Neuropilin-2 expression is inhibited by secreted Wnt antagonists and its down-regulation is associated with reduced tumor growth and metastasis in osteosarcoma
- Tao Ji†1, 2,
- Yi Guo†1,
- Kapjun Kim1,
- Peter McQueen1,
- Samia Ghaffar1,
- Alexander Christ1,
- Carol Lin3,
- Ramez Eskander4,
- Xiaolin Zi5 and
- Bang H Hoang1, 6Email author
© Ji et al.; licensee BioMed Central. 2015
Received: 11 September 2014
Accepted: 6 April 2015
Published: 17 April 2015
Neuropilin 2 (NRP2) isa multi-functional co-receptor to many receptors, including VEGF receptor, c-Met and others. NRP2 has recently been implicated in tumor angiogenesis, growth, and metastasis of many other cancers. However, its role in osteosarcoma remains poorly understood.
NRP2 was overexpressed in osteosarcoma cell lines and tissues, and associated with poor survival of osteosarcoma patients. Knockdown of NRP2 expression by short-hairpin (Sh) RNA resulted in reduced tumor growth, metastasis, and blood vessel formation of osteosarcoma. Knockdown of NRP2 expression by ShRNA also inhibited the recruitment of HUVEC cells to osteosarcoma cells. Inhibition of Wnt signaling by overexpression of secreted Wnt antagonists soluble LRP5, Frzb, and WIF1 markedly down-regulated mRNA and protein expression of NRP2 in osteosarcoma cell lines.
Regulation of NRP2 receptor expression may represent a novel approach for treatment of osteosarcoma through retarding osteosarcoma growth, metastasis and blood vessel formation. In addition, down-regulation of NRP2 expression can be achieved by expression of secreted Wnt antagonists.
Osteosarcoma (OS) is the most common primary malignancy of bone in children and adolescents. Despite recent advances in multimodality treatments consisting of neo-adjuvant chemotherapy and wide surgical excision, 40-50% of adolescent patients develop lung metastasis and 80% of patients with metastasis at diagnosis will relapse . The survival rate has not significantly changed over past 20 years and novel therapeutic targets need to be developed.
Neuropilins, including neuropilin-1 (NRP1) and neuropilin-2 (NRP2), are multi-functional coreceptors for class 3 semaphorins (SEMA) and vascular endothelial growth factor (VEGF), essential for both neuronal guidance and cardiovascular development [2,3]. NRP1-/ mice exhibited early embryonic mortality with obvious cardiovascular defect . NRP2−/− mice displayed abnormal development of peripheral lymph vessels . In the vascular system, NRP1 is expressed mainly in arteries whileNRP2 is expressed in vein and lymphatic vessels [5,6]. During angiogenesis and lymphangiogenesis, NRP1 and 2 were involved in the regulation of endothelial cell properties and mediate sprouting of blood vessel and lymphatic vessels, respectively [7,8]. These findings showed the crucial role of NRP1 and 2 in the development of the vascular and lymphatic systems, respectively.
Besides being found in vascular and lymphatic channels, NRP1 and NRP2 are also expressed in a wide variety of human cancers, such as lung, breast, prostate, colon, pancreas, neuroblastoma, melanoma, etc. [3,9-14]. Oncologic studies have demonstrated that over-expression of NRP1 and NRP2 is correlated with increased vascularity, metastatic potential, advanced stage, and poor prognosis. Generally, NRP1 is predominantly found in carcinoma while NPR2 is expressed in non-epithelial tumors, such as melanoma, leukemia, neuroblastoma , and OS . A study by Handa et al. reported that 80% of OS samples expressed NRP2 and NRP2-positive tumors showed a significant increase in vascularity, and portended a poorer prognosis . However, there is still no direct evidence that blocking NRP2 in OS results in decreased blood vessel formation, tumor growth, or metastatic potential. In breast , colorectal  and pancreatic cancer , blocking NRP-2 resulted in suppressed tumor growth, reduced lymphangiogenesis/angiogenesis and metastasis, although the underlying mechanisms are still poorly understood.
Given the implication of NRP2 in tumor growth, angiogenesis, and metastasis, understanding the regulation of NRP2 expression is of importance. We have reported that blocking Wnt signaling by secreted antagonists resulted in a suppression of tumor growth and lung metastasis [20-24]. Angiogenesis may play a role in the regulation of tumor growth and metastasis by the Wnt signaling pathway. VEGF-A has been reported as transcriptional target gene of Wnt signaling . Therefore, the effects of Wnt signaling on angiogenesis in OS and on the expression of NRP2 deserve further exploration.
In this study, we examined the expression of NRP2 in OS cell lines and tumor tissues, and correlated the expression levels with patients’ survival. By knocking down NRP2 using ShRNA, we examined the potential role of NRP2 in modulating tumor growth, invasion, metastasis and blood vessel formation in OS. In addition, we used Wnt antagonists as a means to elucidate the regulatory effect of Wnt signaling on NRP2 expression.
Results and discussion
NRP2 expression is correlated with metastasis and poor prognosis of OS
Knockdown of NRP2 by ShRNA resulted in reduced in vitro and in vivo growth of OS
NRP2 knockdown resulted in reduced tumor invasion, migration, cell-cell adhesion, and lung metastasis in vivo
NRP2 knockdown is associated with decreased blood vessel density in OS
NRP2 knockdown inhibited endothelial recruitment by OS cells
NRP2 expression is regulated by canonical Wnt signaling
In the present study, we show that NRP2 is significantly elevated in OS cell lines compared to normal osteoblasts. Furthermore, the expression of NRP2 correlates with a poor prognosis of OS patients. To the best of our knowledge, this study also represents the first line of evidence that transcriptional regulation of neuropilin involves the Wnt signaling pathway. Our in vitro data suggest that NRP2 modulates the recruitment of endothelial cells as a means to enhance tumor angiogenesis. Our in vivo experiments corroborate these data by demonstrating that inhibiting NRP2 by ShRNA impairs blood vessel formation, tumor growth, and metastatic potential of OS. These data suggest that NRP2 serves a tumor promoting function in OS. Therefore, suppression of NRP2 may be a novel strategy for the treatment of OS metastasis and progression.
Knockdown of NRP2 by ShRNA only resulted in a moderate inhibition of in vitro cellular growth and a mild apoptotic effect in OS. However, NRP2 knockdown significantly abrogated the in vivo growth of OS tumors in a mouse model. These findings indicate that the effects of NRP2 knockdown in vivo is not a direct result of inhibiting tumor cell proliferation. Interestingly, our study showed that tumor samples from the ShNRP2 group displayed lower blood vessel density, suggesting NRP2 enhances blood vessel formation in OS. This finding is consistent with previous reports in breast , colorectal , and pancreatic cancer . However, none of those reports investigated the interaction of NRP2 suppressed tumor cells and endothelial cells. In this study, we used tumor cell-HUVEC co-culture model to examine the effect of NRP2 knockdown in tumor cells on HUVEC tube formation and recruitment. Unexpectedly, knockdown of NRP2 in OS cells preferentially inhibit the recruitment of HUVEC rather than inhibiting the capacity of HUVEC to form endothelial tubes. To the best of our knowledge, NRP2-mediated endothelial recruitment by OS cells represents a novel finding in this study as this phenomenon has not been well described. Vascular endothelial cells recruitment plays a pivotal role in vessel sprouting and angiogenesis . Blocking recruitment of endothelial progenitor cells by anti-angiogenic drugs has been associated with a reduction in tumor size and blood flow . Molecular mechanisms underlying endothelial cell recruitment by NRP2 in tumor cells remains to be explored.
VEGF, SDF-1 , and CXC chemokine  have been reported to mediate angiogenesis including endothelial cell recruitmeng . In the present study, our data indicated that NRP2 knockdown did not affect the secretion of VEGF from tumor cells. A series of other soluble factors deserve further exploration. In addition, the recruitment of angiocompetent BMDCs (bone-marrow-derived dendritic cells), TEMs (Tie2-expressing monocyte), TAMs (Tumor-associated macrophages), neutrophils, mast cells and CD11b + GR-1 + myeloid-derived suppressor cells, which release angiogenic factors such as VEGF, and MMP  may also play an important role in endothelial recruitment and angiogenesis in tumor. The recruitment of angiocompetent immune cells by NRP2 depleted tumor cells deserves further study as well.
Tumor-endothelial communication has mutual influence on both sides. Our data showed that NRP2 knockdown in tumor cells not only changed the behavior of tumor cells but also altered the interaction between OS and endothelial cells. Interestingly, during co-culture with endothelial cells, the NRP2-suppressed OS cells developed significant morphological change. The significance and mechanism underlying the morphological change of Sh-NRP2 cells remains to be explored. Our previous study demonstrated decreased metastatic capacity of morphologically changed OS cells by Wnt antagonists [22,32]. Further experiments are needed to determine if the co-culture and NRP2 knockdown induced OS cell morphology change is one of the mechanisms that resulted in the decreased lung metastasis in OS.
Pulmonary metastasis represents a poor prognostic factor that still remains as a therapeutic bottleneck in OS. NRP2 expression has been shown to correlate with aggressiveness and metastasis of several types of malignancy . In this study, our tissue microarray data clearly shows that NRP2 expression correlates with a worse prognosis, strongly implicating its role in OS progression and metastasis. NRP2 knockdown in OS cells exhibited reduced motility and invasion, suggesting a direct effect of NRP2 on metastatic capacity of OS cells. Others have shown that NRP2 promotes extravasation and metastasis in renal cell carcinoma by interaction with endothelial α5 integrin . Here, our in vivo studies demonstrated that NRP2 knockdown significantly inhibited pulmonary metastasis of OS in a xenograft mouse model. Cancer cell adhesion involves interacting with adjacent cancer cells as well as endothelial cells and extracellular matrix. NRP1 was initially identified as a cell-cell adhesion molecule . Therefore, it is of interest to determine whether NRP2 is involved in cancer to endothelial cell adhesion. Goel and colleagues reported that NRP2 regulated α6β1 integrin and enabled the formation of focal adhesion of breast cancer . Cao et al. used atomic force microscopy to precisely measure the attachment and detachment of cancer cells to endothelial cells via NRP2 binding to α5 integrin . Using endothelial adhesion assays, we demonstrated that NRP2 is required for OS cell adhesion to endothelial cells, consistent with recent reports in the literature. Clearly, findings from this study and others have deepened our understanding of the important role of NRP2 in tumor metastasis, indicating its potential as a novel therapeutic target.
VEGF-A has been reported as a transcriptional target of Wnt signaling in colon cancer . Unlike NRP2, we found that VEGF-A expression was not suppressed in OS cells by the Wnt antagonist sLRP5. Due to diverse functions of Wnt antagonists, we also sought to use other secreted antagonists to examine the consequence of Wnt blockade on NRP2. Blocking Wnt signaling by additional antagonists such as Wif-1 and DKK3 led to a similar suppression of NRP2, strongly implicating this receptor as a downstream Wnt target. Furthermore, chromatin IP assays confirmed the existence of TCF-binding sequences within 3kbp upstream of the transcription start site for the NRP2 gene. These regions presumably function as transcriptional regulatory elements. Whether the NRP2 promoter responds to the β-catenin/TCF complex still remained undetermined. However, these findings suggest a novel role for Wnt signaling as a modulator of tumor angiogenesis by regulating NRP2.
In this study, we found that blocking Wnt signaling by DKK3 resulted in variable inhibitory effects on NRP2 in different OS cell lines. The reason for this variation may be related to the ability of Dkk-3 to inhibit Wnt signaling being cellular context-dependent. We previously demonstrated Wnt inhibition by DKK3 in OS Saos-2 cells as evidenced by antagonism of cytoplasmic β-catenin . However, ectopic Dkk-3 expression in prostate cancer cells activates c-Jun NH2-terminal kinase (JNK) leading to apoptosis but did not affect β-catenin level, suggesting a role for Dkk-3 in the Wnt/PCP rather than in the Wnt/β-catenin pathway . Despite this variation, secreted Wnt antagonists appear to down-regulated NRP2 expression in OS cells, suggesting that Wnt signaling modulates tumor angiogenesis via NRP2.
We demonstrated that inhibition of NRP2 expression by shRNA knockdown impaired tumor growth, invasion, and blood vessel formation in OS. NRP2 modulates tumor blood vessel formation by altering the recruitment of endothelial cells to OS tumor cells. In addition, NRP2 can be down-regulated by overexpression of secreted Wnt antagonists such as sLRP5, Frzb, and WIF1. Our study also suggests that NRP2 expression is transcriptionally regulated by canonical Wnt signaling.
Cell lines and plasmids
Normal Human Osteoblasts (NHOST) were obtained from Cambrex Bio Science and maintained in Osteoblast Growth Media (Lonza). Saos-LM7 was a gift from Dr. Eugenie Kleinerman (MD Anderson Cancer Center, Houston, TX). Human OS cell lines 143B, 143.89.2, Saos-2, MNNG/HOS and U2OS (American Type Culture Collection), Saos-LM7, and OS160 were maintained in MEMα medium supplemented with 10% fetal bovine serum (FBS), supplemented with penicillin/streptomycin. Human Umbilical Vein Endothelial Cells (HUVEC) were from ATCC (American Type Culture Collection, Manassas VA) and maintained in EGM-2 medium supplemented with 2% FBS and VEGF. All cells were cultured at 37°C in a humidified incubator with 5% CO2. PCDNA3.1 Directional TOPO Expression vector was obtained from Invitrogen. An Ultimate ORF WIF-1 clone (ID: IOH11153) was obtained from Invitrogen and subcloned into the PCDNA3.1 TOPO vector. The dominant-negative, soluble LRP5 plasmid (sLRP5, a generous gift of Matthew Warman, Case Western Reserve University, Cleveland, OH), was constructed by deleting the transmembrane and cytoplasmic domains of LRP5, resulting in a secreted protein that binds and prevent Wnt ligands from activating the native LRP5 receptor.
Tissue microarrays (TMA) and survival analysis
Patient OS tissue microarrays (TMA) were purchased from IMGENEX. NRP-2 staining was conducted by using rabbit anti-NRP2 antibody and anti-rabbit immunostaining kit from R&D system. NRP2 staining intensity of the tumor tissue was scored as no staining (−), weak staining (+), moderate staining (++), and strong staining (+++). The clinical information of tissue microarray samples included follow-up duration and survival status. Kaplan-Meier survival curve was created to represent disease–specific mortality for patients with or without NRP2 expression. The log-rank test was used to compare differences between two groups.
For NRP2 knockdown experiment, OS cell lines were transfected with Lipofectamine 2000 (Life Technologies) with pGFP-V-RS HuSH shRNA vectors (Origene) containing either the scrambled shRNA cassette TR30013 (control) or human NRP2 targeting shRNAs. 143B or Saos-2 cells constitutively expressing the puromycin resistance gene and human NRP2 shRNA were selected and expanded in media containing 1 μg/mL puromycin. The pooled stable transfectants (to avoid cloning artifacts) were examined.
RNA isolation and real time quantitative RT-PCR
Total RNA was isolated using TRIzol reagent (Invitrogen) according to the manufacturer’s instructions. Reverse transcription of total RNA was performed using the Reverse Transcription System kit (Promega, Madison, WI) with random primers. Real-time RT-PCR was performed as previously described . PCR condition was as follows: 45 cycles of 30 seconds at 95°C, 30 seconds at 58°C, 60 seconds at 72°C. Relative fold change in mRNA expression compared to control was calculated using the comparative Ct method. Ct is the cycle number at which fluorescence intensity first exceeds the threshold level. ∆ Ct is Ct (target gene) -Ct (actin). Gene-specific primer sequences are available upon request. Specificity of amplification products were verified by agarose gel electrophoresis and melting curve analysis .
Twenty to 80 μg of protein lysate was separated electrophoretically on denaturing SDS-polyacrylamide gel, transferred to nitrocellulose membranes, and probed with primary antibodies. Blots were exposed to horseradish peroxidase-conjugated secondary antibodies and visualized by an ECL detection system according to the manufacturer’s protocol (Amersham Biosciences, Piscataway, NJ). For loading control, the initial western blot was placed in Restore Western stripping buffer (Thermo Scientific) for 15 min to remove the antibody (primary and secondary), washed in water for 5 min, blocked with 5% milk for 1 hour, and probed with β-actin antibody (Santa Cruz Biotechnology, Santa Cruz, CA; Catalog # sc-130301) [20,24]. The primary antibodies used in western blot included NRP2, GAPDH (Santa Cruz Biotechnology, Santa Cruz, CA. NPR2 catalog # sc-13117; GAPDH catalog # sc-137179); VEGF, DKK3 (Abcam, Cambridge, MA. VEGF catlog # ab46154; DKK3 catalog # ab136101); Wif-1 (Cell Signaling Technology, Danvers, MA, Catalog # 5652); Each western blot was repeated 3 times. Blots were quantitated by densitometry using Image J (Software, NIH, Bethesda, MD, USA) and normalized to a housekeeper marker β-actin or GAPDH . The intensity of each tested marker is presented as a ratio of a tested mark/β-actin or GAPDH.
Tumor and lung tissues were fixed in formalin and sectioned. Antigen retrieval was done using 10 mmol/L sodium citrate (pH 6.0) at 95°C for 15 min. After blocking with PBS containing 3% bovine serum albumin for 1 h, cells were incubated with an NRP2 antibody (Santa Cruz Biotechnology, Santa Cruz, CA, Catalog# sc-13117) for 12 h. After washing, cells were incubated with an Alexa-488 conjugated secondary antibody (Molecular Probes, Eugene, OR, Catalog # A-11059) and mounted in Vectashield with 4’, 6-diamidino-2-phenylindole (DAPI, Vector Laboratories, Burlingame, CA). Localization of immunostaining was analyzed by laser scanning confocal microscopy (X40 magnification) using the 488-excitation wavelength .
For apoptosis detection, cells were stained with FITC-labeled annexin V and propidium iodide (PI) (BD Biosciences, San Jose, CA). After incubations, floating cells were first harvested and adherent cells were trypsinized and pooled together. Cells were washed twice with cold PBS and resuspended in 1× binding buffer at a concentration of 1 × 106 cell/ml. Transfer 100ul of the solution (1 × 105 cells) to a 5 ml culture tube. Add 5ul of FITC Annexin V and 5ul PI. Gently vortex the cells and incubate for 15 min at room temperature in the dark. After the incubation period, 400ul of 1 × binding buffer was added to each tube. The stained cells were analyzed by flow cytometry in one hour. Each flow-cytometry experiment was repeated three times .
Blood vessel density assay
Immunofluorescence was used to determine blood vessel density with CD31 (Abcam), a marker for vascular endothelium, and the blood vessel staining was analyzed with a Nikon Eclipse TE2000-S fluorescent microscope (magnification, 100X) using the 488-excitation wavelength. The vessel density was determined by counting the number of blood vessels in 10 fields (magnification, 100X) of slides from each group and the result was recorded as mean number of blood vessels per field.
Motility and invasion assay
Motility and invasion assays were performed using 24-well invasion chamber system (BD Biosciences, MA) as previously described . The matrigel coated inserts were used for invasion assay. The uncoated inserts were used for motility assay. 1 × 105 cells for invasion assay and 5 × 104 cells for motility assay were seeded in the upper chamber in serum-free MEMα medium. MEMα medium with 10% FBS (used as a chemoattractant) was placed in the bottom well. Incubation was carried out for 48 h for invasion assay or 24 h for migration assay, at 37°C in humidified air with 5% CO2. Non-invasive or non-migrating cells in the upper chamber were then removed with a cotton swab. Invading or migrating cells on the bottom of the inserts were fixed with methanol and stained with hematoxylin. The number of invading or migrating cells was determined by counting five fields (100×) under the microscope, and calculated as mean number of cells per field. All experiments were performed in triplicate.
Twenty thousand tumor cells were seeded into 24-well plates approximately 24 h before the start of the recruitment assay. HUVEC cells were serum starved in EGM-2 medium supplemented with 0.2% FBS for 24 h. HUVEC cells were then suspended at 4 × 104 HUVECs per ml of 0.2% FBS EGM-2. 500 μl of the suspension was then added into each insert and the recruitment assay was allowed to proceed for 12–16 h depending on tumor cell lines. After completion of the assay, the inserts were fixed with methanol for 5 min and stained with hematoxylin. The number of migrating or invading cells was determined by counting 5 fields at × 100 magnification.
Endothelial adhesion assay
HUVEC cells were cultured in 6-well plate and allowed to grow to confluence. 2 × 104 tumor cells were added into the wells pre-cultured HUVEC cells for 30 minutes at 37°C. The wells were washed with PBS gently to remove non-adherent cells. Five images were taken. The number of tumor cells adhering to the HUVEC cell was then quantified using ImageJ (NIH).
Soft agar colony formation assay
Soft agar colony formation assay was performed using six-well plates as previously described . Each well contained 2 mL of 0.8% agar in complete medium as the bottom layer, 1 ml of 0.35% agar in complete medium and 6000 cells as the feeder layer, and 1 ml complete medium as the top layer. Cultures were maintained under standard culture conditions. The number of colony was determined with an inverted phase-contrast microscope at × 100 magnification. A group of >10 cells was counted as a colony. The data are shown as mean number of colony ± SEM of four independent wells at 20 days after the start of cell seeding .
In vivo tumorigenesis model
4-week old male nu/nu nude mice (Taconic) were purchased and housed in pathogen-free conditions for additional 4 weeks before tumor inoculation. The animal protocol was approved by the Institutional Animal Care Utilization Committee (IACUC). Sh-NRP2 transfected and vector control transfected 143B cells were grown to 80% confluence, and re-suspended in PBS and injected subcutaneously (S.C.) into the flank of 8-week old nude mice at 1 × 106 cells/0.1 ml. Tumor size was measured every 3 days using a caliper. The tumor volume was calculated by the formula 1/6 πab2 (π =3.14, a = long axis and b = short axis of the tumor). Growth curves were plotted from the mean tumor volume ± SEM from 10 animals in each group. 21 days after injection, the animals were sacrificed and tumors were harvested, measured, weighed, and fixed in 10% formalin [20,24]. Each experiment was repeated 3 times.
In vivo lung metastasis model
4-week old male nu/nu nude mice (Taconic) were were purchased and housed in pathogen-free conditions for additional 4 weeks before tumor inoculation. shNRP2 transfected and vector control transfected 143B cells were grown to 80% confluence, and re-suspended in PBS. 0.03 ml of cell suspension (1 × 107 cells/ml) was injected percutaneously into the tibia of anesthetized 8-week old nude mice. After 4 weeks, the animals were sacrificed according to an IACUC-approved protocol. Lungs were harvested, fixed in Bouin’s solution, and the number of lung surface metastatic nodules was counted and graphed. To determine the number of lung surface metastatic nodules per field, we count 10 fields (×100) to calculate the mean value for each group. Mean number of lung nodules was compared between shNRP2 transfected and vector control transfected groups. Each group contained 10 mice and each experiment was repeated 3 times. Microscopic lung metastases were visualized on 5-μm paraffin embedded sections stained with H & E .
HUVEC Tube Formation Assay
In order to examine the effect of NRP2 knockdown on angiogenesis, matrigel tube formation assay was performed using Human Umbilical Vein Endothelial Cells (American Type Culture Collection, Manassas VA). Tube formation assay was performed according to the manufacturer’s protocol (BD, Endothelial Cell Tube Formation Assay). Briefly, HUVEC cells were serum starved in EGM-2 media supplemented with 0.2% FBS for 24 h. 96-well culture plates were coated with 50 μl Matrigel (BD Biosciences, San Hose, CA), that was allowed to solidify for 1 hour at 37°C. The pre-treated HUVEC cells were then seeded in the well at 3 × 104 cells/well. Meanwhile, the conditioned medium was collected and added in each wells. Then the HUVEC cells were incubated at 37°C for 6 hours. For tumor cell-HUVEC co-culture model, HUVEC cells were labelled with CellTracker Red CMTPX dye (Invitrogen) for 30 min and subsequently treated in EGM-2 media supplemented with 2% FBS for 30 min. The tumor cells and HUVEC cells were trypsinized and re-suspended at 4 × 104/ml and 2 × 105/ml respectively in EGM-2 media supplemented with 2% FBS. The tumor and HUVEC cell suspensions were then mixed at a 1:1 ratio and 100 μl of each mixture was seeded into each well of the tube formation assay plate. The assay plate was incubated at 37°C for 12 h. Images of each well were taken and processed using Angiogenesis Analyzer for ImageJ software (NIH) to obtain the number of tubules and total tubule length per image.
Chromatin immunoprecipitation (ChIP) analysis
By analysis of promoters using Genebank and MatInspector software, five TCF/LEF binding sites in NRP2 promoter region were found. In order to verify the binding of TCF/LEF on NRP2 promoter region, Chromatin immunoprecipitation (CHIP) analysis was performed using Upstate Chromatin immunoprecipitation (CHIP) Assay Kit (Millipore, San Diego, CA). Briefly, 1x106 143B cells were seeded in 10 cm dish. After overnight incubation, 1% formaldehyde was directly added to the culture medium and incubated for 10 minutes at 37°C to cross link histones to DNA. Cells were then lysed and sonicated to shear DNA to between 200–1000 base pairs. TCF4 antibody (3 μg/mL) was added and incubated overnight with rotation. 60 μL Protein A Agarose was added to precipitate the DNA/antibody complex. After sequentially washing with low salt immune complex wash buffer, high salt immune complex wash buffer, LiCl immune complex wash buffer, and TE buffer, DNA/antibody complex was eluted from antibody. After histone-DNA crosslink at 65°C for 4 h, DNA was recovered by phenol/chloroform extraction and ethanol precipitation. Polymerase chain reaction (PCR) was performed to amplify the TCF/LEF binding sites. Five pairs of primer for NRP2 promoter, which span each TCF/LEF binding site, were used. The primer sequences are available upon request.
Comparisons of number of colony, fold change in levels of mRNA, and the blood vessel density between different transfection groups were conducted using Student’s t-test. For tumor growth experiments, repeated measures ANOVA was used to examine the differences in tumor volume among different transfection groups at each time points. Additional post-test was done to examine the differences in tumor volume between vector control and Sh-NRP2 transfection groups at each time point by the conservative Bonferroni method. All statistical tests were two sided. P < 0.05 was considered statistically significant.
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