Signaling lymphocytic activation molecules Slam and cancers: friends or foes?

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Oncotarget. 2018; 9:16248-16262. https://doi.org/10.18632/oncotarget.24575

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Gregory Fouquet _, Ingrid Marcq, Véronique Debuysscher, Jagadeesh Bayry, Amrathlal Rabbind Singh, Abderrahmane Bengrine, Eric Nguyen-Khac, Mickael Naassila and Hicham Bouhlal


Gregory Fouquet1,*, Ingrid Marcq1,*, Véronique Debuysscher1, Jagadeesh Bayry2, Amrathlal Rabbind Singh3, Abderrahmane Bengrine4, Eric Nguyen-Khac1,5, Mickael Naassila1 and Hicham Bouhlal1

1INSERM 1247-GRAP, Centre Universitaire de Recherche en Santé CURS, Université de Picardie Jules Verne, CHU Sud, Amiens, France

2INSERM UMRS 1138, Centre de Recherche des Cordeliers–Paris, Paris, France

3Department of Microbiology, Aravind Medical Research Foundation, Anna Nagar, Madurai-India

4Biobanque de Picardie, Centre Hospitalier Universitaire Sud, Amiens, France

5Service Hepato-Gastroenterologie, Centre Hospitalier Universitaire Sud, Amiens, France

*These authors contributed equally to this work

Correspondence to:

Hicham Bouhlal, email: [email protected]

Ingrid Marcq, email: [email protected]

Keywords: SLAMF molecules; cancer; pathophysiology; therapy

Received: October 19, 2016     Accepted: December 03, 2017     Epub: February 26, 2018     Published: March 23, 2018


Signaling Lymphocytic Activation Molecules (SLAM) family receptors are initially described in immune cells. These receptors recruit both activating and inhibitory SH2 domain containing proteins through their Immunoreceptor Tyrosine based Switch Motifs (ITSMs). Accumulating evidence suggest that the members of this family are intimately involved in different physiological and pathophysiological events such as regulation of immune responses and entry pathways of certain viruses. Recently, other functions of SLAM, principally in the pathophysiology of neoplastic transformations have also been deciphered. These new findings may prompt SLAM to be considered as new tumor markers, diagnostic tools or potential therapeutic targets for controlling the tumor progression. In this review, we summarize the major observations describing the implications and features of SLAM in oncology and discuss the therapeutic potential attributed to these molecules.


Molecular characteristics of SLAM family receptors

SLAM family receptors belong to the Immunoglobulin (Ig) superfamily. The SLAM family contains nine members that possess an extracellular segment comprising two or four Ig-like domains (V-like variable and C2-like constant), a transmembrane segment and a cytoplasmic tail. All members of type-1 transmembrane glycoproteins with the exception of SLAMF2, link to the cell membrane through glycosyl-phosphatidylinositol (GPI) anchor [1, 2]. The cytoplasmic portion is characterized by the presence of several tyrosine motifs TxYxxI/V (ITSM), (T is threonine, I is isoleucine, V is valine and X is any amino acid) [35]. However, SLAMF2 lacks ITSM domains due to the absence of C-terminal domain [6]. Meanwhile, even though SLAMF8 and SLAMF9 have a short cytoplasmic tail (~30 amino acid residues), they also lack tyrosine motifs [7, 8]. SLAMF3 exhibits splitting of its two extracellular domains [9, 10]. SLAM members are activated mostly by homophilic interactions via their V-like N-terminal domains except SLAMF2 and SLAMF4, which are activated by heterophilic interactions [11]. The functional importance of SLAM-related receptors in immune response is highlighted by the identification of molecular defect responsible for X-linked lymphoproliferative (XLP) syndrome [12]. Indeed, the gene mutated in XLP is found to code for a small adapter-like protein named SLAM-associated protein (SAP) or SH2D1A (hereafter termed SAP). SAP is composed of almost entire Src homology 2 (SH2) domain, and binds with high specificity and affinity to tyrosines in the intracellular domain of SLAM-related receptors [12]. In human, upon activation, SLAMF receptors interact with SLAMF associated protein (SAP) and Ewing’s sarcoma’s-Activated Transcript 2 (EAT-2) to form a receptor complex. The SAP family also includes EAT-2 related transducer (ERT, also known as SH2D1W) [13].

The newly formed complex undergoes phosphorylation at tyrosine residues by Fyn tyrosine kinase leading to recruitment of additional effector molecules [14]. Several lines of evidence support the idea that SLAM family members can provide a second signal for the stimulation of immune cells. SLAM/SAP-dependent functions in immune regulation include natural killer (NK) and T-cell development, B-cell regulation and antibody production/isotype switching and NK-cell cytotoxicity [14]. EAT-2, a SLAM-associated adaptor is expressed in innate immune cells such as dendritic cells (DCs), macrophages and NK cells and it facilitates SLAM-dependent expression of pro-inflammatory cytokines in these cells [6]. Like other members of SLAM family, SLAMF3 recruits SAP and EAT-2 via its SH2 domain [15] with the exception that SLAMF3 is the only member, which is able to interact with μ2 sub-unit of AP-2 complex through its Y470 motif [16]. The SLAMF3-AP-2 interaction is essential for endocytosis of this complex in immune cells. Upon endocytosis, in T cells, 70 to 80% of SLAMF3 receptors are degraded in the lysosomal compartment, while others are recycled to the surface. In contrast, majority of the receptors are degraded upon internalization in B cells [16]. The internalization of receptor is also regulated by TCR- and BCR-mediated signaling, which, enhance the rate of endocytosis. Thus, endocytosis of the receptor represents an essential mechanism of modulation of surface expression of SLAMF3.

SLAMF3 is the only member of SLAM family, which has ability to bind directly to Grb2. This adaptor protein is known to activate Ras-MAPK signaling pathway through the recruitment of Son of Sevenless molecule (SOS) [17]. In T cells, Grb2-SH2 domain binds to SLAMF3 phosphorylated at Y606 residue. SLAMF3 phosphorylation is performed by Fyn or Lck [18]. Moreover, Grb2-binding site is required for the receptor internalization in T cells following commitment of SLAMF3 or TCR. The co-ligation of SLAMF3 and TCR inhibits ERK phosphorylation as well as cytokine production as opposed to co-ligation of TCR with other members of the SLAM family. It is worth to mention that Grb2-binding site (Y606) is different from those of SAP (Y603 and Y626) and AP-2 (Y470) [1820] (Figure 1).

SLAM members, cellular and molecular characteristics.

Figure 1: SLAM members, cellular and molecular characteristics. HSCs: Hematopoietic Stem Cells; DCs: Dendritic Cells; NK: Natural Killer; PKCƟ: Protein Kinase C Ɵ; BCL10: B-Cell Lymphoma 10; NF-ƙB: Nuclear Factor-ƙB; SHP-1/2: SH2 domain-containing Phosphatase 1/2; SHIP1: SH2-containing Inositol 5'-polyphosphatase 1; SHC: Src Homology 2 domain Containing; Btk: Bruton's tyrosine kinase; Lck: Lymphocyte-specific protein tyrosine kinase; Dok1/2: Docking protein 1/2; Ras-GAP: Ras GTPase-activating proteins; LAT: Linker for activation of T cells; Grb2: Growth factor receptor bound protein 2; AP-2: Adaptor Protein complex-2; ERK: Extracellular signal-Regulated Kinases; PI3K: PhosphoInositide 3-Kinase; mTOR: mammalian Target of Rapamycin; RB: Rétinoblastoma; PLCγ: PhosphoLipase Cγ; Cbl: Casitas B-lineage Lymphoma; CSK: COOH-terminal Src kinase; 3BP2: Abl-SH3 Binding Protein 2. Localisation of ITSM (TxYxxI/V) were determined on Ensembl. [1, 2, 11, 21, 84, 95].

SLAM members in hematopathologies

Members of SLAM family are known to be implicated in the pathophysiology of hematologic complications. For this reason, some of them are targets for the monoclonal antibody therapies that are being tested in different clinical trials. In this section, we summarize the implication of SLAM receptors in hematopathologies with an emphasis on their utility in diagnosis and as therapeutic targets (Table 1).

Table 1: SLAM members implicated in hematological affections and targeted by diagnosis and therapeutic strategies

SLAM Family












B lymphoma


Hodgkin’s lymphoma


Non-Hodgkin’s Lymphoma







B lymphoma

























Abbreviations: MM: Multiple Myeloma; CLL: Chronic Lymphocytic Leukemia; ALL: Acute Lymphocytic Leukemia; AML: Acute Myeloid Leukemia.


SLAMF1 (CD150) is the prototype member of SLAM family that initiates signal transduction networks in T lymphocytes, NK and antigen-presenting cells [6, 14]. During B-T lymphocytes cooperation, SLAMF1 acts as a self-ligand to initiate a signal transduction pathway and to increase lymphocyte activation. SLAMF1 is highly expressed by thymocytes (highest by double positive cells), T and B lymphocytes (overexpressed upon activation), DC, platelets, hematopoietic stem cells (HSCs) and macrophages. Of note, overexpression of SLAMF1 has been reported in monocytes and macrophages of patients with Crohn’s disease and in T lymphocytes from rheumatoid arthritis patients [21, 22].

SLAMF1, in addition to CD86 and CD200, were identified as robust markers that could be added to a routine panel for plasma cell (PC) identification and minimal residual disease evaluation in multiple myeloma (MM) [23]. SLAMF1 expression is also decreased in patients with aggressive chronic lymphocytic leukemia (CLL) and was associated with reduced overall survival [24] (Table 1). Therefore, the loss of SLAMF1 expression (SLAMF1low) could indicate an aggressive form of CLL and hence could help in improving patient management as predictive factor of overall survival (OS). Ex vivo, the SLAMF1 ligation with stimulating monoclonal antibody in CLL cells, induces phosphorylation of p38, JNK1/2 and Bcl-2, and promotes autophagy. On the contrary, cells with silenced-SLAMF1 are resistant to induction of autophagy [24]. Furthermore, SLAMF1 in combination with SKI gene (v-SKI avian sarcoma viral oncogene homolog), was also proposed as robust indicator of prognosis in untreated CLL patients [25].

SLAMF1 also acts as receptor for measles virus (MV) [26]. Studies employing MV as an oncolytic virotherapy agent have suggested that SLAMF1 is a therapeutic target in certain hematological diseases. For instance, in mouse models, this therapeutic strategy has been evaluated using attenuated MV to target certain acute lymphoblastic leukemia (ALL) [27]. Attenuated MV efficiently killed leukemia cells without affecting normal human blood cells and progenitors. A few intravenous injections of attenuated MV were able to eradicate leukemic blasts [27]. Takeda et al. reported higher susceptibility of lymphoma cells to attenuated therapeutic MV vaccine strain (CAM-70)-induced cytolysis due to elevated expression of SLAMF1 in these cells. Similarly, using SLAMF1 expression in cancer cells, the MV oncolytic virotherapy could serve as an alternative therapy against Epstein-Barr Virus (EBV)-positive diffuse large B-cell lymphoma [28]. MV OVT might also target SLAMF1 to fight non-Hodgkin’s lymphoma (Table 3). A vaccine containing MV has been used as an oncolytic agent against mantle cell lymphoma, an aggressive, difficult to cure, but radiosensitive B-cell non-Hodgkin’s lymphoma. Using sodium-iodide symporter loaded MV, a high concentration of iodide was achieved within infected tumor cells. The combination of virotherapy and systemic (131)I resulted in rapid disease regression compared to other therapy alone. The SLAMF1-dependent entry of therapeutic MV allows efficient viral spread, tumor regression, and prolonged survival [29] (Table 2).

Table 2: SLAM members implicated in anti-cancer clinical trials

SLAM family


Treatment type

Treatment name

Study phase




Oncolytic MV vaccine strains




Non-Hodgkin’s lymphoma






anti-SLAMF2 Ab


Phase 1 clinical trial


B lymphoma










2B4 chimeric receptor





CLL and lymphoma

anti-SLAMF6 Ab

994.1 and 480.12




αSLAMF6 and Ibrutinib





CS1-specific peptide




anti-SLAMF7 Ab



[70, 72]

Elotuzumab combined to Bortezomib



Elotuzumab combined to Bortezomib

Phase 1 clinical trial


Elotuzumab combined to Lenalidomide and Dexamethasone

Phase 1 clinical trial


Elotuzumab combined to Lenalidomide and Dexamethasone

Phase 3 clinical trial

(ELOQUENT-1, NCT01335399)

MM with renal impairment

anti-SLAMF7 Ab

10 mg/Kg Elotuzumab, 5-25 mg Lenalidomide and 40 mg Dexamethasone

Phase 1b clinical trial


Refractory or relapsed MM

anti-SLAMF7 Ab


Phase 1 clinical trial


10 or 20 mg Elotuzumab, 25 mg Lenalidomide and 40 mg Dexamethasone

Phase1b-2 clinical trial


10 mg/Kg Elotuzumab, 25 mg Lenalidomide and 40 mg Dexamethasone

Phase 3 clinical trial


10 mg/Kg Elotuzumab, 1,3 mg Bortezomib and 20 mg Dexamethasone

Phase 2 clinical trial


10 mg/Kg Elotuzumab, 200 mg Thalidomide and 40 mg Dexamethasone

Phase 2 clinical trial


Elotuzumab in combination with Lenalidomide and Dexamethasone obtained FDA in November 2015

Abbreviations: MM: Multiple Myeloma; CLL: Chronic Lymphocytic Leukemia; ALL: Acute Lymphocytic Leukemia.

Table 3: SLAM members implicated in solid cancers

SLAM Family





CNS tumors












Abbreviations: HCC: HepatoCellular Carcinoma; CNS: Central Nerve System.

One of the therapeutic strategies used to eliminate cancer cells is induction of apoptosis and/or autophagy. In this scenario, interaction of SLAMF1 expressed on infiltrating T cells with SLAMF1 of Hodgkin’s lymphoma cells inhibits cell proliferation and induces apoptosis in L1236 Hodgkin’s lymphoma cells independent of JNK activity [30]. Because, SLAMF1 regulates phosphorylation of MAPKs Erk1/2 and p38, it has been proposed that it can contribute to the regulation of tumor cell maintenance in low-rate proliferating Hodgkin’s lymphoma cells [30].

In addition to hemophilic interaction of SLAMF1, its ligation to SAP is also suggested to play a crucial role in the activation of Akt signaling [31]. This activation occur in normal tonsillar B cells and Hodgkin’s lymphoma B cells [32]. SLAMF1-mediated phosphorylation of Akt activates the phosphorylation of its downstream targets (GSK-3β and FoxO1) in EBV-transformed and Hodgkin›s lymphoma cells. Thus by triggering one of the mechanisms, SLAMF1 could suppress apoptosis and hence support survival of immortalized B cells [32].


SLAMF2 (CD48, B-lymphocyte activation marker BLAST-1) is reported to be expressed in NK, CD8, γδ T cells, basophils, eosinophils, mast cells and multipotent progenitor [21, 33]. SLAMF2 was described as low affinity ligand for human CD2 [34]. One of the SLAMF2 specificities is the heterophilic interaction with its ligand SLAMF4 [11] (Figure 1). Several studies have targeted SLAMF2 in cancer therapies. Murine anti-SLAMF2 IgM antibody WM63 was used in a pilot CLL phase I clinical trial and results showed a transient reduction in the number of circulating cancer cells [35] (Table 2). The potential application of same anti-SLAMF2 IgM antibody was also reported in case of B lymphoma [36]. Since SLAMF2 is highly expressed on more than 90% MM plasma cells compared to normal lymphocytes (Table 1), this receptor serves as target for mAb therapy in MM [37]. Anti-SLAMF2 antibody induces antibody-dependent cell-mediated cytotoxicity and complement-dependent cytotoxicity against MM cells in vitro. In severe combined immunodeficient mice, anti-SLAMF2 antibody inhibited tumor growth without damaging normal CD34+ hematopoietic stem/progenitor cells (HSC) [37] (Table 2). SLAMF2 maintains hematopoiesis and HSC CD34+ pool by controlling IFN-γ production, which negatively affects self-renewal. Low level expression of SLAMF2, and lack of efficient SLAMF2-SLAMF4-induced signaling, leads to lowered levels of IFN-γ and more long-term quiescent CD34+ HSCs in the bone marrow [38]. More importantly, during chemotherapy cures, the microenvironment around HSC in the absence or presence of low expression of SLAMF2 and IFN-γ renders quiescent cells refractory to molecules such as 5-FU and decreases its therapeutic efficiency [38]. A major concern regarding the use of SLAMF2 as a therapeutic target is its broad expression in normal lymphocytes and monocytes, which might cause severe cytopenia and immunosuppression when anti-SLAMF2 mAb is used as a therapeutic drug. Therefore, due to hematological toxicities, anti-SLAMF2 mAb might not be suitable for a long-term maintenance therapy. The potential hematological toxicity of anti-SLAMF2 mAb should therefore, be carefully tested at the pre-clinical stage. These data indicate that anti-SLAMF2 mAb may well turn out to be an effective tool for the improvement of MM patient survival [39].


SLAMF3 (CD229, Ly9 in mice) was initially described in thymocytes (highest by double negative and single positive cells), T cells, follicular helper T, B cells (increased expression upon activation), DCs, macrophages and NK cells [21] but its function remains unclear. This receptor is recruited to the contact site between T cells and B cells during antigen presentation process and it is involved in the formation of the immunological synapse [40]. The triggering of SLAMF3 on human T cells induces the rapid phosphorylation of its tyrosine residues and decreases the activation of ERK and the production of CD3-induced IFN-γ [18]. Endocytosis of SLAMF3 blocks lymphocyte activation pathways indicating that the expression of SLAMF3 at the cell surface could regulate lymphocyte functions. In mice, stimulation of SLAMF3 decreases the production of IFN-γ, IL-2, IL-4, IL-6, IL-10 and TNF-α by CD3-activated T cells [41]. However, analysis of T cells from SLAMF3 (Ly9-/-)-deficient mice demonstrated the role of SLAMF3 in T cell activation, as well as in the production of IL-2 and Th2-type cytokines [42]. SLAMF3 expression has been recently shown to correlate with the certain autoimmune disorders. SLAMF3 and SLAMF6 co-stimulation increases IL-17A production by Th17 cells and the correlation between their surface expression and disease activity in systemic lupus erythematosus has been reported [43].

One of the conditions for an effective cancer immunotherapy is the identification of tumor-associated antigens (TAAs), which are increased during neoplastic transformation. These antigens have to be processed and presented by major histocompatibility complex molecules allowing recognition by T cells. Studies with peptides derived from human TAAs indicated that most tumors expressing these antigens could be attacked by specific cytotoxic T cells [4446]. Some antigen presenting cells, such as B-CLL cells, are ineffective antigen presenting cells and poor stimulators of a primary immune response because they are lacking in costimulatory and adhesion molecules [47]. SLAMF3 is highly expressed in B-CLL cells, processed and efficiently presented as TAA [48, 49] (Table 1). Presenting SLAMF3 allows the expansion of autologous tumor-specific T cells and function as a unique TAA for this malignancy [49]. Importantly, SLAMF3 may serve as marker of bone marrow from MM patients and thus allowing identification of myeloma cells by flow cytometry and immunohistochemistry. Silencing of SLAMF3 in MM cells decreased the number of viable myeloma cells and enhanced the anti-tumor activity of conventional chemotherapeutics. These findings suggest that SLAMF3 can be considered as a therapeutic target to induce complement and cell-mediated lysis of myeloma cells [50]. These suggestions were further reinforced by Atanackovic et al. who showed that SLAMF3 is the only over-expressed/phosphorylated immunoreceptor in myeloma cell lines and primary CD138- negative cell population, which have previously been recognized as myeloma precursors cells [50] (Table 1). High expression of SLAMF3 has been described in patients with monoclonal gammopathies of uncertain significance, smoldering myeloma, and leukemia. The SLAMF3-targeting strategy was extended successfully to plasma cells from patients with MGUS [51]. Above all, the high expression of SLAMF3 correlates well with chemotherapy-resistant cells and myeloma-propagating phenotype. Thus, designing monoclonal antibodies specific to SLAMF3 could improve the treatment and help to obtain prolonged remissions in MM patients.


SLAMF4 (CD244, 2B4) expression is reported on CD8+ T cells, γδ T cells, NK cells, macrophages, basophils, mast cells and eosinophils. Following interaction of SLAMF4 with its natural ligand, SLAMF2, its cytoplasmic domain binds to SAP [21] (Figure 1). This interaction activates NK cell and induces IFN-γ secretion [52]. SLAMF4-mediated activation of NK cells involves complex interactions involving LAT, Ras, Raf, ERK and p38 [53]. In SLAMF4-deficient mice, NK cells are ineffective in eliminating cancer cells because they are inactivated. Functional impairment of NK cells in the absence of SLAMF4/SLAMF2 interactions is associated with defective calcium signaling as well [54].

In acute myeloid leukemia patients, polyclonal large granular lymphocytes (LGLs) were reported to have anti-tumor activity. The LGLs are CD3+/CD8+/CD56+, polyclonal cells that do not express NK cell receptors for MHC class I molecules. SLAMF4 expressed by LGLs largely contributes to their ability to lyse leukemia cells of patients [55]. SLAMF4 might potentiate the activator signal through T lymphocyte receptor (TCR) ζ chain. Indeed, the chimeric SLAMF4-TCRζ receptor induces more specific cytolysis of leukemia cells than SLAMF4 alone. This observation has also been extended to memory T cells stimulated by the tumor antigen [56]. SLAMF4 receptor has potent stimulatory effect in NK cells when expressed alone or as an antigen-specific SLAMF4- TCRζ chimeric receptor. Thus, SLAMF4 could be considered as powerful new tool for adoptive immunotherapy of leukemia and other malignancies [57] (Table 2).


SLAMF5 (CD84) expression has been described in thymocytes (highest by single positive cells), T cells, TFH cells, B cells (overexpressed with activation), macrophages, DCs, platelets, basophils, mast cells and eosinophils. SLAMF5 is involved in T cells activation by enhancing IFN-γ secretion [58] and in the stimulation of platelets [21, 59]. SLAMF5 could also serve to distinguish two splenic B cells populations: SLAMF5Low and SLAMF5high. SLAMF5high sub-population represents a subset of memory B cells as demonstrated by increased cell size, co-expression of the memory B cell-specific marker CD27, somatically mutated Ig variable region genes, and increased proliferation compared to SLAMF5Low B cells. The ligation of SLAMF5 with a specific mAb induces rapid phosphorylation of tyrosine residues in ITSM motif. Then, SLAMF5 recruits the cytoplasmic adaptor proteins SAP and EAT-2 [60] (Figure 1).

Among the CLL characteristics are the accumulation of CD5+ B lymphocytes in peripheral blood, in lymphoid organs and in bone marrow and the accumulation of the malignant cells due to reduced apoptosis sensitivity. CLL may be classified based on mutational status of the immunoglobulin variable heavy-chain gene, ZAP-70 overexpression, cytogenetic abnormalities (13q-, + 12, 11q-, 17p-) and expression of several cell surface antigens (CD38, CD49d) that correlate with risk of disease progression (Rai or Binet staging system) [61]. In the context of CLL, SLAMF5 expression is significantly higher during early stages of disease and is regulated by macrophage migration inhibitory factor and its receptor CD74 (Table 1). The activation of SLAMF5 initiates Akt signaling cascade that increases the anti-apoptotic Bcl-2 gene expression and consequently enhances CLL cell survival. Thus, the blockade of the SLAMF5-dependent survival pathway in CLL cells might represent a new therapeutic strategy [62]. Indeed, the blockade of SLAMF5 inhibits the interaction between CLL cells and their microenvironment inducing cell death as a consequence [63]. Several studies have reported a panel of clusters of differentiation (CD) antigens that are known to correlate with the prognosis of CLL. Huang et al. identified the profiles of surface CD antigens that distinguish clinically stable from progressive or slow progressive CLL. In the case of progressive CLL, 27 CD antigens including SLAMF5, are differentially abundant (CD11a, CD11b, CD11c, CD18, CD19, CD20, CD21, CD22, CD23, CD24, CD25, CD38, CD40, CD43, CD45, CD45RA, CD52, CD69, CD81, CD98, CD102, CD148, CD180, CD196 and CD270). This profiling provided the basis for a rapid test to identify patients with CLL according to the probability of clinical progression and the potential of earlier requirement for treatment [61].


SLAMF6 (CD352, NTB-A, SF2000, Ly108 in mice) expression is reported in thymocytes (highest by double negative and single positive cells), T cells, B cells (overexpressed with activation), DCs, NK cells, neutrophils, eosinophils. It is also expressed under two distinct isoforms (LY108–1 and LY108–2) in lupus-prone mice [21]. In NK cells, SLAMF6 activation is implicated in the cytotoxic activities and cytokine production [64]. SLAMF6 plays a key role in T cell activation [65] and neutrophil functions [66]. In pathological conditions, SLAMF6 is highly expressed in CLL and B lymphocytes of lymphoma patients (Table 1). For this reason, Korver et al., used two mAbs (994.1 and 480.12) to target SLAMF6 in a preclinical study of CLL and lymphoma, (Table 3). Indeed, they showed 86% decrease of tumor volume in a xenograft nude mouse CA46 model treated with 300μg of mAbs twice a week. Moreover, in a xenograft SCID mouse and in systemically disseminated Raji human lymphoma cells model, authors observed significant increase in survival of animals injected with 100 μg of mAbs [67]. These promising findings highlight the importance of targeting SLAMF6 as an immunotherapy for B-cell malignancies.

The decrease in CLL progression observed by Yigit in xenografted SCID mice model after the administration of anti-SLAMF6 confirmed the implication of this receptor in CLL pathophysiology. The effect of anti-SLAMF6 is amplified when it was administered concomitantly with Ibrutinib, a Bruton tyrosine kinase inhibitor. Anti-SLAMF6 decreased the number of CLL cells everywhere except in peritoneal cavity and Ibrutinib increased the efficiency of anti-SLAMF6 by inducing the release of CLL cells from their niche. All these data suggest that the combination of anti-SLAMF6 and Ibrutinib might be an efficient new treatment against CLL [68].


NK cells, T lymphocytes, activated B cells and macrophages are the cells that majorly express SLAMF7 (CD319, CS1, CRACC) [21] (Figure 1). The cytoplasmic domain of SLAMF7 contains two ITSM that are involved in the interaction with SAP. The SLAMF7 homophilic interaction regulates NK cell cytolytic activity [69]. SLAMF7 is highly expressed by more than 97% of myeloma cells while its expression is restricted in normal cells [70, 71]. In some preclinical studies, SLAMF7 was targeted by humanized mAb, HuLuc63 (Elotuzumab), which stained CD138+ myeloma cells, NK cells, NK-like T cells, and CD8+ T cells [70] (Table 2). HuLuc63 inhibits MM cells binding to bone marrow stromal cells and induces antibody-dependent cellular cytotoxicity against MM cells (Figure 3). This effect is SLAMF7-specific and dose-dependent, and leads to tumor regression in multiple xenograft models of human MM [70, 72]. Moreover, Elotuzumab, promoted the ligation between NK and myeloma cells by the intermediary of SLAMF7 and induced NK cytotoxicity against myeloma cells independent of ADCC [73, 74]. In addition, SLAMF7-derived peptides showed efficacy to induce the activation of some cytotoxic T cells clones. Later, Bae et al. suggested SLAMF7239–247 as SLAMF7-specific HLA-A2 peptide capable of activating cytotoxic T lymphocytes and inducing specifically the lysis of the primary MM cells and HLA-A2+-CS1+ MM cell line [75] (Table 3).

Mechanisms of Elotuzumab against myeloma cells.

Figure 2: Mechanisms of Elotuzumab against myeloma cells. SLAMF7 and CD16 on NK cells can bound to Elotuzumab. The binding to SLAMF7 induces NK cell activation and enhances cytolysis function against myeloma cells. While the binding to CD16 receptor can induce the release of Perforin/Granzyme by NK cells and subsequently enhance ADCC against myeloma cells overexpressing SLAMF7. Moreover, CD16 (NK cells), Elotuzumab and SLAMF7 (Myeloma cells) can enhance NK cell cytotoxicity against myeloma cells independent of ADCC. Furthermore, Elotuzumab-SLAMF7 interaction can inhibit the adhesion between myeloma cells and BMSC.

SLAMF3 implication model as hepatocellular carcinoma (HCC).

Figure 3: SLAMF3 implication model as hepatocellular carcinoma (HCC). Left quadrant, shows the schematic representation of the role of SLAMF3 as negative regulator of MAPK / mTOR pathway. In HCC hepatocyte, the rate of SLAMF3 is lowered. In this cell, the triggered signals by growth factors through their specific receptors activate signalization pathways, including the MAPK pathway, which will be constitutively active. This pathway stimulates, among others, the expression of certain resistance transporters such as MRP-1 that are responsible for the resistance to chemotherapies molecules. The MAPK pathway also modulates the formation of the nuclear complex RB / E2F, whose target genes are among that regulating the cell cycle and mitosis such as Plk-1. The resultant of these pathways activation state are enhanced cell proliferation, unblocked cell cycle and apoptosis escape leading to the progression of the tumor mass. Right quadrant, represents the hypothetic therapeutic model of SLAMF3 in HCC. The restoration of a high expression of SLAMF3 induced a down phosphorylation of MAPK ERK and mTOR. First, the strong expression of SLAMF3 reduced phosphorylation ratio of RB permitting its binding to the E2F factor which induces its inhibition. The decreased Plk-1 expression, one important E2F target is implicated in the inhibition of mitosis induced by the high expression of SLAMF3. Second, the high expression of SLAMF3 inhibits expression and function of MRP-1, that sensitize the cancer cell to drugs. Finally, the high expression of SLAMF3 in the cancer cell controls proliferation, blocks mitosis and sensitizes to apoptosis which controls progression of the tumor mass.

Several studies showed that Elotuzumab could trigger autologous ADCC against primary MM cells resistant to conventional or novel therapies like Bortezomib and HSP90 inhibitors. Pretreatment with conventional or novel anti-MM drugs enhance HuLuc63-induced MM cell lysis [71] (Figure 2). Therefore, these results prove that SLAMF7 play a pivotal role in the elimination of MM and provide the preclinical rationale to test it alone or in combination with other drugs in clinical trials. Bortezomib is a reversible proteasome inhibitor with significant activity in MM that could enhance Elotuzumab activity. When tested in MM xenograft model, the combination of Elotuzumab and Bortezomib, exhibited a significant enhancement of in vivo antitumor activity [71]. These preclinical results encouraged phase I and II clinical trials of Elotuzumab in patients with relapsed or refractory MM. When tested in phase I, Elotuzumab alone failed to reproduce the same efficiency as in animal model [76]. On the other hand, when administered to patients under Bortezomib treatment, Elotuzumab improved the objective response rate from 45% to 48% [77]. In a phase II trial, the combined use of Elotuzumab with Lenalidomide and dexamethasone in 150 patients with refractory/relapsed MM, seems to increase the progression-free survival from 6.9 to 9.7 months with stable ORR from 66% to 63% [78]. Importantly, a positive effect of Elotuzumab is reported to improve the ORR to 82% when used in combination with Lenalidomide and low-dose of dexamethasone [79].

In a phase II, randomized, multicenter, open-label, intravenous Elotuzumab (10 or 20 mg daily) in combination with oral Lenalidomide (25 mg daily) and dexamethasone (40 mg daily) improves the efficacy with an acceptable safety in patients with relapsed MM. These results seem to be better when only Lenalidomide and dexamethasone are used [80]. In patients with renal impairment, (about 50% of patients with MM), Elotuzumab might be used without dose adjustment but Lenalidomide needed a dose adjustment [81]. All these findings allowed the realization of a phase III testing of Elotuzumab in combination with Lenalidomide and dexamethasone in relapsed MM and in untreated MM patients [82]. In patients with relapsed or refractory MM, combination of Elotuzumab, Lenalidomide, and dexamethasone (Elotuzumab group: 325 patients) significantly reduced the risk of disease progression or death by 30% compared to control (control group: 321 patients treated with Lenalidomide and Dexamethasone). However, this study did not integrate Lenalidomide untreated patients as control group. This lack of control makes it difficult to conclude about the real effect of adding Lenalidomide. It has to be noted that the adverse events reported in 25% of the patients were principally common hematologic toxic effects (lymphocytopenia, anemia, thrombocytopenia and neutropenia). Serious adverse events were reported in 65% and 57% of patients in the Elotuzumab and the control group, respectively. In the Elotuzumab group, 34% patients had grade 3 or 4 neutropenia, as compared with 44% in the control group. Grade 3 or 4 lymphocytopenia was reported in 77% patients in the Elotuzumab group and 49% in the control group. Other reported side effects were non-hematologic toxic effects like fatigue, diarrhea and muscle spasms [82]. The above-mentioned findings allowed the FDA, in November 2015, to issue the authorization of Elotuzumab use in combination with Lenalidomide and dexamethasone in MM.

Lately, the combination of Elotuzumab with Thalidomide and dexamethasone was tested in a phase II trial involving 40 patients with refractory/relapsed MM. The results show an ORR of 38% with median progression-free survival of 3.9 months. This combination might constitute a potential alternative to the Elotuzumab, Lenalidomide and dexamethasone combination [83].

SLAM in solid cancers

Other cell types outside the immune system also express SLAM members. The reported detection of SLAMF2 in melanoma and SLAMF3 in hepatocellular carcinoma (HCC) assigned new roles to SLAM receptors in physiology and pathology. These recent observations reveal numerous potential therapeutic applications targeting SLAM members in solid cancers (Table 3).


Quite often, SLAMF1 is expressed on normal and malignant cells of the immune system [84]. However, little is known about its expression outside the hematopoietic system. Although SLAMF1 is not found in different regions of normal brain tissues, immunohistochemical study revealed its expression in 77.6% of human central nervous system (CNS) tumors, including glioblastoma, anaplastic astrocytoma, diffuse astrocytoma and ependymoma. These observations have proposed the expression of new isoform of SLAMF1 nCD150 as new diagnostic marker in CNS tumors [85] (Table 2).

Mehrle et al. reported that the up-regulation or silencing of SLAMF1 in human lymphocytes was accompanied by increased or decreased cytotoxic activity respectively, and suggested the implication of SLAMF1 in cytotoxicity against human colon cancer. Moreover, increased cytotoxic activity against cancerous cells and IFN-secretion are the result of the up-regulation of SLAMF1 in T cells that decrease the tumor progression index in xenografted mice [86]. Following its activation, SLAMF1 co-localizes to the lipid rafts (specific membrane compartments) in cytotoxic CD8+ T cells.


NK cells play a crucial role in the anti-cancer immunity. In patients with advanced-stage HCC, Attenuated infiltration and dysfunction of NK cells in the intratumoral region was positively associated with the increased level of activated monocytes/macrophages in peritumoral stroma of HCC tissues. Accordingly, activated monocytes isolated from HCC tissues caused transient activation and consequently their apoptosis. This process was mediated by cell-cell interactions by way of SLAMF2-SLAMF4, but not NKG2D and NKp30 [87].

In Melanoma, targeting the interaction of SLAMF2-SLAMF4 or use of anti-SLAMF4 mAb are promising therapeutic strategies. The activation of SLAMF4 or SLAMF2 in murine tumor model by injecting specific antibodies resulted in a five-fold reduction of melanoma cells metastasis. This anti-tumor effect involves cytolytic function and IFN-γ production of NK cells as expected [88].

The implication of SLAMF2-SLAMF4 in melanoma anti-tumor effect is subject of some controversies. For instance, in one study involving SLAMF4 (-/-) mice, it was difficult to confirm the role of SLAMF2-SLAMF4 interaction in anti-melanoma response. When injected with SLAMF2+ and SLAMF2- metastatic B16 melanoma cells, wild-type mice poorly rejected the SLAMF2+ melanoma cells compared to SLAMF2- tumor cells, suggesting an inhibitory effect of SLAMF4-SLAMF2 interaction on melanoma cells [89].


Recently, it has been reported that SLAMF3 is the only member of its family expressed in hepatocytes [90] (Figure 1). Identifying SLAMF3 in non-blood tissue such as liver tissue opened new avenues to investigate other physiological functions of this receptor. SLAMF3 expression is high in human healthy primary hepatocytes and is reduced in HCC cells. SLAMF3 low expression was confirmed in several HCC cell lines suggesting its negative regulation in cancer cells [90] (Table 3). The restoration of SLAMF3 expression in these cells inhibited cell proliferation, migration and enhanced apoptosis (Figure 3). This finding suggested that SLAMF3 is involved in the control of hepatocyte proliferation and in carcinogenesis.

SLAMF3 controls proliferation in part by decreasing MAPK Erk1/2, JNK and mTOR phosphorylation [90]. SLAMF3 expression in HCC retains Retinoblastoma (RB) factor in its hypo-phosphorylated active form, which in turn inactivates E2F transcription factor, thereby repressing the expression and activation of Polo-like kinase Plk-1 (Figure 3). A clear inverse correlation was also observed between SLAMF3 and Plk-1 expression in patients with HCC [91]. Thus, the inhibitory effect of SLAMF3 on cell cycle progression occurs through Plk-1 and RB activation [91]. These findings attributed new functions to SLAMF3 as molecular regulator of cell proliferation, cell cycle progression and apoptosis and qualify SLAMF3 to be considered as potential therapeutic candidate to control tumor progression at least in the liver.

In HCC, the expression of multi-drug resistance proteins, MRP-1, correlates with the resistance to chemotherapy and to treatment failure. MRP-1 (ABCC1), a member of the ABC superfamily transporters is expressed in all organs. MRP-1 mediates active efflux of a broad range of physiological substrates like glucuronide, glutathione and sulfate conjugates [92]. Chemotherapy drugs including Doxorubicin, Vincristine, Etoposide and Methotrexate also induce these reagents [93]. In HCC cells, induction of SLAMF3 expression decreased the expression of MRP-1. Furthermore, restoring high SLAMF3 expression in vitro model inhibited the efflux of therapeutic molecules [94] (Figure 3). Elevated SLAMF3 expression might thus play a key role in eliminating cancer cells by the chemotherapy drugs [95].


SLAM molecules are of particular interest for diagnosis and therapy of various cancers. Targeting these molecules is already under clinical investigations and has the potential to open new therapeutic options to improve management of cancer patients (Table 2). The most advanced therapeutic strategy is targeting of SLAMF7 (CS1) using humanized mAb in MM management. Completion of phase III studies and validation of therapeutic efficacy and safety of Elotuzumab in MM requires addressing of key issues regarding the biology of SLAMF7.

Another key finding is the SLAMF3 expression in hepatic tissue and its role as cell proliferation regulator and apoptosis inductor. This regulation involves several pathways constitutively activated in HCC such as MAPK pathways. However, comprehensive investigations are needed to identify SLAMF3 molecular partners to clarify the link between receptor expression and regression of tumors in xenografts Nude mice model. The implication of immune cells (innate and adaptive) cannot be ignored and requires further investigation. In parallel, various risk factors that promote transformation of cells like viral factors, metabolic abnormalities or the intake of alcohol could have an impact on the SLAM receptor expression or function. Further work is needed to determine the cross talk between these risk factors and SLAM.


No conflicts of interest are reported for this study.


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