Maintenance of stemness is associated with the interation of LRP6 and heparin-binding protein CCN2 autocrined by hepatocellular carcinoma

The overall response rate of hepatocellular carcinoma (HCC) to chemotherapy is poor. In our previous study, oxaliplatin-resistant HCC is found to exhibit an enhanced stemness, and increased levels of CCN2 and LRP6, while the role of CCN2 and LRP6 in the prognosis of HCC patients, and the interaction regulation mechanism between CCN2 and LRP6 are still unclear. The expression levels of CCN2 and LRP6 were detected in large cohorts of HCCs, and functional analyses of CCN2 and LRP6 were performed both in vitro and in vivo. The roles of cell surface heparin sulfate proteoglycans (HSPGs) in the mutual regulatory between CCN2 and LRP6 were verified in HCC, and the interventions of low molecular weight heparin sodium (LMWH) were explored. CCN2 and LRP6 were overexpressed in HCCs, and the CCN2 and LRP6 levels were positively associated with the malignant phenotypes and poor prognosis of HCCs. LRP6 could significantly upregulate the expression of CCN2. Meanwhile, CCN2 was able to enhance malignant phenotype of HCC cells in a dose-dependent manner through binding with LRP6; and knock-down of LRP6 expression, perturbation of HSPGs, co-incubation of CCN2 with LMWH could significantly block the adhesion of CCN2 to LRP6. LMWH enhanced the therapeutic effect of oxaliplatin on HCC with a high CCN2 expression. CCN2 plays a promoting role in HCC progression through activating LRP6 in a HSPGs-dependent manner. Heparin in combination with chemotherapy has a synergic effect and could be a treatment choice for HCCs with a high CCN2 expression.

of stem cells [3][4][5][6]. The cells with a more malignant potential contribute to the "stemness", including maintenance of quiescence, sphere formation, high tumorigenicity, and resistance to hypoxia and chemoradiation [7]. Wnt signaling is one of the key pathways in regulating the cancer cell stemness [8]. Low-density lipoprotein receptor-related protein-6 (LRP6), which is a coreceptor in Wnt signaling, forms a signaling complex with Wnt ligand to activate downstream signaling. In HCC, aberrant expression and phosphorylation of cell surface LRP6 contributes to the activation of Wnt/β-catenin signaling pathway and play an important role in the hepatocarcinogenesis [9]. However, the role of LRP6 in the progression and prognosis of HCC patients is still unclear.
The CCN family is a small, six-member family of cysteine-rich regulatory proteins in humans, which share a multimodular structure with an N-terminal secretory signal domain followed by four conserved functional domains [10]. Therefore, CCN proteins not only behave like traditional growth factors or cytokines since it does not just appear to have a unique receptor to which it binds with high affinity to induce signal transduction. In the earlier years, several studies had described the role of CCN2 in proliferation, chemotaxis, adhesion, migration, and cell fate in different cell types and tissues [11][12][13][14]. By cDNA microarrays, we also found oxaliplatin-pretreated hepatocellular carcinoma exhibited the enhanced stemness and increased expression of CCN2 and LRP6 [15]. It was reported that LRP6 was one of the HSPGs-dependent adhesion receptors for CCN2, and co-incubation of CCN2 and heparin or perturbation of cell surface heparan sulfate proteoglycans (HSPGs) with heparinase completely blocked the adhesion of hepatic stellate cells to CCN2 [16]. Segarini also proved cells deficient for the receptor LRP6 were partly affected to bind with CCN2, with the notion that a principal function of CCN2 is to modulate receptor/ligand interactions [17]. In the field of cancer research, especially for HCC, the negative role of CCN2 and the interaction regulation mechanism between CCN2 and LRP6 are still unclear.
We hypothesize that LRP6 is positively regulated by CCN2, and is essential for the activation of the Wnt/βcatenin pathway directed by binding to the Wnt coreceptor LRP6 on HCC in a HSPGs-dependent manner, which is associated with enhanced stemness and poor prognosis in HCC. The study described herein demonstrated that malignant phenotype and poor prognosis were positively related to LRP6 and CCN2 in human HCC. And then, overexpression of LRP6 and CCN2 together was proved a major contributor to the enhanced stemness phenotype of HCC, and LRP6 could upregulated the expression of CCN2. Finally, this study showed that the mechanism of co-adhesion between LRP6 and CCN2 is dependent on cell surface HSPGs, highlighting the potential for heparin to be explored further as a therapeutic candidate for combination therapy in a subgroup of HCC patients with high expression of CCN2.

Results
CCN2 and LRP6 are up-regulated in human HCC and invasive HCC cell Lines To determine the role of CCN2 and LRP6 in HCCs, we first detected the mRNA expression levels of CCN2 and LRP6 in 96-paired HCC and adjacent non-tumor liver tissues. As compared with non-tumor liver tissues, upregulation of CCN2 and LRP6 was observed in 68.75% (66/96) and 76.04% (73/96) HCC samples, respectively (Fig. 1a). Similar results in their proteins levels were found by Western blot in randomly selected 16 HCC samples (Fig. 1b) and immunohistochemical staining (IHC) in 144 HCC samples (Additional file 1: Figures S1 and S2). In IHC staining, positive staining for CCN2 was observed in cytoplasm, and LRP6 was observed in both cytoplasm and membrane (Fig. 1c). The alterations of CCN2 and LRP6 expression levels were further validated using IHC staining in tissue microarrays (TMA) containing tumor and non-tumor tissues from 374 HCC patients (validation cohorts). Although the CCN2 and LRP6 expression levels exhibited considerable heterogeneity in HCC tissues, the alteration tendency was consistent to the training set ( Fig. 1d; Additional file 1: Figure S3A, B).
Previously, we found the up-regulated expression of CCN2 and LRP6 in oxaliplatin-resistant subcutaneous tumor mice screened by cDNA microarrays [15]. In the present study, increased expression levels of CCN2 and LRP6 were proved in oxaliplatin-resistant HCC cell lines and subcutaneous tumor tissues. [15] (Additional file 1: Figure S4). Increased CCN2 and LRP6 expression levels were also observed in seven HCC cell lines, especially in those with high malignant potential, whereas relatively lower expression levels were detected in liver cells (Fig. 1e).
High expression levels of CCN2 and LRP6 are associated with malignant phenotype and poor prognosis of HCCs To illustrate the clinical relevance of CCN2 and LRP6 expression in HCC, the 374 patients in the validation cohort were dichotomized according to high or low expression of CCN2 and LRP6. High expression of CCN2 was detected in 190 out of 374 HCCs (50.80%), which was significantly correlated with tumor number (p = 0.029), vascular invasion (p = 0.022), and tumor encapsulation (p = 0.034); however, no significant association was found between CCN2 expression level and the other clinical and pathological characteristics. On the other hand, high expression of LRP6 was found in 222 of 374 HCCs (59.35%), which was significantly correlated with vascular invasion (p = 0.016), and tumor encapsulation (p = 0.042); but no significant association was found between LRP6 expression and the other clinicopathological characteristics. (Additional file 2: Table S1).
Univariate analysis revealed that tumor size (p = 0.026; p = 0.019), tumor number (p = 0.010; p = 0.007), and vascular invasion (p = 0.003; p = 0.002), as well as the expression levels of CCN2 (p = 0.001; p = 0.004) and e Relative CCN2 and LRP6 mRNA and protein levels in HCC cell lines and normal liver cell line L-02, and GAPDH was used as a loading control LRP6 (p < 0.001; p < 0.001) were significantly associated with the post-operative OS and CCR of HCC patients. AFP level (p = 0.003) was just associated with the CCR of HCC patients. However, no significantly prognostic significance was found in the other characteristics, including age, gender, HBsAg, HCV background, and liver cirrhosis (Additional file 2: Table S2). The multivariate Cox proportional hazards model revealed that overexpression of CCN2 (p = 0.002; p = 0.018) and LRP6 (p = 0.006; p = 0.014), vascular invasion (p = 0.019; p = 0.041), and tumor size (p = 0.013; p = 0.006) were independent prognostic indicators for OS and CCR of HCC patients; and AFP level (p = 0.039) was independent risk factor for the CCR of HCC patients. However, Fig. 2 Up-regulation of CCN2 and LRP6 correlates with poor prognosis and in HCC patients. a, b, c Kaplan-Meier's curves for OS and TTR according to CCN2 and LRP6 expression in the validation cohort (n = 374). High expression levels of CCN2 and/or LRP6 are associated with poor prognosis of HCCs. d CCN2 and LRP6 expression in tumor with early recurrence (<24 months) and those without (n = 8) no significantly prognostic significance was found with the tumor number (Additional file 2: Table S3).
In 2003, Ye et al. [18] compared the gene expression profiles of 30 HCCs with or without metastasis. We reanalyzed the results and found LRP6 was significantly upregulated in HCC with metastasis (p = 0.0013) (Additional file 1: Figure S5). To further confirm the prognostic value of CCN2 and LRP6 level for HCC, we also analyzed them by immunoblotting in frozen tissue samples from HCC patients with and without early recurrence. Similarly, much higher levels of CCN2 and LRP6 expression were detected in HCC tissues with early recurrence compared with those non-recurrence HCCs (Fig. 2d).
Similarly, to examine the role of LRP6 in HCC, MHCC-97H cells were selected and successfully transfected with specific shRNA to silence LRP6 expression. Among the three LRP6-shRNA tested, LRP6-sh2 was able to induce the knock-down of LRP6 most efficiently.
In addition, the specific LRP6 inhibitor DKK1 was used to examine the role of LRP6 in Wnt activation induced by CCN2. DKK1 treatment significantly inhibited the Wnt signal, and CCN2 couldn't significant reverse the downward trend without any change of p-LRP6, GSK3β, P-GSK3β (Ser9), β-catenin, or SOX2 levels (Fig. 5d). To further clarify the role of LRP6 in Wnt signal activation, the LRP6 knockdown cell MHCC-97H-LRP6-Sh was treated with CCN2 in step-increasing concentrations, but no any significant change in Wnt signaling was observed (Fig. 5e). Expression of CCN2 in HCC is related to malignant phenotypes. a Endogenous CCN2 was silenced in MHCC97H cells using specific vshRNA. CCN2-Sh1 was validated as yielding the most efficient interference of CCN2 by western blot and ELISA. b Expression of LRP6, p-LRP6, E-cadherin, CD90, and ALDH, was determined following downregulation of CCN2 in MHCC97H cells by shRNA CCN2-Sh1 and gene rescue of CCN2. c Invasiveness, migration, adherent colony formation, and the anoikis ability were assessed among MHCC97H-Mock, MHCC97H-shRNA-CCN2 and CCN2 rescued cells. d Subcutaneous tumor growth capacity was determined for xenografts with MHCC97H-CCN2-sh1 cells or MHCC97H-Mock cells in nude mouse models CCN2 Binds with LRP6 in a HSPGs-dependent Manner, and co-incubation of CCN2 with LMWH blocks the binding In the present study, dose-dependent promotion of adhesion was observed in MHCC-97H cells when they were incubated in 96-well plates that had been precoated with 0-3 μg/ml recombinant human CCN2 (Fig. 6a). To determine the potential role of LRP6 on cell surface in CCN2-mediated adhesion, we found that MHCC-97H-LRP6-sh cells exhibited a significant decrease in cell adhesion of compared to untreated MHCC-97H cells (0.43 ± 0.02 vs. 0.52 ± 0.03, p = 0.0012). Adhesion of MHCC-97H cells to CCN2 was significantly blocked after the destruction of HSPGs with heparinase (0.25 ± 0.01 vs. 0.52 ± 0.03, p < 0.001) or inhibition of HSPG sulfation with NaClO 3 (0.25 ± 0.02 vs. 0.52 ± 0.03, p < 0.001) (Fig. 6b). In addition, co-incubation of CCN2  (Fig. 6c).
In addition, to gain more insights on the CCN2-LRP6 interaction, HCC-97H cells were transfected with Flag-CCN2 or empty vector. Co-IP assays showed CCN2 formed a complex with Wnt signal co-receptor LRP6, and this complex could be significantly blocked by LMWH (Fig. 6d).

Discussion
For HCC patients diagnosed at early stages, potentially curative treatments are available, such as radiofrequency ablation, resection, and liver transplantation. While, more than 70% of patients are at an advanced stage when HCC diagnosed, and are not eligible for curative therapy. Therefore, transcatheter hepatic arterial chemoembolization (TACE) and systemic chemotherapy are the most common methods of treatment. Unfortunately, the overall response rate of HCC to such treatments is poor, due in part to the relatively high stemness of these cancer cells [15]. And the reducing of stemness may have the potential to favourably make up for the deficiencies of treatment options and thus benefit the patients. In cancer, Wnt signaling is one of the key signaling pathways related to stemness, which is frequently activated, and plays an important role in hepatocarcinogenesis and malignant progression. Activation of Wnt/β-catenin signaling results in β-catenin translocation into the nucleus, where this factor activates target genes that regulate stemness. LRP6, which is a co-receptor for Wnt ligand and this complex, activates Wnt downstream signaling [19,20]. In 2003, our group collaborated with the United States' National Cancer Institute to compare the gene expression profiles of HCC with or without metastasis, and found LRP6 was significantly upregulated compared with the liver tissue of nonmetastatic HCC [18]. Overexpression of LRP6 in HCCs was also proved in the present study, and which was positively associated with malignant phenotypes and poor prognosis of HCC patients. Then, we found the increased expression of LRP6 in oxaliplatin-resistant hepatocellular carcinoma with enhanced stemness. In HCC cell lines, we also proved enhanced stem-like characteristics of cancer cells were related to high expression of LRP6. Meanwhile, we also found there was a positive relationship between the phosphorylation of LRP6 and CCN2. Then, the negative role of CCN2 and the mutual regulatory mechanism between CCN2 and LRP6 were explored in HCC. The CCN family, first described by P. Bork in 1993, is a small, six-member family of cysteine-rich regulatory proteins found in humans, which share a multi-modular structure with an N-terminal secretory signal domain followed by four conserved domains, including an IGF binding domain (IGFBP), a von Willebrand type C domain (VWC), a thrombospondin-1 domain (TSP1), and a cystine knot domain (CT) [21]. Cause of their four conserved domains, they can modulate the activities of many peptide growth factors [22,23]. CCN2 as one of the CCN family proteins has been implicated in various biological processes including cell migration and tumor progression [24]. In diabetic nephropathy, the activation of Wnt signaling in mesangial cells by CCN2 was along with stimulated phosphorylation of LRP6, nuclear localization of β-catenin, and expression of Wnt targets [25]. Previously, we had proved oxaliplatin-resistant HCC exhibited increasing pulmonary metastatic potential with 267 significantly up-regulated genes by DNA microarray analysis, including CCN2 [15]. Thus, in HCC, we speculate CCN2 could regulate Wnt signaling pathway probably because of its ability to bind to the Wnt co-receptor LRP6. In the present study, we confirmed the increased expression of CCN2 in oxaliplatin-resistant hepatocellular carcinoma with enhanced stemness. And the downregulation and rescue of CCN2 altered the phosphorylation level of LRP6, as well as the expression of the associated downstream Wnt signaling factors. The enhanced stemness and the related biomarkers were also studied after the upregulation or overexpression of CCN2, and our findings support the notion that CCN2 is responsible for LRP6 receptor interactions. And inhibition of CCN2 could downregulate Wnt signaling and inhibite the stemness of HCC. According to the structure characteristic, LRP6 is one of the HSPGs-dependent adhesion receptor for CCN2 [10,26]. Thus, it will be very exciting to understand the associated mutual regulation of CCN2 and LRP6 in HCC, and such information may underscore a novel implication of heparin in anti-HCC therapy.
The diverse but specific interactions of CCN2 with cell surface receptors permits their participation in a broad spectrum of cellular processes, whereas cell surface HSPGs serve as binding sites for all CCN family proteins, including CCN2. Gao et al. [16] demonstrated that co-incubation of CCN2 with heparin or perturbation of cell surface HSPGs with heparinase completely blocks the adhesion between CCN2 and hepatic stellate cells. In the present study, we also proved dose-dependent adhesion of recombinant human CCN2 to an HCC cell line MHCC97H. The role of LRP6 on the HCC cell surface in CCN2-mediated adhesion was also demonstrated. Adhesion of HCC cells to CCN2 was nearly completely blocked after the destruction of HSPGs with heparinase or inhibition of HSPGs sulfation with NaClO3. Co-incubation of CCN2 with heparin also completely blocked the adhesion between LRP6 and CCN2. Together, these results indicated that CCN2 binding with LRP6 is a HSPGs-dependent process in HCC, and these findings are critical for us to develop treatment regimens to downregulation of Wnt signaling and inhibition of stemness of HCC, for those with high expression of CCN2.
In clinical trials with cancer patients, low molecular weight heparin sodium (LMWH) appears to prolong survival of patients with advanced malignancy [27][28][29]. Altinbas et al. [30] found small cell lung cancer (SCLC) was a chemotherapy responsive tumor and associated with alterations in the coagulation system, and addition of LMWH to combination chemotherapy resulted in increase in survival. Jong et al. [31] found that LMWH use was an independent predictor of improved survival in men with metastatic castration resistant prostate cancer receiving docetaxel. Our research group also proved LMWH could inhibit tumor growth and metastasis by inhibiting tumor angiogenesis in nude mice HCC models [32]. Evidence suggests that heparin species inhibit mitogenic signaling mainly through inhibition of growth factors and their receptors [33], and/or by inhibition of the enzyme heparanase [34]. Another possibility is that heparin inhibits metastasis by blocking platelet-tumor cell interactions, thereby inhibiting aggregates of tumor cells lodging in the microvasculature. In the present study, we demonstrated LMWH exhibited no significant proliferation inhibition but showed increased sensitivity to oxaliplatin when combined with LMWH. Interestingly, LMWH partially inhibited the tumors that had been established with MHCC97H cells with the high expression of CCN2, but did not significantly inhibit proliferation of tumors established with MHCC97H-CCN2-Sh cells. Through our research, this anti-tumor effect of LMWH in this study may be contributed to the interfering core regulatory functions of CCN2 proteins that function to orchestrate the Wnt co-receptor LRP6 (Fig. 8).

Conclusions
In conclusion, we have demonstrated that CCN2 plays an adverse role that is directed by the phosphorylation of the Wnt co-receptor LRP6 in HCC in a HSPGs-dependent manner. Combination treatment with oxaliplatin and LMWH resulted in an enhanced chemotherapeutic effect on HCC tumors with high expression of CCN2. While, the utility of heparin and LMWH as anticancer drugs is limited due to their anticoagulant activity, nonanticoagulant heparins are preferable for potential clinical use because they could be administered at high doses, thereby fully exploiting the antimetastatic component of heparin, and because they could be applied to cancer patients with bleeding complication, such as HCC.

Cell lines and animals
The human HCC cell lines with high metastatic potential used in this study were HCCLM3 and MHCC97H cells (established at Fudan University) [35], and which were supplied and authenticated in the year 2010 during study initiation by Biosyn, Inc. using DNA profiling of short tandem repeat markers. The human HCC cell lines with low metastatic potential were SMMC-7721 cells (established at Second Military Medical University), and PLC, Bel7402, and Hep3B cells (obtained from American Type Culture Collection), and the human liver cell line LO2 (obtained from Chinese Academy of Science) were all conserved and supplied by our Liver Cancer Institute in the year 2010 during study initiation, and no authentication was done. All cells were maintained in DMEM (GICBO, Grand Island, NY) supplemented with 10% fetal bovine serum (GICBO) at 37°C in a humidified incubator with 5% CO 2 . It was routinely screened for presence of mycoplasma (Mycoplasma Detection Kit, Roche Diagnostics) during the study period.
Male BALB/c nu/nu mice (aged 4-6 weeks and weighing approximately 20 g) were obtained from the Chinese Academy of Science (SLRC, Shanghai, China) and maintained under standard pathogen-free conditions. The experimental protocol was approved by the Shanghai Medical Experimental Animal Care Commission.

Patients and follow-up
A total of 630 tissue specimens were obtained for this study. In training set, 104 paired HCC samples were used for immunohistochemistry, 96 paired HCC samples were used for real-time PCR, and 16 paired HCC samples were used for Western blot. In validation set, 374 patients who underwent curative resection between January 2004 and December 2006 at the Liver Cancer Institute, Zhongshan Hospital, Fudan University provided the samples for immunohistochemistry. 374 Patients were followed after surgical treatment until December 2013, and the median follow-up was 63 months (range, 0-110 months). The follow-up procedures were described in detail in a previous report [36]. Curative resection was defined as complete resection of tumor nodules, leaving tumor margins free of cancer upon histologic examination. The histopathologic diagnosis was based on World Health Organization criteria. The detailed clinicopathologic characteristics of all HCC study patients in the study are listed in Additional file 2: Tables S1-S3.
Ethical approval was obtained from the Zhongshan Hospital Research Ethics Committee, and informed consent was obtained from each patient.

Vector construction, transfection and lentivirus transduction
The human full-length cDNA of CCN2 (NM_001901.2) and LRP6 (NM_002336) were obtained from Genesent (shanghai China) and then cloned into the pCDH Fig. 8 Cell surface HSPGs consists of a protein core linking several linear heparan sulfate (HS) chains. HS chains ensure CCN2 bind to the cell surface, and decisively regulate their accessibility, LRP6 phosphorylation, and Wnt activation. Co-incubation of LMWH with CCN2 could significantly block the adhesion of CCN2 to cell surface HSPG, and inhibit the function of CCN2. Oxaliplatin could upregulate CCN2 expression and activate Wnt signaling, while, co-incubation of CCN2 with heparin also completely blocked the adhesion between LRP6 and CCN2, and activation of Wnt signaling pathway lentiviral expression vector (System Biosciences). Using the In-Fusion HD Cloning Kit (Takara), the amplified fragment was inserted into the plasmid pCDH (between XbaI and EcoRI sites). Flag-tagged CCN2 in pCDH vector was from Genesent (shanghai China). The primers were listed in Additional file 2: Table S6. Lentiviral shRNA expression plasmids PLKO.1, three different shRNAs against CCN2 and LRP6 mRNA are listed in Additional file 2: Table S7.
Cell binding assays CCN2 was diluted in PBS and used to coat 96-well plates (50 μl/well) for 20 h at 4°C. Wells were then blocked with 1% BSA for 1 h at 37°C. A volume of 50 μl of cell suspension containing 1.5 × 10 4 MHCC97H cells was added to each well for 20 min at 37°C, and then the wells were washed three times with 200 μl PBS. Alternatively, 2 μg/ ml heparin was mixed with MHCC97H cells just prior to plating. Adherent cells were counted using the Cell Counting Kit 8 (Dojindo,Kumamoto, Japan).

Immunoprecipitation assay
For purifying Flag-tagged CCN2 fusion proteins, HEK-293 T cells with Flag-tagged CCN2 stable overexpression were harvested in RIPA lysis buffer supplemented with complete protease inhibitor and phosphatase inhibitor (Roche Applied Science). The lysate was cleared by centrifugation at 12000 g before being loaded to M2 anti-Flag mAb agarose beads (Sigma, St. Louis, MO, USA) pre-equilibrated in RIPA buffer overnight at 4°C. The beads were washed with RIPA buffer five times and 30ul RIPA buffer was added to cover the beads. The RIPA buffer containing beads and Flag-tagged CCN2 fusion proteins were stored at 4°C for the next experiment. For the extraction of membrane proteins, MHCC97H cells were grown to 75% confluence. The membrane proteins were extracted using a ProteoExtract Native Membrane Protein Extraction Kit (M-PEK Kit; Calbiochem, La Jolla, CA, USA) according to manufacturer's instruction. For the binding assay, Flag-tagged CCN2 bind to the beads was incubated with membrane proteins with or without LMWH (2 μg/ml, Santa Cruz Biotechnology) overnight at 4°C in RIPA buffer. Then, the beads were washed with RIPA buffer five times and bound proteins eluted using Flag peptide (Sigma). The washed protein was boiled in loading buffer, resolved on SDS-PAGE. Subsequent immunoblots were probed with the appropriate antibody and detected by ECL.

Animal model and treatment procedures
MHCC97H-CCN2-sh2 cells and the associated MHCC 97H-Mock control cells, or MHCCC97H-LRP6-sh2 and the associated MHCC97H-Mock control cells were injected subcutaneously into the upper left flank region of 4 mice per group to produce tumors. Four weeks later, subcutaneous xenografts were measured as previously described.
In addition, 24 mice were injected with MHCC97H cells subcutaneously into the upper left flank region. Seven days later, these 24 mice were randomly divided into four groups: control group, heparin group, oxaliplatin group, and heparin + oxaliplatin group. The control group was injected with 0.1 ml 5% glucose solution (GS) and 0.1 ml 0.9% normal saline (NS) via intraperitoneal and subcutaneous injections, respectively. The heparin group was treated with 0.1 ml heparin (250 U/kg) via subcutaneous injections once a day. The oxaliplatin group was treated with 0.1 ml oxaliplatin (10 mg/kg) via intraperitoneal injection, and the heparin + oxaliplatin group was treated with both heparin and oxaliplatin as described above. Four weeks later, all subcutaneous xenografts in the four groups were measured and performed as described in previous publication [18,37].
Finally, six mice were injected with MHCC97H-CCN2-SH2 cells subcutaneously into the upper left flank region to produce tumors. Seven days later, the six mice were randomly divided into two groups. The control group was treated with 0.1 ml 0.9% normal saline (NS), and the heparin group was treated with 0.1 ml heparin (250 U/kg). After four weeks, all subcutaneous xenografts in the two groups were measured. For additional methods please find in the Additional file 3.

Additional files
Additional file 1: Figure S1. Expression of CCN2 and LRP6 was analyzed in 144-paired HCC samples and adjacent nontumor liver samples in training cohorts. (A) Upregulation of CCN2 in HCC samples. (B) Upregulation of LRP6 in HCC samples. Figure S2. Up-regulation of CCN2 and LRP6 correlates with poor prognosis and in HCC patients. Kaplan-Meier's curves for OS and TTR according to CCN2 and LRP6 expression in the validation cohort (n=144). Figure S3. Expression of CCN2 and LRP6 was analyzed in 374-paired HCC samples and adjacent nontumor liver samples in validation cohorts by tissue microarrays. Figure S4. Oxaliplatin-treated HCC cell lines and subcutaneous tumor tissues showed increased expression of CCN2 and LRP6. (A) Upregulation of CCN2 and LRP6 in Oxaliplatin-treated HCC cell lines. (B) Upregulation of CCN2 and LRP6 in Oxaliplatin-treated subcutaneous tumor tissues. Figure S5. Expression of CCN2 and LRP6 from the gene expression profiles of 30-paired HCC samples with or without metastasis was analyzed. LRP6 was significantly upregulated in HCC with metastasis, while no significant association was found in the expression of CCN2. Figure S6. LMWH demonstrate no significant inhibitory effect on the in vitro proliferation of MHCC-97H for 24, 48, 72h, with the IC50 645±99.33, 699±87.88, and 469±72.77 U/ml respectively. Figure S7. The synergetic effect of LMWH combined with chemotherapy was evaluated, and LMWH (2 U/ml) significantly increased the sensitivity MHCC-97H cells to oxaliplatin. (ZIP 8918 kb) Additional file 2: Table S1. Correlations between CCN2/LRP6 and clinicopathology feature in 374 patients with HCC. Table S2. Univariate analysis of factors associated with survival and recurrence in 374 patients with HCC. Table S3. Multivariate analysis of factors associated with survival and recurrence in 374 patients with HCC. Table S4. Primary antibodies used for western blot and immunohistochemistry.