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. 2020 Apr 30;10:452. doi: 10.3389/fonc.2020.00452

Table 2.

MicroRNAs (miRNAs) targeting breast cancer stem cells (BCSCs).

miRNA Target Result on BCSCs References
miR-7 KLF4 -Reduces stemness phenotypes
-Inhibits pluripotent potential of stem cells
(22)
miR-9 Notch signaling Reduces metastasis (23)
miR-16 WIP1 -Reduces self-renewal
-Increases sensitivity to doxorubicin (Dox)
(24)
miR-23b MARCKS -Inhibiting cell cycle
-Inhibiting motility
(25)
miR-29b -SPIN1
-Wnt/β-catenin and Akt signal pathways
-VEGFA
-PDGFA/B/C
-MMP2/9, ITGA6,
-ITGB1, TGFβ2/3
-Inhibits self-renewal and growth
-Inhibits invasion and metastasis
(26)
miR-30a Protein AVEN -Inhibits the growth
-Induces apoptosis
(27)
miR-30e -Ubc9
-ITGB3
-Inhibits self-renewal
-Induces apoptosis
(28)
miR-34 family (miR-34a and miR-34c) -Notch signaling
-Notch4
-Reduces cancer stem cell phenotypes
-Suppresses EMT
-Suppresses metastasis
-Increases sensitivity to Dox and paclitaxel
(23, 29, 30)
miR-93 Sox4 -Reduces stemness phenotypes
-Promotes differentiation
-Inhibits pluripotent potential of stem cells
(31)
miR-126/miR-206/miR-335 -Sox4
-Tenascin C
-Reduces stemness phenotypes and proliferation
-Inhibits metastasis and migration
(32)
miR-128 -Nanog
-Snail
-Reduces stemness phenotypes
-Inhibits pluripotent potential of stem cells
(33, 34)
miR-140 -Sox9
-ALDH1
-Reduces stemness phenotypes
-Inhibits pluripotent potential of stem cells
(35)
miR-148 -BMI1
-ABCC5
-Inhibits progression
-Induces apoptosis
-Increases sensitivity to Dox
(33, 34)
miR-153 HIF1α Inhibits angiogenesis (36)
miR-200 family (miR-200a, miR-200b, and miR-200c) -BMI1
-Suz12
-Notch pathway components, Jagged1, Maml2/3
-ZEB1/2
-Suppresses colony formation
-Suppresses tumor formation
-Suppresses invasion
-Suppresses EMT
(3739)
miR-600 -SCD1 enzyme
-Wnt/β-catenin pathways
Promotes differentiation (40)
miR-708 Neuronatin ERK/FAK pathway Inhibits migration and metastasis (41)
let-7 -H-RAS
-MYC
-HMGA2
-IL-6
-ERα
-Inhibits self-renewal
-Inhibits pluripotent potential of stem cells
(42, 43)

KLF4, Kruppel-like factor 4; WIP1, wild-type p53-induced phosphatase 1; MARCKS, myristoylated alanine rich protein kinase C substrate; SPIN1, Spindlin 1; VEGFA, vascular endothelial growth factor A; PDGFA/B/C, platelet-derived growth factor A/B/C; MMP2/9, matrix metalloproteinases 2/9; ITGA6, integrin subunit alpha 6; ITGB1, integrin subunit beta 1; TGFβ2/3, transforming growth factor beta 2/3; Protein AVEN, apoptosis and caspase activation inhibitor; Ubc9, hypothetical protein; ITGB3, integrin subunit beta 3; EMT, epithelial–mesenchymal transition; ALDH1, aldehyde dehydrogenase 1; BMI1, B lymphoma Mo-MLV insertion region 1 homolog, a member of the polycomb repression complex 1 family; ABCC5, multidrug resistance-associated protein 5; HIF1α, hypoxia-inducible factor 1α; Suz12, polycomb repressive complex 2 subunit; Maml2/3, mastermind-like Notch coactivators 2/3; ZEB1/2, zinc finger E-box binding homeobox 1; SCD1, stearoyl-CoA desaturase-1; HMGA2, high-mobility group AT-hook 2; IL-6, interleukin 6; ERα, estrogen receptor α.