The miR-200 family is comprised of five members: miR-200a, miR-200b, miR-200c, miR-141 and miR-429. These members are then divided into two clusters based on chromosomal location, with cluster one consisting of miR-200b, miR-200a, and miR-429, located on chromosome 1 in humans, and cluster two consisting of miR-200c and miR-141, located on chromosome 12 in humans [3]. The gene sequence between the two clusters only differs by a single nucleotide, which suggests that the members of miR-200 can potentially target a common subset of genes for similar physiological effects [32,33]. Due to the relatively high degree of overlap in target genes between the two clusters, all members of the miR-200 family are good candidates for targeting common subsets of genes, such as those that are involved in breast cancer metastasis [34,35].

Metastasis and cell invasion are both characteristic of malignant tumor progression [36]. Further research shows that the acquisition of epithelial-to-mesenchymal transition (EMT) typically results in invasion and metastasis by promoting cell detachment, which thereby increases tumor cell mobility [6]. EMT also contributes to the malignant transformation of many human cancers. The loss of epithelial differentiation and transition to mesenchymal phenotype is linked to progression of most cancer malignancies. Epithelial cells typically have normal cell-to-cell junction and adhesion, while mesenchymal cells have weaker cell wall adhesion, making them more motile and likely to enhance invasive characteristics. EMT has been found to play an essential role in tumor invasion, metastatic dissemination, and the acquisition of resistance to current cancer therapies [37]. It is activated by EMT-inducing transcriptional repressors, which include members of the Snail family and the ZFH family of transcription factors [7,38]. Emerging studies indicate that the miRNA-200 family could regulate the EMT process by targeting specific molecular markers of EMT [12].

The miR-200 family targets specific molecular markers of EMT, including E-cadherin, which is the marker for epithelial phenotype, vimentin, and ZEB1 and ZEB2, which are the markers of mesenchymal phenotype [3,39]. Furthermore, ZEB1 has been shown to be an essential EMT activator in human cancers, including breast cancer, and promoted metastasis of tumor cells in mouse models [7,40,41]. The miR-200 family has been shown to induce epithelial phenotype by suppressing the expression of EMT inducers, ZEB1 and ZEB2 [42,43]. In a pioneering work by Gregory et al. [43], it was suggested that the entire miR-200 family is downregulated upon exposure to transforming growth factor-β (TGF-β). TGF-β is a cytokine that is known to induce the EMT phenotype [37,44,45]. Reexpression of the miR-200 family significantly inhibited EMT that was induced by TGF-β, while inhibition of the miR-200 family resulted in the induction of EMT phenotype. Furthermore, there were increased levels of ZEB1 and ZEB2 following the induction of EMT, which suggests that the miR-200 family is a negative regulator of the mesenchymal markers, ZEB1 and ZEB2. Another study [46] that focused on miRNAs suppressed by ZEB1 also showed that the most affected miRNAs were members of the miR-200 family. It was revealed that ZEB1 can bind to highly conserved sites in the promoter and directly suppress transcription of an entire cluster of the miR-200 family. Furthermore, ZEB1 is also a target of miR-200c, which indicates that there is an EMT-inducing feed-forward cycle.

A recent study on miR-200 revealed that three miRNA clusters, miR-200c-141, miR-200b-200a-429, and miR-183-96-182, are all involved in the regulation of self-renewal in cancer stem cells (CSCs) and normal stem cells [47]. The three miRNA clusters are downregulated in human breast CSCs, normal human cells, and mouse mammary cells. Emerging evidence has demonstrated that the BMI1 gene, which promotes stem cell self-renewal, was directly inhibited by these miRNA clusters. In addition, ectopic overexpression of miR-200c in embryonal carcinoma cells resulted in neural differentiation and suppressed tumorigenicity of breast CSCs in vivo [48]. Our own investigations into the mechanisms of phosphoglucose isomerase (PGI)/autocrine motility factor (AMF)-induced metastases of breast cancer cells in vitro as well as in vivo have suggested the involvement of miR-200s [12]. We found that the PGI/AMF-induced EMT is marked by induced E-cadherin expression and reduced vimentin/ZEB1/ZEB2 expression. Furthermore, we observed a mechanistic involvement of miR-200s in this regulation of EMT by PGI/AMF, where overexpression of miR-200s was found to reverse the PGI/AMF-induced EMT and, conversely, silencing of miR-200s was found to induce EMT even in the PGI/AMF-silenced breast cancer cells. We further confirmed our results in vivo in an experimental pulmonary metastases model where PGI/AMF or silencing of miR-200s induced lung metastases and downregulation of PGI/AMF or overexpression of miR-200s significantly reduced these lung metastases. Thus, evidence from all these studies suggests that the miR-200 family plays a crucial role in regulation of breast cancer metastasis and aggressiveness.

The miR-125 has two known isoforms in humans: miR-125a and miR-125b. Altered expression of miR-125 has been observed in several malignancies, including breast cancer [49,50]. The miR-125a and miR-125b were both found to be significantly downregulated in breast cancer patients. Guo et al. [51] explored the role of miRNA-125 in breast cancer after observing [22,52] that there were decreased levels of miRNA-125 in breast tumors in comparison to normal breast tissues. Their work [51] showed that miRNA-125a is inversely correlated with HuR expression in various breast carcinoma cell lines. HuR is an RNA binding protein (RBP) that is upregulated in several different cancers. The miR-125a represses translation of HuR through a target site in the 3′ UTR. Overexpressing miR-125a led to decreased HuR protein levels, suppressed cell growth, and reduced cell migration and proliferation. These results suggest that miR-125a can potentially aid in tumor suppression in breast cancer by utilizing HuR as a direct and functional target.

Further research showed that miR-125a and miR-125b are both downregulated in HER2-overexpressing breast cancers [53]. HER2, the human epidermal growth factor receptor 2, has no ligand-binding domain and thus cannot bind growth factors. It binds to other ligand-bound epidermal growth factor receptor family members to create a heterodimer [7]. Amplification of HER2 is common in numerous cancer patients, including those with breast tumors. The miR-125a and miR-125b function as tumor suppressors in SKBR3 cells, a HER2-overexpressing human breast cancer cell line, by suppressing HER2 mRNA and protein levels. This results in reduced cell growth, motility and invasiveness [54]. The c-Raf has also been proposed as a target of miR-125b leading to its antiproliferative effect [55].

Lethal-7 (let-7), one of the first mammalian miRNAs to be identified, was initially discovered to play a role in the developmental timing of Caenorhabditis elegans and is conserved throughout the animal phyla [4,7,56]. The let-7 family consists of 12 members: let-7-a1, let-7-a2, let-7-a3, let-7-b, let-7-c, let-7-d, let-7-e, let-7-f1, let-7-f2, let-7-g, let-7-i and miR-98 [3,57]. Studies have shown that let-7 is often absent in cells that are less differentiated, exhibit a mesenchymal phenotype and represent more advanced cancer [58]. Thus, in accordance, higher levels of let-7 are expressed in cells that are more differentiated, exhibit an epithelial phenotype and represent less advanced cancer. An in vivo study of let-7 showed that its administration was effective against lung and breast cancers in mice and further computational analysis suggested that let-7 would be effective in estrogen receptor positive (ER+) metastatic breast cancer [6]. let-7 also regulates apoptosis and CSCs differentiation, which suggests that it has high potential of being utilized in cancer therapy [59].

An earlier study investigated the expression of let-7 in breast cancer cells and demonstrated that let-7-fl is expressed in multiple breast cancer cell lines [60]. Further research investigated the role of let-7 in distinguishing breast tumor-initiating cells (BT-IC) from other differentiated progeny. There was reduced expression of let-7 in BT-IC, but the level of let-7 increased with differentiation [61]. Administration of let-7 in BT-IC also resulted in reduced proliferation and reduced metastasis in vivo. On the other hand, when let-7 was silenced, non-T-IC experienced higher self-renewal ability. The research suggests that let-7 affects self-renewal ability of cancer cells, so cancer therapy by targeting let-7 in breast cancer patients could be beneficial and could serve as a novel treatment option.

Dangi-Garimiella et al. proposed a role for let-7 in the metastasis of breast cancer. Their study showed that signaling through let-7 regulates the repressive action of Raf kinase inhibitory protein (RKIP) on metastasis of breast cancer cells [62]. RKIP is a suppressor gene in human breast cancers that inhibits MAPK, G protein-coupled receptor kinase-2 and NF-κB signaling cascades [63,64]. Its expression is thus expected to be reduced in invasive cell lines. RKIP, in accordance, inhibited invasion by metastatic breast cancer cells and repressed breast tumor cell intravasation in mouse models. Inhibition of MAPK resulted in decreased transcription of LIN28, which led to the downregulation of let-7 targets. The let-7 targets are mechanistically linked to metastasis of carcinomas, and thereby their downregulation enhances the process by which RKIP exerts its tumor suppressor abilities [3,65]. Elevated levels of let-7 family members results in the downregulation of its targets, such as HMGA2, which are mechanistically linked to metastasis of cancer cells.

Another proposed role for let-7 is its involvement in signaling through estrogen receptor. Previous research revealed that estradiol (E2) may encourage increased levels of eight members of the let-7 family [66]. E2 also acts as a ligand for both estrogen receptor alpha (ER-alpha) and estrogen receptor beta (ER-beta). Recent analysis reported that there is an inverse association between the expression of ER-alpha and various members of the let-7 family [67]. The let-7 family miRNAs were found to be downregulated in human breast cancer cells at stages of ductal carcinoma in situ (DCIS) and invasive ductal carcinoma (IDC) in comparison to the benign stage. Overexpression of let-7 family members in ER-positive cells resulted in downregulated ER-alpha activity, reduced cell proliferation and induced apoptosis. Furthermore, it was found that let-7 family members target similar genes and have similar functions.

Studies surrounding let-7 suggest that it can be used as a future cancer therapeutic. It is now widely accepted that let-7 levels are high in normal cells and reduced in invasive cancer cell lines. However, the mechanism of let-7 deregulation and its role in tumorigenesis is currently not fully understood. Further studies on the molecular mechanisms behind let-7 activity in cancer would improve treatment plans for therapeutic applications.

The miR-205 has been implicated as a tumor suppressor in breast cancer [68]. The miR-205 expression is reduced in breast cancer tissue samples in comparison to normal breast tissue. Furthermore, its expression is limited to myoepithelial cells and is reduced in matching tumor samples, which indicates that it is associated with a good prognosis. The miR-205 was shown to negatively modulate ZEB1 and is thereby negatively linked to the acquisition of EMT [43,69]. This suggests that miR-205 activity is very similar to that of the miR-200 family, which is also associated with negative regulation of EMT. Further support for miR-205’s potential to identify breast tumors from normal tissue revealed reduced expression in breast cancer cell lines MCF-7 and MDA-MB-231 in comparison to normal MCF-10A breast epithelial cells. In addition, transfecting miR-205 in cancer cells resulted in the inhibition of cell proliferation, clonogenicity and invasion [68]. The downregulation of miR-205 in metastatic breast cancer cell lines suggests that it is an ideal therapeutic target in cancer treatment.

Another study explored miR-205 target genes in breast cancer patients. It revealed that miR-205 directly targets HER3, a receptor tyrosine kinase of the epidermal growth factor receptor (EGFR) family [70]. Members of EGFR are typically involved in tumorigenesis when their signaling functions are deregulated [71]. The miR-205 inhibits HER3, inactivating the downstream mediator Akt, which results in the suppression of the PI3K/Akt signaling pathway. In breast cancer, overexpression of HER2 is characteristic of an aggressive subset of tumors [72]. HER2 activity is dependent on the transinteraction with other HER family members. In particular, its relationship with HER3 leads to the activation of the PI3K/Akt pathway, progression of tumor and resistance to chemotherapy [73]. HER3 thus plays a critical role in HER2-mediated tumorigenesis. The miR-205 can contribute to cancer therapeutics due to its negative regulation of the HER3 receptor, which affects survival and proliferation of breast cancer cells. The miR-205 can inhibit breast cancer cell proliferation and improve response to specific targeted therapies as well.

The miR-206 has been shown to suppress breast cancer migration [74,75]. It was first discovered by using miRNA microarrays to compare miRNA expression between normal and breast cancer cells [22]. The miR-206 is upregulated in estrogen receptor negative (ER−) breast cancers and also inhibits the expression of the estrogen receptor gene ERα (ESR1) through two binding sites in the ESR1 3′ UTR [76]. Other work also showed that miR-206 expression was reduced in ERα-positive human breast cancer tissues and that miR-206 suppresses ESR1 expression in addition to inhibiting the growth of MCF-7 breast cancer cells [77]. The miR-206 was shown to induce cell cycle arrest and inhibit estrogen-induced proliferation. The tumor suppressive role of miR-206 was further confirmed in another study that demonstrated miR-206 to be downregulated in metastatic breast cancer cells in comparison to normal parental cells [78]. Reexpression of miR-206 resulted in reduced invasive capacity and altered cell morphology, which can also limit the migration of metastatic cells. These findings suggest a potential role for miR-206 in breast cancer therapy.

The miR-34a is a transcriptionally regulated miRNA by the p53 network, which has been shown to be downregulated in multiple cancers [52]. A previous study has demonstrated that in breast cancer, miR-34a levels are lower in triple negative and mesenchymal-type breast cancer cell lines when compared to the normal epithelial cell lines [79]. The study proposed that p53 mutations may contribute to lower miR-34a expression. In terms of investigating the miRNA’s sensitivity to radiation, the authors compared the sensitivity of the normal breast epithelial cell line HMEC, the HER-2+ cell line UACC-812, and the mesenchymal-type cell line MDA-MB-231. Results have indicated that MDA-MB-231 cells, which have low miR-34a levels, showed increased sensitivity to radiation in comparison to HMEC and UACC-812, which both express high levels of miR-34a [79]. In addition, MDA-MB-231 cells were protected from radiation-induced death if miR-34a levels were increased. In accordance, downregulating miR-34a levels would enhance radiation-induced deaths. The results of this study suggest that miR-34a is essential for MDA-MB-231 cell survival when considering radiation sensitivity.

Another study examined the effect of miR-34a on breast cancer development and found that its levels are downregulated in five different breast cancer cell lines in comparison to the normal epithelial cell line 184A1 [80]. Ectopic expression of miR-34a levels in breast cancer cells also led to reduced cell proliferation, invasion, and induced apoptosis. It was also found that miR-34a targets, Bcl-2 and SIRT1, are in reverse correlation with ectopic expression of miR-34a. The study concluded that miR-34a is able to inhibit breast cancer cell proliferation and migration through downregulation of Bcl-2 and SIRT1. Since manipulating miR-34a levels affects radiation sensitivity in breast cancer cells, miR-34a could have great potential for breast cancer therapy.

The miR-31, which is known to have pleiotropic effects on breast cancer metastasis, has been shown to inhibit metastasis at multiple steps by inhibiting the expression of prometastatic genes [81]. Normal levels are exhibited in normal breast epithelial cells, but miR-31 is almost undetectable in metastatic breast cancer cells in vivo. It is also expressed in decreased levels in non-metastatic breast cancer cell lines. Investigations that explored miR-31 expression in MDA-MB-231 and SUM-159 breast cancer cells found that ectopic expression of miR-31 in vivo and in vitro hindered invasion and metastatic colonization [81]. The experiment showed that even though overexpressing miR-31 in breast cancer cells resulted in larger tumors and increased proliferation, the cancers were encapsulated and less invasive. Furthermore, miR-31 also reduces cell survival and the ability to form secondary tumors. In accordance, inhibiting miR-31 resulted in increased invasiveness and metastasis in vivo.

The miR-31 may regulate at least 200 different mRNAs in mammalian cells. At least six targets have been identified, which include frizzled3 (Fzd3), integrin α-5 (ITGA5), myosin phosphatase-Rho interacting protein (M-RIP), matrix metallopeptidase 16 (MMP16), radixin (RDX) and RhoA [82]. In order to investigate whether miR-31 regulation of these target genes affects metastatic function, the six identified target genes were reexpressed in miR-31-expressing cells. Results showed that only ITGA5, RDX, and RhoA could reverse the motility defects and impaired invasion, which suggests that these three genes are important targets of miR-31. These findings indicate that miR-31 inhibits metastasis, which suggests that it may be an ideal therapeutic target for breast cancer.

The miR-342 was revealed to play a tumor suppressive role in regards to tamoxifen resistant breast cancer. Tumor resistance to tamoxifen, which is a selective estrogen receptor (ERα) modulator, remains a serious problem in clinical applications today, particularly in patients with carcinoma that overexpress the HER2 receptor tyrosine kinase. Although tamoxifen is one of the most common prescribed endocrine therapies, about 30%–40% of patients will fail adjuvant tamoxifen therapy and almost all of these patients with metastatic cancer will develop tamoxifen resistance as well [83]. Various studies have implicated HER2 as a significant factor in resistance to tamoxifen. Recent research found that there is an oncogenic splice isoform of HER2, HER2Δ16, which is also associated with metastatic breast cancer and resistance to endocrine therapy [84]. The miR-342 was revealed to contribute to tamoxifen resistance in several models, including cell lines that overexpress HER2Δ16 [85]. The miR-342 is downregulated in tamoxifen resistant breast cancer cell lines as well as in tamoxifen refractory breast cancers. Furthermore, the study also showed that miR-342 regulates gene expression in regards to tamoxifen-mediated apoptosis and proliferation. Reexpression of miR-342 may present a therapeutic approach in suppressing the growth of tamoxifen resistant breast cancer cells.

The miR-10b was one of the first miRNAs discovered to influence cancer metastasis. miR-10b is highly expressed in metastatic breast cancer cells and has a positive influence on cell migration and invasion in vitro [10,86]. It also initiates tumor invasion and metastasis in vivo. The metastatic MDA-MB-231 breast cancer cells were reported to express significantly higher levels of miR-10b in comparison to MCF-7 cells, which typically have little capacity to metastasize. Transduction of miR-10b into non-invasive SUM149 breast cancer cells resulted in increased size and invasiveness of tumors found in mice in comparison to tumors from nonmetastatic control SUM149 cells [10]. This study also emphasized the correlation between miR-10b expression levels in primary breast cancer and clinical progression in cancer treatment. Mechanistically, miR-10b was found to be activated by the transcription factor twist, which then causes an interruption of homeobox D10 (HOXD10) mRNA translation [87]. This results in increased expression of Ras homolog gene family member C (RhoC), which promotes cell invasion and metastasis [10].

Further research on the role of miR-10b in the metastasis of breast cancer showed that downregulation of miR-10b is one of the mechanisms by which breast cancer metastasis suppressor 1 (BRMS1) inhibits metastasis [88]. When BRMS1 was transfected into metastatic MDA-MB-231 and MDA-MB-435 breast cancer cells, the cell lines showed reduced metastasis [88]. The BRMS1 transfection also resulted in downregulated expression of miR-10b and RhoC, which suggests that miR-10b does affect the metastasis of breast cancer cells [89].

Recent exploration of miR-10b also demonstrated that treating cancer in mouse model with miR-10b antagonistic miRNAs (antagomirs) suppresses breast cancer metastasis [90]. Antagomirs, which are chemically engineered anti-sense RNA oligonucleotides against cognate miRNAs, are efficient and specific silencers of endogenous miRNAs. Silencing the miR-10b regulator resulted in decreased levels of miR-10b in vivo [3]. When mouse models with metastatic cancer were treated with miR-10b antagomirs, there was no resultant inhibition of primary tumor growth. Instead there were signs of decreased lung metastasis. These results suggest that miR-10b may be a good predictor of breast cancer metastasis because high levels are expressed in tumors that are more likely to metastasize into distant organs [91].

The miR-21 has been found to be consistently overexpressed in many carcinomas, including breast cancer [92–94]. In accordance with these findings, further research revealed that miR-21 is also highly upregulated in breast cancer cell lines when compared to normal breast samples, which suggests that miR-21 may act as an oncogene [95]. Among the 157 human miRNAs that were analyzed by real-time RT-PCR arrays, miR-21 was considerably overexpressed in breast cancer tissues [93]. To further explore the role of miR-21 in breast cancer development and progression, the miRNA was suppressed in breast cancer samples by anti-miR-21, which inhibits cell growth in vitro and tumor growth in vivo. Suppression of miR-21 was found to be linked with reduced cell proliferation and increased apoptosis [96,97]. Another study also confirmed that miR-21 targets the tumor suppressor tropomyosin 1 (TPM1), and overexpressing TPM1 in breast cancer cells resulted in suppressed clonogenic potential [98]. Therefore, it can be concluded that the downregulation of TPM1 by miR-21 suppression may explain the inhibition of tumor invasion.

Additional analysis of metastatic MDA-MB-231 breast cancer cells demonstrated that suppressed miR-21 results in decreased invasion and lung metastasis [98]. This investigation also helped identify two more targets of miR-21, which are programmed cell death-4 (PDCD4) and maspin [99]. PCDD4 and maspin both negatively enhance invasion and metastasis and thereby provide more targets for miR-21 in human breast cancers. Another important target of miR-21 includes the tumor suppressor gene phosphatase and tensin homolog (PTEN) [100–102]. In a study involving 40 invasive ductal carcinoma samples from breast cancer patients, expression of miR-21 was revealed to be negatively correlated with expression of PTEN [103,104]. The inverse relationship between PTEN and miR-21 suggests that tissues with miR-21 expression represent an aggressive phenotype. However, other studies have also shown that although the upregulation of miR-21 correlates with invasive tumors, there is still no clear pattern observed for the target genes, such as PTEN and PDCD4 [102]. Further studies should explore miR-21 targets in order to appreciate the benefit of targeted therapy for breast cancer.

As mentioned above, miR-21 has been found to be overexpressed in breast tumors in comparison to normal breast tissue, and is also associated with advanced stage, lymph node positivity, and reduced survival time [45]. The role of miR-21 is not only important in its activity as a biomarker, but also as a functional target. A study in which MCF-7 breast cancer cells were transfected with anti-miR-21 oligonucleotides resulted in reduced in vitro cell growth and in vivo tumor growth in a xenograft mouse model [45]. The reduced cellular proliferation was associated with increased apoptosis and reduced levels of the BCL-2 anti-apoptotic protein. Overall, miR-21 has been shown to affect several targets, including PDCD4, TPM1, maspin, and PTEN. Studies on miR-21 suggest that miR-21 is an oncogenic miRNA and plays a role not only in tumor growth, but also in invasion and metastasis by targeting multiple anti-metastatic genes [7,105,106].

The miR-155 is overexpressed in several human carcinomas, including breast cancer [92]. It is an effective suppressor of apoptosis, due to its effects on caspase 3, the most important caspase that is involved in the execution-phase of apoptosis [107]. Recent studies have investigated the targets of miR-155. The tumor-suppressor gene suppressor of cytokine signaling 1 (SOCS1) has been identified as a target of miR-155 in breast cancer cell lines [108,109]. The expression of SOCS1 was found to be inversely correlated to miR-155 expression in human breast cancer cells. Ectopic expression of miR-155 also enhanced proliferation of breast cancer cells and the development of tumors in vivo. Furthermore, silencing of SOCS1 in breast cancer cells reestablishes the oncogenic effects of miR-155, while restoring SOCS1 expression promotes the pro-tumorigenesis function of miR-155, which indicates that miR-155 negatively regulates SOCS1.

Another study also showed that miR-155 is upregulated in normal mouse mammary gland epithelial cells (NMuMG cells) by the TGF-β pathway and it mediates TGF-β-induced epithelial-to-mesenchymal transition (EMT) and cell invasion [110]. Researchers have found that the ectopic expression of miR-155 in NMuMG cells disturbs proper tight junction formation between cell walls and promotes cell migration and invasion. Furthermore, miR-155 also directly inhibits the expression of RhoA, a gene that regulates various cellular processes, including cell adhesion, motility, and polarity. The miR-155-induced phenotypes were reestablished by expressing a miR-155 insensitive version of RhoA in miR-155 overexpressing cells. These results indicate that miR-155 is regulated by the TGF-β pathway and also downregulates the RhoA protein expression to enhance the acquisition of EMT phentype. Also, by demonstrating that miR-155 is highly expressed in invasive tumors but not in noninvasive cancer samples, it was shown that miR-155 is linked to cancer invasiveness in human breast cancers [45]. Therefore, the miR-155 appears to play an essential role in breast cancer metastasis due to its implications in the acquisition of EMT and increased potential for invasion and metastasis.

Another role of miR-155 in the regulation of cell survival is seen through the downregulation of its direct target FOXO3a in breast cancer. Ectopic expression of miR-155 induced cell survival and chemoresistance to several agents, while the knock-down of miR-155 resulted in apoptosis and increased chemosensitivity [111]. In this investigation, it was found that overexpression of miR-155 led to repressed FOXO3a protein with consistent mRNA levels, and the knock-down of miR-155 resulted in increased FOXO3a. This study revealed that there is an inverse correlation between miR-155 and FOXO3a in breast cancer cell lines, which suggests that miR-155 is an essential therapeutic target in breast cancer.

The miR-373 and miR-520c are prometastatic miRNAs [79,112]. In a genetic screen that overexpressed approximately 450 miRNAs in the nonmetastatic MCF-7 breast cancer cell line, authors found that miR-373 and miR-520c promoted migration and invasion in vivo and in vitro. Furthermore, several cancer lines even required miR-373 for migration and the miRNAs also elicited a migratory phenotype by inhibiting the expression of the metastasis repressor CD44 [113]. Ectopic overexpression of CD44 reduced migration of MCF-7 cells that express miR-373 and miR-520c, which indicates that the downregulation of CD44 is essential to the migration of these cells [114]. Finally, miR-373 was also shown to be upregulated while CD44 was decreased in metastatic breast cancer tissue specimens [115], which additionally implicate these miRNAs for their roles in breast cancer metastasis.

Studies on miR-375 show conflicting results in both oncogenic and tumor suppressive roles. One particular study investigated miR-375 levels in estrogen receptor α (ERα)-positive breast cancer cell lines. Upregulation of ERα results in abnormal cell proliferation in the majority of breast cancers, but understanding of the mechanism behind this phenomenon is still unclear. Research showed that overexpression of miR-375 in ERα-positive breast cell lines contributed to proliferation [116]. In accordance, inhibiting miR-375 expression in ERα-positive MCF-7 breast cells resulted in reduced proliferation and ERα activation. The study also identified RASD1 as a potential target of miR-375. The miR-375 regulates RASD1 by targeting the 3′ untranslated region in RASD1 mRNA [116]. RASD1 contributes to cell proliferation by negatively regulating ERα expression. This suggests that there is a positive feed-forward loop, and that miR-375 plays an oncogenic role in breast cancer.

On the other hand, a conflicting study reveals that miR-375 may also have tumor suppressive role. Research on EMT and its role in initiating tumor cell invasion and metastasis showed that the acquisition to EMT exhibits resistance to a variety of cancer therapies, including tamoxifen [117]. To investigate the role of miRNAs in regards to resistance to tamoxifen, MCF-7 breast cells were exposed continually to tamoxifen to create a tamoxifen-resistant (TamR) model, which subsequently developed mesenchymal characteristics and increased invasiveness. Data showed that miR-375 was one of the top downregulated miRNAs in resistant cells and that the reexpression of miR-375 showed increased sensitivity of tamoxifen-resistant cells, and also partly reversed EMT phenotype [117]. The study also revealed that miR-375 directly targets metadherin (MTDH) and that there is an inverse correlation between the expression of miR-375 and MTDH in primary breast cancer cell lines. Furthermore, patients who were also exposed to tamoxifen were found to express higher levels of MTDH and experience shorter disease-free survival, and they also faced increased risk of relapse. Thus, concentrating on reexpression of miR-375 may serve as a potential therapeutic approach for breast cancer treatment.

The miR-221 and miR-222 have both been identified as basal-like subtype-specific miRNAs, expressed in a basal-like subtype of breast cancer [118]. Both miRNAs function as regulators of EMT and the expression of these miRNAs results in increased cell migration and invasion. The miR-221 and miR-222 repress their target tricho-rhino-phalangeal syndrome type 1 protein (TRPS1), which in turn increases the EMT-promoting protein zinc finger E-box-binding homeobox 2 (ZEB2) [118]. Another study also demonstrated that miR-221 and miR-222 both directly target estrogen receptor alpha (ERα) and that overexpression of these miRNAs in breast cancer aid in the progression of the more aggressive basal-like breast cancer [119]. They repress proteins p27/Kip1 and p57, which are both cell cycle inhibitors, which results in increased proliferation [120]. These characteristics also aid in developing tamoxifen resistance in basal-type breast cancers. These findings suggest that both miRNAs play important roles in the promotion of clinically aggressive basal-like breast cancer.

Further insight revealed that miR-221 and miR-222 are differentially expressed and that both miRNAs are overexpressed in estrogen receptor negative (ER−) breast cancer [119]. Transfections of miR-221 and miR-222 synthetic mimetics into a nontransformed mammary cell line MCF10A resulted in induced EMT-like phenotypes, increased invasion and migration, and increased the levels of the mesenchymal marker vimentin. In addition, inhibiting miR-221 and miR-222 in the metastatic MDA-MB-231 breast cancer cell lines induced a reverse phenotype.