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HAX-1 has been described as a protein potentially involved in carcinogenesis and especially metastasis. Its involvement in regulation of apoptosis and cell migration along with some data indicating its overexpression in cancer cell lines and tumors suggests that HAX-1 may play a role in neoplastic transformation. Here we present the first systematic analysis of HAX-1 expression in several solid tumors.
Using quantitative RT-PCR, we have determined the mRNA levels of HAX1 splice variant I in several solid tumors. We have also analyzed by semiquantitative and quantitative RT-PCR the expression of five HAX-1 splice variants in breast cancer samples and in normal tissue from the same individuals. Quantitative PCR was also employed to analyze the effect of estrogen on HAX1 expression in breast cancer cell line. Immunohistochemical analysis of HAX-1 was performed on normal and breast cancer samples.
The results reveal statistically important HAX1 up-regulation in breast cancer, lung cancer and melanoma, along with some minor variations in the splicing pattern. HAX-1 up-regulation in breast cancer samples was confirmed by immunohistochemical analysis, which also revealed an intriguing HAX-1 localization in the nuclei of the tumor cells, associated with strong ER status.
HAX-1 elevated levels in cancer tissues point to its involvement in neoplastic transformation, especially in breast cancer. The connection between HAX-1 nuclear location and ER status in breast cancer samples remains to be clarified.
HAX-1 (HS1 associated protein X-1, encoded by the HAX1 gene) is an important target of study in the field of cancer research on account of its involvement in regulation of apoptosis and cell migration, key processes in carcinogenesis and metastasis.
The anti-apoptotic, cell-protecting properties of HAX-1 as well as its interactions with apoptosis-related proteins have been widely reported [1-3]. HAX-1 was demonstrated to interact with proteins involved in mitochondrial membrane permeabilization and elements of the mitochondrial mega-channel [4,5] as well as with proteins directly involved in initiation and execution of apoptosis [2,6,7] and with several viral proteins important for cell survival [1,8,9]. Recently, it was observed that HAX-1 is required for suppression of apoptosis in lymphocytes and neurons, by presenting Omi/HtrA2 to Parl processing . Nevertheless, in spite of the large body of data indicating its role in apoptosis, molecular mechanisms of HAX-1-mediated cell protection still remain to be clarified.
The most explicit role of HAX-1 has been suggested by the studies on the pathogenesis of severe congenital neutropenia (Kostmann disease). This immuno-deficiency syndrome is characterized by the paucity of neutrophils in peripheral blood caused by a block in promyelocyte/myelocyte maturation, associated with their apoptosis. HAX1 mutations, leading to the inactivation of the protein, were found in Kostmann patients, indicating the involvement of HAX-1 in the functioning of the immunological system as well as in apoptosis .
HAX-1 multifunctionality manifests itself in a number of reported interactions with other proteins. One of these proteins is prohibitin. Prohibitin was initially identified as a repressor of estrogen-dependent transcriptional activity, but was subsequently shown to localize in the mitochondrial inner membrane and form a complex with VDAC, ANT2 and HAX-1, implying its role in apoptosis . It has been reported that in the presence of ERα and estradiol, prohibitin translocates to the nucleus, providing a possible link between HAX-1 and estrogen-receptor signaling. Another possible connection to estrogen signaling is suggested by data from microarray analysis, which has classified HAX1 (as one of 172 out of 20,000 human genes) as estrogen-responsive [11,12]. Thus, further analysis of HAX1 responsiveness to estrogen seems to be worthwhile.
Besides its involvement in apoptosis, HAX-1 has been also implicated to function in regulation of cell migration [13,14]. The HAX-1 protein partner, HS1 , is highly homologous to cortactin, a cytoskeletal protein frequently overexpressed in cancer. Considering the similarity between HS1 and cortactin , it is not surprising that HAX-1 also binds the latter . It has been suggested in several reports [17,18] that cortactin promotes tumor invasiveness and metastasis. While HS1 is expressed mostly in hematopoietic cells, cortactin is present in all other tissues [19,20]. It interacts with the Arp2/3 complex, promoting actin polymerization during actin network reconstruction in motile cells. HAX-1 was shown to form a complex with cortactin, the small GTP-ase Rac and regulatory protein Gα13. Accordingly, a model was proposed, in which Gα13, when bound to HAX-1, stimulates migration, while in the absence of HAX-1 it activates cell adhesion . A more recent report  demonstrates the role of HAX-1 in regulation of carcinoma cell migration and invasion via clathrin-mediated endocytosis of intergin αvβ6. The interaction of HAX-1 with the IL-1α precursor which has been shown to regulate human endothelial cell migration in vitro  provides additional support for a role in regulation of cell migration.
Since the inhibition of apoptosis and the induction of cell invasiveness are crucial for carcinogenesis, it is logical to expect that HAX-1 overexpression in neoplastic cells should contribute to tumor resistance to apoptosis as well as to the enhancement of metastatic potential.
HAX-1 overexpression has been observed in lesional psoriasis, a chronic inflammatory disease in which differentiation of keratinocytes is disturbed due to abnormal resistance to apoptosis . In the same report, HAX-1 was shown to be overexpressed in melanoma cell lines. HAX-1 overexpression was also observed in oral squamous cell carcinoma (SCC) samples . HAX-1 up-regulation in skin cancer samples and cell lines, its involvement in pathology of skin disease and the chromosomal location of the HAX1 gene within the epidermal differentiation complex (chromosome 1q21) suggests its role in maturation of the human epidermis. This conclusion points to its possible involvement in development of melanoma.
Except for the reports demonstrating HAX-1 overexpression in SSC samples and a few cancer cell lines, to date, the only available results concerning its expression in cancer consist of data from microarray and SAGE analyses. According to Oncomine, , a cancer microarray database, HAX1 is overexpressed in hepatoma, lung cancer, lymphoma, melanoma, leukemia and myeloma - in order of decreasing statistical significance. Downregulation of expression was observed for brain cancer, ovarian cancer and seminoma. In breast cancer, statistically significant overexpression correlated with carcinoma grade. In a gene expression profiling study utilizing SAGE, HAX1 overexpression was demonstrated to be specifically induced by hypoxia in renal cell carcinoma (RCC) cells . Although these reports indicate HAX1 overexpression in cancer, their reliability is not as high as in the focused study, so they still need to be verified by more systematic analysis.
HAX1 was shown to be expressed quite ubiquitously in human tissues, with relatively higher expression in testis, liver and skeletal muscle . It has also been shown to be alternatively spliced, producing at least five splice variants with the same open reading frame in human cells [25,26]. Expression analysis ascertained so far for variants I and II in normal tissues  shows prevalent expression of splice variant I. The role of the other variants in processes like apoptosis, cell signaling and migration, remains unclear. Analysis of the potential variations in HAX1 splicing patterns in tumors may shed some light on the role of splice variants in cancer pathology.
The involvement of HAX-1 in processes crucial to carcinogenesis as well as demonstration of its overexpression in several tumor cell lines provides strong arguments for a detailed analysis of its role in neoplastic transformation and metastasis. In this report, we present for the first time a focused analysis of HAX1 expression in several solid tumors, identifying three malignant neoplasms (breast cancer, lung cancer and melanoma) in which HAX1 is significantly up-regulated. Detailed analysis of expression of five splice variants of HAX1 in breast cancer revealed tumor-specific variations in the pattern of splicing. HAX-1 elevated expression in breast cancer was confirmed at the protein level, by immunohistochemistry, which also revealed its nuclear localization in ER-positive tumors. Expression results were validated against clinical data, including stage and grade of tumor, receptor and nodal status. Additionally, the influence of estrogen on HAX1 expression was estimated in a breast cancer estrogen-responsive cell line (MCF-7) and found not significant.
Breast cancer samples were obtained from 15 breast cancer patients (median age 64 years, range 32-81 years) undergoing surgery at the Cancer Center - Institute of Oncology in Warsaw. Samples were diagnosed according to histopathological reports as primary invasive carcinomas (ductal, lobular, papillary and mixed). Paired samples of breast carcinoma and normal tissue adjacent to the carcinoma were collected from each patient. These tissues are referred to as 'normal' breast tissues, although they cannot be regarded as completely 'healthy normal' specimens. A detailed description of the breast carcinomas of the 15 patients is shown in Table Table1.1. This study was approved by the local ethics committee and the patients gave an informed consent about the usage of tissues for research purposes.
The following oncology qPCR arrays were purchased from OriGene Technologies (Rockville, MD, USA) and used to asses human HAX-1 mRNA expression levels: TissueScan Oncology Survey Tissue qPCR Array I, TissueScan Breast Cancer Tissue qPCR Array II, TissueScan Lung Cancer Tissue qPCR Array III, TissueScan Melanoma Tissue qPCR Array. All the clinical and pathological information associated with samples in each of the panels can be found on the OriGene website http://www.origene.com/geneexpression.
Breast cancer and adjacent normal tissue samples were selected by a pathologist from surgically removed tissues of breast cancer patients immediately after surgery. Samples were flash-frozen, pulverized in liquid nitrogen using Microdismembrator II (Braun Biotech, Aylesbury, UK) and stored at -80°C prior to RNA isolation.
RNA from 30 - 90 mg of pulverized breast cancer tissue and normal controls from the same patient was isolated using NucleoSpin RNA II kit (Macherey - Nagel, Düren, Germany). RNA from 5×105 MCF-7 or Hela cells was isolated using PureLink Micro-to-Midi Total RNA Purification Kit (Invitrogen, Carlsbad, CA, USA). The amount and purity of RNA were measured spectrophotometrically on NanoDrop ND-1000 (NanoDrop Technologies, Wilmington, DE, USA). Overall RNA integrity and quality was assessed on a denaturing agarose gel. Genomic DNA was removed from RNA samples by digestion with recombinant DNase I, RNase-free (Roche, Mannheim, Germany) according to the manufacturer's instructions. First strand cDNA was synthesized from 50 ng (for semi-quantitative PCR on patient samples), 200 ng (for quantitative PCR on patient samples) or 1 μg (MCF-7 and Hela cells) of total RNA using 25 ng oligo(dT)18 primers (Fermentas, Burlington, Canada) and SuperScript II, RNase H - Reverse Transcriptase (Invitrogen) according to the manufacturer's instructions. Reverse transcription was repeated at least twice to minimize the effects of possible differences in reverse transcription efficiency amongst samples.
Expression of HAX-1 splicing variants in breast cancer versus normal tissue was analyzed using reverse transcription semi-quantitative PCR. Splice variant nomenclature is presented as in Carlsson et al. . Primers for PCR were designed to amplify HAX1 variant I, II and III specifically, primers for variants IV and V have been described previously . Primers for GAPDH were described elsewhere . Primer sequences are presented in Table Table2.2. The amount of cDNA template corresponding to 2.5 ng (for HAX1 variant I and GAPDH), 5 ng (for HAX1 variant II) or 10 ng (for HAX1 variant III, IV and V) of total RNA was amplified using Taq DNA Polymerase (Invitrogen), 200 nM dNTP (Fermentas) and 100 nM of the appropriate primers. PCR conditions were: 95°C (5 minutes) followed by cycles of 95°C (30 seconds), 57°C (30 seconds), and 72°C (30 seconds). Cycle numbers for linear amplification of HAX1 were as follows: variant I - 35, HAX1 variant II - 35, HAX1 variant III - 40, HAX1 variant IV and V - 40, GAPDH - 30 cycles. The experiment was independently repeated thrice.
Expression levels of HAX1 splicing variants in oncology qPCR arrays and breast cancer samples versus normal tissues as well as transcripts levels in cells treated with beta-estradiol were assessed using quantitative PCR on an ABI Prism 7000 Sequence Detection System (Applied Biosystems, Foster City, CA, USA) with human ACTB as a reference gene. Amplification mixtures (25 μl) contained 10 ng (samples obtained from patients) or 20 ng (MCF-7 and Hela cells) of cDNA template, 1×SYBR Green I Master Mix Buffer (Applied Biosystems) and 100 nM of the appropriate forward and reverse primer. Primers used for amplification of HAX1 variant I were the same as in semi-quantitative PCR. Primer sequences for HAX1 variant II and cathepsin D (CTSD) are shown in Table Table2.2. Primers for the reference gene ACTB were described previously . The cycling conditions for HAX1 splicing variants were as follows - precycling hold at 95°C for 10 minutes, 40 cycles: 95°C for 30 seconds and 60°C for 60 seconds; for CTSD - precycling hold at 95°C for 10 minutes, 40 cycles: 95°C for 30 seconds, 57°C for 30 seconds, 72°C for 30 seconds; for ACTB - precycling hold at 95°C for 10 minutes, 40 cycles: 95°C for 30 seconds, 55°C for 30 seconds, 72°C for 30 seconds. To assess specificity, amplification products were subjected to melting curve analysis. Raw data were analyzed using ABI Prism 7000 SDS Software Version 1.1 (Applied Biosystems). Relative expression levels were calculated using efficiency-corrected Ct model which takes into account amplification efficiencies of each primer pair .
MCF-7 estrogen-dependent breast cancer cells and HeLa (human cervical carcinoma) cells were preconditioned for a week in D-MEM (Invitrogen) with charcoal-stripped FBS (Sigma-Aldrich, MO, USA) and subjected to the treatment with the indicated concentrations of beta-estradiol (Sigma-Aldrich) for 48 h . cDNA obtained from the treated cells was analyzed by qPCR with primers specific for HAX1, variants I and II (as above), CTSD and ACTB.
Immunohistochemical stainings were performed on paraffin-embedded material after heat-induced epitope retrieval (HIER). A mouse monoclonal anti-HAX-1 antibody was used at a concentration of 1:75 (BD Transduction Laboratories, USA). Antigens were retrieved by heating the sections in 0.01 M citrate buffer (pH 6.0) 6 × 5 min. in a microwave oven at 700 W. Non-specific tissue and endogenous peroxidase reactivity were blocked with 10% BSA and 3% H2O2, respectively. The sections were incubated with primary antibodies overnight at 4°C. The binding of the primary antibody was detected by a Vectastain Elite ABC kit (Vector Laboratories, Burlingame, CA, USA) and DAB was used as a chromogen. Slides were counterstained with Mayer's hematoxylin. Normal mouse IgG of the same subclasses and concentrations as the primary antibody served as negative controls.
Statistical analysis was performed using Statistica 6.0 (StatSoft, Inc., OK, USA). Nonparametric Mann-Whitney test and Wilcoxon test for matched pairs' analysis were used to analyze mRNA expression data. Fisher's exact test was used to determine statistical significance of the IHC data. A P-value of < 0.05 was regarded as statistically significant.
In a preliminary screen, performed in order to asses HAX1 expression levels in different solid tumors, a survey panel containing cDNA from 96 tissue samples, covering 8 different cancers (breast, colon, kidney, liver, lung, ovarian, prostate, thyroid) was used (TissueScan Oncology Survey Tissue qPCR Array I). The samples represented disease stages from 0 to III or IV. Expression levels of all panel data were ascertained by quantitative PCR. Expression of splice variant I was assessed and considered as representative for overall HAX1 expression, on the basis of its prevalence in respect to other variants (as shown in this study in section "HAX1 splice variants expression in normal vs. tumor samples of breast cancer" and in Carlsson et al., 2008 ). Statistical significance for panel data was assessed using the nonparametric Mann-Whitney test. The highest levels of expression, significantly exceeding the level of normal control, were observed in breast and lung cancers (Fig (Fig1A1A and and1B).1B). In these two panels, up-regulation is significant in the most advanced stages of the disease (stages III-IV, P = 0.025 and 0.049 for breast and lung cancer, respectively). For the rest of the analyzed tumors, no significant overexpression or relation was observed, except for colon cancer, where significant up-regulation was detected for stages I-II (Fig 1C, D, E, F, G and and1H).1H). Since our study was focused on finding a relationship between HAX1 expression levels and factors related to metastasis, such as stage, nodal status and grade of the disease, colon cancer was excluded from further analysis because of a non-significant p-level value for stages III-IV.
To further verify the results obtained from the survey panel, and to narrow the analysis, three other panels - breast cancer, lung cancer and melanoma - were analyzed, each containing cDNA from 48 tissue samples for each cancer type. Melanoma was included because of the potential role of HAX-1 in skin diseases and its reported overexpression in melanoma cell lines . Panels contained samples from different stages of disease, including metastatic carcinomas (2, 7 and 40 cases for breast cancer, lung cancer and melanoma, respectively).
Detailed analysis of the expression data obtained from these specific panels was performed using non-parametric Mann-Whitney test and confirmed HAX1 significant up-regulation in tumors, though not as high as previously detected in the survey panel (Fig (Fig2).2). The most marked results were obtained for breast cancer samples, with significant overexpression (in regards to stage 0) for all subsequent stages of the disease (Fig (Fig2A).2A). In lung cancer samples, significant overexpression was obtained for stages I and IV, with higher expression levels and higher significance for stage IV (Fig (Fig2B).2B). The melanoma tissue panel was composed of normal and exclusively metastatic carcinoma samples from stages III and IV. Significant overexpression was obtained for both groups, with higher significance for stage IV (Fig (Fig2C2C).
Human HAX1 pre-mRNA is alternatively spliced to generate at least 8 splice variants [25,26]. Five of these variants remain in the same reading frame, while the rest contains a frameshift, generating a different protein product. In this analysis we ascertained the expression levels for the first five splice variants in the same reading frame (Fig (Fig33).
Since the previous study in which the expression of splice variants I and II was compared  revealed that variants' expression levels vary considerably (with the prevalence of splice variant I), to further demonstrate possible differences in expression the relative mRNA levels of the all five variants were assessed by standard RT-PCR. The results show that while variant I is quite abundant and easily detectable by 30 PCR cycles (Fig (Fig4A),4A), the expression of the other variants is quite weak (visible bands at 40 cycles, Fig Fig4A4A).
Samples of normal (adjacent to tumor) and tumor tissues from the same patient were analyzed for 15 breast cancer cases (Table (Table1).1). This type of material enables matched pair analysis, which eliminates differences in expression arising from the variability of genomic background. Expression of splice variants I, II, III, IV and V were analyzed by standard RT-PCR, with GAPDH as a reference (Fig (Fig4B).4B). The most marked difference in expression was detected in case of variant III. In 8 paired samples the expression of the splice variant III was detected only in tumors, while in the remaining 7 samples expression of variant III was detected neither in tumors nor in normal tissues, except for one case, in which the expression was detected in normal tissue and not in tumor. For the other variants the differences in expression were not detectable in the standard PCR experiment, apart from slight overexpression of variant V in six cases out of fifteen (Fig (Fig4B4B).
Expression of variants I and II was relatively high (although much higher for variant I), which made it possible to reliably and precisely assess its levels by quantitative PCR. For both variants up-regulation in tumors was statistically significant (P = 0.047 and P = 0.02 for variants I and II, respectively, nonparametric Wilcoxon test for matched pairs). The results also demonstrated, that although the high expression of the splice variant I in respect to the other variants (observed previously for the normal tissues, ) remains very high in tumors, the median value of the variant I/variant II expression ratio is considerably lower in tumor than in the matching normal tissues: 9 (6.63-11.23) and 15 (10.97-17.01), for tumor and normal tissues, respectively (Fig (Fig5A).5A). Accordingly, the relative tumor overexpression level in most cases (13 patients, 87%) is higher for variant II than for variant I (Fig (Fig5B5B).
HAX1 expression levels were analyzed in respect to prognostic markers other than stage of the disease, in order to establish possible relationships. Factors like tumor size, grade of the disease, nodal status and histology were used to categorize data, followed by statistical analysis of the groups. For breast cancer, receptor status (ER, PR and HER2) was additionally included in the analysis. Data from the cDNA panel of breast cancer samples showed a significant relationship between HAX1 expression levels and tumor size (P = 0.004 and P = 0.0015 for T0 vs. T1 and T0 vs. T2-4, respectively) and grade (P = 0.003 and P = 0.0015 for G0 vs. G1-2 and G0 vs. G3, respectively), but for the other prognostic markers no significant relation was detected. For the other two panels, pathology reports concerning tumor size and grade were not sufficient to perform the analysis in the case of melanoma, and showed no relationship in the case of lung cancer.
Data from the matched pairs of normal and tumor tissue samples from the 15 patients were analyzed separately. The relationships between variants I and II expression levels and the established breast cancer prognostic factors were calculated and are summarized in Table Table3.3. The most significant relationship was found, again, for tumor size (P = 0.005, same value for variants I and II). Relationships of weak significance (borderline) were found for nodal status (inverse relationship, variants I and II), progesterone-negative cancers (variants I and II) and HER2-negative cancers (variant II). Estrogen receptor status had no relation to HAX1 expression level, which confirms the results obtained from the panel data analysis.
The MCF-7 estrogen-dependent breast cancer cell line was subjected to treatment with the indicated concentrations of beta-estradiol (Fig (Fig6A).6A). Concurrently, the same experiment was performed in HeLa cells as an estrogen-independent reference (Fig (Fig6B).6B). The levels of HAX1 expression for the two splice variants (I, II) in estradiol-treated cells were established by quantitative PCR. The effect of estrogen was assessed in comparison to the known up-regulation of expression observed for cathepsin D mRNA . No significant HAX1 up- or down-regulation was observed for any of the splice variants. This result is consistent with the lack of relation between HAX1 expression levels and the ER status, in the samples from cDNA panels and from patients (Table (Table22).
HAX1 up-regulation detected at the mRNA level was confirmed at the protein level by immunohistochemical analysis. Paraffin sections of the paired normal and tumor tissues from all fifteen patients were analyzed. HAX-1 up-regulation was detected in most of the tumor samples (Table (Table4,4, Fig Fig7A7A and and7B).7B). Intensive HAX-1 staining was observed not only in the cytoplasm (Table (Table4,4, Fig Fig7B),7B), but also in the nuclei of the tumor cells (Table (Table4,4, Fig Fig7A).7A). In the matching normal cells cytoplasmic staining was minimal (Table (Table4,4, Fig Fig7G7G and and7H)7H) and nuclear staining was not detected (Table (Table4,4, Fig Fig7G).7G). IgG controls of the analyzed tissue sections were negative (Fig (Fig7E7E and and7F).7F). It was observed, that strong nuclear HAX-1 staining was associated with strong ER staining (Table (Table4,4, Fig Fig7A7A and and7C),7C), while cytoplasmic HAX-1 staining coincided with weak ER staining (Table (Table4,4, Fig Fig7B7B and and7D);7D); this relation was calculated by the Fisher's exact test and found significant (P = 0.026).
HAX-1 nuclear localization was also observed by immunofluorescence in about 21% of cells in HAX-1-GFP-transfected MCF-7 breast cancer cell line, thus confirming IHC data, indicating that HAX-1 is present, at least to some extent, in the nuclei of breast cancer cells (Additional files 1 and 2).
HAX-1 protein has been reported to play a role in apoptosis and cell migration, its overexpression has been detected in cancer cell lines and - mostly by microarray analysis - in tumors, but hitherto, no systematic screen of its expression in cancer has been performed. This report represents the first preliminary analysis of HAX1 expression levels in solid tumors.
The initial survey, performed for a cDNA panel containing samples from eight different solid tumors revealed significant HAX1 overexpression for stages III-IV of breast and lung cancer. The samples derived from the other six cancers (colon, kidney, ovary, liver, prostate, thyroid) did not show significant changes in HAX1 expression, except for stages I-II of colon cancer.
An extended analysis of specific cDNA panels, containing a larger number of samples from different disease stages, confirmed the presence of statistically significant overexpression in breast and lung cancer and additionally, in melanoma. Detailed statistical analysis of these data has shown that for breast cancer and melanoma HAX1 is significantly overexpressed in subsequent stages, with higher significance for later stages. For breast cancer, a similar relation was observed for tumor size and histological grade, but no relation was detected for other prognostic markers such as nodal status and receptor status (ER, PR and HER2). The number of cases with metastatic disease for breast and lung cancer was not sufficient to calculate a relation between HAX1 overexpression and the presence of distant metastases. In the case of melanoma all tumor samples were derived from cancers with distant metastases, which also excluded the possibility of comparing the expression in primary and metastatic tumors. Detailed examination of the data from the lung cancer panel did not confirm high overexpression status detected previously in the survey panel, but nevertheless, a significant overexpression was observed for the samples from stages I and IV. Therefore, panel analysis provided evidence for the expected HAX1 overexpression in tumors and identified specific tumors in which such overexpression takes place. Our results indicate the relation of HAX1 expression to tumor size, stage and grade of the disease but more detailed analysis is needed to confirm if the observed relationships are in any way connected to a potential role for HAX-1 in metastasis. The lack of relationship between HAX1 expression and nodal status does not support such a hypothesis, but it still needs to be verified on a larger scale.
cDNA panel analysis produced results which are partially consistent with the microarray-generated data deposited in Oncomine (overexpression in lung cancer and melanoma, grade-specific overexpression in breast cancer), but there are also substantial differences (lack of significant overexpression in hepatoma).
To further analyze HAX1 up-regulation in breast cancer, matching pairs of tumor and normal adjacent tissues from 15 breast cancer patients were examined, confirming significant overexpression in tumor tissue. The differential samples under analysis represented several types of tumor (ductal, lobulary, papillary and mixed carcinomas) with different tumor size, nodal and receptor status. The group was too uniform in respect of grade and stage of the disease to confirm the relationship of these factors to HAX1 expression level. The analysis of other prognostic markers demonstrated a significant relation between HAX1 expression level and tumor size, which confirms the results obtained from the cDNA panel. No relation was detected for receptor status, again, confirming the results from the panel. The relationships found for nodal status, progesterone and HER2 status were of borderline significance and since they were not confirmed by the panel data, their reliability is doubtful. In general, data from matched-pair analysis are largely consistent with the data obtained from the cDNA breast cancer panel. The discrepancies are minor and can be explained by the small number of cases in the matched-pairs analysis.
Matched pairs of tumor and normal tissues were also used to determine the variations of HAX1 splicing pattern in breast cancer samples. Detailed quantitative analysis was possible only for splice variants I and II, because the expression of the other variants is barely detectable, and is therefore likely to produce ambiguous quantitative results. All five variants were however analyzed by standard RT-PCR. The results revealed that HAX1 splicing pattern in breast cancer is indeed slightly, but recurrently different than in normal tissues. Variant I expression remains high in normal and tumor tissues, compared to the expression of the other variants, but variant II levels are reproducibly higher in tumors (Fig (Fig5),5), pointing to its specific up-regulation. The most marked difference in the splicing pattern was detected for splice variant III; its expression in normal samples could not be detected by standard RT-PCR, probably due to combined effects of its very low expression level and a relatively small amount of the obtained cDNA, but in more than a half of the samples a clear PCR product was detected in tumor samples (Fig (Fig4).4). These results suggest that variant III expression could be tumor-specific. Up-regulation of the HAX1 alternative splice variants in cancer indicates their specific role, but cannot be explained until specific functions would be attributed to the different splice variants and their corresponding putative protein products.
HAX-1 overexpression in breast cancer samples was confirmed at the protein level by immunohistochemistry. Although the reaction is not standardized (as in the case of known markers), the expression was clearly up-regulated in almost all tumor tissue sections analyzed (Table (Table4).4). Overexpression was detected, as expected, in the cytoplasm, but also in the nuclei of tumor cells, which is inconsistent with previous findings, associating HAX-1 with cytoplasmic structures (ER and lammelipodia, ; ER and mitochondria, [1,15]; mitochondria, [7,9]. Suzuki et al.,  observed HAX-1 at the nuclear envelope, but this location was never confirmed in subsequent reports. Location of Hax-1 in the nuclear matrix was previously detected in normal rat testis . Nuclear localization of HAX-1 has also been observed in systemic sclerosis fibroblasts . The latter represents so far the only report suggesting that this localization might be disease-dependent. Results presented here implicate, that the nuclear localization of HAX-1 might be also associated with some types of cancer.
HAX-1 overexpression detected in breast cancer, where estrogen receptor status is an obvious prognostic factor, combined with some literature data indicating possible induction of HAX1 by estrogen [11,12] provided reasons to ascertain the influence of the estrogen treatment on HAX1 expression. The results show clearly that, in spite of previous predictions, HAX1 mRNA expression level is estrogen-independent. This finding is in agreement with the lack of a relation between HAX1 expression levels and ER status in breast cancer samples. However, estrogen may regulate HAX-1 activity in some other, non-genomic way. The observed relation between nuclear localization of HAX-1 and estrogen receptor up-regulation suggests that estrogen may influence HAX-1 cellular localization. It has been observed  that HAX-1-interacting protein, prohibitin, is translocated to the nucleus upon estrogen treatment, and acts as a repressor of ER activity. It remains to be established if nuclear translocation of HAX-1 is also directly associated with estrogen activity, but the observed correlation points to this conclusion. There must be, however, some other factors affecting HAX-1 localization, since HAX-1-GFP-transfected MCF-7 breast cancer cells show nuclear localization of this fusion in about 21% of the analyzed cells (Additional Files 1 and 2), while estrogen treatment enhances nuclear localization only slightly, to about 26% (data not shown).
This report provides evidence for HAX-1 up-regulation in several types of solid tumors, confirming previous estimations based on its anti-apoptotic activity, overexpression in cancer cell lines and scattered high-throughput data. These preliminary results call for a more detailed analysis to establish HAX-1 relation with tumorigenesis and a highly probable association with metastasis, along with clarification of the molecular mechanisms behind HAX-1 cellular functions.
3'UTR: 3' untranslated region; ACTB: beta-actin gene; ANT2: adenine nucleotide translocator 2; Arp2/3: actin-related protein 2/3; CTSD: cathepsin D gene; ERα: estrogen receptor alpha; GAPDH: glyceraldehyde-3-phosphate dehydrogenase gene; HS1: hematopoietic lineage cell specific protein 1; IHC: immunohistochemistry; Omi/HtrA2: Omi/high temperature requirement protein A2; Parl: presenilin associated rhomboid-like; qPCR: quantitative polymerase chain reaction; Rac: Ras-related small GTP-binding protein; RT-PCR: reverse transcription polymerase chain reaction; SAGE: serial analysis of gene expression; VDAC: voltage dependent anion channel.
The authors declare that they have no competing interests.
AT carried out the molecular genetic studies and participated in statistical analysis and drafting the manuscript, AR carried out the immunoassays, KC participated in molecular studies, KP carried out tissue sample selection and classification for immunohistochemistry, SR participated in immunoassays, sample collection and management, JK and JS participated in coordination of the study and helped to draft the manuscript, EG conceived of the study, participated in its design and coordination, carried out statistical analysis and drafted the manuscript. All authors read and approved the final manuscript.
The pre-publication history for this paper can be accessed here:
HAX1 nuclear localization detected by immunofluorescence. Methods and Results sections for detecting HAX-1-GFP fusion protein in transfected MCF-7 breast cancer cell line. Nuclear localization of the fusion protein was detected in about 21% of the cells.
We thank Antek Łączkowski for assistance in statistical analysis, Elżbieta Brewczyńska for assistance in patients' classification and Ania Wilczyńska for helpful comments. This work was supported by Polish Ministry of Science and Higher Education research grant N301004 32/0437.