Open Access

Anaplastic lymphoma kinase protein expression predicts micrometastases and prognosis for patients with hepatocellular carcinoma

  • Authors:
    • Jianhua Liu
    • Haosheng Jin
    • Hongxia Tian
    • Guoda Lian
    • Shaojie Chen
    • Jiayu Li
    • Xuchao Zhang
    • Dong Ma
  • View Affiliations

  • Published online on: November 4, 2015     https://doi.org/10.3892/ol.2015.3859
  • Pages: 213-223
  • Copyright: © Liu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

The present study aimed to investigate anaplastic lymphoma kinase (ALK) status in hepatocellular carcinoma (HCC) and to evaluate whether abnormalities in expression were associated with patient prognosis. ALK status was investigated using immunohistochemistry (IHC), reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR) and fluorescence in situ hybridization (FISH) assays in 342 HCC patients. In addition, rapid amplification of complementary DNA ends‑coupled PCR sequencing was performed, in order to confirm the presence of ALK abnormalities in patients exhibiting ALK messenger RNA (mRNA) overexpression. The correlation between ALK expression and the clinicopathological features and prognosis of the HCC patients was statistically analyzed. The results of the present study revealed overexpression of ALK protein and mRNA; furthermore, ALK gene copy number gains were observed via IHC (44.7%; 153/342), RT‑qPCR (47.4%; 162/342) and FISH (32.7%; 112/342) analyses, although ALK rearrangement or mutation was not demonstrated in the results of any of these assays. ALK protein expression levels were significantly associated with hepatitis C virus (HCV) status (P<0.001) and the presence of micrometastases (P=0.011). Within the entire patient cohort, ALK expression was associated with poor progression‑free survival (PFS; P=0.041). Subsequent analysis in patient subgroups that demonstrated hepatitis B surface antigen positivity, HCV negativity, stage III‑IV disease, recurrence and micrometastasis positivity revealed that overall survival (OS) and PFS were significantly reduced in those patients exhibiting ALK expression compared with those patients who were negative for ALK expression. Multivariate analysis revealed that ALK expression was an independent risk factor for OS (P=0.042) and PFS (P=0.033), particularly for patients with stage III‑IV tumors. Thus, ALK may serve as a novel indicator for the metastatic behavior and prognosis of HCC.

Introduction

Hepatocellular carcinoma (HCC) is the fifth most frequently diagnosed malignancy and the third most common cause of cancer-associated mortality globally (1). Previous evidence has suggested the existence of marked geographic variation, with a high prevalence of HCC in East Asian countries, particularly China (2). Although significant advances have been made with regard to surgical resection, ablation and chemotherapy (3), the prognosis of HCC remains unfavorable. As our understanding of the molecular mechanisms underlying the initiation and progression of HCC increases, targeted therapy has become a promising alternative to currently used treatments, representing a landmark in drug development and a significant step towards the development of personalized medicine for the treatment of HCC (4). However, the efficacy of existing targeted drugs has plateaued in recent years due to increasing drug resistance (5). Therefore, the discovery of novel molecular targets is urgently required for the development of more effective and efficient therapeutic agents.

In general, receptor tyrosine kinases (RTKs), which are crucial for signal transduction, are dysregulated in a diverse range of tumor types (6). The anaplastic lymphoma kinase (ALK) gene, a proto-oncogene that encodes a transmembrane RTK, was initially identified in anaplastic large cell lymphomas carrying an abnormal t(2;5)(p23;q35) translocation (7). Subsequently, its fusion variants were additionally identified in inflammatory myofibroblastic tumors (8) and diffuse large B-cell lymphomas (9). The human ALK gene has a significant role in brain and neuronal development during embryogenesis, however, is downregulated in adults (10). It is well-known that genetic abnormalities involving ALK include translocation (also known as ‘rearrangement’), amplification and mutation, as well as ALK overexpression (11,12). DNA amplification and point mutations were originally identified in neuroblastoma, indicating that the ALK gene may possess high carcinogenic and neoplastic potential (13). In addition, ALK fusion oncogenes, resulting from chromosomal translocations, proved to be the most commonly observed ALK aberrations in cancer, and were able to induce constant ALK kinase activity via their own constitutive self-association, as well as acting as an oncogenic addiction pathway (14). A number of specific small-molecule ALK inhibitors are capable of efficiently suppressing such activity (15).

Echinoderm microtubule-associated protein-like 4 (EML4)-ALK fusion variant was initially reported in 2007, as an oncological driver in non-small cell lung carcinoma (NSCLC) (16), and this led to a focus on the development of novel targeted agents for cancer diagnosis and therapy (11,15). Subsequently, the success of crizotinib (PF-02341066), a targeted agent against EML4-ALK, in the treatment of advanced ALK-rearranged NSCLCs, led to an interest in the significance of ALK status in various other epithelial malignancies, and represented the beginning of a novel era of the targeting of ALK abnormalities for therapeutic purposes in solid tumors (17). Aberrant ALK genes have been reported in various solid tumors (often in addition to hematological malignancies), including esophageal (18), breast (19), colorectal (20) and renal carcinoma (21), indicating an association between ALK abnormalities and human cancer development. However, little research has been conducted to evaluate the abnormalities and clinical significance of the ALK gene in HCC.

In order to improve our current knowledge, the present study comprehensively detected ALK gene status in a large HCC cohort, and investigated whether ALK abnormalities are associated with patient clinicopathological features and prognosis.

Materials and methods

Clinical specimens and follow-up

A total of 342 HCC tumor specimens and corresponding normal non-cancerous tissues were obtained from patients who had undergone surgical resection at Guangdong General Hospital (Guangzhou, China), between June 2005 and October 2010. For the performance of immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH) assays, sections of the resected malignant tissues were fixed using 10% formalin and subsequently embedded in paraffin, followed by longitudinal slicing into 4-µm thick serial sections. The remaining HCC tissues were frozen using liquid nitrogen and stored at −80°C, until required for intensive investigation by reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and rapid amplification of complementary DNA (cDNA) ends (RACE)-coupled PCR sequencing. All patients had not received any anticancer therapy prior to surgery. Micrometastases were defined in accordance with the criteria proposed by Hu et al (22). Disease staging was based on the tumor-node-metastasis staging system of the Union for International Cancer Control (23). Clinical history was extracted from patient medical records. All patients received post-operative follow-up by telephone every 3 months for the initial 2 years of the study, and subsequently every 6 months until mortality or the study endpoint was reached. Overall survival (OS) and progression-free survival (PFS) were measured from the date of surgery until mortality/censoring or local recurrence/distant metastasis/censoring, respectively. The survival analysis utilized in the present study was designed to compare OS and PFS among patients. Each participant signed written informed consent for the use of their resected tissues and personal information for research purposes, and approval was obtained from the Ethics Committee of Guangdong General Hospital (Guangzhou, China).

ALK IHC analysis

ALK IHC staining was performed as previously described (24). In brief, unstained slides were successively submerged in xylene (Guangzhou Yikang Biological Science Technology Co., Ltd., Guangzhou, China), graded alcohol series and tap water for deparaffinization. Following deparaffinization, the intrinsic peroxidase activity of samples was inhibited using 3% hydrogen peroxide. Antigen retrieval was performed by microwave heating at 95°C, following submersion of the sections in ethylenediaminetetraacetic acid buffer (pH 8.0; Shanghai Xibao Biological Technology Ltd., Shanghai, China). The samples were incubated with rabbit monoclonal anti-human ALK [D5F3®; Cell Signaling Technology, Inc., Danvers, MA, USA; 1:50 dilution in antibody diluent (Dako, Glostrup, Denmark)] at 4°C overnight; non-specific protein binding sites were blocked with 5% goat serum (Shanghai Xibao Biological Technology Ltd.). Subsequent to being washed, immunoreaction was visualized using biotinylated goat anti-rabbit IgG secondary polyclonal antibodies (dilution, 1:200; Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA) for 1 h, and thereafter, streptavidin-horseradish-peroxidase complex (Shanghai Xibao Biological Technology, Ltd.) and 3-amino-9-ethyl carbazole (Shanghai Xibao Biological Technology, Ltd.) were added. Finally, all samples were counterstained using hematoxylin (Shanghai Xibao Biological Technology, Ltd.), dehydrated and sealed with cover slips for microscopic examination (CX31; Olympus Corporation, Tokyo, Japan). Two experienced investigators, who were blinded to the patient clinicopathological profiles, confirmed the immunostaining levels separately. The scoring scheme utilized to assess staining was as follows: 0, absent staining; 1+, weak cytoplasmic staining; 2+, moderate and smooth cytoplasmic staining, and 3+, strong and granular cytoplasmic staining in ≥10% of tumor cells (24).

ALK FISH analysis

FISH, a gold standard for confirming gene status, was applied to 342 unstained HCC samples with the Vysis ALK Break Apart FISH Probe kit (Abbott Laboratories, Chicago, IL, USA) according to standard FISH protocols. Following deparaffinization, dehydration and treatment with citric acid, the tumor sections were washed with phosphate-buffered saline, followed by dehydration in alcohol and air-drying at 37°C. Subsequently, the slides were added to 5 µl of diluted ALK probe and denatured. The probe was hybridized and the slides were washed. The reagent was comprised of two DNA probes labeled with Spectrum Orange (red) and Spectrum Green (green), which were able to test various genetic rearrangements of ALK at 2p23, by hybridizing and breakpoint flanking. FISH signals were evaluated under a fluorescence microscope (IX72; Olympus Corporation) using an oil immersion objective. Two pathologists independently analyzed all FISH results. ALK translocation positivity was defined as the separation of red and green signals, or a single red signal, in at least 15% of analyzed cells. However, since the criteria for gain of ALK copy number have not been established, the present study adopted the previously published cut-off values for colorectal cancer in the current analysis (25). Briefly, the positivity for gain of ALK gene copy number was considered to be 3–5 copies of ALK per cell in ≥10% of all detected cells, and amplification was regarded to be ≥6 copies of ALK per cell in ≥10% of all detected cells.

ALK RT-qPCR analysis

Total RNA was isolated from matching pairs of frozen HCC tissue blocks with TRIzol® reagent (Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA) according to the manufacturer's protocols. Each tissue was trimmed at low temperature to protect the RNA from degradation. Prior to amplification, the purity and concentration of the extracted RNA were assessed using gel electrophoresis and absorbance at A260/A280. Reverse transcription for cDNA was subsequently conducted with a cDNA synthesis kit (Invitrogen; Thermo Fisher Scientific). cDNA was synthesized using 2.5 µg of total RNA as template and 1 mmol/l oligo(dT) primer in 25 µl of a solution that included 200 units of M-MLV reverse transcriptase. Subsequently, 5 µl of cDNA was applied as the template in a 20-µl reaction for RT-qPCR analysis with SYBR® GreenER™ qPCR SuperMix (Invitrogen; Thermo Fisher Scientific) and the ABI 7500 cycler (Applied Biosystems; Thermo Fisher Scientific) under the following thermal cycling conditions: 95°C for 2 min, 40 cycles of 95°C for 15 sec and a final extension at 72°C for 5 min. The remaining generated cDNA was stored at −20°C for further RACE-coupled PCR sequencing. β-actin served as the internal control. The primers were purchased from Shanghai GeneChem Co., Ltd. (Shanghai, China) and synthesized as follows: Sense, 5′-CCTGGAGCTGGTCATTACGA-3′ and antisense, 5′-TGGTTTGTGAAGGAGCCATT-3′. The melting curve of each sample was analyzed in order to guarantee the product specification. As stated in a previous study (26), RT-qPCR analysis for ALK was defined as positive when the specimen Cq value was <30.

RACE-coupled PCR sequencing analysis

Cases with RT-qPCR positivity were selected for RACE-coupled PCR sequencing analysis. Stored cDNA was purified using a High Pure PCR Product Purification kit (Roche Diagnostics, Indianapolis, IN, USA). Subsequently, reactions mixing purified cDNA were initiated by incubation at boiling temperature followed by incubation on ice. The following procedure was performed for targeted capture of rearranged sequences using previously published protocols (11). Following two successive runs of PCR, amplification of desired cDNA segments spanning exon 20 of the ALK gene and upstream sequences, which may possess the transcript sequences of ALK fusion partners, was achieved. The primers used were selected according to the study by Zhang et al (11), and were obtained from Shanghai GeneChem Co., Ltd. The first and second pairs of primers used were as follows: Sense, 5′-CGCGTCCACTAGTACGGGGGGGGGG-3′ and antisense, 5′-GGCACCTCCTCGACGTCACTGATG-3′; and sense, 5′-GCGCACGGCTCCACTAGT-3′ and antisense, 5′-ACCAGGAAACAGCTATGACCGGTCTTGCCAGCAAAGCAGTAG-3′, respectively. Following purification and labeling of the PCR products with M13 sequencing primer, 5′-GAAACAGCTATGACC-3′, the amplified fragments were sequenced using the Genetic Analyzer 3730×l (Applied Biosystems; Thermo Fisher Scientific). The resulting files were aligned to the ALK reference sequence (National Center for Biotechnology Information accession number, NM_004304.3) in order to determine whether ALK mutations or fusions were present.

Statistical analysis

The χ2 test was performed in order to estimate the association between ALK protein expression and clinicopathological features. Kaplan-Meier survival curves were plotted with significance calculated using log-rank statistics. Independent prognostic markers of OS and PFS were assessed using univariate and multivariate proportional Cox models. P<0.05 was considered to indicate a statistically significant difference. All data analysis was performed using SPSS version 18.0 (SPSS Inc., Chicago, IL, USA).

Results

ALK protein is detectable using IHC

ALK protein expression was investigated using IHC staining in all HCC biopsies (Fig. 1). In the normal non-cancerous (confirmed by histopathological examination) biopsied samples adjacent to the tumor samples, cytoplasmic ALK staining was absent or poor, and occurred in very few cells (Fig. 1A). Of the 342 enrolled patients, 153 exhibited various degrees of brown cytoplasmic staining in the majority of tumor cells (Fig. 1B–D).

ALK status dectection via FISH

No HCC specimens demonstrated any evidence of rearrangement or amplification in the ALK locus using a break-apart FISH assay. However, in 112/342 images, gain of ALK gene copy number was observed, which was regarded as indicating FISH-positivity (Fig. 2A), and the remaining samples were regarded to be FISH-negative (Fig. 2B). Among the 112 FISH-positive patients, 108 were additionally positive for ALK protein expression identified via IHC.

ALK status detection via RT-qPCR and RACE-coupled PCR sequencing assays

In order to compare the levels of ALK messenger RNA (mRNA) in 342 HCC specimens with that of adjacent non-cancerous tissues, RT-qPCR was performed. The results of the present study revealed that ALK mRNA was significantly increased in 162 HCC samples. Notably, of the 162 cases exhibiting RT-qPCR positivity, 139 were IHC-positive and 101 were additionally FISH-positive (Table I). Fig. 3A illustrates nine representative cases. Furthermore, ALK status was detected in 162 cases that were RT-qPCR positive using RACE-coupled PCR sequencing. Following alignment of the gene sequence with the ALK reference sequence based on a previous study (11), no mutations or fusions with potential partners were detected (Fig. 3B).

Table I.

Concordance among IHC, FISH and RT-qPCR results for anaplastic lymphoma kinase expression in 342 hepatocellular carcinoma patients.

Table I.

Concordance among IHC, FISH and RT-qPCR results for anaplastic lymphoma kinase expression in 342 hepatocellular carcinoma patients.

RT-qPCRFISHIHC-positive (n=153)IHC-negative (n=189)
PositivePositive101     2
PositiveNegative  38  21
NegativePositive     7     2
NegativeNegative     7164

[i] IHC, immunohistochemistry; FISH, fluorescence in situ hybridization; RT-qPCR, reverse transcription-quantitative polymerase chain reaction.

Certain clinicopathological features are associated with ALK protein overexpression

The present study evaluated the association between ALK gene expression and clinicopathological features of HCC patients (Table II). All analyses were performed according to IHC outcomes, as ALK protein was more stable than DNA and RNA, which assured comparability among histological specimens. The results of the present study indicated that ALK protein expression was highly correlated with hepatitis C virus (HCV) status (P<0.001) and micrometastases (P=0.011), however, it was not significantly associated with patient age, gender, hepatitis B surface antigen (HBsAg), α-fetoprotein (AFP), cirrhosis, tumor size, tumor multiplicity, clinical stage, vascular invasion, Child-Pugh classification, recurrence and lymph node metastasis (P>0.05).

Table II.

Correlation between clinicopathological features and negative (n=189) and positive (n=153) anaplastic lymphoma kinase (ALK) protein expression in hepatocellular carcinoma patients.

Table II.

Correlation between clinicopathological features and negative (n=189) and positive (n=153) anaplastic lymphoma kinase (ALK) protein expression in hepatocellular carcinoma patients.

ALK protein

Clinicopathological featurenNegative, n (%)Positive, n (%)P-value
Age at diagnosis, years
  <60265  153 (57.7)112 (42.3)   0.088
  ≥60  77     36 (46.8)  41 (53.2)
Gender
  Male270  145 (53.7)126 (46.7)   0.165
  Female  72     45 (62.5)  27 (37.5)
Hepatitis B surface antigen
  Negative  81     45 (55.6)  36 (44.4)   0.952
  Positive261  144 (55.2)117 (44.8)
Hepatitis C virus
  Negative324  189 (58.3)135 (41.7)<0.001
  Positive  18     0 (0.0)     18 (100.0)
α-fetoprotein, ng/ml
  <20169     90 (53.3)  79 (46.7)   0.460
  ≥20173     99 (57.2)  74 (42.8)
Cirrhosis
  Absent155     90 (58.1)  65 (41.9)   0.343
  Present187     99 (52.9)  88 (47.1)
Tumor size, cm
  <5189  108 (57.1)  81 (42.9)   0.437
  ≥5153     81 (52.9)  72 (47.1)
Tumor multiplicity
  Single276  151 (54.7)125 (45.3)   0.674
  Multiple  66     38 (57.6)  28 (42.4)
Clinical stage
  I–II163     90 (55.2)  73 (44.8)   0.986
  III–IV179     99 (55.3)  80 (44.7)
Vascular invasion
  No210  117 (55.7)  93 (44.3)   0.832
  Yes132     72 (54.5)  60 (45.5)
Child-Pugh score
  A316  177 (56.0)139 (44.0)   0.331
  B  26     12 (46.2)  14 (53.8)
Recurrence
  No250  144 (57.6)106 (42.4)   0.152
  Yes  92     45 (48.9)  47 (51.1)
Lymph node metastasis
  No288  153 (53.1)135 (46.9)   0.066
  Yes  54     36 (66.7)  18 (33.3)
Micrometastases
  No297  172 (57.9)125 (42.1)   0.011
  Yes  45     17 (37.8)  28 (62.2)
Survival analysis

By the cutoff day on June 1, 2013, 68.4% (234/342) of the enrolled patients, all of whom exhibited recurrence or uncontrolled HCC, had succumbed. The median follow-up duration was 36.0 months (range, 0.6–79 months), and 13 (3.8%) cases were lost during the follow-up period. The potential effect of the ALK gene on survival was assessed. In the total patient cohort, it was observed that OS did not significantly differ between patients with positive or negative ALK expression (χ2=3.238; P=0.072; Fig. 4A. However, PFS for patients with positive ALK expression was significantly poorer compared with that of patients with negative ALK expression (χ2=4.187; P=0.041; Fig. 4B. Following additional stratification of 342 HCC patients, OS and PFS were found to be markedly reduced in patients exhibiting ALK expression compared with patients without ALK expression, in subgroups that were HBsAg positive (P=0.026 vs. 0.015; Fig. 5A–B), HCV negative (P=0.043 vs. 0.021; Fig. 5C–D), stage III–IV (P=0.002 vs. 0.001; Fig. 5E–F), recurrence positive (P=0.029 vs. 0.034; Fig. 6A–B) and micrometastasis positive (P=0.039 vs. 0.036; Fig. 6C–D). However, in the HBsAg-negative (P=0.863 vs. 0.869), HCV-positive (no comparison analysis), stage I–II (P=0.895 vs. 0.825), recurrence-negative (P=0.375 vs. 0.267) and micrometastasis-negative (P=0.184 vs. 0.152) subgroups, ALK expression exerted no impact on OS or PFS. Furthermore, ALK expression was not associated with survival stratified by age, gender, AFP, cirrhosis, tumor size, tumor multiplicity, vascular invasion, Child-Pugh classification and lymph node metastasis.

In addition, Cox proportional hazards model was applied in order to reveal the independent impacts of the following features on OS and PFS: Age, gender, HBsAg, HCV, AFP, cirrhosis, tumor size, tumor multiplicity, clinical stage, vascular invasion, recurrence, lymph node metastasis, micrometastases, Child-Pugh classification and ALK protein expression. The results of univariate and multivariate analyses indicated that ALK protein expression exerted a significant prognostic effect on PFS in HCC patients (hazard ratio, 1.365; 95% confidence interval, 1.029–1.810; P=0.031; Table III), although it was not an independent prognosticator for OS (hazard ratio, 1.290; 95% confidence interval, 0.973–1.709; P=0.076). ALK protein expression may be an independent risk factor for OS (P=0.041 vs. 0.042) and PFS (P=0.029 vs. 0.033; Table IV), particularly for stage III–IV patients.

Table III.

Univariate and multivariate analyses of progression-free survival in 342 hepatocellular carcinoma patients.

Table III.

Univariate and multivariate analyses of progression-free survival in 342 hepatocellular carcinoma patients.

A, Univariate analysis

ParameterVariableHazard ratio (95% confidence interval)P-value
Age at diagnosis, years<60 vs. ≥601.012 (0.747–1.372)   0.938
GenderMale vs. female0.880 (0.635–1.219)   0.443
Hepatitis B surface antigenPositive vs. negative1.068 (0.787–1.449)   0.673
Hepatitis C virusPositive vs. negative0.816 (0.433–1.538)   0.529
α-fetoprotein, ng/ml<20 vs. ≥200.932 (0.721–1.205)   0.591
CirrhosisAbsent vs. present1.026 (0.791–1.330)   0.849
Tumor size, cm<5 vs. ≥51.143 (0.883–1.478)   0.310
Tumor multiplicitySingle vs. multiple1.050 (0.763–1.447)   0.763
Clinical stageI–II vs. III–IV1.228 (0.949–1.589)   0.118
Vascular invasionNo vs. yes1.113 (0.854–1.450)   0.430
RecurrenceNo vs. yes1.002 (0.749–1.340)   0.990
Lymph node metastasisNo vs. yes1.099 (0.779–1.550)   0.591
MicrometastasesNo vs. yes1.397 (0.974–2.004)   0.069
Anaplastic lymphoma kinase proteinPositive vs. negative1.304 (1.005–1.691)   0.045
Child-Pugh classificationA vs. B  6.220 (3.764–10.278)<0.001

B, Multivariate analysis

ParameterVariableHazard ratio (95% confidence interval)P-value

Anaplastic lymphoma kinase proteinPositive vs. negative1.365 (1.029–1.810)   0.031
Child-Pugh classificationA vs. B  7.198 (4.261–12.159)<0.001

Table IV.

Univariate and multivariate analyses of overall survival for 179 stage III–IV hepatocellular carcinoma patients.

Table IV.

Univariate and multivariate analyses of overall survival for 179 stage III–IV hepatocellular carcinoma patients.

A, Univariate analysis

ParameterVariableHazard ratio (95% confidence interval)P-value
Age at diagnosis, years<60 vs. ≥601.026 (0.700–1.505)   0.894
GenderMale vs. female0.958 (0.625–1.499)   0.883
Hepatitis B surface antigenPositive vs. negative1.062 (0.708–1.593)   0.770
Hepatitis C virusPositive vs. negative0.885 (0.389–2.014)   0.771
α-fetoprotein, ng/ml<20 vs. ≥200.875 (0.648–1.240)   0.453
CirrhosisAbsent vs. present1.137 (0.804–1.609)   0.468
Tumor size, cm<5 vs. ≥51.095 (0.569–1.407)   0.631
Tumor multiplicitySingle vs. multiple1.264 (0.725–2.203)   0.408
Vascular invasionNo vs. yes1.104 (0.609–1.224)   0.410
RecurrenceNo vs. yes1.091 (0.744–1.599)   0.656
Lymph node metastasisNo vs. yes1.081 (0.636–1.361)   0.711
MicrometastasesNo vs. yes1.230 (0.832–1.816)   0.299
Anaplastic lymphoma kinase proteinPositive vs. negative1.416 (0.999–2.006)   0.041
Child-Pugh classificationA vs. B  6.898 (3.593–13.240)<0.001

B, Multivariate analysis

ParameterVariableHazard ratio (95% confidence interval)P-value

Anaplastic lymphoma kinase proteinPositive vs. negative1.894 (1.023–3.507)   0.042
Child-Pugh classificationA vs. B  8.610 (4.246–17.786)<0.001

Discussion

To the best of our knowledge, the results of the present study demonstrated the first evidence that ALK expression was increased at a transcriptional level, and additionally at a translational level, in human HCC samples compared with adjacent normal tissue samples. ALK rearrangement was not observed in any of the examined samples. The expression of ALK protein was significantly correlated with the aggressiveness and prognosis of primary HCC.

HCC is a pathologically and clinically heterogeneous neoplasm, exhibiting high malignancy and a consequent poor prognosis due to its aggressive features (27). Despite the complexity of hepatocarcinogenesis, the discovery of additional prognostic predictors and therapeutic targets for HCC has attracted particular interest. As a result, a number of genes, including epidermal growth factor receptor, transforming growth factor β and c-MET, have been identified as molecular targets of HCC (28). Recently, much attention has been paid to the ALK gene, a member of the RTK family, the dysregulation of which is associated with abnormal development and malignant transformation in human cancer (29). However, to the best of our knowledge, the clinical value of ALK abnormalities in human HCC has not previously been comprehensively evaluated.

In the present study, ALK status was investigated in a large cohort of HCC patients. IHC, RT-qPCR and FISH analyses revealed that increased expression of ALK protein and mRNA, as well as ALK gene copy number gain, occurred in HCC, with the rates of expression observed in patients being 44.7% (153/342), 47.4% (162/342) and 32.7% (112/342), respectively. Notably, there was concordance in the assessment of ALK expression levels among IHC, RT-qPCR and FISH detection methods, demonstrating that ALK gene upregulation was present at post-transcriptional and transcriptional levels. Meanwhile, the results of the present study revealed that RT-qPCR possessed a higher sensitivity (90.8%) and that FISH had increased specificity (97.9%) compared with IHC staining, which demonstrated similar results to those of a previously published study (30). However, it is notable that ALK overexpression or ALK gene copy number gain is not indicative of ALK rearrangement. To the best of our knowledge, in patients exhibiting NSCLC, copy number gain and amplification of the ALK gene are reportedly highly expressed, while ALK translocations are rare (13). Similar results have also been described in esophageal carcinoma (18). In the present study, no rearrangement, amplification or mutation of the ALK locus was identified using FISH and RACE-coupled PCR sequencing assays. A recent retrospective study (12) reported that ALK gene copy number gain was common in HCC investigated with FISH analysis, whereas ALK rearrangement was not observed. These previous results supported the results of the present study, which indicated that the ALK gene was upregulated in HCC, and that this may be a potential biomarker for HCC.

The present study additionally characterized the association between ALK protein and the clinicopathological features of HCC. The results of the present study demonstrated that ALK protein overexpression possessed significant correlation with HCV status and micrometastases. Briefly, ALK may be a valuable indicator for the identification of subsets of HCC cases with HCV infection and increased invasive tendency. Various experimental model systems have proved that ALK gene overexpression contributes to cell migration and invasion (10,31,32), which are crucial steps in the metastatic cascade, and may lead to distant organ involvement and tumor aggressiveness (33). Furthermore, Shao et al (34) reported that ALK protein was overexpressed in HCC and may be involved in the progression of HCC tumors, although the patient cohort investigated in this previous study was small. Similarly, the results of the present study suggested a significant impact of ALK overexpression on the promotion of the development and metastasis of HCC.

Activation of proto-oncogenes and inactivation of tumor suppressors contributes to the occurrence and progression of malignancies. Specifically, the ALK oncogene is activated by its endogenous ligands, midkine and pleiotrophin, which serve as mitogenic and angiogenic factors in cancer (10). Given that the activated ALK gene induces an intricate system of downstream signaling cascades, including phosphoinositide 3-kinase/protein kinase B and mitogen-activated protein kinase pathways, it is possible that the ALK gene may mediate cellular proliferation, motility and apoptosis, and thereby possess a significant role in the promotion of tumorigenesis and development in vitro and in vivo (35). Recently, Hasan et al (33) illustrated that MYC proteins that targeted key proliferative pathways in the cancer development process, and thus contributed to tumor growth and metastasis in neuroblastoma, regulated ALK expression. Notably, Di Paolo et al (36) reported that the RNA interference-based knockdown of ALK, independent of fusion gene status, resulted in the downregulation of proliferation and the upregulation of apoptosis in neuroblastoma tumor cells, thereby ultimately inhibiting tumor growth and prolonging survival in vivo. Therefore, these previous results confirm that ALK has a significant role in the progression and metastasis of HCC.

In addition, ALK overexpression has been documented as possessing an unfavorable prognosis in multiple human cancers, including neuroblastoma (36), breast carcinoma (37) and basal cell carcinoma (38). Similarly, the present study revealed that ALK protein was significantly correlated with poor PFS in the entire study cohort, particularly for patients with HBsAg positivity, HCV negativity, advanced stage tumors, recurrence or micrometastases. Notably, there were certain differences between the results of the present study and the previous findings of Jia et al (12), which demonstrated that ALK gene copy number gain predicted the survival of patients exhibiting HBsAg negativity, however, did not impact on the survival of patients with HBsAg positivity. The primary reasons for the disagreement between these sets of results may be due to the genetic backgrounds and research methods utilized (protein versus gene copy number). The results of the current study concluded that the prognosis of HCC patients exhibiting ALK overexpression tended to be poorer.

Due to the retrospective nature of the present study, a number of patients and their clinical information were lost to follow-up, particularly those patients who were not hospitalized following surgery, which may have led to bias in the results. Accordingly, additional experiments in vitro and in vivo are required to confirm the results of the present study. In addition, it remains to be elucidated whether HCC patients exhibiting ALK overexpression may benefit from treatment with ALK inhibitors. Further research focusing on these issues is required.

In conclusion, ALK may serve as a valuable predictor of micrometastases and poor survival. Therefore, radiological diagnosis in combination with ALK detection may assist with the prognostic evaluation of novel HCC cases, as optimal individualized therapeutic strategies remain to be devised.

Acknowledgements

The present study was supported by a grant from the Program of Science and Technology Commission Foundation of Guangzhou City, Guangdong Province, China (grant no. 2011B031800285).

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January-2016
Volume 11 Issue 1

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Spandidos Publications style
Liu J, Jin H, Tian H, Lian G, Chen S, Li J, Zhang X and Ma D: Anaplastic lymphoma kinase protein expression predicts micrometastases and prognosis for patients with hepatocellular carcinoma. Oncol Lett 11: 213-223, 2016
APA
Liu, J., Jin, H., Tian, H., Lian, G., Chen, S., Li, J. ... Ma, D. (2016). Anaplastic lymphoma kinase protein expression predicts micrometastases and prognosis for patients with hepatocellular carcinoma. Oncology Letters, 11, 213-223. https://doi.org/10.3892/ol.2015.3859
MLA
Liu, J., Jin, H., Tian, H., Lian, G., Chen, S., Li, J., Zhang, X., Ma, D."Anaplastic lymphoma kinase protein expression predicts micrometastases and prognosis for patients with hepatocellular carcinoma". Oncology Letters 11.1 (2016): 213-223.
Chicago
Liu, J., Jin, H., Tian, H., Lian, G., Chen, S., Li, J., Zhang, X., Ma, D."Anaplastic lymphoma kinase protein expression predicts micrometastases and prognosis for patients with hepatocellular carcinoma". Oncology Letters 11, no. 1 (2016): 213-223. https://doi.org/10.3892/ol.2015.3859