A role for endothelial nitric oxide synthase in intestinal stem cell proliferation and mesenchymal colorectal cancer
- Jon Peñarando1,
- Laura M. López-Sánchez1, 2,
- Rafael Mena1,
- Silvia Guil-Luna1,
- Francisco Conde1, 2,
- Vanessa Hernández1,
- Marta Toledano1, 2,
- Victoria Gudiño6,
- Michela Raponi6,
- Caroline Billard6,
- Carlos Villar3,
- César Díaz4,
- José Gómez-Barbadillo4,
- Juan De la Haba-Rodríguez1, 2, 5,
- Kevin Myant6,
- Enrique Aranda1, 2, 5 and
- Antonio Rodríguez-Ariza1, 2, 5Email authorView ORCID ID profile
© The Author(s). 2018
Received: 7 November 2017
Accepted: 14 December 2017
Published: 10 January 2018
Nitric oxide (NO) has been highlighted as an important agent in cancer-related events. Although the inducible nitric oxide synthase (iNOS) isoform has received most attention, recent studies in the literature indicate that the endothelial isoenzyme (eNOS) can also modulate different tumor processes including resistance, angiogenesis, invasion, and metastasis. However, the role of eNOS in cancer stem cell (CSC) biology and mesenchymal tumors is unknown.
Here, we show that eNOS was significantly upregulated in VilCre ERT2 Apc fl/+ and VilCre ERT2 Apc fl/fl mouse intestinal tissue, with intense immunostaining in hyperproliferative crypts. Similarly, the more invasive VilCre ERT2 Apc fl/+ Pten fl/+ mouse model showed an overexpression of eNOS in intestinal tumors whereas this isoform was not expressed in normal tissue. However, none of the three models showed iNOS expression. Notably, when 40 human colorectal tumors were classified into different clinically relevant molecular subtypes, high eNOS expression was found in the poor relapse-free and overall survival mesenchymal subtype, whereas iNOS was absent. Furthermore, Apc fl/fl organoids overexpressed eNOS compared with wild-type organoids and NO depletion with the scavenger carboxy-PTIO (c-PTIO) decreased the proliferation and the expression of stem-cell markers, such as Lgr5, Troy, Vav3, and Slc14a1, in these intestinal organoids. Moreover, specific NO depletion also decreased the expression of CSC-related proteins in human colorectal cancer cells such as β-catenin and Bmi1, impairing the CSC phenotype. To rule out the contribution of iNOS in this effect, we established an iNOS-knockdown colorectal cancer cell line. NO-depleted cells showed a decreased capacity to form tumors and c-PTIO treatment in vivo showed an antitumoral effect in a xenograft mouse model.
Our data support that eNOS upregulation occurs after Apc loss, emerging as an unexpected potential new target in poor-prognosis mesenchymal colorectal tumors, where NO scavenging could represent an interesting therapeutic alternative to targeting the CSC subpopulation.
Advances in understanding the molecular pathways in colorectal cancer (CRC) have resulted in the development of novel targeted therapeutics . However, CRC remains the third most frequent cancer and the fourth leading cause of cancer deaths worldwide . The cancer stem cell (CSC) model provides an attractive explanation to these mortality data and therapy failure . In the CSC model, a small subpopulation of tumor cells possesses unlimited proliferative potential and chemoresistance, ultimately resulting in a tumor spreading and metastasis . Thus, this cellular subset with tumor-initiating properties has the capacity to evade conventional therapies, which contributes to the adverse survival rates, so new specific targets must be found . Moreover, the heterogeneity of CRC hinders the selection of patients who will respond better to therapy and the detection of new targeted agents . To solve this problem, several gene-expression-based CRC classifications have been reported, dividing the disease into different clinically relevant CRC subtypes [6–10]. Recently, the International CRC Subtyping Consortium analyzed different CRC data sets and have described four robust consensus molecular subtypes (CMSs) associated with clinical variables : CMS1 (microsatellite instability), CMS2 (canonical), CMS3 (metabolic), and CMS4 (mesenchymal). Interestingly, although these classifications differed in the number of tumor subtypes, they all agree in the identification of a stem-like mesenchymal subtype, which is associated with poor patient outcome in CRC , so new specific targets must be discovered to improve current treatments.
Nitric oxide (NO) has been highlighted as an important agent in different physiopathological conditions, including colon cancer . It has been shown that NO has a dual role in tumoral processes, being cytotoxic or cytostatic at high levels whereas low levels can have the opposite effect and promote tumor growth . This molecule is synthesized by three different NO synthase (NOS) isoforms using L-arginine and molecular oxygen as substrates: neuronal NOS (nNOS), inducible NOS (iNOS), and endothelial NOS (eNOS) . The inducible isoform has been the center of attention in the study of its role in tumorigenesis . However, there is a huge controversy about the expression and role of iNOS in human colon carcinogenesis. Whereas some authors seem to detect iNOS expression in 60% of human colon adenomas , other studies reported that levels of this isoenzyme were low or absent at all stages of colon cancer [17, 18]. Moreover, conflicting results for the role of iNOS in colon tumorigenesis have been found by independent groups using the same Min mouse model [19, 20]. On the other hand, recent works in the literature indicate that eNOS may be implicated in different tumor processes, such as resistance to hormonal therapy , angiogenesis, invasion, and metastasis . Furthermore, high levels of eNOS have been correlated with an angiogenic phenotype and predict poor prognosis in human gastric cancer . Despite the relation between tumor-expressed eNOS and tumor maintenance , there are no data about the role of this protein in the stem-cell-like population responsible for the initiation and maintenance of tumor growth.
In the present study, by employing three different independent mice models, we show that eNOS upregulation is an early event in CRC after Apc loss and it is also upregulated in the human mesenchymal CRC subtype. Moreover, we demonstrated that iNOS was absent in all these models as well as in human mesenchymal tumors. We showed that specific removal of eNOS-produced NO with the scavenger carboxy-PTIO (c-PTIO) impaired stem-related signaling pathways essential for CSCs, which decreased in vitro tumorsphere and organoid formation and in vivo tumor formation.
eNOS is overexpressed in hyperproliferative regions and tumors of Apcfl/fl, Apcfl/+, and Apcfl/+ PTENfl/+ intestinal mouse tissue
Deletion of both copies of Apc leads to a Wnt-driven hyperproliferative phenotype. On the other hand, the conditional deletion of a single copy of Apc (VilCre ERT2 Apc fl/+ ) leads to mice carrying 10–20 discrete adenomas following spontaneous loss of the wt Apc allele . An analysis of the tumors that arose in this mouse model showed that an increase of eNOS expression was observed in tumor regions. However, normal areas of the intestine that still remained organized and where tumors were absent did not show any staining at the bottom of intestinal crypts (Fig. 1a). We also found this upregulation of eNOS in intestinal adenomas from Apc fl/+ mouse tissue by RT-qPCR compared with normal intestinal tissue from the same animal (Fig. 1b). The above results suggest that the increase of NO production in mutant crypts through overexpression of eNOS isoenzyme occurs following loss of Apc. Again, iNOS was not induced after the loss of just one Apc allele (Fig. 1a). Similarly, invasive tumors from the more invasive VilCre ERT2 Apc fl/+ Pten fl/+ mouse model showed an overexpression of eNOS in tumors whereas normal crypts did not show any expression of this isoenzyme (Fig. 1a). Accordingly, RT-qPCR analyses confirmed that eNOS was almost threefold upregulated in the intestine of VilCre ERT2 Apc fl/+ Pten fl/+ mice compared with normal tissues (Fig. 1b). As found in the other two mouse models, iNOS expression was absent in both tumor and normal epithelium adjacent to the tumor (Fig. 1a).
Therefore, the above results suggest that there may be a relevant role for the upregulation of eNOS expression in the early stages of CRC, where the Lgr5-positive stem cell population is in expansion, and also that the upregulation of this NOS isoform is maintained in more advanced and invasive genotypes.
eNOS is upregulated in the mesenchymal poor-prognosis subtype and poorly differentiated human colorectal tumors
We next evaluated the expression of NOS isoforms in different CRC subtypes. We classified 40 human colorectal adenocarcinomas according to Sadanandam et al.  and De Sousa et al. . Thus, we obtained a supervised classification of tumors into five molecularly distinct subtypes, which are associated with different clinically relevant characteristics: transit-amplifying, enterocyte, goblet-like, inflammatory, and stem-cell-like (Additional file 1: Figure S1 and Additional file 2: Figure S2).
The expression of iNOS was found in some human colorectal tumors and it was restricted to just some aberrant crypts or even individual cells, unlike the general high expression of eNOS in mesenchymal tumors (Fig. 3). The induction of iNOS occurs in punctual regions where proper inductive signals may lead to a massive increase in its expression. This produces just temporary high levels of NO, since this is energetically unsustainable over time. Interestingly, immunohistochemical analyses of unclassified high-grade poorly differentiated tumors from CRC patients also showed the upregulation of eNOS compared with non-proliferative areas (Additional file 5: Figure S5). In line with these results, a significantly decrease was found in 5-year survival in patients with CRC, colon adenocarcinoma, and rectum adenocarcinoma when eNOS was upregulated. However, a low expression of iNOS isoform decreased the 5-year survival of these patients (Additional file 6: Figure S6). Thus, as found for mesenchymal CRC tumors, the overexpression of eNOS and low expression of iNOS resulted in a poor prognosis in CRC. Overall, the above results suggest that the eNOS isoform is the main source of NO in mesenchymal poor-prognosis tumors.
eNOS is upregulated in intestinal epithelial organoids derived from Apcfl/fl mice and NO scavenging decreases their proliferation and stem-cell marker expression
NO depletion abolishes the capacity of CRC cells to form tumorspheres and organoids in vitro and impairs CSC-related pathways
The above results demonstrate a regulatory role for NO in the CSC phenotype and emphasize the importance of the production of this molecule by eNOS in maintaining this phenotype. Moreover, NO scavenging is shown to be an appealing alternative to the typically used iNOS inhibitors in cancer, particularly in stem-cell-like or mesenchymal tumors.
NO scavenging reduces the capacity of mesenchymal CRC cancer cells to form tumors in xenograft mouse models
Although there is emerging evidence indicating that CSCs are responsible for cancer aggressiveness, chemoresistance, and relapse, which results in high mortality rates , there is a little knowledge about their regulation. Different biological mediators in tumor microenvironments may cause reversible changes in a CSC population . The iNOS isoform has been shown to be the predominant enzyme that promotes tumor progression through NO production  and has prompted the search for new therapies based on inhibitors against the iNOS isoform . Nevertheless, there is a huge controversy about the role of iNOS in colon cancer [16–20], and this approach offers a limited therapeutic benefit in contexts where constitutive isoforms are the main or even the only source of NO . Moreover, there are non-enzymatic sources of NO, which are not blocked by NOS inhibitors . Furthermore, NO scavenging shows a second-order reaction kinetic, decreasing NO preferentially in regions of aberrant overproduction and having a light impact on essential basal NO levels . Thus, NO scavengers emerge as an alternative approach to targeting this molecule before it can exert its effects, trapping NO from all sources.
In 1997, Takahashi et al. showed there was increased expression of eNOS in endothelial cells of azoxymethane-induced rat colon tumors . Although the effects of NO from the eNOS isoenzyme on tumorigenesis have been mainly related to its expression in endothelial cells , tumor-expressed eNOS and its role in initiation and maintenance of the tumorigenic process have been previously shown in other tumors . Actually, an upregulation of eNOS expression was found in undifferentiated regions compared to differentiated tumor areas in a murine mammary tumor model, and strongly eNOS-positive tumor cells have been found in lung metastatic sites .
Here, to elucidate the role of NO in CSC biology, we used the early tumorigenesis VilCre ERT2 Apc fl/fl mouse model, where the deletion of both copies of this gene results in a crypt progenitor-like phenotype characterized by augmented proliferation and CSC subset expansion . Epithelial cells from intestinal Apc fl/fl crypts showed intense immunostaining of eNOS, whereas crypts from wt mice did not show any expression of this isoenzyme. In fact, the conditional VilCre ERT2 Apc fl/+ mouse model showed that the haploinsufficiency of the Apc gene is enough to upregulate the expression of eNOS and increase the production of NO in tumors. These results support the relevance of eNOS isoform in this context of Lgr5-positive stem cell expansion. The production of NO in the colon has been linked with a higher risk of colon cancer  and our results suggest that the eNOS isoenzyme seems to be an important source of these molecules in early mutational events of the disease. Similarly, invasive tumors from the more invasive VilCre ERT2 Apc fl/+ Pten fl/+ mouse model showed that eNOS was upregulated in tumors whereas normal crypts did not show any expression. Interestingly, iNOS expression was absent in all three independent mouse models, supporting the hypothesis that eNOS is the most relevant NOS during the first stages of the disease.
We also classified 40 human colorectal tumors into five molecular subtypes according to Sadanandam et al.  and De Sousa et al. . The stem-like subtype matches the mesenchymal CMS group of the most robust classification system currently available for CRC and has the worst relapse-free and overall survival . This mesenchymal phenotype has been shown to be regulated by different pleiotropic-acting molecules, including miRNAs . Here, we obtained a significant signature of 11 miRNAs, which differentiates the mesenchymal subtype from the other tumors. Similarly, we obtained a specific immune response in the classified human mesenchymal tumors. In particular, a significant increase of dendritic cells, CD45 cells, macrophages, and mast cells was found in mesenchymal tumors. This is consistent with the fact that the stromata of these tumors are infiltrated with endothelial cells, cancer-associated fibroblasts, and also innate immune cells [11, 52]. Moreover, these tumors showed an upregulation of immune response genes such as complement signaling genes, whose overexpression has been shown in mesenchymal tumors . These three signatures generate a robust classification of the mesenchymal tumors, which differentiates them from the other tumors. Notably, gene expression analysis of NOS isoforms revealed that eNOS was significantly upregulated in the mesenchymal subtype whereas iNOS was absent. This result suggests that eNOS is the most relevant enzymatic source of NO in this poor-prognosis tumor subtype and may represent an active stem-cell regulatory point in cancer as well as a possible target for therapy against aggressive human tumors.
In vitro tumor organoid models could be used to interrogate the sensitivity toward different drugs and to predict patient response . Here, we found that eNOS was significantly upregulated in Apc fl/fl organoids compared to their normal counterparts whereas iNOS was downregulated. Moreover, we showed that scavenging NO with the highly specific NO scavenger c-PTIO  significantly decreased the proliferation of Apc-deleted organoids, markedly decreasing the Lgr5 population and downregulating the expression of other stem-cell markers including Troy , Vav3 , and Slc14a1 . These results support again the implication of NO in maintaining the CSC phenotype. Moreover, the withdrawal of NO with c-PTIO impaired the CSC phenotype of CRC cells, decreasing their self-renewal capacity and the expression of key proteins considered as putative targets in CSC signaling pathways, such as Notch, β-catenin, and Bmi1 . The effect was molecule-specific since the use of NO donors allowed tumor cells to recover their initial phenotype and abrogated the anti-CSC effect of c-PTIO. Furthermore, scavenging NO with c-PTIO in iNOS-knockdown HCT-116 cells also resulted in an impairment of the CSC phenotype, highlighting the relevance of eNOS-produced NO. These results suggest that targeting CSC self-renewal through NO scavenging could be a valuable approach in cancer therapy.
According to the CSC model, only this subset of tumor cells has the capacity to generate tumors in xenotransplantation experiments with immunocompromized mice due to its self-renewal properties and wide proliferative potential . Herein, the abrogation of NO for 24 hours generated tumors with 50% less volume in a xenograft model with mesenchymal HCT-116 CRC cells. This result supports the idea that NO trapping causes long-term changes in the CSC phenotype of tumor cells, decreasing their enormous proliferative capacity. Furthermore, we found an impaired tumor growth capacity in c-PTIO-treated mice, which formed tumors significantly smaller than those of untreated mice. These tumors did not show iNOS expression, whereas intense immunostaining of eNOS was found. Moreover, tumors formed in c-PTIO-treated animals showed a downregulation of β-catenin and Bmi1 expression, which is a key protein required for CSC function in colorectal tumors and represents an effective target for controlling tumor growth .
In summary, our data show that eNOS upregulation is as an early event in CRC together with Apc loss and this overexpression is maintained in other more advanced tumor genotypes. This isoenzyme is upregulated in different scenarios where the CSC phenotype is enhanced, including different mice conditional CRC models, human mesenchymal CMS tumors, and poorly differentiated aggressive adenocarcinomas. Moreover, the NO scavenger c-PTIO has been shown to impair the stem-related signaling pathways essential for CSCs in vitro and to have an antiproliferative effect in vivo, decreasing β-catenin and Bmi1 expression in a xenograft mouse model. Since targeting the CSC population is increasingly becoming a priority in cancer research, our results indicate that eNOS is an unexpected potential new target in human poor-prognosis mesenchymal colorectal tumors.
Patients and inclusion criteria
Forty patients over 18 years of age with resectable CRC and submitted to surgery in Reina Sofía Hospital (Córdoba, Spain) were included in the study, which was approved by the Reina Sofía Hospital ethical committee. Signed informed consent was obtained from each patient.
Classification into colon cancer subtypes
We used the nCounter Element system from NanoString to analyze the RNA expression of a set of genes and classify CRC samples according to Sadanandam et al.  (five subtypes) and De Sousa et al.  (three subtypes), both classifiers strongly relating to each other. Data analysis was performed using nSolver software (NanoString Technologies, Seattle, WA, USA) to manage the raw data generated for the expression of each gene. Then, the raw data expression readouts were normalized and an overall average (mean) was established for each gene. The positive expression of one particular gene indicates that the number of RNA molecules is above the average, whereas negative expression indicates that it is below the mean of the number of RNA molecules. An miRNA signature from different tumor subtypes was obtained using the nCounter human v3 miRNA expression assay from NanoString. Tumor immune response in the different tumor subtypes was obtained using the nCounter PanCancer immune-profiling panel from NanoString.
First, 4-μm-thick sections were mounted on poly-L-lysine coated slides, deparaffinized in xylene, and rehydrated using graded alcohols. Antigen retrieval was accomplished with a 10 mM citrate buffer (pH 6.0) at 95–98 °C for 20 min. Endogenous peroxidase was neutralized using EnVision FLEX peroxidase-blocking reagent (Dako, Denmark) for 10 min. Tween-phosphate-buffered saline (PBS) was used as the washing solution. Tissue sections were blocked with 3% bovine serum albumin and the mouse-on-mouse staining protocol (Abcam) was used for mouse samples with eNOS mouse-produced antibody. Anti-eNOS (6H2) (1:200, Cell Signaling, Danvers, MA, USA, ref 02/2016, lot 2, RRID AB_10850618), anti-iNOS (1:100, Invitrogen, lot RJ2276825, RRID AB_2537941), anti-Bmi1 (1:400, Abcam, lot GR301384-1, RRID AB_2065390), and β-catenin (BD, East Rutherford, NJ, USA, 1:100, lot 5121508, RRID AB_397554) were used as primary antibodies. EnVision FLEX + mouse (linker) (Dako) was use for eNOS staining in mouse samples. EnVision FLEX/HRP (Dako K8000) was used as the secondary antibody for 30 min at room temperature, followed by 3,3'-diaminobenzidine (DAB) staining (Dako liquid DAB + substrate chromogen system, Dako). Sections were then counterstained with hematoxylin, dehydrated, and mounted.
Quantitative real-time reverse-transcriptase polymerase chain reaction
Total RNA extraction was performed using RNeasy Mini Kit (Quiagen, Hilden, Germany) following the manufacturer’s recommendations. iScript gDNA clear cDNA synthesis kit (Bio-Rad) was used to obtain cDNA and real-time PCR was performed using Sensifast SYBR NO-ROX mix (Bioline, London, UK). Expression levels of eNOS, iNOS, Lgr5, Troy, Vav3, and Slc14a1 were measured by quantitative real-time PCR (qPCR) using LightCycler 480 Instrument II (Roche, Basel, Switzerland). Primer sequences are described in Additional file 8: Table S1. Results were normalized to glyceraldehyde 3-phosphate dehydrogenase (GADPH) and relative expression was determined by the 2-∆∆Ct method.
c-PTIO was purchased from Sigma-Aldrich (St Louis, MO, USA) and DETANONOate from Cayman Chemical (Ann Arbor, MI, USA). S-nitrosocysteine (CSNO) was synthesized as previously described  by incubation of L-cysteine with acidified sodium nitrite and quantification by absorbance at 334 nm using a molar absorption coefficient of 0.74/mM/cm. IL-1β, IFN-γ, and TNF-α were purchased from R&D Systems.
HCT-116 cells (DSMZ, Braunschweig, Germany) were grown in McCoy’s 5A medium (Biowest) containing 10% fetal bovine serum (FBS) (PAA Laboratories, Pasching, Austria). Caco-2 cells (ECACC, Salisbury, UK) were grown in MEM medium (Biowest, Nuaillé, France) containing 15% FBS (PAA Laboratories) and MEM non-essential amino acids (Biowest). Culture media were supplemented with 2 mM glutamine (Biowest) and Zell Shield antibiotics (Minerva Biolabs, Berlin, Germany). Cells were maintained in a humidified atmosphere at 37 °C and 5 °C CO2.
Western blot analysis
Cells were treated with c-PTIO, c-PTIO and DETANONOate, or CSNO for 24 hours and protein lysate extraction and immunoblotting were performed as described elsewhere . Primary antibodies recognizing Notch1 (Abcam, Cambridge, UK, 1:2000, lot GR215257-19, RRID AB_881725), Bmi1 (Abcam, 1:5000), β-catenin (BD, 1:2000) and Sox2 (R&D Systems, Minneapolis, MN, USA 1:1000, lot KOY0212101, RRID AB_355110) were used. Stain-free technology (Bio-Rad, Hércules, CA, USA) was used as loading protein control and densitometric analysis was performed with Image Lab software (Bio-Rad).
Colonosphere formation assay
Cells were treated while growing in adherence and then trypsinized and seeded at clonal density (1 cell/μL) in ultra-low attachment surface 96-well plates (Costar, Corning, NY, USA) with serum free Dulbecco’s MEM Nutrient Mixture F + 12 HAM (Sigma-Aldrich) supplemented with 1× B27 (Invitrogen, Carlsbad, CA, USA), 10 ng/ml bFGF (Prepro Tech, London, UK), 20 ng/ml EGF (Santa Cruz Biotechnology, Heidelberg, Germany) and 1% (v/v) methylcellulose (R&D Systems) to prevent cell aggregation. Every 2–3 days, freshly supplements were added. The number and size of colonospheres were analyzed by optical microscopy 1–2 weeks after seeding.
Organoid formation assay
Cells were treated while growing in adherence and then trypsinized and embedded in Matrigel (growth factor reduced, phenol red free; BD) on ice and seeded in 24-well plates (10–25 single cells/μL of Matrigel per well). The Matrigel was polymerized for 10–15 min at 37 °C and then 500 μL/well basal culture medium (advanced DMEM/F12) supplemented with Zell Shield antibiotics (Minerva Biolabs), 1× B27 and 1× N2 (Thermo Scientific, Waltham, MA, USA) was added. The number and size of organoids were analyzed by optical microscopy 1–2 weeks after seeding.
For wt or VilCre ERT2 Apc fl/fl mouse organoids, crypts, fragments of epithelium, or single cells were seeded in 24-well plates (50 and 10 fragments per 10 μL of Matrigel per well, respectively). After 24 hours, organoids were treated with c-PTIO for 48 hours and proliferation was determined by analyzing the images with ImageJ software.
Confocal immunofluorescence: in situ staining of organoids within Matrigel
Cells were plated in 60 μL of Matrigel in μ-slide eight-well ibiTreat chamber slides (Ibidi, Martinsried, Germany) and overlaid with advanced DMEM/F12 supplemented with Zell Shield antibiotics, 1× B27 and 1× N2 supplement. Cell-derived organoids were observed for 16 days and then they were fixed in situ for 5 min each with −20 °C 100% methanol and 2% formaldehyde in PBS. The chambers were washed twice for 5 min with PBS and once for 5 min with PBS-Tween. The slides were blocked with 3% bovine serum albumin for 30 min and incubated with β-catenin antibody (BD, 1:50) at 4 °C overnight and washed three times for 5 min with PBS-Tween. Organoids were then incubated with Alexa Fluor 488 secondary antibody (Thermo Fisher, 1:200) at 4 °C overnight and were washed three times for 5 min with PBS-Tween. Nuclei were stained with DAPI and serial images were taken using a Zeiss LSM 710 confocal microscope.
Lentiviral particles transduction and iNOS-silenced clone selection
HCT-116 cells were seeded (12,000 cells/well) in 96-well plates to be transduced at 50–80% confluency. To enhance the transduction, 8 μg/ml hexadimethrine bromide (Sigma-Aldrich) was added to the cells. Then, viral particles containing iNOS shRNA or non-target control shRNA were added at 5× multiplicity of infection and the cell–viral particle mixture was incubated at 37 °C overnight. After incubation, the viral-particle-containing medium was removed and replaced with fresh complete culture medium. Cells were expanded to obtain a sufficient amount for selection of transduced cells. Then, cells were harvested in filtered (0.2 μm) basic sorting buffered (1× phosphate buffer, 2 mM EDTA, 25 mM HEPES pH 7.0, 2% FBS, and Zell Shield antibiotics) and green fluorescent protein-positive cells were sorted by flow cytometry (FACSAria III, BD) with a 100-μm nozzle in a cloning 96-well plate. Clones were grown in 50% FBS complete medium and iNOS downregulation was confirmed by RT-qPCR.
Mouse xenograft model
The experiment with mice was approved by the Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC) Ethical Committee and followed all the ethical protocols established. To establish a subcutaneous colorectal xenograft model, control cells or cells treated with c-PTIO for 24 hours (2.5 × 106 HCT-116 in 100 μL Matrigel) were implanted subcutaneously into the flanks of 5-week-old immunocompromized male NOD/SCID mice (NOD.CB17/AlhnRj-Prkdcscid, Janvier Labs). The experiment was terminated 37 days post injection and tumor volume was analyzed. To evaluate the in vivo effectiveness of c-PTIO, both hind flanks of 6-week-old male NOD/SCID mice (NOD.CB17/AlhnRj-Prkdcscid, Janvier Labs) were injected subcutaneously with 4 × 106 HCT-116 cells in 100 μL Matrigel. Eight-week-old mice were treated with one intraperitoneal injection per week of c-PTIO (320 mg/kg) or vehicle (PBS). Tumor growth was measured weekly using a digital caliper. The apparent tumor volume was calculated as lw2/2 and final tumor volume as (π/6) × lw ×h (l:lenght; w:width; h:height).
Student’s test was used to test for statistical significance. Error bars represent mean ± standard deviation.
We would like to acknowledge the following founding sources: Instituto de Salud Carlos III through the projects PI13/00553 and PI16/01508 (co-funded by the European Regional Development Fund/European Social Fund) “Investing in your future”). ARA was funded with a researcher contract through the program “Nicolás Monardes” from Junta de Andalucia. We also acknowledge the technical help of Álvaro Jiménez and Esther Peralbo from the Genomics and Microscopy Units at the IMIBIC.
Availability of data and materials
All data generated or analyzed during this study are included in this published article and its supplementary information files.
JP designed and performed most of the experiments, analyzed the data, and wrote the manuscript. LMLS helped to perform the xenograft experiments. RM helped to perform the CRC molecular classification. SGL helped to perform the immunohistochemistry assays. FC, VH, MT, VG, MR, CB, and JDR provided technical and material support. CV, CD, and JGB contributed to the collection and clinical characterization of human tumor samples. KM provided Apc mice models and technical support. EA and ARA conceived the project, designed the experiment, and revised the manuscript. EA and ARA share the senior authorship of this work. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The study was approved by the Reina Sofía Hospital ethical committee and signed informed consent was obtained from each patient. All animal work has been conducted according to national guidelines and animal experiments described herein were approved by the IMIBIC Ethical Committee.
The authors declare no competing interests.
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