Genetic aberrations are observed in >80% of CLL patients (9). The most frequent alteration is del13q14, which accounts for >50% of CLL cases. Calin et al(10) determined that a cluster of two miRNA genes, miR-15a and miR-16-1, were absent or downregulated in CLL patients with a 13q deletion and this downregulation correlated with allelic loss at 13q14. This was the first study to demonstrate that two miRNAs may act as suppressor genes of human cancer. A minimally deleted region containing deletions in the leukemia 2 (DLEU2) gene and the miR-15a/miR-16-1 genes has been identified in this region (10,11). However, Lia et al(12) determined that the size of the 13q14 deletion was related to the penetrance and aggressiveness of lymphoproliferative diseases, which suggested another tumor suppressor function of genetic elements in addition to DLEU2/miR-15a/miR-16-1. Therefore, other genes are located in 13q14 as well as miR-15a and miR-16-1. miR-15a and miR-16-1 function as tumor suppressor genes through targeting several molecules involved in cell proliferation and apoptosis, such as B-cell CLL/lymphoma 2 (BCL2), cyclin D1 and D3 (CCND1 and CCND3) and cyclin-dependent kinase 6 (CDK6) (13,14).

Another common aberration in CLL is trisomy 12 (10–20%). It has previously been determined that NOTCH1 mutations were detected in approximately half of IGVH unmutated/ZAP70⁺ trisomy 12 CLL patients (41.9%), which indicated that NOTCH1 activation is strongly correlated with trisomy 12 (15). However, López et al(16) suggested that the distribution of NOTCH1 mutations in CLL with trisomy 12 is heterogeneous and other chromosomal abnormalities including trisomy 18 altered the prognosis of these patients. Further studies are required to determine the correlation between NOTCH1 and trisomy 12 in CLL. The involvement of miRNAs in NOTCH1 mutations have been identified in T cell acute lymphocytic leukemia (T-ALL), including miR-181-a-1, miR-181-b-1 and miR-223 (17,18).

Deletion of 11q22-23 is observed in ~20% of patients with advanced CLL (9) and predominantly impacts the ataxia-telangiectasia mutated (ATM) gene. Mutations of the ATM gene were detected in 12% of all CLL patients and ~1/3 of the CLL cases with del11q23 (19). ATM functions in regulating cell cycle progression and controlling the integrity of DNA repair. CLL patients with this deletion or mutation have a significantly shorter treatment-free interval (23.5 months) compared with those without such abnormalities (64.2 months) (20). A combination of an 11q deletion and an ATM mutation in CLL resulted in a shorter overall survival (OS) and progression-free survival (PFS) time following first-line therapy with alkylating agents and purine analogs (20). ATM is important in the regulation of miRNA biogenesis. It directly phosphorylates KH-type splicing regulatory protein (KSRP, a key component in Drosha and Dicer miRNA-processing complexes) upon DNA damage, facilitating the interaction between KSRP and pri-miRNAs and promoting miRNA maturation (21). Wang et al(22) demonstrated that miR-181 was directly targeted by ATM in breast cancer. Moreover, miR-34b and miR-34c are located in the 11q23 region, thus deletion of this region led to the downregulation of these two miRNAs (23).

Deletion of 17p13 was observed in ~5–10% of CLL cases at first diagnosis or treatment (9). Over 80% of CLL cases with 17p deletion carried TP53 (a tumor suppressor involved in cell cycling and cell death) mutations in the remaining allele. Inactivation of the second TP53 allele by point mutation was identified in numerous CLL cases and was correlated with chemorefractiveness and reduced survival (24). Expression of miR-34a, miR-29c and miR-17-5p were significantly downregulated in CLL with TP53 abnormalities (25).

All blood cell lineages are generated from the hematopoietic stem cells (HSCs) in the bone marrow. miRNAs contribute to B cell development by targeting different transcription factors. Developmental arrest at the progenitor (pro) B cell to precursor (pre) B cell transition and an influence on antibody diversity is induced by knocking out Dicer in early B cells (26). The involvement of miRNAs during B cell development are shown in Fig. 2. Homeobox (HOX) family members, which are essential in modulating HSC homeostasis, are directly repressed by the miR-196b and miR-10 families, leading to the promotion of HSC differentiation. The development of progenitor cells is also blocked by miR-126, through the direct inhibition of the mRNAs encoding polo-like kinase 2 and HOXA9 (27). Constitutive expression of miR-150, a hematopoietic-specific miRNA, blocks the transition from pro-B cell to pre-B cell by inhibiting the expression of the translation factor, c-myb (28,29). It has been demonstrated that the miR-17-92 cluster (miR-17-5p, miR-18a, miR-19a, miR-19b-1, miR-20a and miR-92) suppressed the expression of tumor suppressor phosphatase and tensin homolog (PTEN), which is often mutated in human lymphomas, and the pro-apoptosis protein BCL2-interacting mediator of cell death (30). This cluster is required for B cell development in normal hematopoiesis and increased expression of these genes was demonstrated to be oncogenic promoting the transition from pro-B cell to pre-B cell during B cell development (31). There are multiple putative binding sequences for miR-181b in the 3′UTR of activation-induced cytidine deaminase (AID) and these sequences are directly inhibited by miR-181b (32). miR-223 inhibits LMO2 in the transition from naïve B-cell to germinal center (GC) B-cell and GC B-cell to memory B-cell (33). Expression of miR-155 was observed to be at a moderate level in HSC, a high level in the germinal center and relatively lower level in mature B cells during normal lymphopoiesis (34). Upregulation of miR-155 has been observed in various human B-cell neoplasms, including diffuse large B cell lymphoma, Hodgkin’s lymphoma and CLL. Numerous studies have demonstrated that miR-155 is important in the immune system and in homeostasis. Mice lacking miR-155 exhibited a normal steady condition of immune cell populations; however, showed a defective humoral response when immunized (35). miR-155 is upregulated subsequent to B cell activation in the GC, defective antibody class switching and reductive differentiation into plasma cells occurs in miR-155 deficient B cells (36). PU.1 and AID are two targets through which miR-155 functions. However, miR-155 and miR-181b do not exhibit overlapping functions in regulating AID expression as miR-181b prevents premature AID activity in the early stages of activation and miR-155 functions at a relatively later activation time. High levels of miR-34a also restricts the transition from pro-B to pre-B cell through inhibiting forkhead box transcription factor 1 (37).

Numerous studies have demonstrated that the Wnt signaling pathway is significant in embryonic development and fundamental cellular functions throughout life. It has recently been demonstrated that the Wnt/β-catenin signaling pathway is significant in tumorigenesis and angiogenesis (38). Constitutive activation of β-catenin inhibits multilineage differentiation from HSCs, including the development of B cells (39). Lu et al(40) observed the activation of the Wnt signaling pathway in CLL. Significantly higher expression levels of Wnt3, Wnt5b, Wnt6, Wnt10a, Wnt14, Wnt16, Fzd3 and LRP5/6, as well as LEF1 were observed in CLL cells compared with that in normal B cells. Survival of CLL lymphocytes was enhanced by SB-216763, an inhibitor of GSK3β. Two small molecule inhibitors of the LEF-1/β-catenin complex, CGP049090 and PKF115-584, were observed to efficiently induce the apoptosis of CLL cells in vitro and in vivo, whereas the normal B cells were not significantly affected (41). The Wnt canonical signaling pathway may be significant in the survival of CLL cells.

Several studies demonstrated the correlation between miRNAs and the canonical Wnt/β-catenin signaling pathway. Valastyan et al(42) observed that Fzd3 was directly targeted by miR-31 in breast cancer and may have been a mechanism causing miR-31 to oppose metastasis. Analyses of the mRNA and protein levels determined that Wnt1 is transcriptionally inhibited by miR-21. Differentiation of monocyte-derived dendritic cells is inhibited by the antagonism of miR-21, either by adding exogenous Wnt1 or transfected with miR-21 inhibitors (43). PTEN is an important tumor suppressor and the loss of PTEN results in the upregulation of anti-apoptotic factor myeloid cell leukemia 1 (MCL1) in HSC. PTEN was also shown to be targeted by miR-21 in hepatocellular cancer and epithelial ovarian cancer (44,45). In addition, Rossi et al(46) suggested the 21FK (miR-21 expression, fluorescence in situ hybridization and karyotype) score, a three-category score model (scores of 0, 1 or 2) to stratify the CLL patients according to OS. The lower the score, the longer the OS time in CLL patients. One point was allocated for miR-21 expression with a 17p deletion, and no points were allocated for low miR-21 expression or a normal karyotype. Patients with a score of zero exhibited a significantly higher survival rate than those with a score of 1 or 2. An miR-29a/Wnt positive feedback loop was discovered in osteoblastic differentiation. Transcription of miR-29 was induced by the canonical Wnt signaling pathway. Dikkopf-1, Kremen2 and secreted frizzled related protein 2, which are negative regulators of the canonical Wnt signaling pathway were directly inhibited by miR-29a. The expression levels of these Wnt signaling inhibitors were increased in miR-29a antagonist transfected cells (47). Furthermore, miR-315 and miR-135a/b directly targeted Axin and APC, respectively, in the canonical Wnt pathway (48). Few studies are available concerning miRNAs in the Wnt/β-catenin signaling of CLL. miRNAs are involved in several components of the canonical Wnt signaling pathway; however, the majority of the specific mechanisms remain unknown possibly due to the crosstalk between Wnt/β-catenin signaling and other pathways.

Patients with aggressive CLL usually express the unmutated immunoglobulin heavy-chain variable-region gene (IgV_H) and a high level of the 70-kDa ζ-associated protein (ZAP-70), whereas patients with mutated IgV_H and low ZAP-70 expression present with indolent CLL (49). Through an miRNA microarray composed of 190 human genes, Calin et al(50) identified a significant correlation between miRNAs and CLL with ZAP-70 expression and unmutated IgV_H. A signature of 13 miRNAs was identified, with upregulation of miR-15a, miR-16-1, miR-16-2, miR-23b, miR-24-1, miR-146, miR-155, miR-195 and miR-221, and downregulation of miR-223, miR-29a-2, miR-29b-2 and miR-29c in CLL with high ZAP-70 expression and unmutated IgV_H. Therefore, the expression of certain miRNAs may act as prognostic markers of CLL. The predictive value of circulating miRNAs in CLL disease stratification has been demonstrated (51). Expression levels of certain circulating miRNAs present in CLL patient plasma, such as miR-150 and miR-135, were significantly different from that in control groups. Circulating levels of certain miRNAs in CLL with ZAP-70⁺ were also different from those in ZAP-70⁻ CLL patients. The level of miR-150 in the ZAP-70⁻ CLL plasma was increased, which was thought to be correlated with the disease stage (51). Bomben et al(52) observed a significantly higher expression level of miR-17 (the prototypic member of the miR-17-92 family) in IgV_H unmutated CLL cells with high ZAP-70 compared with that in CLL cells with mutated IgV_H and a low ZAP-70 phenotype.

The prognostic value of TP53 mutations in CLL has been shown in numerous studies. Zenz et al(53) demonstrated that the TP53 mutation acted as a central prognostic factor for PFS and OS in CLL independent of 17p deletions. TP53 mutation and/or 17p deletions were identified in ~29% of CLL patients refractory to fludarabin in first-line treatment settings. Notably, the correlation between TP53 mutations and certain other factors, such as IGHV gene mutations, CD38 and ZAP-70 expression, or any chromosomal abnormality (other than 17p deletion) was of no significance (24). Therefore, TP53 mutations may be beneficial if added to the genetic tests for CLL. microRNA/TP53 feedback circuitry was demonstrated to be correlated with CLL pathogenesis and outcome (54). In this feedback circuit, TP53 acts as a molecular linker between miR-15a/miR-16-1 and miR-34b/miR-34c clusters, which are located on chromosome 13q and chromosome 11q, respectively. miR-15a and miR-16-1 directly bind to the 3′UTR of TP53 and inhibit its expression. TP53 binds directly to a TP53 binding site on pre-miR-34b/miR-34c to promote their translation and the downstream signal is activated. In CLL cases with a 13q deletion only, downregulated or absent miR-15a/miR-16-1 resulted in increased levels of BCL, MCL1 and TP53, further activated the expression of miR-34a, miR-34b and miR-34c and induced ZAP-70 inhibition. Thus, in CLL patients with a 13q deletion, the number of apoptotic cells may be decreased due to the increased levels of anti-apoptotic proteins; however, the increase in tumor burden is relatively low due to the enhancement of the TP53 tumor suppressor pathway (54). This feedback circuitry provides a novel mechanism for the involvement of miRNAs in CLL with 13q deletions and their interaction with TP53. Mraz et al(55) demonstrated the involvement of miRNAs in cases of CLL with TP53 mutation. Thirty-five miRNAs were detected in CLL samples with TP53 mutations (n=12) and wild type TP53 samples (n=18), as a consequence, miR-34a, miR-29 and miR-17-5p were significantly downregulated in CLL with mutated TP53. miR-34a, which is located in 1p36 and is frequently deleted in numerous types of tumors, was the most differentially expressed miRNA with an ~9-fold decrease in CLL with mutated TP53. miR-29 was reported to directly downregulate the expression levels of TCL1 and MCL1 in CLL. As a member of the miR-17-92 family, miR-17-5-p directly targeted E2F1, p21 and cyclin D1, and other genes involved in the G1/S-phase cell-cycle transition.

Leong and Karsan (56) observed the activation of NOTCH1 in leukemia through the study of the chromosomal translocation t(7;9)(q34;q34.3) in T cell acute lymphoblastic cases (56). Activating mutations of NOTCH1 were observed in 8.3% of CLL at diagnosis, 31% in CLL transformation to Richter’s syndrome and 20% in CLL chemorefraction (57). CLL patients with a NOTCH1 mutation presented with a more advanced clinical stage at diagnosis and a shorter 10-year OS (21%) compared with those without NOTCH1 mutations (56%) (58). NOTCH1 mutation in CLL generates a premature stop codon and leads to a constitutively activated and more stable form of the NOTCH1 protein, which lacks the C-terminal domain which contains a PEST sequence. Mutations of NOTCH1 act as an independent prognostic marker of CLL, which is prone to be mutually exclusive with TP53 mutations and a poor prognosis (59). Microarray profiling of miRNAs in T-ALL cells was performed prior to and following inhibition of Notch signaling with γ-secretase inhibitor (GSI). The expression level of miR-223 significantly increased ~1.5-fold when Notch signaling was inhibited by GSI. miR-223 targeted the 3′UTR of the insulin-like growth factor 1 receptor (IGF1R) and downregulated its expression. Thus, Notch signaling inhibits the miR-223 expression level in T-ALL cells and the total IGF1R protein levels are negatively regulated by miR-223 (18). miR-181a and miR-181-b-1, miRNAs related to NOTCH1, are also observed in T-ALL. Deletion of miR-181a-1/miR-181b-1 significantly inhibits the NOTCH1 oncogene-induced T-ALL by downregulating the negative regulators downstream of the NOTCH and pre-TCR signaling pathway (17). In addition, miR-181a/miR-181-b promoted the development of NK cells from CD34⁺ hematopoietic progenitor through the suppression of nemo-like kinase (NLK), a protein kinase that negatively regulates Notch signaling by inhibiting the formation of the Notch active transcriptional complex. Transcription levels of miR-181a/b increased during NK cell development from NK progenitor cells to final CD56⁺ NK cells. Moreover, miR-181a/miR-181b also increased IFN-γ production in primary CD56⁺ NK cells, possibly by regulating the Notch signaling pathway (60). In addition, expression of miR-451 and miR-709 were repressed by intracellular NOTCH1 in a T-ALL mouse model through induction of the degradation of the E2A tumor suppressor (61).

In conclusion, the results of these studies suggest that miRNAs involved in the NOTCH1 mutation are important in several diseases, particularly T-ALL. A previous study demonstrated that NOTCH1 may be added to the hierarchical prognostic classification in CLL (62). However, few studies have been conducted concerning the correlation between miRNAs and NOTCH1 mutation in CLL at present. Thus further studies regarding the mechanism of miRNAs and NOTCH1 in CLL may aid in a more accurate prognosis for CLL patients.