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Introduction

Multiple myeloma (MM) is the second most common haematological malignancy worldwide. However, MM is incurable for the majority of patients (1). Malignant plasma cells expand in the bone marrow, in which they constantly develop, acquire resistance to apoptosis and eventually cause patients to exhibit symptomatic MM (CRAB: High calcium, renal impairment, anemia and bone lesions) (2). In most cases, MM is preceded by an asymptomatic premalignant disease known as monoclonal gammopathy of undetermined significance (MGUS) (3). It has been reported that ~2% of the population over the age of 50 are affected by MGUS, with 1% of cases progressing to MM every year (4).

MM acts as osteolytic bone metastasis, and this behavior differs from that of other hemotologic malignancies that infiltrate the bone marrow. The bone marrow is a semi-solid tissue that occupies cavities within spongy or cancellous bone. Bone marrow is composed of interstitial cells and blood vessels that are associated with haematopoiesis, bone marrows primary function (5). The bone marrow microenvironment (BMME), which is also known as the bone marrow niche, consists of a cellular and non-cellular component. The cellular component includes stromal cells, endothelial cells, osteoclasts (OCs), osteoblasts (OBs) and immune system cells, and the non-cellular component includes the extracellular matrix (ECM) and liquid milieu, which contains chemokines, cytokines and growth factors (6). The BMME has been previously demonstrated to be a scaffold for haematopoietic stem and progenitor cells (HSPCs) (7–9). Further studies (10–12) have reported that the BMME serves an important role in haematopoiesis and in neoplastic disease. The stability of the BMME is essential for the maintenance of normal cell proliferation, differentiation, metabolism and mobilization. An abnormal BMME has been revealed to lead to cell lesions or tumorigenesis. An abundance of research has been undertaken into elucidating the biological features of MM, and the association with the BMME (13,14). It can be concluded from these studies that the BMME serves a key role in the differentiation, proliferation and drug resistance of malignant plasma cells. These studies also provide preclinical evidence that MM cells and bone marrow stromal cells (BMSCs) can be targeted as antitumor strategies and used in disease treatment (15). The present article elaborates on the complex interaction that exists between the BMME and MM.

The bone marrow microenvironment

Cellular compartment

Bone marrow stromal cells (BMSCs)

The components of the BMME, especially the BMSCs and the extracellular matrix (ECM) proteins, serve a key role in the pathogenesis of MM (16) (Fig. 1). The adhesion that occurs between MM plasma cells and both BMSCs and ECM proteins has been well-established. These adhesions can influence the growth, proliferation, invasion and drug resistance of MM cells and cause angiogenesis and lytic bone lesions (13,17). The very late antigen 4 (VLA-4), which is located on the MM plasma cell surface, mediates the binding between tumor cells and ECM proteins, including type I collagen and fibronectin, and can bind to BMSC vascular cell adhesion molecule-1 (VCAM-1). The tumor cells that adhere to BMSCs can stimulate numerous pathways, and result in the upregulation of cytokines, which regulate the cell, and antiapoptotic proteins (18), including interleukin-6 (IL-6), RANKL and Activin A (19,20). The interaction between MM and BMSC cells can be mediated via the Notch-signaling pathway. The notch-signaling pathway in MM and BMSCs can be stimulated by the interaction with Notch-Notch ligand, and can lead to the secretion of IL-6, vascular endothelial growth factor (VEGF) and insulin-like growth factor 1 (IGF-1). Additionally, the adhesion of MM cells to BMSCs also induces NF-κB-dependent transcription and IL-6 secretion. IL-6 promotes MM cell production and secretion of VEGF, and regulates malignant plasma cell apoptosis and OC differentiation (21). Conversely, the inhibition of NF-κB activity abrogates this response (22). It has been previously demonstrated that in patients with MM, exosomes may be released by BMSCs and transferred to MM cells, leading to MM progression and the induction of drug resistance (23,24). Recently, a study has demonstrated that MM exosomes that are derived from BMSCs can promote BMSC growth and angiogenesis by modifying the BM microenvironment. This modification can increase MM cell proliferation, disease progression and interfere with drug resistance (25). Although the specific mechanism governing this remains unclear, these findings revealed that cell exosomes may be associated with the intercellular transfer of genetic information in clonal plasma cell disorders (24). Understanding MM cell exosomes and their associated miRNA may enable the discovery of a novel therapeutic strategy for the treatment of MM.

Figure 1. Interactions between MM cells and the BM microenvironment. In healthy individuals, an equilibrium exists between bone resorption and new bone deposition. Osteoblastic differentiation is inhibited by the secretion of Wnt signal inhibitors, DKK1 and sclerostin. OCs are also inhibited by OPG, which is secreted by osteocytes. As MM develops, MM cells induce osteoclastogenesis directly via the secretion of MIP-1α, IL-6, and indirectly via increased RANKL expression in stromal cells. OCs secrete anti-apoptotic cytokines, including IL-6, BAFF and APRIL. Endothelial cells also secrete IL-6, which stimulates MM cell proliferation. An increased number of MM cells can promote angiogenesis via the secretion of VEGF. MM, multiple myeloma; BM, bone marrow; DKK1, dikkopf1; OCs, osteoclasts, OPG, osteoprotegerin; IL-6, interleukin-6; MIP, macrophage inflammatory protein; VEGF, vascular endothelial growth factor.

Angiogenesis and endothelial cells

BM angiogenesis is considered to indicate MM progression (6). BM samples from patients with MM have demonstrated that angiogenesis serves an important role in MM pathogenesis (26). BM angiogenesis is assessed using measurements of microvessel density (MVD). These results are compared with patients who have inactive disease or MGUS as MVD has been demonstrated to consistently increase in patients with progressive MM (27). In the BM, a mutual interaction of cells, cytokines and growth factors exists inside an intricate ecosystem, in which pericytes and endothelial cells survive and proliferate with fibroblasts, inflammatory cells and hematopoietic stem cells. The growth of malignant cells in the BM has been revealed to disrupt this balance, resulting in an increase in vascularity and tumor progression (28). The release of pro-angiogenic cytokines/molecules, including VEGF, basic-fibroblast growth factor (bFGF) and the cell surface matrix metalloproteinases (MMPs), from malignant plasma cells, BMSC and OCs, can cause angiogenesis (29,30). VEGF can stimulate proliferation and chemotaxis in stromal cells via VEGF receptor-1, (VEGFR-1) and in endothelial cells (ECs) via VEGFR-2 (31). VEGFR-1 expression is common in MM cell lines and in patients with MM. The mutual interaction between VEGF and VEGFR-1 induces MM cell proliferation and facilitates VEGF secretion. VEGF enhances angiogenesis and also contributes to cell growth and survival by inducing IL-6 secretion (32). VEGF interacts with pro-angiogenic factor osteopontin (OPN), which is secreted by OCs, to induce osteoclastogenic activity and enhance vascular endothelial cell angiogenesis (33). OCs produce MMP-9, which has been demonstrated to be responsible for OC-induced angiogenesis (34). In MM, BM sinusoids allow MM cells to receive O2 and nutrients, and contribute to the removal of catabolites from the circulation (35). Through the paracrine and cell adhesion-mediated interactions between MM cells and BMSCs, elevated BM neovascularization promotes MM plasma cell proliferation, survival and drug resistance. This occurs when insufficient nutrients and O2 are delivered to MM cells, which causes the upregulation of numerous cytokines associated with angiogenic activity, including VEGF and bFGF. This has been supported by in vitro data that has demonstrated that the elevated proliferation of MM cell lines and primary MM cells can be triggered by both human umbilical vein endothelial cells, and endothelial cells originating in BM aspirate samples of patients with active MM (36).

Osteoclasts (OCs)

Normal bone is composed of mineralized and organic components. In a normal BM microenvironment, osteocytes, OCs and OBs sustain homeostasis by maintaining a balance between bone formation and bone resorption. Osteocytes constitute the majority of all bone cells, and OCs and OBs constitute <10% (37). The balance between the generation of new OBs and OCs is disrupted in MM, leading to the rapid development of bone lesions and bone resorption (38–40), which are the major primary clinical features of this disease (41). Patients with MM exhibit a decreased number of live osteocytes due to the presence of bone lesions, which may be involved in MM-induced OC formation (42). Bone destruction caused by osteoclast activation usually occurs close to MM plasma cells, and not in normal bone marrow. A number of cytokines are associated with osteoclast activation, including RANKL, interleukin-3 (IL-3) and MIP-1a (6). IL-3 expression significantly increases in patients with MM, and this can upregulate OC activity and inhibit osteogenic protein-2 (bone morphogenetic protein-2), which subsequently inhibits OB differentiation (43,44). OCs produce OPN and IL-6, and the adhesion of OCs to MM plasma cells has been demonstrated to increase IL-6 production, a key growth factor involved in MM progression (45). Osteoclastic resorption induces the release of matrix-bound factors which promote the development of MM. This process has been named ‘the vicious cycle’ (46). Additionally, as a member of the tumor necrosis factor (TNF) family, RANK ligand has been associated with increased osteoclastogenesis, which is also involved with MM. In the bone marrow, the adhesion of MM plasma cells and neighboring BMSCs leads to an increase in RANKL expression. RANKL binding to its associated receptor indirectly increases osteoclast precursor cell activity, which increases OC differentiation via the c-Jun N-terminal kinase pathway and NF-κB (47). Osteoprotegerin (OPG) is a soluble decoy receptor that is attracted to OBs and stromal cells. The RANKL and OPG molecules, which are mutually competitive receptors, serve an important role in the regulation of bone resorption (48). In patients with MM, higher RANKL expression and decreased OPG is exhibited in the bone marrow microenvironment, which leads to increased osteoclast activation and bone osteolysis. RANKL is the most important protein associated with the prolonged survival of MM plasma cells. This is due to RANKL inhibiting osteoclast apoptosis. It has been previously demonstrated that obstructing RANKL, with its soluble form, RANK, can accelerate bone loss and regulate tumor pressure in MM animal models (49). Recently, it has been reported that OC activity is associated with the excitation of resting MM cells in bone marrow. These results revealed that OCs may serve an important role in remodeling the terminal ‘vicious cycle’, as well as inducing tumor growth and increasing the possibility of relapse (50). Therefore, OCs are considered to be associated with tumor growth in MM (51).

Osteoblasts (OBs)

It is not yet clear what effects osteoblasts exhibit on MM cells. In patients with MM, OC proliferation and differentiation is inhibited due to bone cell abnormalities (52). Numerous factors are associated with the suppression of osteoblast activity and new bone growth, including the secretion of DKK1, soluble Wnt inhibitor frizzled-related protein 2 (sFRP-2) and transforming growth factor-β (TGF-β) (53). DKK1, a Wnt-signaling antagonist, is secreted by MM cells and is overexpressed in patients with MM who exhibit lytic bone lesions (54). A previous study has demonstrated that the inhibition of DKK1 can reduce bone resorption and tumor burden in a severe combined immunodeficient 11-rabbit (SCID-rab) myeloma model (55). Additionally, OB differentiation has also been revealed to be suppressed by sFRP-2, which is produced by the majority of MM cells, including in RPMI8226 and U266 cell lines (56). A similar effect has been indicated subsequent to the induction of osteocyte overexpressing sclerostin (SOST) (57). However, intriguing findings are emerging in this field of research (58). Whether OBs are inhibitory or supportive in MM has been revealed to depend on the source of the MM cells (59). A previous study has indicated that OBs contributed to MM cell survival and growth, and also increased osteolysis development, which enhanced MM pathogenesis (19). The capacity of OBs to secrete IL-6 close to MM plasma cells may result in this phenomenon and promote increased bone resorption and MM cell proliferation (60). It has also been reported that OBs serve a key role in activating MM cell survival, and this may be due to the release of OPG inhibiting MM cell apoptosis, which is mediated by TNF-related apoptosis-inducing ligand (TRAIL) (61). Yaccoby et al demonstrated that the majority of MM plasma cells obtained from active MM patients, in triple-cultures with OBs+OCs, exhibited fewer viable cells compared with cells co-cultured with OCs and MM plasma cells alone. In myelomatous severe combined immunodeficiency (SCID) exhibited in mice implanted with fetal human bone (SCID-hu mouse model), OBs were revealed to inhibit tumor growth and increase bone mineral density (59). Overall, further research is required to determine an efficient method to target OBs and alter tumor cell survival and growth. This could be used as a novel therapeutic strategy in the treatment of patients exhibiting bone disease and tumor growth (46). Future research should aim to elucidate the mechanisms behind the interaction between OBs and MM plasma cells. Elucidating the mechanisms behind this interaction may support the potential use of osteoblastic mediators in the treatment of MM.

Non-cellular compartment

IL-6

The association between cytokines, proteolytic enzymes, chemokines and adhesion molecules provides survival signals that are used in MM plasma cells and are associated with the development of MM drug resistance. Among these, IL-6 has been reported to serve a key role in a variety of tumor activities, including cell migration, invasion, tumor growth, apoptosis, angiogenesis, the differentiation of tumor cells and inflammation or infection (62,63). IL-6 was initially cloned as a B cell stimulating factor (BSF) and designated interferon β2. IL-6 has been demonstrated to stimulate cytotoxic T cells and promote osteoclast precursor cells to differentiate into mature and active osteoclasts (64). In fact, the cellular sources of IL-6 in MM-infiltrated bone marrow are highly controversial, with their origin usually described as paracrine or autocrine (65). Initially, IL-6 was regarded as an autocrine factor produced by certain MM cells. However, the most recent consensus opinion is that the BM environment constitutes the main source of this cytokine (Fig. 2). Several recent studies have also confirmed the paracrine origin of IL-6 in murine models of plasmacytomas and MM (66,67). Frank myeloma cells and myeloma progenitors in the BMME have been suggested to use two sources of IL-6 to promote tumor maintenance and proliferation in vivo (68). Numerous molecules and cytokines can upregulate the secretion of IL-6 derived from BMSCs. It has been previously reported that IL-6 can be detected in the supernatant of MM cells using stimulation with anti-CD40 antibody (69,70). Additionally, IL-1β has also been indicated to be a major cytokine that contributes to the production of BMSC IL-6 via the paracrine loop, which promotes the growth and survival of MM cells (71). After binding to its receptor (IL-6R), IL-6 triggers the activation of the PI3K/Akt/mTOR (72–74) and Ras/Raf/MEK/Erk (35) signaling pathways. IL-6 has also been revealed to serve a key role as an MM growth factor by stimulating IL-6R and triggering the phosphorylation of STAT3 via JAK1 (75). The Janus kinase (JAK)-signal transducer and activator of transcription (STAT) pathway was initially revealed to be associated with interferon-α (IFN-α), IFN-γ and IL-6-mediated downstream signaling (76). Blocking the IL-6R/STAT3 pathway has been indicated to induce apoptosis in MM cell line NCI-H929 (77). NF-κB has been demonstrated to be associated with cytokine- and adhesion-mediated IL-6 upregulation. Therefore, the inhibition of NF-κB can prohibit the secretion of IL-6 (78). In previous studies, it was suggested that the non-specific inhibition of IL-6 could be performed due to its highly pleiotropic effects (with drugs including lenalidomide and associated immunomodulatory drugs), or IL-6 could be specifically targeted in MM and BMSCs (79). Presently, it is well-known that effective inhibition methods include the use of monoclonal antibodies (mAbs) to IL-6 (siltuximab) (80–82) or IL-6R (tocilizumab), or recombinant proteins, which act as IL-6R antagonists (83). Small molecules that inhibit the cellular IL-6 signaling pathway or cross-talked pathways in MM can also be used (84). Additional therapeutic treatments are performed using compounds, which either block the biochemical pathways that promote IL-6 signaling directly, or activate biochemical pathways which can inhibit IL-6 signaling indirectly (85). The study of mice models is invaluable in providing key evidence for the potential preclinical use of IL-6-targeted therapies for MM treatment.

Figure 2. The roles of IL-6 in the BM microenvironment. IL-6 increases the expression of some survival proteins, including Bcl-2, Bcl-XL and Mcl-1, to decrease apoptosis in MM cells. IL-6 also serves a key role in promoting metastasis in a number of other organs, including the liver and lung. In MM cells, IL-6 upregulates VEGF via the JAK/STAT-3 signaling pathway to remodel vascular structure and increase angiogenesis. Additionally, IL-6 decreases the activity of NK cells by inhibiting the expression of CD80, CD86 and IL-12 in dendritic cells. IL-6 induces MM cell RANKL production and inhibits OB differentiation, via MM cell DKK-1 expression, to enhance bone degradation. IL-6, interleukin-6; BM, bone marrow; MM, multiple myeloma; VEGF, vascular endothelial growth factor; JAK, Janus kinase; STAT, signal transducer and activator of transcription; NK, natural killer; OB, osteoblast; DKK1, dikkopf1.

IGF-1

Within the past decade, the insulin-like growth factor (IGF) system has been demonstrated to serve a key role in the establishment and progression of MM (86,87) (Fig. 3). It has been previously reported that IL-6 inhibition is not sufficient to induce effects in MM. Therefore, an increased interest has emerged into the IGF system, which can compensate IL-6 signaling and may induce the proliferation and survival of IL-6-independent MM cells (88). This suggests that IGF-1R inhibitors may contribute to the drug resistance exhibited, both in vitro and in vivo, to well-known anti-myeloma medicines (89,90). In the extracellular environment, the IGF system is composed of six high-affinity insulin-like growth factor binding proteins (IGFBP1-6), IGF1, IGF2, IGF-1R and a minor free fraction of total IGF (91). The binding of free IGF to its receptor initiates a signaling cascade that results in the proliferation and viability of MM cells. In MM, IGF-1 is largely available in the BMME due to its secretion from BMSCs and OBs. It has been previously revealed that, through the activation of IGF-1R, IGF-1 serves an important role in MM cell growth, increases DNA synthesis and has been demonstrated to enhance the survival and proliferation of some MM cell lines. However, anti-IGF-IR blocking antibody use can inhibit the aforementioned effects (92,93). A number of studies have indicated that MM cells exhibit high IGF-1 and IGF-1R expression and, through an autocrine cascade, IGF-1/IGF-1R signaling contributes to the survival, growth and drug resistance in MM cells (86,94). Furthermore, in MM cell lines, it has been revealed that autocrine IGF-1 is an important self-clonogenic growth factor (95). Recent research has also demonstrated that IGF-1 can reverse the inhibition of cell proliferation induced by the knockdown of EEN. EEN, an endocytosis-regulating molecule, promotes the proliferation and viability of MM cells by stimulating IGF-1 secretion (96). In MM, the role of IGF-1/IGF-1R signaling in the inhibition of apoptosis and the induction of tumor cell proliferation occurs via activation of the PI3K/AKT and MAPK pathways (97). Which of these two activities (apoptosis or cell proliferation) is initiated depends on which pathway is induced. For example, apoptosis can be inhibited by IGF-IR through the activation of the PI3K/AKT pathway, which inhibits the ability of mitochondria to release cytochrome c. Subsequent to this, pro-apoptotic protein BAD is phosphorylated by activated AKT, separated from anti-apoptotic protein Bcl-2 and sequestered by the adaptor protein 14-3-3, leading to the inhibition of apoptosis in PCM cells (72,98). Additionally, IGF-1/IGF-1R is associated with MM cell proliferation, including migration, adhesion and invasion. These processes differentiate monoclonal malignant plasma cells in the BM microenvironment (99). IGF-1 serves a chemo-attractant role in murine 5T33MM cells and has been revealed to enhance cell adhesion to the extracellular matrix glycoprotein fibronectin in vitro by activating IGF-IR downstream targets, such as the PI3K/AKT pathway (100). IGF-1R is also upregulated in MM cells subsequent to interaction with the BMME (101). It has also been reported that enhanced IGF-1 signaling, through increased IGF-1 secretion and IGF-1R activation, is associated with bortezomib drug-resistance. This resistance may be overcome by inhibiting downstream targets such as PI3K and mTOR (90). IGF-1 signaling promotes the activation of AKT. However, the AKT signaling pathway is not the sole downstream kinase that can be activated by IGF-1. The MAPK pathway has been revealed to be activated by IGF-1 to promote MM proliferation in six MM cell lines (98). Conversely, one study reported that the MAPK pathway could only be activated in IL-6-dependent MM lines. Numerous downstream signaling pathways may also be activated by IGF-1, including the Janus kinase pathway (102). Therefore, further research is required to elucidate which additional signaling pathways lie downstream of IGF-1.

Figure 3. The roles of IGF-1 in MM-specific hallmarks. IGF-1 serves an important role in the homing process, and moves MM cells from the PB into the BM microenvironment. IGF-1 is also associated with bone disease through the promotion of OC activity and maturation, which subsequently inhibits OB activity. Insulin-like growth factor 1, IGF-1; MM, multiple myeloma; PB, peripheral blood; BM, bone marrow; OC, osteoclast; OB, osteoblast.

VEGF

An increase in BM vascularization has been demonstrated to be positively associated with an adverse prognosis in MM patients (103). New blood vessel growth enhances oxygen and nutrient transport to cells and can promote tumor growth. VEGF is a highly conservative homodimeric glycoprotein with a relative molecular mass of 45 kDa. VEGF is the only mitogen that is associated with endothelial cells (104). VEGF is a peptide growth factor that belongs to the platelet-derived growth factor (PDGF) superfamily, which exhibits high homology across species. VEGF has been previously described as a vascular permeability factor (VPF), and is now denoted VEGF-A (105). VEGF serves a key pro-angiogenic role in MM and is induced by MM cells and BMSCs (99). The secretion of VEGF can be stimulated by numerous cytokines and cell growth factors, including IL-6, bFGF, TGF-β and tumor necrosis TNF-α. VEGF serves a role in the formation of new blood vessels by binding to its receptors VEGFR-1 and VEGFR-2. This induces the survival, proliferation, migration and differentiation of BMSCs and ECs, through a number of signaling pathways, including Ras, GAP, PI3K/Akt, STAT and MEK/ERK (103). As aforementioned, angiogenesis is the formation of new vasculature from pre-existing vasculature, and has been demonstrated to be essential for tumor growth, invasion, and metastasis in a variety of cancer types (106). If the pro- and anti-angiogenic balance is broken and angiogenesis is favored, MGUS can turn into MM (107–109). VEGF has been revealed to be crucially implicated during osteoclastogenesis in MM (110). Research has also revealed that when VEGF binds to the VEGFR-1 receptor, which is expressed in OCs, OC cells are stimulated. However, OCs can also be activated indirectly, since MM cells can secrete VEGF subsequent to IL-6 stimulation (111). VEGF directly enhances osteoclastic bone resorption and the survival of mature OCs (33). Furthermore, VEGF is also correlated with high expression and activation of adhesion proteins and has been demonstrated to activate the secretion of proteases and ECM components, which can subsequently remodel ECM structures and modulate tumor cell-tumor cell and tumor cell-ECM interactions.

Exosomes

In recent years, rising evidence has emphasized the role of exosomes in the cross-talk between MM cells and the BMME, and exosomes are now considered to be associated with cell to cell communication (24,112,113). Exosomes, a sub-fraction of extracellular vesicles (EVs), range in size from 30–100 nm. They transport a large variety of mRNAs, proteins and growth factors to target cells, and are secreted either via endocytosis, which occurs in MM cells and cells composing the BMME, or by direct fusion with the cell membrane (114–116). MicroRNAs (miRNAs), a class of small non-coding RNAs, are transported by exosomes and can suppress target gene expression at the post-transcriptional/translational level via hybridization with mRNA transcript sequences (117). It has also been reported that exosomes are associated with various biological processes, including inflammation, embryonic development, hematopoiesis, the immune response and tumorigenesis (118). In MM cells, upregulated miR-146a increases the expression and release of cytokines, including IL-6, CXCL1, IP-10 and CCL5, which enhance MM cell viability and migration (119). miR-146a has also been demonstrated to activate numerous signaling pathways, including NF-κB, Notch and JAK/STAT, and in turn, the Notch pathway contributes to the secretion of cytokines that are induced by miR-146a (120). Previous studies have indicated that MM cell-derived exosome treatment can increase the expression of OC-specific markers, including tartrate-resistant acid phosphatase (TRAP), cathepsin K (CTSK) and matrix metallopeptidase 9 (MMP9) (121). Amphiregulin (AREG), the epidermal growth factor receptor (EGFR) ligand, is expressed by MM cells and is associated with MM-derived exosomes, which participate in MM-induced osteoclastogenesis (122). AREG arises from the activation of the EGFR pathway and, subsequent to MM-derived exosome treatment, its presence is often confirmed by a significant increase in SNAIL mRNA, which is a downstream target of EGFR (122). In vitro studies have indicated that osteoblast differentiation and functionality can be inhibited by exosomes derived from 5TGM1 cells. This study also indicated that DKK1 expression was upregulated in MC3T3-E1 cells containing 5TGM1 exosomes (123). Aberrant angiogenesis has been demonstrated to be associated with exosomes in MM-infiltrated bone marrow (124). A previous study revealed that exosomes that are derived from hypoxia-resistant cells significantly increased angiogenesis, and exosomal miR-135b was considered to be a specific miRNA that is associated with chronic hypoxia (125). Numerous animal model studies have demonstrated that exosomes that are derived from normal BMSCs are effective in the treatment of cardiovascular disease (126) and kidney injury (127). Antitumor drugs, such as doxorubicin, could potentially be loaded into liposomes to improve osteosarcoma chemotherapy treatment (128). Additionally, liposomal doxorubicin could be used in conjunction with bortezomib or dexamethasone in the treatment of patients exhibiting MM (129). A recent study also revealed that in endothelial cells, miR-340 can inhibit angiogenesis via the hepatocyte growth factor/c-MET (HGF/c-MET) signaling pathway (130). Therefore, it can be expected that additional RNA or protein components that are associated with exosomes derived from MM cells or BMSCs exist, and are associated with the cell-cell communication among them. Research into exosomes provides important insights into the methods by which MM can be promptly diagnosed. Exosomal miRNAs, which are derived from young BMSCs, can be utilized in the formation of a novel strategy for MM treatment.

Conclusion

The present review investigated the strong interaction exhibited between MM cells and the surrounding BMME. The present review demonstrated that OBs, OCs, BMSCs and immune cells serve key roles in the promotion of MM cell growth and survival, inhibit autonomous or drug-induced MM cell apoptosis and therefore contribute to the development of osteolysis. Therefore, these cells should be considered in research into potential new treatment strategies for MM. The more research that investigates the interactions between healthy cells in the BMME, the better understanding will be gained into how MM disrupts the BMME. The development of novel MM treatment targets is ongoing. In recent years, the introduction of agents targeting MM cells and their interactions with the BMME, including proteasome inhibitors (bortezomib and carfilzomib) and immunomodulatory agents (thalidomide, lenalidomide and pomalidomide), has reduced mortality in patients with MM. Although bortezomib has been indicated to inhibit VEGF, IL-6 and IGF-1 secretion in BMSC and endothelial cells (36,131), and the OB differentiation and OC apoptosis (132), further elucidation into the molecular mechanisms of MM-bone interactions and the MM niche are required to determine novel target approaches that exhibit beneficial effects on bone disease and MM tumor progression.

Currently, controversy exists as to whether a constant disease control approach should be pursued, which impacts patient quality of life and overall survival, or whether MM should be treated with an aggressive multidrug strategy that exhibits a complete recovery. Younger patients with poor prognosis may benefit more from the aggressive multidrug strategies as these patients are more likely to benefit long-term. However, for elderly, frail or non-high-risk patients who are newly diagnosed with MGUS, the treatment strategy should be to control the disease. This can be done by achieving stable renal function, which exhibits stable non-progression of bone disease, low toxic effects, high quality of life and increased survival rate. Future study should focus on developing combination therapies for a variety of patient subgroups to ensure patients in the low-risk stage or those who do not tolerate concentrated interventions will not be overtreated.

In conclusion, MM remains incurable and exhibits a complex pathophysiology. The interaction between MM plasma cells and BM has been demonstrated to serve a crucial role in the pathogenesis and progression of MM. The current standard treatment, and the majority of active anti-MM drugs, work against MM cells and BMME. Through targeting these diseased cells and their microenvironment, novel treatment strategies may be determined that can improve the outcome of this incurable blood cancer.

Acknowledgements

The authors would like to thank all Lab members, and CYG and YY for collecting literature and discussion.

Funding

The present study was supported by the National Natural Science Foundation of China (nos. 81670200, 81770220 and 81600177; to YY and CG); the 2016 Outstanding Youth Fund of Jiangsu Province BK20160048 (to YY); the Natural Science Foundation of Jiangsu Province BK20161041 (to CG); the National Key Research and Development Program-Precision Medicine sub-program 2016YFC0905900 (to YY); The Priority Academic Program Development of Jiangsu Higher Education Institutions for Chinese Medicine; the Innovation Team of Six Talent Peaks Project in Jiangsu Province TD-SWYY-015 (to CG).

Availability of data and materials

Not applicable.

Authors' contributions

YY, CG and ZF were involved in the conception of the review. JH and RW wrote the manuscript. JQ analyzed the data and plotted the graphs. CG and RW edited the manuscript. All authors have read and approved the final manuscript and agree to be accountable for all aspects of the research in ensuring that the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References