Clinical significance and gene expression study of human hepatic stellate cells in HBV related-hepatocellular carcinoma
- Rui Liao†1, 2,
- Han Wu†1, 2,
- Yong Yi1, 2,
- Jia-Xing Wang1, 2,
- Xiao-Yan Cai1, 2,
- Hong-Wei He1, 2,
- Yun-Feng Cheng3,
- Jian Zhou1, 2,
- Jia Fan1, 2,
- Jian Sun1, 2Email author and
- Shuang-Jian Qiu1, 2, 3Email author
© Liao et al.; licensee BioMed Central Ltd. 2013
Received: 25 February 2013
Accepted: 14 April 2013
Published: 19 April 2013
Peritumoral activated hepatic stellate cells (HSCs) are versatile myofibroblast-like cells closely related with hepatocellular carcinoma (HCC) progression. So far, comprehensive comparison of gene expression of human HSCs during hepatocarcinogenesis is scanty. Therefore, we identified the phenotypic and genomic characteristics of peritumoral HSCs to explore the valuable information on the prognosis and therapeutic targets of HBV related HCC.
A tissue microarray containing 224 HBV related HCC patients was used to evaluate the expression of phenotype markers of HSCs including α-SMA, glial fibrillary acidic protein (GFAP), desmin, vinculin and vimentin. HSCs and cancer associated myofibroblasts (CAMFs) were isolated from normal, peritumoral human livers and cancer tissues, respectively. Flow cytometry and gene microarray analysis were performed to evaluate the phenotypic changes and gene expression in HCC, respectively.
Peritumoral α-SMA positive HSCs showed the prognostic value in time to recurrence (TTR) and overall survival (OS) of HCC patients, especially in early recurrence and AFP-normal HCC patients. Expression of GFAP positive HSCs cell lines LX-2 was significantly decreased after stimulation with tumor conditioned medium. Compared with quiescent HSCs, peritumoral HSCs and intratumoral CAMFs expressed considerable up- and down-regulated genes associated with biological process, cellular component, molecular function and signaling pathways involved in fibrogenesis, inflammation and progress of cancer.
Peritumoral activated HSCs displayed prognostic value in HBV related-HCC, and their genomic characteristics could present rational biomarkers for HCC risk and promising therapeutic targets.
Cancer is now recognized as a functional organ caused by deregulated oncogenes including proto-oncogenes and tumor-suppress or anti-oncogenes, which may well contribute to certain mutational events in the cancer phenotype [1, 2]. Indeed, equally numerous reports have indicated smoldering inflammation in the tumor microenvironment shared the capacity to induce genetic instability or mutation and subsequently fostered the carcinogenic process [3, 4]. Therefore, genetic events and phenotypic variation have shed new light on the relationship between inflammation and cancer. Typically, hepatocellular carcinoma (HCC) is a malignancy characterized by a high degree of genetic heterogeneity and often associated with hepatitis viral infection and cirrhosis [5, 6]. Of note, some immune/inflammation-related gene signatures were identified as sensitive “readout” screening for high-risk patients likely to experience HCC recurrence after resection [7, 8]. Moreover, a subtype of human HCC sharing a gene expression pattern with fetal hepatoblasts has been linked to poor prognosis, which was supposed to be derived from hepatic progenitor cells . This study revealed the malignant biological phenotypes may result from activation of different oncogenic pathways during tumorigenesis and/or different cells of origin including activated inflammatory cells, like tumor-associated macrophages , neutrophils  and mast cells , which may acquire more potent tumor-promoting activities and result in dismal outcome of HCC. Thus, regulation of gene levels in tumor activated inflammatory cells could provide crucial information on the progress and prognosis of HCC.
Interestingly, hepatic stellate cells (HSCs), myofibroblast-like inflammatory cells under activated state, display plastic phenotypes and properties of progenitor cells [13, 14]. In a most recent study , we found triggering receptor expressed on myeloid cells (TREM)-1, a potential functional gene in HSCs, enhanced the aggressiveness of HCC cells. Moreover, we have previously demonstrated  that the density of peritumoral activated HSCs, including their putative functional genes (SPARC, TNC and FAP), were selectively associated with poor prognosis of HCC, revealing that HSCs could reroute the direction from pro-inflammatory response to promoting tumor. Furthermore, a recent integrative genomic analysis revealed that hepatoma cells induced the functional deregulation of relevant gene networks in HSCs, which correlated to the poor outcome of HCC patients . Also, considerable changed gene expression signatures of activated HSCs have been confirmed to have specific contribution to cirrhosis [18–20] and HCC . However, so far, less attention has been paid on the comprehensive comparison of gene expression of human HSCs during hepatocarcinogenesis.
Here, we depicted that peritumoral HSCs were unfavorable predictors in HBV related HCC following resection, especially in early recurrence and AFP-normal HCC patients. To specifically address the possible heterozygous effects and the functional impact of activated HSCs in the aggressive phenotype of HCC, we also characterize the gene expression profile of peritumoral human HSCs and observed numerous regulated genes potentially influencing the malignant behavior of activated HSCs. These alterations presented potential biomarkers and therapeutic targets to interrupt the pivotal pathways in HCC development.
Material and methods
Patients and specimens
Peritumoral α-SMA expression according to characteristics of 224 hepatitis B virus related HCC patients
Low expression (n = 44) (cell numbers ≤ 72)
High expression (n = 180) (cell numbers > 72)
Tissue microarray design and immunohistochemistry
A tissue microarray (TMA) was constructed and immunohistochemistry was carried out as described previously [15, 22]. Under low-power magnification (100X), positive staining cells were screened and photographs of four representative fields were captured under high-power magnification (400X) in Leica DMLA light microscope (Leica Microsystems, Wetzlar, Germany). The positive cell density of each core was counted by two independent investigators blind to clinical outcome and knowledge of the clinicopathologic data. Data were expressed as mean value (±SE) of the triplicate cores taken from each patient. Primary antibodies were mouse anti-human monoclonal antibodies combined with α-SMA (1:100; DAKO), glial fibrillary acidic protein (GFAP 1:100; Cell signaling), desmin (1:50; DAKO), vinculin (1:200; Upstate, Millipore) and vimentin (1:100; Sigma-Aldrich), respectively.
Collection of tumor conditioned medium (TCM) and generation of tumor-induced activated HSCs in vitro
As described previously , tumor conditioned medium (TCM) was collected from HCC cell lines MHCC97L, HCCLM3 and HCCLM6, respectively. Briefly, 5 × 106 tumor cells were seeded into 100-mm dishes containing 10 mL of DMEM with 10% fetal bovine serum for 24 hours and thereafter washed twice with serum-free DMEM, and then cultured in serum-free DMEM. After another 24 hours, the supernatant was centrifuged, filtered and stored at −20°C until use. HSC cell line LX-2 was cultured in T25 flasks (0.6x106) with 5 ml TCM supplemented with 5% FBS for 24 hours.
Flow cytometric analysis
According to previous report [18, 23], four identified phenotypes of activated HSCs including GFAP, fibronectin, CD56 and IL-17R (antibody from ebioscinece, Santa Cruze and R&D Systems, respectively) were used for flow cytometric analysis. Nonspecific IgG of the corresponding class was used as the negative control.
Isolation and culture of cells
HSCs/myofibroblasts were isolated as our described previously . We isolated HSCs from surgical peritumoral tissues and CAMFs from matched cancer tissues, respectively. Quiescent HSCs were isolated from normal liver tissues from hepatic hemangiomas and prolong culture cells were used as in vitro activated HSCs. HSCs/myofibroblasts were isolated by collagenase-pronase perfusion and subsequent density centrifugation on Nycodenz gradients. After collagenase-pronase digestion, the resulting cell pellets were centrifuged at 50 g for 2 minutes to remove hepatocytes. Before collecting HSCs/CAMFs, obtained cells were seeded for 15 min in serum free medium to allow Kupffer cells attachment. To further purify non-attached cells, magnetic anti-CD45 beads (MACS, Miltenyi Biotec, Germany) were used to deplete contaminating leucocytes. Peritumoral HSCs and intratumoral CAMFs were studied at 24 hours after isolation. HSCs from normal livers were studied at 24 hours after isolation (quiescent HSCs) or after 10 days culture (in vitro activated HSCs) without passage, respectively. CD45 and CD31 positive cells were not found in isolated cells by immunocytochemistry staining, demonstrating no contaminating pan-leucocytes and endothelial cells. HSCs purity was assessed by the autofluorescence property and morphology, the populations were more than 95% pure. Primary cells, HSC cell lines LX-2 (as gifts by professor Jin-sheng Guo in Zhongshan hospital) and three HCC cell lines (MHCC97L, HCCLM3, and HCCLM6) initially established and preserved by our institute  were cultured in DMEM supplemented with 10% fetal calf serum (FCS) and 1% penicillin-streptomycin in 95% air and 5% CO2 at 37°C.
Gene expression analysis
Total RNA was extracted from HSCs/CAMFs for microarray analysis. Microarray hybridization was performed using whole human genome oligo array (4 × 44K, Agilent Technologies) based on the manufacturer’s standard protocol. Differentially expressed genes with statistical significance between two groups were identified through volcano plot filtering. The threshold is fold change ≥2.0, p-value <0.05. Pathway analysis and gene ontology (GO) analysis were applied. Finally, hierarchical clustering was performed to show the distinguishable gene expression pattern among samples.
Quantitative polymerase chain (qPCR) reaction validation of microarray data
A total of 49 genes were confirmed by qPCR as previous protocol  using commercially available primer-probe sets (Applied Biosystems, Foster City, CA) and SYBR Green PCR Master Mix (SABiosciences). Primers for these genes are listed in Additional file 1. Expression of GAPDH was used as an internal control. The gene expression was quantified by the 2-△△ CT method.
Statistical analysis was performed by Student t test, Fisher’s exact tests, χ2 tests, Spearman ρ coefficients tests. The “minimum p value” approach [11, 12] was used to get an optimal cut-off (high α-SMA expression >72) by X-tile 3.6.1 software (Yale University, New Haven, CT, USA). P < 0.05 was considered statistically significant.
Expression and predictive value of distinct phenotype markers of HSCs in HCC
Prognostic factors for survival and recurrence
HR (95% CI)
HR (95% CI)
AFP (≤20 v >20 ng/ml)
Tumor number (single v multiple)
Vascular invasion(yes v no)
Tumor encapsulation (yes v no)
TNM stage (IvII- III)
Peritumoral α-SMA density (low v high)
Prognostic factors for early and late recurrence
HR (95% CI)
HR (95% CI)
AFP(ng/ml)(≤20 v >20)
Tumor size (≤5.0 v >5.0)
Vascular invasion(yes v no)
TNM stage (IvII- III)
Peritumoral α-SMA density (low v high)
Secretion of HCC cells lines partly affected the phenotype modulation of HSCs
Global comparison in gene expression between different activated/quiescent phenotypes of HSCs and CAMFs
Verification of the DNA microarray results
To validate the results of DNA microarray, some identified genes of interest involved in liver fibrogenesis and hepatocarcinogenesis were assessed by qRT-PCR. Similar up- and down- regulated trends with DNA microarray were detected in the genes encoding key molecules implicated in inflammation (e.g. IL-17RA, TLR-2), tumor invasion and metastasis (e.g. MMP25), adhesion (e.g. CD36, VCAM1), extracellular matrix degradation (e.g. TIMP2), cytoskeletal organization (e.g. ACTG2, ACTA2). Other genes (e.g. COL1A2, MMP1, GK, PPARG) associated with certain pathways such as ECM-receptor interaction and PPAR signaling pathway also confirmed the results obtained in DNA microarray (Additional file 5).
The plasticity of HSCs phenotype and the lack of specific marker proteins hampered an in depth analysis of the nature and functional properties of these fibroblastic cells in human normal and diseased liver. In particular, heterogeneity of phenotypic features among HSCs present in HCC was seldom noticed. In this present study, our immunohistochemical analysis displayed various distribution and expression intensity of four most prominent HSCs phenotype/gene markers including α-SMA, desmin, GFAP and vimentin  as well as a recently reported marker vinculin , which probably exhibited their different in vivo biological behaviors and cellular response to injurious stimuli in the progress of HCC. Although desmin and GFAP were markers of rat/mouse HSCs [14, 27] and GFAP has also been identified as an early marker of human HSCs activation [28, 29], our study showed they were not expressed in human HCC tissues. Also, vimentin and vinculin were not specific markers for human HSCs, at least in HCC. These results suggested the complexity and the difference of HCC milieu compared to other chronic liver diseases. Excitedly, as a canonical marker of activated HSCs, high expression of α-SMA still showed specificity in HSCs and a good prognostic performance in HBV related HCC patients, which therefore could provide us a reliable monitoring indicator in at-risk HBV related HCC patients.
In line with our previous studies [15, 16], peritumoral HSCs were demonstrated as independent predictors for HCC patients with higher recurrence rate and reduced survival times, also closely related to adverse HCC characteristics like tumor size, tumor differentiation and TNM stage. These data supported the protumor function of activated HSCs. A more important finding was observed that peritumoral HSCs served as unfavorable prognostic predictors in several subgroups including early recurrence group (≤ 24 months)  and AFP-normal patients in HBV related HCC. These results implied activated HSCs could participate in intrahepatic metastases probably involved in the conversion of pro-inflammatory response into promoting tumor . Furthermore, for the AFP-normal HCC patients who were difficult to be supervised, peritumoral HSCs were potential monitoring indicators because of their better prognostic values in the AFP-normal group.
In HCC tissues, different expression patterns of phenotype markers of HSCs probably were cellular response to long-term injurious stimuli in HCC microenvironment. Thus, the early effects of HCC on HSCs (HSC cell line LX-2) were further evaluated by flow cytometry. Here, GFAP showed decreased expression in LX-2 after tumor stimulation, which can partly interpret its transform from an activated marker in chronic liver disease [28, 29] to negative expression in HCC tissues. Moreover, GFAP was identified as a tumor suppressor gene in astrocytoma  and glioma pathogenesis . Loss of GFAP expression in tumor progression could be secondary loss of a differentiation marker and represented a step in tumor development .
On base of the clinical analysis results as aforementioned, we conjectured that there could be more potential key molecules or genes in HSCs which were related with their functional properties and triggered their activation during the development of HCC. Although our colleagues  recently assessed the features of rat HSCs cultured in conditioned medium of HCC cell lines, no study has directly investigated gene expression patterns of HSCs in liver specimens from patients with HCC. A number of genomic analysis of HSCs have been performed, but majority of these studies were restricted to cirrhosis or chronic liver diseases induced HSC activation [18–20]. Therefore, we investigated gene expression of primary HSCs/CAMFs from normal, peritumoral and intratumoral livers. Detailed genomic analysis will contribute to study of their different roles during hepatocarcinogenesis.
To our knowledge, this is the first study about gene expression profile of HSCs freshly isolated from human HCC tissues. COL1A2, ACTG2 and ACTA2, as typical HSC or myofibroblast-like cell activation markers, were increased significantly in activated HSCs and CAMFs compared to quiescent HSCs. These findings, as well as the validated genes suggested the reliability of DNA microarrays data. Moreover, high correlation coefficients between the same types of cells demonstrated small gene expression variances in each group (Additional file 2: Table S2). Consistent with previous studies [18, 20], lower correlation coefficients between culture-activated HSCs and in vivo activated HSCs/CAMF suggested culture-activated HSCs can only partly reflect the underlying gene expression changes of in vivo activated HSCs. Compared with in vivo activated HSCs/CAMFs, different gene expression patterns were detected in culture-activated HSCs probably due to different in vivo stimulus effects and the lack of cell-cell contact and cell–matrix interaction . Importantly, our study identified a large number of previously known and unknown functional genes in activated HSCs/CAMFs during the process of hepatocarcinogenesis. First, peritumoral HSCs and intratumoral CAMFs shared similar gene expression profile (r = 0.936, P < 0.001) and relatively minor gene changes in HCC, which therefore suggested the important roles of these changed genes in hepatocarcinogenesis and the possible evolution from HSCs into myofibroblasts. Compared with upregulated genes, more downregulated genes (188 v 467) in intratumoral CAMFs than peritumoral HSCs may be associated with loss-of-function mutation of genes in intratumoral immunosuppression microenvironments. Second, according to biological process in GO analysis, considerable inflammation/immune response related genes (e.g. IL-18, TNFRSF1B) upregulated in peritumoral HSCs compared with intratumoral CAMFs, indicating activated HSCs were sensitive target cells respond to peritumoral inflammatory stimulus and can be driven into malignant phenotypes fostering the carcinogenic process. Third, pathway analysis of differentially expressed genes further extended the information on the roles of peritumoral HSCs and intratumoral CAMFs in development of HCC. For example, compared with quiescent HSCs, down-regulate of apoptosis related genes in CAMFs may be implicated in their increased proliferative abilities. Compared to CAMFs, lower expression levels of genes in p53 pathway in peritumoral HSCs may attribute to the protumor power of activated HSCs. Fourth, identification of novel genes associated with tumor activated HSCs can benefit an in depth analysis of the nature and functional properties of HSCs in HCC. However, further studies need to test these hypotheses.
Recent epidemiologic data indicate that one of the most important risk factors for HCC development is HBV infection, especially in east Asian [33, 34]. Here, in absence of a direct association between HBV infection and HSCs activation, but we highlighted HSCs function as regulators in inflammation-mediated liver injury after HBV infection. An in-depth comparison with other etiologies including hepatitis C virus or alcohol-related HCC could find the association between HBV and HSCs activation. Consist with previous survey , our most tissue samples were obtained from patients with typical cirrhosis (192/224, Table 1). Accordingly, we conjecture that cirrhosis might influence the gene expression level in HSCs to a great extent. Further investigation in HCC patients with different grades of fibrosis may provide further insight into the mechanisms of malignant transformation from fibrosis and cirrhosis to HCC.
In conclusion, we demonstrated that peritumoral activated human HSCs were poor prognostic factors for HBV related HCC after resection, especially in early recurrence and AFP-normal subgroups. Moreover, we showed for the first time that in HCC milieu, peritumoral HSCs markedly expressed fibrogenesis and hepatocarcinogenesis related genes. In this regards, these alterations had potential to be responsible for the acquirement of malignant phenotypes and behavior of activated HSCs during the process of HCC, therefore providing us available multi-target to constitute a promising therapeutic strategy for HCC.
The authors thank KangChen Bio-Tech Co Ltd, Shanghai, China, for help in cDNA microarray construction. Supported by the National Key Sci-Tech Special Project of China (Nos. 2012ZX1000 2010-001-002), National Natural Science Foundation of China (Nos. 81071707 and 81071995; key program No. 81030038), the Open Project of the State Key Laboratory of Oncogene and Related Gene (No. 90-09-03).
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