The uncertain role of unmodified mesenchymal stem cells in tumor progression: what master switch?
© BioMed Central Ltd 2013
Published: 18 March 2013
Mesenchymal stem cells (MSCs) are emerging as promising gene vectors for cancer therapy because of their unique characteristics, including the ease of their expansion and genetic modification and their remarkable tumor-tropic properties. However, there remains a concern that MSCs may promote cancer progression. Surprisingly, there are conflicting reports within the literature describing both the promotion and inhibition of cancer progression by MSCs. The reasons for this discrepancy are still unknown. The surface markers, differentiation ability, and tumorigenic roles of MSCs, as well as their effect on immunoregulation, produce heterogeneity. In this review, we describe the heterogeneity of MSCs by the species from which they are derived, the methodology for their isolation and the context of their interactions with cancer cells. The conflicting roles of MSCs in tumor progression may be attributable to the bimodal effect of unmodified MSCs on immunoregulation. MSCs have been reported to suppress T-cell function and inhibit graft-versus-host disease (GVHD). On the other hand, MSCs elicit the graft-versus-tumor (GVT) effect in some cases. Selective allodepletion may be used to dissociate GVHD from the GVT effect. Understanding the conditions that balance GVHD and the GVT effect of MSCs may be crucial to advance cancer therapy research with respect to MSCs.
Cancer is a highly prevalent, life-threatening disease that affects people around the world. The major limitation of cancer therapeutic strategies is the lack of tumor specificity . Pre-clinical and clinical studies have shown that stem cell-based therapies hold tremendous promise for the treatment of human disease . Mesenchymal stem cells (MSCs) have been considered as potential therapeutic cells for tissue repair, bone fracture, cartilage defects, graft-versus-host disease (GVHD), inflammatory disorders and type I diabetes [3–5]. The potency of MSCs for differentiation is the basic premise on which regenerative medicine is established. MSCs have the ability to differentiate into osteocytes and chondrocytes. Because of their multipotency, MSCs have also been used for treating heart failure and for neural repair [6, 7]. In addition to their ability to differentiate into damaged tissues, MSCs secrete cytokines and chemokines that provide the beneficial effects of regenerative medicine .
Recently, the extension of the therapeutic potential of MSCs to cancer therapy has raised great interest. For cancer gene therapy, it is important to achieve the expression of the therapeutic gene at specific tumor sites. Gene vectors are vehicles that deliver and express the corrective genes to specific sites. To date, gene vectors can mainly be divided into two categories: viral and non-viral. Although there has been intensive research focus on developing cancer cell-targeting viral and non-viral vectors, the benefits are still modest. MSCs have inherent tumor-tropic migratory properties, which allow them to serve as vehicles for delivering effective, targeted therapy to primary tumors and metastatic sites . Despite their tremendous potential, the effects of MSCs as therapeutic agents in cancers still need to be explored. Expression of exogenous anticancer molecules in MSCs by retroviruses or lentiviruses raises concerns regarding the potential risks associated with insertional mutation. In addition, it remains controversial whether unmodified MSCs promote tumorigenesis.
Bimodal nature of MSCs in tumorigenesis
Conflicting reports within the literature have indicated that MSCs act to either promote or inhibit cancer progression. The reason for this discrepancy is still unknown. It is important to elucidate the effects of MSCs on tumor progression before they are considered for use in clinical trials for cancer therapy.
There is substantial evidence supporting an inhibitory role of MSCs on cancer progression. MSCs are thought to inhibit tumor growth by increasing inflammatory infiltration , inhibiting angiogenesis , and suppressing Wnt signaling [11, 12] and AKT signaling , which have been reviewed in detail elsewhere . Human MSCs have been shown to inhibit the proliferation of tumor cells and induce apoptosis in tumor cells in vitro via soluble factors . Agents derived from extracts of umbilical cord MSCs have been reported to have tumor-inhibitory properties . Additionally, human skin-derived MSCs significantly inhibit glioblastoma growth in two different tumor models by releasing high amounts of transforming growth factor-β and down-regulating vascular endothelial growth factor, which might contribute to decreased tumor cell invasion and the number of tumor vessels . Bone marrow-derived MSCs can be safely expanded in vitro and are not susceptible to malignant transformation, suggesting these cells are suitable for cancer cell therapy .
On the other hand, the role of MSCs in promoting cancer progression is also supported by several studies. There is evidence suggesting that some cancers may originate from normal stem cells . Although genomic stability of MSCs in long-term cell cultures has been described, concerns regarding the possibility that MSCs undergo malignant transformation have still been raised. Spontaneous malignant transformation of MSCs in vitro was reported in adipose tissue and bone marrow-derived MSCs [20–22]; however, one of these that reported malignantly transformed MSCs was later confirmed to be cross-contaminated with human fibrosarcoma or osteosarcoma cell lines during the primary culture . Murine MSCs have been shown to be less stable and more prone to malignant transformation than their human counterparts . MSCs have been described to localize to tumor sites, where they integrate into the tumor-associated stroma [24, 25]. MSCs interact with tumor cells to promote tumor growth directly or indirectly in an autocrine or paracrine manner. Cancer cell-derived cytokines induce secretion of soluble factors by MSCs. The resulting factors operate in an autocrine manner to induce expression of a group of cytokines by the MSCs, then proceed to act in a paracrine fashion on the cancer cells . These cancer-promoting effects are mostly dependent on inflammatory cytokines secreted by MSCs . MSCs could be involved in cell survival, invasion, and motility through cytokine signaling [24, 27, 28]. MSCs are efficient in the chemoattraction of endothelial cells and promote angiogenesis  and are also able to differentiate into endothelial cells and vessel pericytes, thus contributing to neovasculogenesis [30–32]. The immunosuppressive properties of MSCs can also partly explain their cancer-promoting functions. A discrepancy also exists between in vitro and in vivo behavior, suggesting the involvement of the tumor microenvironment .
Some research has attributed the discrepancy of the effects of MSCs on tumorigenesis to the timing of MSC introduction into tumors . In vivo studies were performed injecting mixed MSCs and cancer cells or MSCs alone into animal models with established tumors. The presence of MSCs during early tumor growth may facilitate angiogenesis . The injection timing actually reflects the ratio of MSCs and cancer cells. In many co-injection studies, MSCs are usually injected at an equal number with their cancer counterparts, whereas when injected into the established tumor animal model, much fewer MSCs reach the tumor site compared to the cancer cells. When MSCs are the primary component of the tumor microenvironment, they have a tendency to promote metastasis [24, 27, 34]. The minimized direct contact of MSCs during tumor initiation may have a tendency to inhibit tumor cell growth . This finding strongly indicates that the interaction between MSCs and tumor cells is important to fully understand the impact of MSCs on tumor progression. MSCs along with other bone marrow-derived cells migrate to the sites of the primary tumor and prime distant tissues for tumor cell implantation and proliferation [24, 35, 36]. MSCs that are recruited to the tumor stroma create a cancer stem cell niche via cytokine networks [26, 37]. They interact with cancer cells and tumor-resident neighbors such as fibroblasts and macrophages. They also provide the homing sites for metastatic cells, leading to the establishment of metastatic foci. The primary tumor-derived vascular endothelial growth factor, placental growth factor (PlGF) or recently recognized exosomes induce reprogrammed bone marrow progenitors toward a pro-vasculogenic phenotype and support tumor growth and metastasis [36, 38, 39]. The multipotent differentiation of MSCs may be the decisive factor affecting cancer behavior. In addition to having the potential to differentiate into osteocytes, chondrocytes and adipocytes, MSCs have been described to have the potential to differentiate into neurocytes, heart cells and tumor-associated fibroblasts (TAFs). TAFs are part of the tumor stroma and provide functional and structural support for tumor progression and development. In addition to promoting angiogenesis and the proliferative capacity of tumor cells, TAFs have been implicated in enhancing tumor cell invasiveness, possibly through the induction of epithelial-mesenchymal transition . There are several suggested origins for TAFs, including tissue-resident cells, circulating cells and epithelial-mesenchymal-transformed cells . It is postulated that TAFs are derived from a subset of 'specialized' MSCs due to the high degree of similitude between the two cell types [25, 41]. It was reported that under long-term tumorigenic conditions in vitro, MSCs expressed TAF-like proteins . MSCs are supposed to lack hematopoietic cell markers such as CD34 and CD45; however, under tumorigenic conditions, CD11b, CD34 and CD45 were also expressed in MSCs [42, 43]. When co-implanted with metastatic cancer cells, all bone marrow-derived MSCs persisted and integrated into tumor stroma, but only CD11b-positive subsets of MSCs significantly promoted tumor growth and metastasis . Under tumorigenic conditions, MSCs underwent hematopoietic differentiation and showed characteristics of macrophage cells . Considering the close relationship between macrophages and tumor cells, the roles of MSCs in tumor progression become more elusive. The hematopoietic differentiation potential of MSCs makes cancer and the tumor micro-environment more complex.
Phenotypically and functionally heterogeneous MSCs
The isolation methods and sources of MSCs vary in different labs. Bone marrow is the main source of MSCs. In addition, MSCs can be isolated from adipose tissue, human umbilical cord Wharton's jelly, and synovial membranes. Although putative surface markers can be found on MSCs, the specificity of these markers is always under a shadow of doubt. These surface markers can also be found on non-stem cells. In addition, a particular marker may only be expressed on stem cells at a certain stage or under certain conditions . This discrepancy of surface marker expression as well as other heterogeneous properties of MSCs may be attributable to the isolation method and source of MSCs. MSCs isolated from human umbilical cord Wharton's jelly by the collagenase/trypsin method are enriched in expression of C-kit and Oct-4 . MSCs from bone marrow and Hoff's fat pad show a high potential to differentiate into chondrocytes whereas MSCs from subcutaneous fat demonstrate a poor potential for chondrogenesis . Rabbit and sheep MSCs were able to differentiate into chondrocytic lineages much more easily than human MSCs . Traditional culture medium for MSCs includes Dulbecco's modified Eagle's medium (DMEM) or minimum essential medium alpha (MEM-α) supplemented with fetal bovine serum (FBS). Growth factors such as basic fibroblast growth factor (bFGF) are sometimes added to keep the MSCs undifferentiated. Because of the complexity of FBS, the undefined components in FBS may cause inconsistent results . Some alternative serum free media with recombinant growth factors such as platelet-derived growth factor (PDGF), bFGF and transforming growth factor-β were confirmed to retain the phenotype, differentiation and colony-forming unit potential of MSCs . The presence of glucose in the medium affects the differentiation status and senescence of MSCs . Although MSCs have been isolated on the basis of plastic adherence in most studies, some researchers isolated a low-adherent subfraction of MSCs with the CD45(-)CD14(+)CD34(+) phenotype that also express common MSC markers. They confirmed that this subpopulation of MSCs is capable of differentiating into endothelial cells that highly express angiogenic markers and exhibit functional properties of the endothelium . Endometrial MSCs express genes involved in angiogenesis/vasculogenesis and steroid hormone/hypoxia responses .
Bimodal effect of unmodified MSCs on immunoregulation
The bimodal nature of unmodified MSCs is not exclusive to tumorigenesis, for MSCs have bimodal function with regard to immunoregulation . MSCs are considered to be 'immunologically privileged', as they express a relatively small complement of the molecules that are required for fully activating T cells . These cells have a reduced expression of both class I and II major histocompatibility complex (MHC) as well as a lack of surface expression of the co-stimulatory molecules CD80, CD86 and CD40 . These properties allow the use of mismatched MSCs in vivo without provoking a proliferative T-cell response .
GVHD is a major complication of hematopoietic stem cell transplantation. Co-transplantation of MSCs and hematopoietic stem cells results in fast engraftment and 100% donor chimerism . Both preclinical and clinical studies have shown that allogeneic transplantation of adipose-derived stem cells is able to control GVHD . Our previous work showed that tumor-bearing mice withstood persistent engraftment of xenogeneic bone marrow-derived MSCs for an extended period of time . Immunosuppression occurs most effectively under conditions in which MSCs make physical contact with an allogeneic tissue and release soluble factors . Adipose-derived stem cells have been shown to lack MHC II expression and its immunosuppressive effects mediated by prostaglandin E2. The suppressive effects of MSCs on immune cells, including T cells, B cells, natural killer (NK) cells and dendritic cells suggest MSCs may be used as a novel therapeutic tool for GVHD and other autoimmune disorders . However, MSCs apparently play multiple roles in immunoregulation in a circumstantial manner. For example, they can act as immune suppressors or stimulators and their expression of MHC-II can either increase or decrease following IFN-gamma stimulation . Additionally, the immunosuppressive property of bone marrow-derived MSCs is altered when they are differentiated . Differentiated MSCs in the tumor microenvironment may show different allogeneic or xenogeneic responses . MSCs from different patients show functional heterogeneity in immunoregulation. The immunosuppressive effect of chronic myelogenous leukemia-derived MSCs on T-cell proliferation is dose dependent . Chronic myelogenous leukemia patient-derived Flk1(+)CD31(-)CD34(-) MSCs have a normal morphology, phenotype and karyotype but appear to have an impaired capacity for T lymphocyte inhibition . In comparison to normal MSCs, MSCs from multiple myeloma patients exhibit a normal capacity for differentiation and long-term hematopoietic support but show reduced efficiency in inhibiting T-cell proliferation and produce abnormally high amounts of IL-6 . MSCs from immune thrombocytopenic purpura patients have been shown to have an impaired proliferative capacity and a lower capability of inhibiting activated T-cell proliferation in comparison to cells isolated from healthy donors. Additionally, caspase 9 expression is higher in MSCs from these patients .
The tumor microenvironment may influence the immunosuppressive properties of MSCs. The inflammatory factor TNF-α is sufficient to reverse the immunosuppressive effect of MSCs on T-cell proliferation, and this effect was due to an increase in IL-6 secretion . When co-cultured with MSCs at normoxic conditions, the percent of activated HLA-DR(+) T cells is much higher than that observed under hypoxic culture conditions (at 5% O2) . Stro-1-enriched populations elicit a significantly more profound dose-dependent inhibition of lymphocyte proliferation in a mixed lymphocyte reaction than other populations of MSCs . MSCs were also reported to be antigen presenting cells [65, 74].
The immunological effect of mesenchymal stem cells may be a critical element in tumorigenesis
MSCs are a particularly attractive option for cell therapy and tissue engineering applications because they can be used in autologous or allogeneic transplantation, thus avoiding any complications associated with immune rejection. As mentioned above, several studies have demonstrated the suppression of GVHD by MSCs in transplanted recipients . The infusion of donor MSCs to engraftments in the recipient's body may suppress the immune system. Unfortunately, this is the exact property that may promote cancer progression. For cancer therapies, it may be beneficial to elicit the graft-versus-tumor (GVT) effect. Doctors have found that patients with cancer achieved spontaneous remission following a severe infection. Patients who develop acute or chronic GVHD have lower cancer recurrence rates than patients who did not develop GVHD [75, 76].
MSCs have great potential for cancer therapy. They can be used as gene carriers for targeted cancer gene therapy, and unmodified MSCs demonstrate a marked capacity for inhibiting tumor progression in some cases. MSCs are a heterogeneous subset of stromal cells, and differences in their surface marker composition, differentiation ability and influence on immunoregulation establish this heterogeneity. They exhibit different characteristics in the tumor microenvironment. The phenotypic heterogeneity among MSCs may reflect their functional heterogeneity. Thus, the discrepancies among research results may be explained by the heterogeneity of MSCs. An important determinant that switches the tumor promoting and inhibiting roles of MSCs may be related to the immunoregulation of different subsets of MSCs. It will be important to balance GVHD and the GVT effect of MSCs when considering MSC-mediated cancer therapy. Selective allodepletion may be used to dissociate GVHD and the GVT effect before the advancement of MSC-mediated cancer gene therapy.
basic fibroblast growth factor
fluorescence-activated cell sorting
fetal bovine serum
major histocompatibility complex
mesenchymal stem cell
This work was supported by national natural science foundation, China (project number 81272255, 30971497, 91229122), Innovation subject foundation for doctoral student, Hunan province, China (project number CX2010B039), Hunan Natural Science Foundation (10JJ7003), National Training and Research Base for Talents of principles of carcinogenesis foundation (111 project: 111-2-12)
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