Background
Bone sarcomas, a heterogeneous group of rare malignant tumors of mesenchymal origin [
1], occur primarily in adolescents and young adults. Bone sarcomas are classified genetically into two categories: osteosarcoma (OS) is characterized by complex karyotypes indicative of severe genetic and chromosomal instability [
2], while Ewing’s sarcoma (EWS) is characterized by the presence of tumor-specific translocations. OS is the most common primary tumor of the bone and it is usually found at the end of long bones, often around the knee [
3]. The etiology of OS is not well understood, as well as a clear link between OS and inherited genetic mutations or specific genetic changes has not been established, although patients with Li-Fraumeni syndrome have a high risk of developing OS by inheriting mutations that silence the p53 tumor suppressor gene (for a comprehensive review see [
4]). EWS typically develops in the femur and tibia. The most common mutation associated with EWS involves a translocation of chromosomes 22 and 11 (t (11;22)), which fuses a portion of the
EWSR1 gene with a portion of the
FLI1 gene to create a
EWS/FLI-1 fusion. This is a non-inheritable somatic mutation acquired only in tumor cells during a person’s lifetime [
5,
6].
Despite considerable improvements in the diagnosis and treatment of OS and EWS, progress in patient survival has remained stagnant for more than two decades [
7‐
9]. Current OS and EWS treatments consist of multiple modalities, traditionally including amputation or limb-sparing surgery, with the goal of complete tumor removal. Adjuvant therapies—such as radiation and chemotherapy—are used selectively in an effort to minimize both local recurrence and distant metastasis of the disease. Tumor resection often causes a massive bone defect that is difficult to treat. Thus, OS and EWS patients could benefit from a mesenchymal stem cell (MSC)-based therapeutic approach to bone reconstruction, alone or in combination with biomaterials to provide a structural support.
Recognition of the regenerative potential of MSCs is one of the most exciting fields in cell-based therapy; their safety and efficacy has been reported in > 250 clinical trials [
10]. MSCs are appealing because they can be isolated easily from bone marrow (BM) and several other human tissues, can be expanded
in vitro, have a high proliferative capacity, lack immunogenicity, display immunomodulatory properties, retain the ability to secrete soluble factors that regulate crucial biological functions, such as proliferation and differentiation over a broad spectrum of target cells [
11], and target damaged tissues and tumor sites (for a review see [
12,
13]). Most importantly, the ability of MSCs to differentiate into several cell lineages makes them ideal for reparative medicine [
14‐
16].
The use of MSCs for clinical applications requires
in vitro expansion. However, there is concern about the chromosomal stability and biosafety of expanded human MSCs, particularly those derived from sarcoma patients (for updated reviews see [
17,
18]). Several studies have indicated that murine MSCs acquire chromosomal abnormalities after a few
in vitro passages and generate OS after the
in vivo transplantation [
19,
20]. In contrast, MSCs derived from healthy human donors or patients with Crohn’s disease do not undergo malignant transformation after the
in vitro expansion [
21‐
26]. Centeno
et al. [
27,
28] reported that 227 patients treated for various orthopedic conditions by implanting autologous MSCs that had been expanded
in vitro using growth factors supplied by a platelet lysate did not experience any evident neoplastic complication with > 2 years of follow-up. Thus, it remains to be determined whether MSCs derived from healthy or sarcoma affected-patients have functional defects that could hamper therapeutic efficacy. In this study, we evaluated the characteristics of BM-derived MSCs from sarcoma patients and healthy controls
in vitro to assess their oncogenic potential before clinical application.
Methods
Study design
The in vitro biosafety profiles of BM-derived MSCs from OS and EWS patients (MSC-SAR) were compared to those of BM-MSCs from control healthy donors (MSC-CTRL) after expansion under the same culture conditions. Potential hallmarks of tumorigenic transformation were assessed by characterizing MSC morphology and immunophenotype, osteogenic and adipogenic differentiation, sequencing genes frequently mutated in OS and EWS, evaluating telomerase activity, assessing the gene expression profile of major cancer pathways, as well as cytogenetic analysis on synchronous MSCs, and molecular karyotyping using a comparative genomic hybridization (CGH) array.
Patients
The study was approved by the Rizzoli Orthopedic Institute Ethics Committee (Bologna, Italy), and all patients provided informed consent. Seven bone sarcoma patients and six healthy donors were included. Detailed information about the bone sarcoma patients is shown in Table
1.
Table 1
Characteristics of patients and bone sarcomas
MSC-SAR 1 | F | 36 | Osteosarcoma | Proximal humerus |
MSC-SAR 2 | M | 45 | Osteosarcoma | Distal femour |
MSC-SAR 3 | M | 17 | Ewing Sarcoma | Iliac crest |
MSC-SAR 4 | M | 20 | Osteosarcoma | Distal femour |
MSC-SAR 5 | M | 12 | Ewing Sarcoma | Femour |
MSC-SAR 6 | M | 63 | Condrosarcoma | Acetabolar |
MSC-SAR 7 | M | 17 | Osteosarcoma | Femour |
Isolation of bone marrow nucleated cells and MSCs expansion
Isolation of BM-derived MSCs was performed as described previously [
29] through gradient separation and plastic adherence. Briefly, 8 mL of undiluted BM aspirate were loaded into a BD Vacutainer® CPT™ tube (Becton Dickinson, Franklin Lakes, NJ, USA) and then processed according to the manufacturer’s instructions. The top layer containing plasma and mononuclear cells was harvested. The cell number was counted and the viability evaluated. For expansion, cells were then transferred to 150-cm
2 culture flasks by seeding 4 × 10
5 cells/cm
2 with α-Modified Minimum Essential medium (α-MEM; BioWhittaker, Lonza, Verviers, Belgium) supplemented with 20% lot-selected fetal bovine serum (FBS; Gibco, Invitrogen-Life Technologies, Paisley, UK) and 1% GlutaMAX™ (Invitrogen-Life Technologies). The flasks were incubated at 37°C in a humidified atmosphere of 5% CO
2 with medium change every 3–4 days. When the cells reached ~70–80% confluence, they were detached by mild trypsinization (TripLe™ Select, Invitrogen-Life Technologies) for 3 min at 37°C and counted. Cells were reseeded into a new 150-cm
2 flask at a density of 4000 cells/cm
2.
Immunophenotypic characterization
Phenotypic characterization of MSCs was performed by fluorescence-activated cell sorting (FACS) analysis of cell-surface markers at passage 2 (P2). MSCs were labeled with monoclonal antibodies against CD34, CD45, CD44, CD90, CD105, CD166 (Beckman Coulter, Fullerton, CA, USA) and CD146 (Miltenyi Biotech, Bergisch Gladbach, Germany). Control samples were labeled with isotype-matched control antibodies (Beckman Coulter, Brea, CA, USA). In brief, cells were trypsinized and aliquoted at a concentration of 1 × 106 cells/mL, fixed in 0.5% formalin for 20 min, and washed once in PBS. Next, samples were incubated with either conjugated specific antibodies or isotype-matched control mouse immunoglobulin G at the recommended concentrations. Labeled cells were washed twice and suspended in FACS buffer. The analysis was performed using a FC500 flow cytometer (Beckman Coulter).
Cell proliferation
Cell number and viability were assessed for each passage using a NucleoCounter® device (ChemoMetec, Lillerød, Denmark) that detects non-viable cells by propidium iodide nuclear staining and determines cell viability by calculating the ratio of non-viable to total cell numbers. The number of population doublings (PD) for each passage was calculated using the formula: log
2
(N
1
/N
0
), where N
0
is the number of cells seeded and N
1
the number of cells harvested at the end of the passage and cumulative population doubling (CPD) refers to the sum of PDs over passages.
Senescence assay
Senescence was detected by staining MSCs with a β-galactosidase (SA-β-gal) staining kit (Cell Signaling Technologies, Danvers, MA, USA) according to the manufacturer’s instructions, and analyzed with a direct-light microscope. Briefly, 1 × 104 cells were plated in a 35-mm2 dish and incubated overnight at 37°C. After removing the growth medium, cells were washed twice with PBS, fixed for 10–15 min at room temperature, and incubated at 37°C overnight in a dry incubator (atmospheric CO2) with fresh β-gal staining solution. β-gal–positive cells were monitored under a microscope for the development of blue color and subsequently imaged.
MSCs differentiation in vitro
Osteogenic differentiation was induced at P3 by seeding MSCs in α-MEM supplemented with 2% FBS in six-well plates at 5 × 10
5 cells per well. The next day, an osteogenic-inducing cocktail composed of 10 mM β-glycerophosphate (Sigma, St. Louis, MO, USA), 50 μg/mL ascorbic acid (Sigma) and 100 nM dexamethasone (Sigma) was added. As a negative control, cells seeded under the same conditions were maintained in a non-inducing medium. Media were changed twice per week. After 14 days, the samples were stained with Alizarin Red-S (AR-S) (Sigma) to reveal the deposition of a calcium-rich mineralized matrix [
30]. Adipogenic differentiation was induced at P3 by seeding 5 × 10
5 MSCs/well in a six-well plate in Dulbecco’s Modified Essential Medium-high glucose (DMEM–HG; Euroclone, Milan, Italy) supplemented with 2% FBS (Gibco) and incubated overnight to allow cell attachment. Then, medium was switched to adipogenic-induction medium composed of DMEM–HG supplemented with 2% FBS, 10 μM bovine insulin (Sigma, St Louis, MO, USA), 1 μM dexamethasone (Sigma), 200 μM indomethacin (Sigma) and 500 μM 3-isobutyl-1-methyl xanthine (IBMX, Sigma). As a negative control, cells seeded under the same conditions were maintained in non-inducing medium. Media were changed twice per week. After 21 days, the presence of lipid depots was visualized by staining samples with Oil Red O. In brief, cells were washed twice with phosphate-buffered saline (PBS; Euroclone, Milan, Italy), fixed in 4% paraformaldehyde (Sigma) for 10 min and stained with 0.18% Oil Red O (Sigma) for 15 min.
Cell-cycle synchronization and cytogenetic analyses
It has been reported [
21] that 20–25 valuable metaphase cells/slides can be obtained by synchronizing MSCs. To synchronize the cell cycle, MSCs at > 80% confluence were detached, re-plated at 7000 cells/cm
2, and maintained in culture medium without FBS for 20 h. After that, complete medium containing FBS was returned to the cultures for 27–28 h and incubated at 37°C with 0.1 mM colcemid solution (Irvine Scientific, Santa Ana, CA, USA). After 4 h, cells were harvested, treated with 0.56 mM KCl, and fixed in methanol/acetic acid (3:1). Cells in metaphase were Q-banded and karyotyped in accordance with the International System for Human Cytogenetic Nomenclature recommendations.
CGH array
Molecular karyotyping was performed by CGH array with the Agilent kit 2 × 105 K (Human Genome CGH Microarray, v. 5.0, Agilent Technologies, Santa Clara, CA, USA), according to the manufacturer’s protocol, as described previously [
24]. The analysis was performed on four MSC-SAR and four MSC-CTRL samples. The minimum positive criteria for an imbalance was considered to be three consecutive oligomeres with a log
2 ratio different from zero; thus, the theoretical resolution of the 105 K 60-mer oligonucleotide platform was ~80 kb. DNA was extracted using QIAamp DNA Blood Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer’s protocol. Array-CGH experiments were analyzed using the Agilent scanner and Feature Extraction software (v. 9.1). A graphical overview was obtained using the CGH Analytics software (v. 3.4.27). Quality control parameters for each experiment were evaluated using the QC metric tool in the CGH Analytics software.
Telomerase activity assay
Telomerase activity was measured by a quantitative real-time PCR-based telomeric repeat amplification protocol (TRAP). MSC-SAR and MSC-CTRL were analyzed by the TeloExpress quantitative telomerase detection kit (Express Biotech International, Thurmont, USA), according to the manufacturer’s instructions. The Huh7 cell line was used as a telomerase-positive control. The results obtained from each MSC sample were compared with a control template standard curve for final absolute quantification of telomerase activity, expressed as attomole of telomerase repeat sequences in 1-μg protein (attomol/μg protein).
Gene sequencing
MSCs obtained from cultures of sarcoma and healthy donors were harvested at early and late passages and washed in PBS buffer. DNA was isolated using the Nucleospin Blood kit (Macherey-Nagel, Dueren, Germany) according to manufacturer’s instructions. DNA quality and quantity were assessed with a NanoQuant Infinite M200 instrument (Tecan Group Ltd, Männedorf, Switzerland) before sequencing.
DNA samples were analyzed for mutational screening of TP53, CDKN1A/p21 and MDM2 genes. The 11 exons of TP53, the 3 exons of CDKN1A along with exon–intron junctions, and SNP309 (rs2279744) in MDM2 were PCR-amplified using primer sequences that will be available upon request. The amplification products were purified using ExoSap-IT reagent (USB Corp., Cleveland, OH, USA) and sequenced in both the forward and reverse directions using BigDye Terminator chemistry version 3.1 (Applied Biosystems, Foster City, CA, USA). Purification of sequencing products was performed with BigDye X-Terminator kit and samples were analyzed using an ABI Prism 3100 automated DNA sequence (Applied Biosystems). Reference sequences for TP53, CDKN1A, and MDM2 were obtained from GenBank (accession numbers NM_000546.4, NM_000389 and NM_002392.3, respectively).
Gene expression analysis
Total RNA from MSC-SAR and MSC-CTRL harvested at early and late culture passages, as well as from subconfluent osteosarcoma cell line U2OS (#HTB-96, ATCC, Teddington, United Kingdom), was isolated using the Qiagen RNeasy mini kit (Qiagen) according to the manufacturer’s instructions. RNA concentration was assessed with a NanoQuant Infinite M200 instrument (Tecan Group Ltd, Männedorf, Switzerland) and RNA integrity was verified spectrophotometrically by 260/280 nm ratios > 2.0 and 260/230 nm ratios > 1.7. An equal amount of RNA (500 ng) was used for reverse transcription using the RT2 First Strand Kit (Qiagen) using protocol steps that eliminated genomic DNA.
qPCR experiments were performed using the Human Cancer Pathway Finder PCR Array (RT
2 Profiler PCR Array PAHS-033R, SABioscience, Frederick, MD, USA) and RT
2 SYBR Green ROX Fast Mastermix (Qiagen) on a Rotor-Gene Q instrument. The total volume of the PCR reaction was 20 μL and reactions were setup with a Biomek® NX Span-8 automated workstation (Beckman Coulter, Indianapolis, IN, USA) equipped with an adaptor designed to hold Rotor-disc 100 (Qiagen). The thermocycler parameters were 95°C for 10 min, followed by 40 cycles at 95°C for 15 s and then at 60°C for 30 s. The PCR array profiles the expression of 84 genes involved in transformation and tumorigenesis. Four housekeeping genes (
B2M, HPRT1, RPL13A, ACTB), RT controls, and PCR controls were included in each run. Relative expression of target genes was determined using the ΔΔCq method, as described by Livak and Schmittgen [
31]. PCR-array data were analyzed using the web-based software “RT2 Profiler PCR Array Data Analysis v. 3.5”, available at the manufacturer’s website [
32]. The analysis was performed on four MSC-CTRL, four MSC-SAR, and three U2OS samples.
Statistical analysis
Linear regression of CPD curves from MSC-SAR (n = 6) and MSC-CTRL (n = 6) was performed using GraphPad Prism version 5.00 for Windows (GraphPad Software, San Diego, California USA). The same software was used to compare the mean best-fit slope of two groups.
Discussion
The most common surgical techniques used to treat osteosarcoma around the knee include resection of the epiphysis and reconstruction with a prosthesis, an osteoarticular allograft, an autoclaved autograft, or a combination of the above. The functional results of prostheses and osteoarticular grafts are not satisfactory because of limited durability, joint instability, incongruity, and gross distortion of the normal anatomy. It has been reported that autologous MSCs loaded onto hydroxyapatite scaffolds can successfully heal segmental bone defects in human and animal models [
42‐
44]. In human bone diseases, MSCs are usually delivered or applied locally, often in combination with suitable scaffolds, when it is necessary to provide mechanical stabilization or support to osteosynthesized fractures of long bones [
45] and in atrophic non-unions. Although controversial, MSCs seeded on hydroxyapatite scaffolds have also been used to heal defects derived from curettage of a bone tumor as an alternative to autologous bone grafting [
46]. However, the possible risks of MCSs transplantation are debated. Major concerns have been raised with regard to the biosafety of the
in vitro expanded MSCs, particularly when intended for autologous transplantation in a cell therapy protocol for bone reconstruction of sarcoma patients. Data from a mouse xenograft model proposed that MSCs are precursors of tumor stromal cells [
47] or might differentiate into tumor-associated fibroblast-like cells when cultured in tumor cell-conditioned supernatant [
48]. Therefore, our
in vitro studies will facilitate the safe use of expanded autologous MSCs for tissue engineering strategies to induce bone reformation.
In the present work, we performed cell expansion experiments under previously standardized culture conditions [
29] and assessed
in vitro the biosafety profile of MSCs isolated from the BM of sarcoma patients compared to control donors. Based on the “hallmarks of cancer” criterion [
49], human cells acquire biological capabilities during tumor development in a multi-step process. These hallmarks include sustaining proliferative signaling, evading growth suppressors and enabling replicative immortality, which are all traits found in OS cell lines. We investigated the hallmarks of cancer in MSC-SAR at several levels; the results suggest that MSC-SAR exhibit comparable morphology, immunophenotype, proliferation rate, differentiation potential, and telomerase activity to MSCs of healthy donors. The
in vitro expansion of both MSC-SAR and MSC-CTRL resulted in a progressive aging mechanism coupled to typical traits of altered cell morphology that are consistent with a previous study [
50].
DNA sequencing of
TP53,
CDKN1A/p21 and
MDM2, which are key players in cell cycle regulation and are involved in tumor of mesenchymal origin, did not detect pathological mutations. In addition, the existence of tetraploid cells in both early and late passages of MSCs cultures raises the crucial question whether MSCs clones with a genomic imbalance may acquire a malignant phenotype
in vivo, although they are able to reach the senescence phase
in vitro. The detection of tetraploid cells at similar percentages from MSC-SAR and MSC-CTRL suggests that this chromosomal aberration is not a distinctive feature of MSCs expanded
in vitro from the BM of sarcoma patients. Rather, this chromosomal aberration may be induced by
in vitro culture conditions during expansion procedures that are optimized to achieve a high proliferation rate and to obtain the large number of cells necessary for the analyses and for cell-based therapy approaches. Moreover, it is worth considering that polyploidies were already present in early culture passages, but these positive clones did not acquire a proliferative advantage during culture. These data are in agreement with a previous report by Tarte
et al. [
51] documenting, by conventional karyotype analysis, donor-dependent chromosomal abnormalities in healthy donor BM-MSCs that did not confer a selective advantage to the affected clone.
Gene expression analysis of 84 genes involved in cancer development provided a comparison of MSC-SAR and MSC-CTRL at a translational level. In this study, we used U2OS as a reference tumor cell line and, as expected, 33 of 84 genes investigated were altered when compared to MSC-CTRL. Interestingly, we observed down-regulation of p16 expression, which is responsible for escape from senescence and restoration of cell proliferation activity. Furthermore, several genes were overexpressed > 100-fold in U2OS compared to MSC-CTRL. As an example, MMP9 was overexpressed 152-fold, which is pertinent since MMPs are involved primarily in the breakdown of extracellular matrix and possibly promotion of tumor invasion.
A comparison of gene expression between MSC-SAR and MSC-CTRL revealed that the expression of 15 genes was significantly different, although none of these genes are principally involved in bone sarcoma etiology. While the expression of these 15 genes was altered in U2OS compared to MSC-CTRL, there was no difference between MSC-SAR and MSC-CTRL. For example,
MMP9 was increased 4.05-fold in MSC-SAR compared to MSC-CTRL at P3, even though no significant difference in
MMP9 expression was found at P10, suggesting that an increase in
MMP9 expression in MSC-SAR was not a stable indicator.
ANGPT2 and
CDC25A maintain higher expression levels during
in vitro culture in MSC-SAR compared to MSC-CTRL, but expression of these genes has not been correlated with bone sarcoma etiology (Figure
6A,B). Our analysis determined that expression of the mitogenic growth factor PDFGB increased with time in culture in MSC-SAR (Figure
6B). Moreover, the level of the tumor suppressor gene
SERPINB5 was higher in MSC-SAR at late culture passages (Figure
6B). Conversely,
VEGFA was slightly underexpressed in MSC-SAR at early stages of culture (Figure
6A), and decreased over time (Figure
6B).
Gene expression analysis could provide a signature that will facilitate routine evaluation of the safety of in vitro- expanded MSCs and assessment of the presence of suspicious modifications. Our results support the hypothesis that MSC-SAR do not present a greater risk of undergoing transformation compared to MSC-CTRL. More extensive analysis should be performed to confirm the dysregulation of cancer pathways and exclude possible effects resulting from MSCs aging. The expression of tumor suppressor genes and oncogenes may in fact shift with time in culture and be influenced by stress response mechanisms that are activated under in vitro culture conditions. Our encouraging in vitro results will be expanded upon using in vivo approaches to confirm MSC-SAR safety in an animal model through long-term follow-up and careful examination of the transplanted animals.
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Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
EL, SD and CB carried out the isolation and in vitro expansion of MSC-CTRL and MSC-SAR, performed immunophenotypic characterization, cell proliferation analysis, and MSC differentiation in vitro. SD performed gene expression analysis, while CB analyzed the data and performed the statistical analysis. SD drafted the manuscript and EL coordinated the study and assisted in drafting the manuscript. MM, MAA and RM participated in the in vitro expansion of MSC-SAR and MSC-CTRL to perform the senescence assay and cytogenetic analyses of cell-cycle synchronized cultures. FN, GA and OZ in vitro expanded the MSC cultures and performed CGH array and the corresponding data interpretation. MZ, MP and LS carried out the DNA sequencing analyses and the relative data interpretation. DL performed the telomerase activity assay. DD carried out the BM harvest of all collected MSC samples (MSC-SAR and MSC-CTRL) used in this paper, conceived the study and participated in its design. All authors read and approved the final manuscript.