSP27 expression, respectively. The meta-analysis showed that HSP27 expression was not associated with disease-free survival (positive: negative: HR =1.54, 95% CI =0.93–2.14, P=0.673; )

Figure 5 Forest plot and funnel plots of studies evaluating the relationship between HSP27 expression and prognosis of HCC patients.

Notes: (A) Overall survival; (B) disease-free survival. Weights are from random effects analysis.
Abbreviations: HCC, hepatocellular carcinoma; HR, hazard ratio.
Figure 5 Forest plot and funnel plots of studies evaluating the relationship between HSP27 expression and prognosis of HCC patients.

Publication bias and sensitivity analysis

No publication bias was found for HSP27 expression (P=0.086), gender (P=0.133), AFP (P=0.296), tumor size (P=1), metastasis (P=0.133), HBsAg (P=0.452), tumor differentiation (P=0.118), TNM stage (P=0.806), overall survival rate (P=0.308), and disease-free survival rate (P=0.734) according to the Begg’s test. However, publication bias existed for vascular invasion (P=0.035) and the sensitivity analysis was calculated to determine whether individual studies influenced the pooled OR. The result indicated that no study substantially influenced the pooled OR, which suggested that more studies needed to be included for further research.

Discussion

HSPs are widely found in prokaryotic and eukaryotic cells. They comprise various groups of conserved proteins that have important physiological functions and play key roles in cell growth, differentiation, and gene transcription.Citation26 In recent years, studies have found that HSPs are involved in the development of tumors.Citation27 HSP27 is a member of the HSP family, which acts as an ATPase-independent chaperone. Several studies suggest that HSP27 is involved in the regulation of cell cycle, inhibition of cell apoptosis, remodeling of skeletal structures, regulation of translation initiation, DNA repair, RNA cleavage, and ubiquitin–proteasome pathway degradation of oxidized proteins.Citation28 Additionally, it has been reported that Hsp27 can promote the metastasis ability of tumors through a variety of different molecular mechanisms. For instance, the mitogen-activated protein kinase kinase 4-mediated enhancement of cell invasion is mainly dependent on the role of Hsp27 and MMP2.Citation29 Moreover, Hsp27 maintains the stem cell characteristics of breast cancer stem cells by upregulating cell epithelial–mesenchymal transition (EMT) and the nuclear factor-kappa-B signaling pathway.Citation30

HSP27 also plays an extremely important role in epidermal growth factor-, hepatocyte growth factor-, and interleukin-6- mediated EMT progression in prostate cancer.Citation11 HSP27 has also been suggested to promote tumor metastasis through the regulation of the transforming growth factor beta signaling pathway by activating the expression of MMP2.Citation31 HSP27 can act as a chaperone and perform different cellular functions due to its specific interaction with different binding proteins. For example, HSP27 interacts with tumor protein, translationally-controlled 1 (TPT1, also known as TCTP) and stabilizes the structure of TPT1, which, in turn, reduces the expression and activity of p53.Citation32 HSP27 also plays a role in inhibiting apoptosis by interacting with cytochrome-c and caspase-3.Citation33,Citation34 HSP27 directly interacts with AKT to increase its stability, which, in turn, leads to increased level of phosphorylation of p21, both of which are essential survival factors in DNA-damaged cells induced by ultraviolet radiation.Citation35 HSP27 interacts with insulin-like growth factor 1 and stabilizes the structure of the Bad/14-3-3 complex, allowing Bad to stay in the cytoplasm and preventing its translocation to the nuclei, thus promoting cell survival.Citation36 A recent report also suggested that HSP27 can also downregulate the hippo tumor suppressor pathway.Citation37 In addition, some studies have also shown that HSP27 can directly interact with 14-3-3ζ to promote the progression of non-small cell lung cancer.Citation38 Indeed, inhibition of HSP27 by small interfering RNA (siRNA) or antisense oligonucleotide significantly was found to increase the therapeutic effect of radiotherapy, paclitaxel, HSP90 inhibitor, MET kinase inhibitor, and gemcitabine.Citation39Citation42 In summary, HSP27 could become one of the molecular target of drugs for the treatment of tumors.

Recently, multiple studies demonstrated that HSP27 was highly expressed in a variety of cancers, and its expression was associated with the clinicopathological features and prognosis of the patients with these cancers.Citation14,Citation43 However, since the role of HSP27 in HCC remains controversial, we conducted this meta-analysis to clarify the association between HSP27 expression and clinicopathological features and prognosis in patients with HCC. The results of this meta-analysis, which included 876 patients from 11 studies, indicated that HSP27 was overexpressed in HCC patients and HSP27 expression is significantly related to AFP level, and tumor differentiation in HCC patients. Moreover, we also found that the positive expression of HSP27 predicted a poor overall survival rate, suggesting that HSP27 may be a reliable prognostic biomarker in HCC patients.

In this study, 2 of the articles included, namely Guo et alCitation21 and Joo et al,Citation24 suggested that HSP27 expression was related to the HBsAg. Additionally, 2Citation15,Citation22 of 6, 2Citation22 of 7, and 1Citation20 of 5 studies indicated that overexpression of HSP27 correlated with metastasis, vascular invasion, and TNM stage. However, the pooled results showed no statistically significant relationship between HSP27 and these clinicopathological features. Also, although King et alCitation17 and Zhang et alCitation19 suggested that expression of HSP27 indicated a poor disease-free survival, the results of this meta-analysis showed no statistical significance.

Recently, studies demonstrated that phosphorylated HSP27 may also play an important role in cancers. It has been reported that p-HSP27 was associated with the tumor diameter and portal vein invasion in HCC.Citation16 Moreover, p-HSP27 was related to EMT, apoptosis resistance.Citation44,Citation45 However, p-HSP27 may play a different role from HSP27. Studies found that reduced p-HSP27 was associated with HCC stage,Citation46 so further research should be performed to explore the various function of HSP27.

Limitations

This meta-analysis has some limitations, including the following: 1) There may be some articles with controversial results that have not been published, which may have led to publication bias. 2) With regard to the experimental method, we only chose studies that used IHC analysis in this study. When we carefully read the contents of the articles, we found that the antibody manufacturer and antibody concentration used in the experiments were not the same, and the cut-off values for HSP27 expression differed among the articles. These differences are likely to affect the final result and cause bias, thus more studies with similar antibody, concentration of antibody, and cut-off criteria are needed in order to verify the results of this meta-analysis. 3) Studies included in this meta-analysis only comprised patients of Asian race, including Chinese, South Korean, and Japanese. Accordingly, these results may only be suitable for Asian races, and thus more studies from other areas are needed. 4) Some articles did not provide specific HRs value, which we extracted by software and may cause bias. 5) The number of studies and sample size included in this meta-analysis are limited. Thus, larger samples and additional high-quality studies are needed to confirm the results of this meta-analysis.

Conclusion

Despite the limitations in this meta-analysis, the results are significant. The pooled results indicated that HSP27 expression was related to the incidence of HCC, AFP level, and tumor differentiation. Additionally, HSP27 may be a biomarker of unfavorable prognosis of patients with HCC. However, more high-quality studies are needed to achieve a more convincing statistical analysis.

Acknowledgments

This study was financially supported by the Beijing Municipal Administration of Hospital Clinical Medicine Development of Special Funding Support (ZYLX201612), Capital Foundation of Medical Development (shoufa2016-2-2053), Beijing Tongren Hospital Municipal Administration of Hospital Clinical Medicine Development of Special Funding Support (trzdyxzy201705).

Disclosure

The authors report no conflicts of interest in this work.

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