Abstract

Introduction

Human esophageal carcinoma, one of the most common causes of cancer death worldwide, occurs at a very high frequency in China [1,2]. Esophageal carcinomas often have poor prognosis due to early lymph node metastasis and invasion of neighboring organs such as the aorta, trachea, bronchus, pericardium and lung [2]. Therefore, disrupting the aggressive metastatic phenotype is essential for developing an effective treatment for esophageal cancer. Although several molecules have been reported to contribute to the ability of esophageal carcinoma cells to metastasize and invade normal tissue, such as N-cadherin [3], TSLC1 [4] and MTA1 [5], the underlying mechanism remains obscure. Considering the complexity of tumor invasion and metastasis, various experimental approaches have been developed to systematically identify genes that are involved in the process. By directly comparing the differentially expressed genes between liver metastatic and primary tumor tissues, POSTN, encoding the periostin protein, was identified as a gene associated with colon cancer and liver metastasis [6]. Cancer metastasis is thought to originate from a small proportion of cancerous cells in primary tumors. Therefore, screening for a subpopulation of cells with high metastatic potential from a parent tumor cell line in experimental models is a well-defined method for discovering genes that play roles in metastasis, especially that which preferentially occurs in specific organs. For example, microarray analysis of sublines of the MDA-MB-231 cell line with high lung or bone metastatic selection in nude mice led to identification of a set of genes that mark or mediates breast cancer metastasis in these tissues [7-9].

In order to derive a subpopulation of cells with high metastatic potential from tumor cell lines, we have established a model system to inspect genes involved in different steps of metastasis including invasion, survival and arrest. We screened for and selected an esophageal tumor cell subline with high invasive potential and analyzed genes which may correspond to this phenotype by gene microarray. Through this analysis, we identified sphingosine kinase 1 (SPHK1) as one such gene that participates in esophageal carcinoma invasion and metastasis.

SPHK1 is a conserved lipid kinase that catalyzes formation of important regulators of inter- and intracellular signaling. It is a ubiquitously expressed, evolutionary conserved enzyme that catalyzes phosphorylation of sphingosine (Sph) and dihydrosphingosine (dhSph) to sphingosine 1-phosphate (S1P) and dhS1P, respectively. SPHK1 is transiently activated in response to a large variety of agonists and has been shown to contribute to signaling cascades elicited by TNF-α [10], VEGF and 17β-estradiol [11]. Accordingly, SPHK1 can mediate biological effects of TNF-α such as induction of COX2 and generation of PGE2 in fibroblastic cells and MCP-1 in endothelial cells [12].

Of interest is that SPHK1 mRNA is frequently overexpressed in a variety of solid tumors, suggesting an important role for its encoded enzyme during tumorigenesis. Overexpression of SPHK1 is thought to be oncogenic and renders transfected cells chemoresistant. Bonhoure et al. [13] reported that targeting SPHK1 overcomes the multi-drug- resistant gene (MDR)-associated chemoresistance of HL60 cells. The oncogenic properties of SPHK1 have been demonstrated both in vitro and in vivo in experimental models based on its overexpression in NIH3T3 cells [14]. Overexpression of SPHK1 facilitates anchorage-independent growth in vitro and leads to tumor formation in SCID mice. Furthermore, more recent studies have demonstrated that phosphorylation of SPHK1 and subsequent membrane translocation are required for its pro-oncogenic function. Overexpression of SPHK1 up-regulates MMP1 mRNA and promoter activity as well as its protein levels, and this action by SPHK1 requires activation of the ERK1/2-Ets1 and NF-kB pathways [12]. In addition, high levels of the SPHK1 enzyme and its downstream product, S1P, correlate with poor survival of glioblastoma patients [15,16], and this unusual enhancement of neural cell invasion requires upregulation of the matricellular protein CCN1/Cyr61. These data suggest that enhanced SPHK1 activity in glioblastoma may drive the invasive potential of these cells.

Few studies by other investigators have specifically analyzed the effect of SPHK1 on invasiveness of cancer cells. Our report is the first to implicate the involvement of SPHK1 in the metastasis of esophageal cancer. We observed the overexpression of SPHK1 transcripts in esophageal carcinoma and identified downstream mediators that may mediate enhanced malignant behavior in these tumor cells. As several of these mediators may be useful as therapeutic targets of esophageal carcinoma, our findings will have implications for cancer drug development.

Materials and methods

Results

SPHK1 is overexpressed in the EC9706-P4 subline with high invasive capacity

To establish an esophageal carcinoma invasion model, EC9706 cells were seeded onto Matrigel-coated transwells. The cells were allowed to invade into the lower chamber of the transwell, collected, expanded and then re-seeded onto another Matrigel-coated transwell. Cells were harvested after four rounds of selection, resulting in the establishment of a relatively stable, highly invasive subline, EC9706-P4. The invasive ability of this line was about 15-fold greater than that of the parent cell line, EC9706, in matrigel invasion tests, but equal to that of the third selection round line, EC9706-P3 (Figure ​(Figure1A),1A), suggesting that the metastatic potential of the sublines reached a plateau by the fourth round of selection. Thus, by Matrigel invasive subpopulation selection, we were able to establish the highly invasive and metastatic esophageal carcinoma cell line EC9706-P4.

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Figure 1

Overexpression of SPHK1 in the esophageal carcinoma EC9706-P4 subline with high invasive capacity. EC9706 cells were seeded onto Matrigel-coated transwells and allowed to invade into the lower chamber of the transwell, collected, expanded and then re-seeded onto another Matrigel-coated transwell. After four rounds of selection, the relatively stable, highly invasive subline, EC9706-P4, was established. (A) Transwell invasion analysis showed the invasive ability of EC9706-P4 was about 15-fold greater than the parent cell line EC9706 (P < 0.05) (B) The differential gene expression profiles of EC9706 and EC9706-P4 were analyzed by microarray, and expression of some genes were confirmed by QRT-PCR. Most of the dysregulated genes were previously associated with tumor invasion and metastasis. Notably, SPHK1 expression gradually increased through each round of selection from EC9706 to EC9706-P4.

The gene expression profiles of EC9706 and EC9706-P4 were then analyzed by microarrays. Between these cell lines, 124 genes were differentially expressed, including 71 upregulated genes and 53 downregulated genes in EC9706-P4 relative to EC9706 (cutoff, fold ≥ 2.0, Additional file 1). Most of the dysregulated genes have been previously shown to be involved in tumor invasion and metastasis, such as TFPI-2 [17], LOXL2 [22-24], ADAM12m [25,26], IGFBP1 [27,28], integrin α6[29,30], CD44 [31]and CYR61 [32]. Expression of some of these genes were subsequently tested by QRT-PCR (Figure ​(Figure1B).1B). One of these genes, SPHK1, was of particular interest to our study. Trojanowska et al. showed that overexpression of SPHK1 up-regulated MMP1 mRNA and promoter activity as well as its protein levels [12], and the MMP1 gene is known to play a very important role in the invasion of esophageal cancer. We found by QRT-PCR analysis that SPHK1 expression gradually increased with each round of selection from the EC9706 parent cells to the highly invasive EC9706-P4 subline (Figure ​(Figure1B1B).

SPHK1 is upregulated in esophageal carcinoma and correlates with invasion and clinical outcome

SPHK1 expression was analyzed by RT-PCR and immunofluorecence in esophageal carcinoma cell lines, including KYSE30, KYSE150, KYSE510, KYSE2, EC9706, and NEC cells (Figure ​(Figure2A).2A). In these cell lines, SPHK1 was detected by PCR after 35 cycles (Figure ​(Figure2B).2B). KYSE2 and KYSE30 cells showed the highest SPHK1 expression at both the mRNA and protein levels, and they were also the most invasive lines among the six cell lines tested (Figure ​(Figure2C).2C). To assess SPHK1 protein expression in esophageal carcinoma tissues, 12 paired samples, each consisting of esophageal carcinoma tissue and normal esophageal tissue from the same patient, were analyzed by Western blotting. SPHK1 protein was found to be overexpressed in seven of the twelve (58%) esophageal carcinoma tissues; that is, SPHK1 expression was higher in the tumor tissue than in the companion normal tissue (Figure ​(Figure3A).3A). We then extended this analysis by performing immunohistochemistry (IHC) on 30 pairs of esophageal-carcinoma and normal tissues. In 23 cases (76%), SPHK1 expression appeared to be upregulated in the tumors when compared to the companion normal tissue with the following immunostaining scores: normal: 0.93 ± 0.173; tumor: 2.06 ± 0.46, P < 0.01 (Figure ​(Figure3B).3B). We then evaluated the expression of SPHK1 protein in an esophageal carcinoma tissue microarray (n = 274 tissue microarray elements from 124 cases of esophageal squamous carcinoma) (Figure ​(Figure3C).3C). The expression rates of SPHK1 in cases from tussue microarrays is that 18/124 (14.5%) cases with no SPHK1 expression, 17/124(13.7%) cases with SPHK1 expression score 1, 32/124(25.8%) cases with SPHK1 expression score 2 and 57/124(46.0%) cases with SPHK1 score 3. Statistical analysis indicated that in the esophageal carcinoma, the SPHK1 expression correlated with the depth of tumor invasion (P < 0.0001) and lymph node metastasis (P = 0.016) (Table ​(Table1).1). There was no significant association with age, sex and tumor differentiation.

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Figure 2

Correlation of SPHK1 expression with invasiveness of esophageal carcinoma cell lines. (A, B) SPHK1 expression was analyzed by RT-PCR and immunofluorecence in the esophageal carcinoma cell lines: KYSE30, KYSE150, KYSE510, KYSE2, EC9706 and NEC. (B) In these cell lines, SPHK1 was detected by PCR after 35 cycles. (C) Invasion assays were carried out by seeding 1 × 10⁴ cells in a 24-well transwell unit on polycarbonate filter with 8-μm pores coated with Matrigel. After a 24-h incubation period, the cells that had passed through the filter into the lower wells were stained, counted and photographed. All experiments were performed in triplicate and repeated twice. KYSE2 and KYSE30 cells showed the highest SPHK1 expression at the mRNA and protein levels, and they were also the most invasive among the six cell lines.

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Figure 3

Upregulation of SPHK1 in esophageal carcinoma and correlation with clinical outcome. SPHK1 protein expression was assessed in esophageal carcinoma tissues. (A) Twelve sample pairs, each consisting of esophageal carcinoma tissue and normal esophageal tissue from the same patient, were analyzed by Western blotting. SPHK1 was overexpressed in seven of twelve esophageal carcinoma tissues (58%) compared to the companion normal tissue. (B) The expression SPHK1 in 30 pairs of esophageal-carcinoma and normal tissues were also analyzed by IHC. In 23 of 30 cases (76%), SPHK1 expression appeared to be upregulated in the tumors when compared to the companion normal tissue with the following immunostaining scores: normal: 0.93 ± 0.173; tumor: 2.06 ± 0.46, P < 0.01. (C-D) SPHK1 protein expression in an esophageal carcinoma tissue microarray (n = 274 tissue microarray elements from 124 cases of esophageal squamous carcinoma). By Kaplan-Meier analysis, strong SPHK1 expression (staining intensity equal to, or greater than, 2) was significantly associated with clinical failure, whereas the weak SPHK1staining (staining intensity less than 2) was found in individuals with delayed clinical failure, P < 0.01.

Table 1

SPHK1 correlated with depth of tumor invasion and lymph node metastasis in esophageal carcinoma

Variables	Score of SPHK1 expression				P value
	0	1	2	3
Age, year					0.374
Mean	61.7	61.2	63.2	60.1
SD	11.0	12.8	11.9	14.3
Gender					0.494
Male	7	11	15	26
Female	11	6	17	31
pT (primary tumor)					< 0.0001*
pT0	0	5	4	0
pT1	1	2	6	6
pT2	6	4	10	11
pT3	11	6	12	40
pN(lymphnode metastasis)					0.016*
pN0	14	10	16	17
pN1	4	7	16	40
Differentiation					0. 737
high	4	15	9	19
moderate	6	2	12	21
low	8	0	11	17

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Expression of SPHK1 protein was analyzed in 124 cases of esophageal squamous carcinoma. After staining, slides were evaluated by two pathologists. SPHK1 expression was determined by scoring intensity and percentage of cell staining. Tissues with no staining were rated as 0; those with faint staining or moderate to strong staining in < 25% of cells as 1; with moderate staining or strong staining in 25-50% of cells as 2; and with strong staining in > 50% of cells as 3. Statistical analysis indicated that in the esophageal carcinoma, SPHK1 expression was correlated with depth of tumor invasion (P < 0.0001) and lymph node metastasis (P = 0.016). There was no significant association with age, sex or tumor differentiation.

We therefore examined whether expression of the SPHK1 protein could be used to predict clinical outcome in esophageal carcinoma patients with available survival information. By Kaplan-Meier analysis, strong SPHK1 expression (staining intensity ≥ 2) was significantly associated with clinical failure, whereas the weak SPHK1 staining (staining intensity less than 2) was found in individuals with delayed clinical failure (P < 0.01) (Figure ​(Figure3D).3D). These findings further suggest that SPHK1 overexpression is significantly associated with aggressive human esophageal carcinoma.

SPHK1 upregulates esophageal carcinoma invasive and spontaneous metastasis potential

We next assessed the impact of transfection-mediated SPHK1 gene upregulation in EC9706 cells. Several SPHK1 stable transfected clones were screened and two of them, SPHK1-C17 and SPHK1-C24, had markedly upregulated expression of SPHK1 in EC970 cells (Figure ​(Figure4A).4A). In the transwell invasion assay, upregulation of SPHK1 significantly increased the invasiveness of EC9706 cells (Figure ​(Figure4B).4B). In the 3D Matrigel culture assays, SPHK1 overexpression significantly increased the diameter and the invasive morphology (Figure ​(Figure4C)4C) as well as the proliferation (Figure 4D, F) of the EC9706 cell clones, but did not influence their apoptosis levels in an Annexin V assay (Figure 4E, F). We also examined whether SPHK1 could increase EC9706 cell growth and spontaneous metastasis in nude mice. The SPHK1-C17 and SPHK1-C24 stable overexpressing clones were tested in animal experiments and showed that the SPHK1 gene promoted tumor growth and tumor burden in nude mice. SPHK1 significantly promoted growth of EC9706 xenografts (SPHK1-C17: 2.62 ± 1.12 cm³; SPHK1-C24: 2.78 ± 1.14 cm³) compared to transfected control (EC9706: 1.42 ± 0.854 cm³) or control EC9706 cells (EC9706-Ve: 1.35 ± 0.432 cm³, ANOVA P < 0.01 Figure 5B, D). Expression of SPHK1 increased weight of tumors (SPHK1-C17: 2.42 ± 0.654 g; SPHK1-C24: 1.82 ± 0.542 g) compared to transfected control (EC9706: 1.12 ± 0.454 g) or control EC9706 cells (EC9706-Ve: 1.03 ± 0.434 g, ANOVA P < 0.01 Figure 5C, D). We also observed that SPHK1 upregulation dramatically increased spontaneous lung metastasis of EC9706 cells (SPHK1-C17:7.42 ± 3.43 cm³; SPHK1-C24: 4.21 ± 1.34 cm³) compared to transfected control (EC9706: 1.34 ± 0.65 cm³) or control EC9706 cells (EC9706-Ve: 0.63 ± 0.064 cm³, ANOVA P < 0.05 Figure 5A, D). These studies support the view that SPHK1 expression is vital for the maintenance of invasive and metastatic potential of esophageal carcinoma cells.

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Figure 4

SPHK1 overexpression increased invasive potential of esophageal carcinoma cells. We assessed the impact of gene transfection-mediated SPHK1 upregulation in EC9706 cells. (A) The two stable expression clones SPHK1-C17 and SPHK1-C24 both had markedly upregulated SPHK1 expression in EC970 cells. (B) In the transwell invasion assay, SPHK1 overexpression significantly increased the invasion of EC9706 cells. The numbers of invaded cells in the SPHK1 overexpressing cells (SPHK1-C17 group = 162.0 ± 16.52; SPHK1-C24 group = 173.0 ± 14.73) were higher compared with that of the vector group (37.33 ± 15.57), EC-9706 group (36.33 ± 4.933) and SPHK1-C7 group (31.33 ± 3.786); ANOVA P < 0.0001. (C) In 3D Matrigel culture assays, SPHK1 overexpression significantly increased the diameter and the invasive morphology of EC9706 cell clones. (D, F) SPHK1 overexpression significantly increased the proliferation of EC9706 cells. The OD450 values of the SPHK1-C17 group (3.664 ± 0.792) and SPHK1-C24 group (3.987 ± 0.632) were higher than that of the vector group (1.432 ± 0.453) and EC-9706 group (2.132 ± 0.334), ANOVA P < 0.031. (E, F) Annexin V assay showed overexpression of the SPHK1 gene did not influence the apoptosis level of EC9706 cells. The percentages of apoptotic cells in the SPHK1-C17 group (10.2 ± 0.2) and SPHK1-C24 group (7.3 ± 0.5) were comparable to that of the vector group (9.4 ± 3.2) and EC9706 group (7.3 ± 4.3), ANOVA P = 0.874.

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Figure 5

SPHK1 overexpression increased esophageal carcinoma spontaneous metastasis potential. SPHK1 overexpression increased EC9706 cell growth and spontaneous metastasis in nude mice. Several stable transfected clones were screened and two of them, (A) SPHK1-C17 and SPHK1-C24 were tested in animal experiments. (B, C) The SPHK1 gene promoted tumor growth and tumor burden in nude mice. SPHK1 significantly promoted growth of EC9706 xenografts (SPHK1-C17: 2.62 ± 1.12 cm³; SPHK1-C24: 2.78 ± 1.14 cm³) compared to transfected control (EC9706: 1.42 ± 0.854 cm³) or control EC9706 cells (EC9706-Ve: 1.35 ± 0.432 cm³, ANOVA P < 0.01, B and D). Expression of SPHK1 increased weight of tumors (SPHK1-C17: 2.42 ± 0.654 g; SPHK1-C24: 1.82 ± 0.542 g) compared to transfected control (EC9706: 1.12 ± 0.454 g) or control EC9706 cells (EC9706-Ve: 1.03 ± 0.434 g, ANOVA P < 0.01, C and D). We also observed that SPHK1 upregulation dramatically increased spontaneous lung metastasis of EC9706 cells (SPHK1-C17:7.42 ± 3.43 cm³; SPHK1-C24: 4.21 ± 1.34 cm³) compared to transfected control (EC9706: 1.34 ± 0.65 cm³) or control EC9706 cells (EC9706-Ve: 0.63 ± 0.064 cm³, ANOVA P < 0.05, A and D).

SPHK1 promotes metastasis via activation of the EGFR pathway

To glean mechanistic insight into the role of SPHK1 in invasion and metastasis, we surveyed potential links between this enzyme and key molecules of known relevance to invasion. Western blot analysis indicated that the expression of SPHK1 significantly correlated with the phosphorylation of EGFR, while knockdown of SPHK1 by RNAi decreased EGFR phosphorylation in EC9706-P4 and KYSE2 cells (Figure 6A, B). From the microarray analysis, we clustered the genes upregulated in the SPHK1 overexpression clones compared with control cells (Figure ​(Figure6C).6C). Expression of SPHK1 was significantly correlated with that of genes such as IL6, ITGA2, IL8, EREG, MMP1, ITGA5, MMP3 and AREG. Most of these genes are the downstream genes of the EGFR pathway, and most of them such as EREG [33,34], MMP1 [35] and AREG [33,34] have been reported to be associated with the invasion of cancer cells. Western blotting indicated that the ligands of EGFR, EGF, EREG and AREGinduced the expression of the SPHK1 protein (Figure ​(Figure6D6D).

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Figure 6

SPHK1 promoted metastasis via activation of the EGFR pathway. To glean mechanistic insight into the role of SPHK1 in invasion and metastasis, we surveyed potential links between SPHK1 and key molecules of known relevance to invasion. (A) Western blotting indicated that the expression of SPHK1 was significantly correlated with the phosphorylation of EGFR. (B) Correspondingly, SPHK1 RNAi decreased the phosphorylation of EGFR in EC9706-P4 and KYSE2 cells. (C) We clustered the upregulated genes in the SPHK1 overexpression clones compared with control cells. Expression of SPHK1 was significantly correlated with the expressions of IL6, ITGA2, IL8, EREG, MMP1, ITGA5, MMP3 and AREG. Most of the genes are the downstream genes of EGFR pathway, and most of them have been associated with the invasion of cancer cells. (D) Western blotting indicated that the ligands of EGFR (EGF, EREG, and AREG) induced the expression of SPHK1 protein.

Discussion

Metastasis is a multi-factorial process, including tumor cells capable of escaping their normal microenvironment, traversing into and out of lymphatic or blood vessels and proliferating in new ''soil'' [36]. Implicit in these stages, invasion is the critical ability for tumor cells to metastasize [36]. During invasion, malignant cells reside on or within two major types of extracellular matrices, the basement membrane and the stromal matrix [37]. The basement membrane is one of the most important barriers against cancer cell invasion [37]. Therefore, for this study, we used Matrigel, a solubilized basement membrane preparation from the Engelbreth-Holm-Swarm (EHS) mouse sarcoma, as a model basement matrix to mimic esophageal carcinoma invasion in vivo. Although EC9706, an esophageal squamous carcinoma cell line, can invade and form spontaneous lung metastasis nodules in nu/nu mice, its metastatic potential is relatively low [38]. The metastatic ability of EC9706 may arise from a few subclones with high metastatic potential among the parental cells. By screening with our in vitro model, the subline EC9706-P4 with high invasion potential was established. This subline also exhibited high spontaneous metastatic potential in vivo. Microarray analysis was used to determine which genes may be involved in invasion and metastasis. However, the microarray analysis of esophageal cancer tissues demonstrated that SPHK1 was significantly overexpressed in these tumor tissues, and that this expression significantly correlated with tumor invasion, lymph node metastasis and clinical stage, indicating that SPHK1 is involved in esophageal carcinoma invasion and metastasis. SPHK1 is up-regulated in many types of cancers and has been suggested as a potentially new therapeutic target. However, it is not yet known what signals the cancer cells use to apparently constitutively up-regulate expression of this enzyme, nor is it clear why it has such a profound role in tumorigenesis. A recent study examined the role of SPHK1 in intestinal tumorigenesis in the Min mouse in which intestinal adenomas develop spontaneously [39]. Deletion of the SPHK1 gene in these mice resulted in reduction of adenoma size. Concomitantly, epithelial cell proliferation in the polyps was attenuated, suggesting that SPHK1 regulates adenoma progression [39].

Exogenous expression of SPHK1 in vitro and in vivo further showed that it is a key factor in esophageal carcinoma cell invasion. In the transwell invasion assay, upregulation of SPHK1 expression significantly increased the invasion of EC9706 cells. Furthermore, upregulation of SPHK1 expression significantly increased the proliferation of EC9706 cells in vitro as well as increased EC9706 cell growth and spontaneous metastasis in nude mice. These studies support the view that SPHK1 expression is vital for the maintenance of invasive and metastatic potential of esophageal carcinoma cells. Interestingly, neutralizing S1P, the product of SPHK1 enzymatic activity, with a specific monoclonal antibody was remarkably effective in slowing progression of cancers, such as lung [40], colon [41], breast [42,43], melanoma [44] and ovarian cancers [21,45] in murine xenograft and allograft models [46]. A critical question raised by these observations is how neutralization of this simple lysophospholipid can have such dramatic effects on tumor progression.

To glean mechanistic insight into the role of SPHK1 in invasion and metastasis, we surveyed potential links between SPHK1 and key molecules related to EGFR. Western blot analysis indicated that the expression of SPHK1 was significantly correlated with the phosphorylation of EGFR. In clustering the upregulated genes in the SPHK1 overexpression clones compared with control cells, SPHK1 expression was significantly correlated with that of IL6, ITGA2, IL8, EREG, MMP1, ITGA5, MMP3 and AREG. Western blotting indicated that the ligands of EGFR, EGF, EREG and AREG induced the expression of SPHK1 protein. These findings provide evidence for cross-talk between SPHK1 and the EGFR pathway and reveal a key role for SPHK1 in integrating events downstream of EGF receptors. An intriguing possibility is that many growth and angiogenic factors such as EGF and AREG involved in tumorigenesis may act through SPHK1 activation [47]. Because both EGF and AREG have been implicated in progression of esophageal cancer, it was of interest to examine the involvement of SPHK1. There are numerous reports of rapid and transient activation of SPHK1 by growth and angiogenic factors [48,49]) that stimulate its phosphorylation at Ser225 [50] and subsequent translocation to the plasma membrane [51] where its substrate sphingosine resides, resulting in local formation of S1P [52]. Some cross-talk models between EGFR and SPHK1/S1P have been proposed previously, Estrada-Bernal, A et al[53] have reported that treatment of glioma cell lines with EGF led to increased expression and activity of SphK1. Expression of EGFRvIII in glioma cells also activated and induced SphK1. In addition, siRNA to SphK1 partially inhibited EGFRvIII-induced growth and survival of glioma cells as well as ERK MAP kinase activation. SphK1 activity is necessary for survival of GBM-derived neurosphere cells, and EGFRvIII partially utilizes SphK1 to further enhance cell proliferation. Shida, D. et al [54]reported that LPA markedly enhanced SphK1 mRNA and protein in gastric cancer MKN1 cells, DLD1 colon cancer cells and MDA-MB-231 breast cancer cells. LPA transactivated the epidermal growth factor receptor (EGFR) in these cells, and the EGFR inhibitor AG1478 attenuated the increased SphK1 and S1P(3) expression induced by LPA. Their research finally showed that SphK1 is a convergence point of multiple cell surface receptors for three different ligands, LPA, EGF, and S1P, which have all been implicated in regulation of motility and invasiveness of cancer cells. In breast cancer, Sukocheva, O et al [55]demonstrated that E2-induced EGFR transactivation in human breast cancer cells is driven via a novel signaling system controlled by the lipid kinase sphingosine kinase-1 (SphK1). E2 stimulates SphK1 activation and the release of sphingosine 1-phosphate (S1P), by which E2 is capable of activating the S1P receptor Edg-3, resulting in the EGFR transactivation in a matrix metalloprotease-dependent manner. These findings reveal a key role for SphK1 in the coupling of the signals between three membrane-spanning events induced by E2, S1P, and EGF. However, it is still difficult to understand how such short-lived activation can be responsible for the profound involvement of SPHK1 in tumorigenicity or how this relates to its up-regulation in cancer. Our results imply that SPHK1 may be the central controller of amplification loops of EGF, AREG and EREG-EGFR interactions that can contribute to cancer progression.

Conclusions

We have established an esophageal carcinoma invasion model and generated a highly invasive tumor cell subline in which SPHK1 was overexpressed. Further investigation revealed SPHK1 was significantly correlated with esophageal cancer invasion and metastasis and may be a valuable prognostic marker. Our studies have demonstrated that SPHK1 is involved in upregulation of EREG and AREG through enhancing EGFR phosphorylation to promote invasion. Thus, modulating SPHK1 expression or activity is an attractive additional therapeutic strategy for treatment of esophageal cancer and perhaps other cancers as well. Implementation of pre-clinical and clinical evaluation of SPHK1 as a novel molecular target for cancer therapy is warranted.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

PJ and NJ designed the study and wrote the manuscript, FX and ZWL participated in data analysis, PJ, WJ, ZYL and TYF finished the most experiment, HSY and WSY performed flow cytometry analysis. CBR and LZ collected the samples and made great contribution in making the tissue microarray. All authors read and approved the final manuscript.

Authors' information

Pan Jian, Ph.D. Immunology. Graduated from State Key Laboratory of Molecular Oncology, Cancer Institute (Hospital), Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, PR China. Now is an associate professor of Department of Hematology and Oncology, Children's Hospital of Soochow University, Suzhou, China, and a gust professor of Translational Research Center, Second Hospital, The Second Clinical School, Nanjing Medical University, Nanjing, China.

Supplementary Material

References