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Netrin-1 overexpression is predictive of ovarian malignancies

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Oncotarget. 2011; 2:363-367. https://doi.org/10.18632/oncotarget.258

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Anastasios D. Papanastasiou, Georgios Pampalakis, Dionyssios Katsaros and Georgia Sotiropoulou _

Abstract

Anastasios D. Papanastasiou1*, Georgios Pampalakis1*, Dionyssios Katsaros2, Georgia Sotiropoulou1

1 Department of Pharmacy, School of Health Sciences, University of Patras, Rion-Patras, 26500, Greece

2 Department of Obstetrics and Gynecology, Gynecologic Oncology Unit, University of Turin, Turin, Italy

* These authors contributed equally

Keywords: Oncogene, cancer, kinase, BRAF V600E, drug resistance, proteomics

Received: April 4, 2011; Accepted: May 1, 2011; Published: May 2, 2011;

Correspondence:

Georgia Sotiropoulou, e-mail:

Abstract

Netrin-1 (NTN1) is functionally important for the development of the nervous system. Interestingly, few recent studies showed that NTN1 may also promote cancer by increasing survival and resistance of lung and breast cancer cells to apoptosis. Our purpose was to investigate whether NTN1 and its receptor DCC may be involved in ovarian cancer. The NTN1 and DCC mRNAs were quantified by real-time RT-PCR in normal (10), benign (8) and cancer (17) ovarian tissues. ALAS1 and TBP housekeeping genes were used for normalization. NTN1 was found overexpressed in 76% of ovarian cancer specimens (13/17) as compared to normal (0/10, p<0.004) and benign (1/8, p<0.008) samples. Increased NTN1 mRNA levels correlated with advanced tumor stage (stage III, n=8, 100%) and grade (grade 3, n=7, 100%). In contrast, DCC was found downregulated in 59% (10/17) of ovarian tumors tested but correlation was not significant when compared to normal or benign specimens. Here, we demonstrated that NTN1 may be involved in ovarian cancer as the expression of NTN1 mRNA is strongly upregulated in ovarian malignant tumors but not in benign tumors. The fact that increased NTN1 is specifically observed in cancerous tissues indicates that NTN1 may represent a novel candidate biomarker for ovarian cancer.


Introduction

Netrin-1 (NTN1) is a diffusible laminin-related protein that has been shown to play a major role in the control of neural navigation in the developing nervous system [1, 2]. Recently, NTN1 was proposed to play crucial roles in tumorigenesis as it is involved in regulation of apoptosis by binding to DCC and UNC5H family of dependence receptors that share the ability to induce apoptosis in the absence of their ligands, a trait that confers tumor suppressor activity on these receptors [3]. Expression of one of these dependence receptors at the surface of a tumor cell is considered to render it dependent on ligand availability for survival, thus, inhibiting uncontrolled tumor cell proliferation and/or metastasis. Accumulating evidence implies that this positive signaling pathway is frequently inactivated in human cancers, as it was shown that expression of DCC and UNC5H is lost during tumor progression, thus, conferring a selective advantage to the tumor cell for survival [3]. In addition, this model predicts that a similar advantage may be obtained by gaining autocrine expression of the NTN1 ligand in tumor cells. Indeed, a high percentage of colorectal [4] and metastatic breast [5] cancers overexpress NTN1.

Binding of NTN1 to its receptors inhibits p53-dependent apoptosis, while p53 is directly involved in transcriptional regulation of NTN1 and its receptors [3]. Thus, NTN1 expression confers resistance to apoptosis, thus, enhancing tumor cell survival. In non-small cell lung cancer (NSCLC), >50% of the analyzed tissue specimens expressed abnormally high levels of NTN1 [6, 7]. Interestingly, a recent study revealed that NTN1 expression is selectively up-regulated in colorectal cancers associated with bowel diseases. Moreover, it was demonstrated that this inflammation-driven NTN1 up-regulation is causal for colorectal cancer development, as interference with the NTN1 autocrine loop inhibited colorectal cancer progression without affecting inflammation in a mouse model for ulcerative colitis-associated colorectal cancer [4].

In this direction, it was shown recently that autocrine production of NTN1 in aggressive neuroblastomas conveys selective advantage for tumor growth and dissemination [8], as it blocks the pro-apoptotic activity of the NTN1 receptors, UNC5H, leading to resistance to apoptosis that is a prerequisite for neuroblastoma progression. NTN1 up-regulation was suggested as a potential marker for poor prognosis in infants diagnosed with stage 4S neuroblastoma [8]. It was proposed that interference with the NTN1 autocrine loop in malignant neuroblasts may represent an alternative therapeutic strategy, as it was shown that disruption of this loop triggers cell death and inhibits metastasis of neuroblastoma in avian and mouse models [8].

Interestingly, NTN1 was proposed to play an important role in embryonic and pathological angiogenesis acting as a survival factor also for endothelial cells by blocking the pro-apoptotic effect of the dependence receptor UNC5B and its downstream death-signaling effector, the serine/threonine kinase DAPK. Thus, the proapoptotic effect of unbound UNC5B and the survival effect of NTN1 on endothelial cells finely tune the angiogenic process [9]. Nonetheless, in a recent study, NTN1 was found strongly up-regulated in pancreatic adenocarcinomas and this aberrant NTN1 overexpression was associated with resistance to apoptosis for both tumor and endothelial cells [10]. Triggered by these recent studies pinpointing to important roles of NTN1 in most common malignancies, we investigated here whether NTN1 expression changes between normal, benign and cancerous ovarian tissues. In addition, we examined the expression of the NTN1 receptor DCC. It must be noted that DCC is considered a tumor suppressor that was originally identified based on allelic deletions at 18q21 associated with colorectal cancer [11].

Results and Discussion

As shown in Figure 1 and Table 1, strong upregulation of NTN1 expression was detected in the majority of ovarian cancer specimens when compared to normal (p<0.004) or benign (p<0.008) which is significant according to the T-test values. Expression was considered high when the ratio NTN1/reporter genes (ALAS1-TBP) was ≥6 and for DCC/reporter genes (ALAS1-TBP) ≥0.1. More importantly, upregulation of NTN1 mRNA correlated well with advanced stage of disease (p<0.005, Mann-Whitney U test). It should be noted that a larger cohort of samples should be analyzed, in order to interrogate whether NTN1 expression can be used to predict disease-free survival and/or overall survival. Contrary, DCC was found downregulated in 10/17 (59%) cancer specimens, which is well in accordance with previous observations that reported decreased DCC in 55% of ovarian cancers when measured by immunohistochemistry and RT-PCR in a much larger number of patients [14, 15]. Interestingy, re-expression of DCC in ovarian cancer cells induced an apoptosis phenotype [15]. DCC deactivation results from loss-of-heterozygosity in a subset of ovarian cancers [16]. We were unable to correlate the decreased DCC expression to tumor grade or stage probably due to the small number of samples analyzed. Nonetheless, it should be noted that 7/17 cancer specimens exhibited high DCC expression which correlated with NTN1 upregulation in 6/7 samples (p<0.098 Pearson correlation). Expression of DCC in this subset of ovarian cancers is counterbalanced by increased NTN1 levels, thus, again leading to evasion of apoptosis. When all 35 samples (normal, benign and cancer) were included in the analysis, no correlation (p<0.519) was derived between NTN1 and DCC expression.

Table 1: Clinicopathological features for patient samples correlated to NTN1 and DCC expression in ovarian tissue specimens.
 

NTN1

DCC

  Cases High expression Low expression p value High expression Low expression p value
Normal   10 0/10 (0%) 10/10 (100%)   6/10 (60%) 4/10 (40%)  
    Age ≥54 4 0/4 (0%) 4/4 (100%) 3/4 (75%) 1/4 (25%)
  <54 6 0/6 (0%) 6/6 (100%) 3/6 (50%) 3/6 (50%)
Benign   8 1/8 (12.5) 7/8 (87.5) 5/8 (62.5%) 3/8 (37.5%)
  relative to normal 0.231   0.829
    Age ≥54 2 0/2 (0%) 2/2 (100%)   1/2 (50%) 1/2 (50%)  
  <54 6 1/6 (17%) 5/6 (83%) 4/6 (67%) 2/6 (33%)
Tumor   17 13/17 (76%) 4/17 (24%) 7/17 (41%) 10/17 (59%)
  relative to normal 0.004*   0.675
relative to benign 0.008* 0.977
    Age ≥54 10 8/10 (80%) 2/10 (20%)   5/10 (50%) 5/10 (50%)  
  <54 7 4/7 (57%) 3/7 (43%) 2/7 (28.6%) 5/7 (71.4%)
Grade 0 1 1/1 (100%) 0/1 (0%) 1/1 (100%) 0/1 (0%)
  1 1 0/1 (0%) 1/1 (100%) 1/1 (100%) 0/1 (0%)
2 5 3/5 (60%) 2/5 (40%) 1/5 (20%) 4/5 (80%)
3 7 7/7 (100%) 0/7 (0%) 4/7 (57%) 3/7 (43%)
  relative to grade ≤2 0.013**   0.414
  U 3 2/3 (67%) 1/3 (33%)   0/3 (0%) 3/3 (100%)  
Stage I 5 2/5 (40%) 3/5 (60%) 1/5 (20%) 4/5 (80%)
  II 1 1/1 (100%) 0/1 (0%) 1/1 (100%) 0/1 (0%)
  III 8 8/8 (100%) 0/8 (0%) 5/8 (62.5%) 3/8 (37.5%)
  relative to stage ≤2 0.005**   0.805
  U 3 2/3 (67%) 1/3 (33%)   0/3 (0%) 3/3 (100%)  
High expression is considered the ratio NTN1/reporter genes (ALAS1-TBP) ≥ 6 and DCC/reporter genes (ALAS1-TBP) ≥ 0.1 U: Unknown characteristics *statistically significant, T-test values **statistically significant, Mann-Whitney U test

Figure 1: NTN1 and DCC mRNA expression in ovarian samples. Relative expression levels of NTN1 (left) and DCC (right) were analyzed in the clinical samples. Changes between benign-normal and cancer-normal are considered significant with both the T-test and Mann-Whitney U test (shown are p values calculated by the T-test).

In summary, we show here for the first time that NTN1 is aberrantly overexpressed in the vast majority of malignant ovarian tumors but not in benign tumors. Moreover, high NTN1 expression correlates well with both tumor stage and grade. The observed alteration in NTN1 expression upon progression to malignancy can safely be considered significant as it pertained to 100% of malignant tumors, while in normal and benign tissues NTN1 was barely expressed. Lack of expression in normal/benign is a desired but rare feature of cancer biomarkers. Our finding that NTN1 expression can possibly be used as a biomarker to distinguish benign from malignant ovarian tumors, also implies that NTN1 may be implicated in the progression of benign disease to malignancy. Our improved understanding of the mechanisms underlying the key emergent property of cancers, their malignancy, is expected to promote our efforts to reduce cancer mortality [17]. Based on the intriguing finding that NTN1 expression is not altered in benign ovarian tumors, we propose that NTN1 expression should be evaluated in prospective studies as a promising candidate biomarker to distinguish benign from malignant tumors of the ovary.

Patients and Methods

Clinical samples

All clinical samples used in this study were collected at the University of Turin, Italy. Tissues were obtained following informed and signed consent of the patient under a general tissue collection protocol approved by the Institutional Review Board and the University of Turin, Italy. The samples were snap-frozen in liquid nitrogen and stored at -80oC.

RNA extraction

RNA extraction was performed with RNeasy (Qiagen) after tissue pulverization with a pestle and mortar under liquid nitrogen. RNA purity and integrity were confirmed by spectrophotometry and agarose gel electrophoresis, respectively.

Reverse Transcription and Quantitative PCR

500 ng of total RNA were reverse-transcribed with Superscript II (Invitrogen) using an oligo dT primer according to the standard protocol. The total volume of the recovered cDNA was 21 μl. Real-time PCR was carried out in 25 μl with SYBR Green (Invitrogen) in a Rotor Gene 3000 (Cobert Research). The following conditions were applied for PCR amplification: 50oC for 2 min, 94oC for 5 min followed by 45 cycles (40 for ALAS1, TBP) of 94oC for 15 sec, 54oC for 20 sec (54oC for 30 sec for ALAS1, TBP), and 72oC for 20 sec (30 sec for ALAS1, TBP). The sequences of NTN1 primers were: 5’-TGC AAG AAG GAC TAT GCC GT-3’ and 5’-GCT CGT GCC CTG CTT ATA CAC-3’ and for DCC were: AGC CAA TGG GAA AAT TAC TGC TTA C and AGG TTG AGA TCC ATG ATT TGA TGA G [8]. ALAS1 and TBP primer sets for real-time PCR were obtained from Qiagen (QuantiTect Primer Assay). Serial dilutions of cDNAs from selected tissue samples were used to determine the amplification efficiency of NTN1, DCC, ALAS1 and TBP. The Pfaffl model [12] and the REST 2009© relative expression software tool [13] were used to determine the amplification efficiency and estimate the relative changes in mRNA levels of NTN1 and DCC. Data normalization was carried out against both ALAS1 and TBP1 housekeeping genes, for improved reliability of results. Efficiency and fold-change were calculated based on cycle-threshold values using the REST software and ALAS1 and TBP1 as controls. All samples were analyzed in triplicates in two independent experiments.

Classical RT-PCR and sequencing

Finally, semiquantitative conventional RT-PCR was performed with OneStep (Qiagen) and the PCR products were resolved by agarose gel electrophoresis (not shown). Two randomly selected products were gel-extracted (Qiagen) and sequenced using the NTN1-specific forward primer (VBC, Austria), in order to verify that the PCR product was indeed NTN1-specific.

Statistical analysis

The Mann-Whitney U test or T-test were used to correlate clinical parameters (stage, grade) and NTN1 or DCC relative mRNA expression levels. Statistical analyses were performed with SPSS (SPSS® release 15.0, Chicago, IL, USA).

References

1. Serafini T, Colamarino SA, Leonardo ED, Wang H, Beddington R, Skarns WC, Lavigne MT. Netrin-1 is required for commissural axon guidance in the developing vertebrate nervous system. Cell 1996; 87: 1001-1014.

2. Forcet C, Stein E, Pays L, Corset V, Llambi F, Tessier-Lavigne M, Mehlen P. Netrin-1-mediated axon outgrowth requires deleted in colorectal cancer-dependent MAPK activation. Nature 2002; 417: 443-447.

3. Arakawa H. Netrin-1 and its receptors in tumorigenesis. Nat Rev Cancer 2004; 4: 978-987.

4. Paradisi A, Maisse C, Coissieux MM, Gadot N, Lépinasse F, Delloye-Bourgeois C, Delcros JG, Svrcek M, Neufert C, Fléjou JF, Scoazec JY, Mehlen P. Netrin-1 up-regulation in inflammatory bowel diseases is required for colorectal cancer progression. Proc Natl Acad Sci USA 2009; 106: 17146-17151.

5. Fitamant J, Guenebeaud C, Coissieux MM, Guix C, Treilleux I, Scoazec JY, Bachelot T, Bernet A, Mehlen P. Netrin-1 expression confers a selective advantage for tumor cell survival in metastatic breast cancer. Proc Natl Acad Sci USA 2009; 105: 4850-4855.

6. Delloye-Bourgeois C, Brambilla E, Coissieux MM, Guenebeaud C, Pedeux R, Firlei V, Cabon F, Brambilla C, Mehlen P, Bernet A. Interference with netrin-1 and tumor cell death in non-small cell lung cancer. J Natl Cancer Inst 2009; 101: 237-247.

7. Schön MP, Schön M. To die or not to die, that’s the question--and the answer may depend on netrin-1. J Natl Cancer Inst 2009; 101: 217-219.

8.Delloy-Bourgeois C, Fitamant J, Paradisi, Cappellen D, Douc-Rasy S, Raquin MA, Stupack D, Nakagawara A, Rousseau R, Combareta V, Puisieux A, Valteau-Couanet D, Bénard J, Bernet A, Mehlen P. Netrin-1 acts as a survival factor for aggressive neuroblastoma. J Expe Med 2009; 206: 833-847.

9. Castets M, Coissieux MM, Delloye-Bourgeois C, Bernard L, Delcros JG, Bernet A, Laudet V, Mehlen P. Inhibition of endothelial cell apoptosis by netrin-1 during angiogenesis. Dev Cell 2009; 16: 614-620.

10. Dumartin L, Quemener C, Laklai H, Herbert J, Bicknell R, Bousquet C, Pyronnet S, Castronovo V, Schilling MK, Bikfalvi A, Hagedorn M. Netrin-1 mediates early events in pancreatic adenocarcinoma progression, acting on tumor and endothelial cells. Gastroenterology 2010; 138: 1595-1606.

11. Fearon ER, Cho KR, Nigro JM, Kern SE, Simons JW, Ruppert JM, Hamilton SR, Preisinger AC, Thomas G, Kinzler KW, Vogelstein B. Identification of a chromosome 18q gene that is altered in colorectal cancers. Science 1990; 40: 49=56.

12. Pfaffl MW. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 2001; 29: e45.

13. Pfaffl MW, Horgan GW, Dempfle L. Relative expression software tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-time PCR. Nucleic Acids Res 2002; 30: e36.

14. Saegusa M, Machida D, Okayasu I. Loss of DCC gene expression during ovarian tumorigenesis: relation to tumour differentiation and progression. Br J Cancer 2000; 82: 571-578.

15. Meimei L, Peiling L, Baoxin L, Changmin L, Rujin Z, Chunjie H. Lost expression of DCC gene in ovarian cancer and its inhibition in ovarian cancer cells. Med Oncol 2011; 28: 282-289.

16. Lassus H, Salovaara R, Aaltonen LA, Butzow R. Allelic analysis of serous ovarian carcinoma reveals two putative tumor suppressor loci at 18q22-q23 distal to SMAD4, SMAD2, and DCC. Am J Pathol 2001; 159: 35-42.

17. Lazebnik Y. What are the hallmarks of cancer? Nat Rev Cancer 2010; 10: 232-233.


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