MicroRNA modulators of epigenetic regulation, the tumor microenvironment and the immune system in lung cancer

One of the most promising molecular entities to have impacted cancer research in recent times is the group of small non-coding RNAs known as microRNAs. Since the first miRNA gene called lin-4 was discovered in Caenorhabditis elegans [1], several others have been identified, and so far over 2500 miRs have been described in the human genome miRBase (www.​mirbase.​org) [2]. MicroRNAs have been described to be involved in several cellular processes including proliferation, development, metabolism, differentiation and apoptosis. Importantly, the deregulation of microRNA expression and function has been linked to many human pathological conditions, including cancer [3,4].

Classically, in cancer, microRNAs have been categorized as either oncogenic or tumor suppressor miRNAs. In the first instance, by post-transcriptionally lowering mRNA and subsequently protein levels of molecules with tumor suppressor functions, microRNAs assume an oncogenic function. Conversely, by targeting oncogenic molecules, they act as tumor suppressors and the altered expression levels of the microRNA(s) between tumor and normal states coupled with the function of the targeted molecule(s) dictate the resulting (end) phenotype. Beyond the classical regulation of oncogenes and tumor suppressor mRNAs, aberrantly expressed microRNAs could in further levels of complexity act: 1) to regulate the epigenetic machinery by a) directly modulating enzymes which take part in methylation-mediated silencing and chromatin remodeling [5] or b) be epigenetically regulated themselves [6]; 2) in a paracrine fashion via exosomes, microvesicles and protein complexes to influence the tumor microenvironment [7-10] and 3) to promote the release of mediators which activate pro- or anti-cancer immune activity [11,12]. These latter mechanisms of microRNA regulation are explained in detail.

The epigenome is both dynamic and highly regulated in order to conserve normal expression patterns in cells. One of the most important components of expression regulation is the methylation of CpG islands within promoter regions both in normal as well as cancer cells [13,14]. The dynamic balance is maintained by a family of DNA methyltransferases: notably DNMT1 (maintenance DNMT) and DNMT3a and 3b (de novo DNMTs). Equally important in epigenetic regulation are covalent changes in histone tails that are orchestrated by histone methyltransferases (HMT), histone acetyltransferases (HAT), histone deacetylases (HDAC) [13,15] and polycomb proteins such as PRC 1 and PRC 2 [16]. MicroRNAs as a part of regulatory networks serve as significant targets for the epigenetic machinery and are also active players in modulating enzymes which take part in methylation mediated silencing and the chromatin remodeling machinery. MiR-127 was the first epigenetically regulated microRNA to be reported in a cancer entity [17]. Since then, many microRNAs were found to undergo epigenetic regulation in different cancer types including colorectal [18,19], urological [20], breast [21], ovarian [22,23], gastric [24] and pancreatic [25] as well as different types of haematological malignancies [26]. Most of the microRNAs are involved in crucial processes in the cell, thus, a great number of epigenetically regulated microRNAs (app. 45%) are implicated in several cancer types (eg., miR −124, −129, −34b at least 7 types, 34a −12 types), however, none of these have so far been found to be particularly involved in lung cancer [27].

The tumor microenvironment is an increasingly appreciated item of interest in cancer development and progression. During cancer progression, sequences of molecular changes arise in the tumor as well as in the neighboring tissue stroma. Since tumor development is driven by physiological responses to an aberrant stromal environment [48] the interaction between the tumor and stromal cells determines the outcome of progression [49]. The tumor microenvironment is a complex structure that in addition to the extracellular matrix (ECM) comprises many other cell types, including endothelial cells, inflammatory cells and most abundantly, fibroblasts [50] While normal fibroblasts have been found to prevent tumor progression [51] the so-called cancer associated fibroblasts (CAFs) generate an environment promoting tumor growth and invasiveness [52]. CAFs are characterized by specific changes in their secretory profile, e.g, chemokines that attract inflammatory cells. Together, they release growth factors that trigger cancer cell proliferation, inhibit apoptosis or indirectly stimulate angiogenesis [53]. Interestingly, one of the major mechanisms by which CAFs are activated is mediated by specific microRNAs, e.g. miR-21, miR-31, −214, and 155 [7,8]. There is ample evidence, that microRNAs are not only present in the cells, but also in extracellular space [54,55]. Importantly, extracellular microRNAs also play a very vital role in cell to cell communication [9] and are capable of contributing to microenvironment-associated processes such as angiogenesis, matrix degradation and stromal remodeling, all which support cancer progression and metastasis [10]. About 90% of microRNAs found in the ECM are bound to RNA- binding proteins (eg. AGO proteins, especially Ago2, NPM1 - nucleoplasmin 1 and GW 182 responsible for microRNA stabilization as well as secretion) and just 10% exist in extracellular vesicles such as exosomes, apoptotic bodies and, mainly microvesicles (MVs) [9,55,56]. Remarkably, most of the microRNAs that are differentially expressed in CAFs are down-regulated as compared with normal fibroblasts, suggesting that they act as suppressors of stromal activation [57]. Evidence for the contribution of microRNAs in lung cancer angiogenesis arising from a specific influence on the tumor microenvironment was hinted at in the study by Jusufovic and colleagues [58] who found significantly higher microvessel density (MVD) together with decreased expression levels of let-7b and miR-126 in tumor and surrounding tissue of 50 NSCLC patients as compared to corresponding normal tissues. Interestingly, there was no difference in expression between tumor and surrounding tissue for both microRNAs and MVD, indicating similar molecular changes in the tumor and surrounding cells in this context [58].

In addition to influencing the local microenvironment, tumor cells have also been shown to secrete exosomes at a significantly higher level compared to normal cells [59]. These so-called tumor-derived exosomes (TD exosomes) contain pro-tumorigenic components, in particular abundant microRNAs which influence and modify stromal cells and recruit them as cancer-associated stromal cells, which in turn influence cancer cells and the ECM contributing to cancer development and progression [10,59]. Additionally, a mechanism based on passive leakage has been proposed, in which microRNAs are released from the cells due to injury, chronic inflammation, necrosis, or from cells with very short half-lives, like platelets [60].

Notable instances of microRNA regulation of the tumor microenvironment in lung cancer include the repression of the angiogenic program by IL-8, ICAM and CXCL1 through the lung tumor cell mediated exosomal release of miR-192 with a consequent reduction in metastatic burden and tumor colonization [61]. In another study, TGF-β induced release of miR-183 by lung cancer cells was found to control DAP12, a critical stimulatory signal adaptor linked to numerous NKC receptors resulting in a suppression of NK cell function [62]. Still, Krysan and colleagues found the inflammatory molecule, prostaglandin E2 (PGE2) to mediate an up regulation of c-Myc in stromal cells, which in turn modulates the expression of the miR-17-92 cluster, that effectively targets the tumor suppressor PTEN. The end effect was an augmentation of apoptosis resistance in non-small cell lung cancer (NSCLC) cells [63]. In what appears to be an interesting example of the microenvironment of one organ affecting the dissemination of cells from a different organ, Subramani et al., found that miR-768-3p released by brain astrocytes targets K-ras, mitigating metastatic potential of lung cancer cells. The down-regulation of this microRNA seen in many brain tumors is thought to enhance K-ras expression, including its downstream effectors ERK1/2 and B-Raf, and thus promoting metastasis [64].

In addition to the processes described above, it has become increasingly clear that microRNAs play multiple roles in the negative regulation of numerous immune responses triggered by rapidly proliferating neoplastic cells. The genetic instability of neoplastic cells is associated with alterations of antigenic patterns that may in turn lead to attenuated recognition of the tumor by immune cells [65]. Some of these alterations are largely influenced by actions mediated by a constellation of different microRNAs (Figure 1). An example of this is miR-9 that is over-expressed in many cancers including lung cancer [66]. MiR-9 is capable of down-regulating the transcription of the MHC class I gene, thereby preventing the recognition of tumor cells by the immune system [11,56]. On the other hand, a down-regulation of miR-29 expression in cancer leads to an up-regulation of B7-H3 gene transcription and the subsequent expression of this molecule on the surface of neoplastic cells [67]. Consequently, B7-H3 delivers an inhibitory signal to T cells and NK cells and therefore inhibits the anti-tumor activity mediated by these cells [68,69]. Similarly, miR-222 and −339 down-regulate the expression of intracellular cell adhesion molecule 1 (ICAM-1) on the surface of tumor cells [70]. The binding of ICAM - to lymphocyte function-associated antigen (LFA-1) has been shown to be essential for optimal activation of cytotoxic T cell (CTLs) [71], thus, miR-222 and −339 in cancer cells contribute to impaired CTL-mediated tumor cell lysis [70]. Moreover miRs-221 and −222 are overexpressed in NSCLC and act in part by targeting TIMP3 [72] which has known functions in controlling cytokine and growth factor homeostasis. Furthermore, several microRNAs, for instance miRs-21 and −126/126*, contribute to the modulation of the tumor microenvironment, which encompasses not only stroma cells but also soluble factors and signaling molecules [73-76] (Figure 1). Regulatory T lymphocytes (Tregs), are important components of the tumor stroma, and are known to predominantly exert immunosuppressive effects. A number of tumor-bound chemokines including CCL22 have been shown to recruit Tregs to modulate immune responses in cancer [77]. Notably, CCL22 production in cancer cells is regulated by miR-34a, which suppresses the expression of this chemokine. On the other hand, increased levels of TGF-β in the tumor milieu down-regulate the expression of miR-34a and thereby increase infiltration of immunosuppressive Tregs. The TGF-β - miR-34a - CCL22 axis is therefore important in modulating the tumor microenvironment [78]. Other chemokines such as CXCL12 (Sdf-1) and CCL2 (MCP-1) are secreted by various cancer types and function as autocrine growth factors as well as chemo-attractants for progenitor cells and monocytes/macrophages [12,79,80]. Interestingly, the transcription of the CXCL12 gene is controlled by miR126/miR126*. This microRNA pair directly inhibits the expression of CXCL12 and down-regulates the production of CCL2 in a CXCL12-dependent process in which stromal cells (mainly mesenchymal stem cells, MSCs) seem to play the crucial role. In cancer cells, decreased miR-126/126* expression results in an increased production and secretion of CXCL12 that in turn attracts MSCs to the tumor microenvironment and increases the secretion of CCL2 [75]. Subsequently, CCL2 recruits monocytes/macrophages to the site of neoplastic growth [81].

During migration, monocytes are exposed to many signals derived from cancer and stromal cells that induce their differentiation towards classically (M1) or alternatively activated (M2) macrophages. Tumor associated macrophages (TAMs) control the majority of immunological processes within tumors exerting both, regressive (M1) or progressive (M2) effects on the tumor development [82,83]. Unfortunately, the vast majority of TAMs exhibit an M2-like phenotype. Remarkably, a significant number of microRNAs like miRs-9, −21 and −146 are involved in the differentiation of the TAMs from peripheral blood monocytes (Figure 2). Both monocytes/macrophages and cancer cells are capable of releasing different pro- and anti-inflammatory cytokines like the immunosuppressive cytokine IL-10, which fosters tumor growth [84]. Substantial amounts of this cytokine are secreted by neoplastic cells including that of the lung [85,86]. Interestingly, the transcription of the IL-10 gene in tumor cells is indirectly regulated by miR-30d, which acts by directly repressing GALNT7. GALNT7 suppression leads to increased production and secretion of IL-10, which in turn promotes monocyte differentiation towards the M2 phenotype [87]. In addition, in human monocytes, IL-10 up-regulates miR-187 expression which down-regulates TNF-α production. Moreover, in macrophages, miR-187 indirectly decreases the expression of IL-6 and IL-12p40 via decreasing MAIL in an NFKBIZ-dependent manner [88]. Along similar lines, the differentiation of monocytes towards M2 macrophages can be induced by M-CSF. M-CSF signaling down-regulates miR-142-3p in monocytes which leads to increased Egr2 (Krox20) expression. This transcription factor can control differentiation of monocytes via activating macrophage-specific genes such as C-FMS, acting in cooperation with Spi-1/PU.1 [89].

Many of the pro-tumorigenic outcomes of TAMs’ are controlled by microRNAs and depend on such factors like HMGB1 and IL-10 [88,90]. These mediators are secreted both by tumor cells and stroma and act via interactions with several cell surface receptors including toll-like receptors (TLR) and the IL-10 receptor. TLR2-, TLR-4- and TLR5-mediated signaling and NF-κβ activation in macrophages up-regulates the expression of miR-146 that in turn targets IRAK1 and TRAF6, proteins which are crucial components of interleukin-1- and TNF-related signaling pathways, respectively. More specifically, miR-146 acts via targeting IRAK1 and TRAF6, members of the TLR-NF-κβ pathway, and therefore contributes to controlling the expression of an array of inflammatory cytokine genes. MiR-146 therefore acts through a negative feedback loop and down-regulates cytokine signaling [91]. On another note, miR-92 is up-regulated following TLR-4 activation and in turn down-regulates the expression of TNF-α and IL-6 [92]. TLR4-mediated up-regulation of miR-21 suppresses programmed cell death protein-4 (PDCD4) expression. This mechanism may limit pro-inflammatory cytokine production in macrophages via suppressing NF-κβ activation, leading to an increased IL-10 production [90]. Notably, miR-21 and miR-29a are expressed at different levels in various cancers including lung cancer [93-95]. Both miR-21 and miR29a can act within cancer cells or can be delivered from cancer cells to macrophages by microvesicles and can subsequently bind intracellular TLR7 or TLR8. This microRNA-TLR interaction leads to the activation of the NF-κβ pathway and an increase in the production of the pro-inflammatory cytokines, IL-6 and TNF-α that in turn activate pro-metastatic responses in TAMs [96]. Some microRNAs also mediate a cross talk between cancer and stromal cells as in the case of TAM-derived miR-223, which down-regulates Mef2c expression in neoplastic cells, leading to an increase of cancer cell invasion, probably through the involvement of the miR-223 – Mef2c – β-catenin pathway [97].

Taken together, substantial evidence supports the dynamic role of microRNAs within the tumor microenvironment and with the immune system culminating in the promotion of tumor growth and immune evasion.

The role of microRNAs in the development and progression of lung cancer as well as other types of cancers is overwhelming; with several reports demonstrating the enormous impact microRNAs have on several cancer-associated processes.

In this review, we have elaborated on how microRNA-target interactions transcend beyond simple post-transcriptional regulation of oncogenes and/or tumor suppressor mRNAs to a more complex setting where they not only modulate networks and pathways, but also affect the tumor microenvironment, the epigenome and immune evasion. In lung cancer, their impact is very relevant, and to a large degree is deeply entrenched in several cascades, which impact lung cancer progression and metastasis. Inherently, microRNAs can target several molecules concurrently, and using this advantage together with the identification of the right molecule in the right context could have great potential, especially when used alongside other therapeutic modalities. Their involvement in several critical cancer associated processes makes them highly interesting molecules. Their effects transcend simple intracellular events, and are able to influence neighboring cells and even those at distant sites. Sufficient evidence indicates that they are significant modulators of our immune system which widens their scope as potential therapeutic agents.

Despite the tremendous amount of knowledge we have already on microRNAs, new publications keep coming out, describing yet other novel functions, making us marvel about the wide-reaching potential of these small molecules. In summary, microRNAs seem to be a very promising research target, however, the complexity of their actions makes keeping this promise very challenging.