miRNA General Information
miRNA Mature ID hsa-miR-211-5p
miRNA Stemloop AC MI0000287
miRNA Stemloop ID hsa-mir-211
Sequence uucccuuugucauccuucgccu
TTD Target(s) Regulated by This miRNA Cyclin-dependent kinase 6 (CDK6) Successful Target Target Info [1]
Phosphodiesterase 3A (PDE3A) Successful Target Target Info [2]
Ribonucleoside-diphosphate reductase M2 (RRM2) Successful Target Target Info [3]
Apoptosis regulator Bcl-2 (BCL-2) Successful Target Target Info [4]
Transforming growth factor beta 1 (TGFB1) Successful Target Target Info [5]
Mannose-6-phosphate receptor (M6PR) Successful Target Target Info [2]
ERK activator kinase 1 (MEK1) Clinical trial Target Target Info [4]
Matrix metalloproteinase-9 (MMP-9) Clinical trial Target Target Info [6]
G1/S-specific cyclin-D1 (CCND1) Clinical trial Target Target Info [1]
Interleukin-11 (IL11) Clinical trial Target Target Info [7]
TGF-beta receptor type II (TGFBR2) Clinical trial Target Target Info [2]
CI Man-6-P receptor (IGF2R) Clinical trial Target Target Info [2]
Facilitates chromatin transcription complex (FACT) Clinical trial Target Target Info [2]
Calcium-activated potassium channel KCa1.1 (KCNMA1) Clinical trial Target Target Info [8]
Omphalocele kinase 1 (NUAK1) Literature-reported Target Target Info [9]
Vitamin D3 up-regulated protein 1 (VDUP1) Literature-reported Target Target Info [10]
IP3 receptor isoform 1 (ITPR1) Literature-reported Target Target Info [4]
Osteonectin (SPARC) Literature-reported Target Target Info [11]
Ras-related protein Rab-22A (Rab22a) Literature-reported Target Target Info [12]
Vascular endothelial cadherin (CDH5) Literature-reported Target Target Info [13]
Protein(s) Regulated by This miRNA AP-1 complex subunit sigma-2 Regulated Protein [2]
Cyclic AMP-responsive element-binding protein 5 Regulated Protein [12]
DNA damage-inducible transcript 3 protein Regulated Protein [2]
DNA-binding protein SATB2 Regulated Protein [16]
Elongation of very long chain fatty acids protein 6 Regulated Protein [12]
Homeobox protein HMX1 Regulated Protein [17]
Interferon-induced GTP-binding protein Mx1 Regulated Protein [10]
Interleukin-10 receptor subunit alpha Regulated Protein [19]
Mucin-4 Regulated Protein [20]
Nuclear factor of activated T-cells 5 Regulated Protein [2]
POU domain, class 3, transcription factor 2 Regulated Protein [21]
Serine incorporator 3 Regulated Protein [2]
Transcription factor 12 Regulated Protein [12]
Transcription factor SOX-4 Regulated Protein [22]
Zinc finger protein SNAI1 Regulated Protein [23]
References
REF 1 miR-211 suppresses epithelial ovarian cancer proliferation and cell-cycle progression by targeting Cyclin D1 and CDK6. Mol Cancer. 2015 Mar 11;14:57.
REF 2 New target genes of MITF-induced microRNA-211 contribute to melanoma cell invasion. PLoS One. 2013 Sep 5;8(9):e73473.
REF 3 miR-211 modulates gemcitabine activity through downregulation of ribonucleotide reductase and inhibits the invasive behavior of pancreatic cancer cells. Nucleosides Nucleotides Nucleic Acids. 2014;33(4-6):384-93.
REF 4 The changes of miRNA expression in rat hippocampus following chronic lead exposure. Toxicol Lett. 2014 Aug 17;229(1):158-66.
REF 5 miR-211 promotes the progression of head and neck carcinomas by targeting TGFRII. Cancer Lett. 2013 Aug 28;337(1):115-24.
REF 6 Epigenetic regulation of miRNA-211 by MMP-9 governs glioma cell apoptosis, chemosensitivity and radiosensitivity. Oncotarget. 2012 Nov;3(11):1439-54.
REF 7 Identification of microRNAs inhibiting TGF--induced IL-11 production in bone metastatic breast cancer cells. PLoS One. 2012;7(5):e37361.
REF 8 The regulation of miRNA-211 expression and its role in melanoma cell invasiveness. PLoS One. 2010 Nov 1;5(11):e13779.
REF 9 Transcription factor/microRNA axis blocks melanoma invasion program by miR-211 targeting NUAK1. J Invest Dermatol. 2014 Feb;134(2):441-451.
REF 10 Genome-wide identification of target genes for miR-204 and miR-211 identifies their proliferation stimulatory role in breast cancer cells. Sci Rep. 2016 Apr 28;6:25287.
REF 11 MiRNA-211 suppresses cell proliferation, migration and invasion by targeting SPARC in human hepatocellular carcinoma. Sci Rep. 2016 May 27;6:26679.
REF 12 Microphthalmia-associated transcription factor (MITF) promotes differentiation of human retinal pigment epithelium (RPE) by regulating microRNAs-204/211 expression. J Biol Chem. 2012 Jun 8;287(24):20491-503.
REF 13 MicroRNA-211 expression promotes colorectal cancer cell growth in vitro and in vivo by targeting tumor suppressor CHD5. PLoS One. 2012;7(1):e29750.
REF 14 New target genes of MITF-induced microRNA-211 contribute to melanoma cell invasion. PLoS One. 2013 Sep 5;8(9):e73473.
REF 15 Microphthalmia-associated transcription factor (MITF) promotes differentiation of human retinal pigment epithelium (RPE) by regulating microRNAs-204/211 expression. J Biol Chem. 2012 Jun 8;287(24):20491-503.
REF 16 miR-211 suppresses hepatocellular carcinoma by downregulating SATB2.Oncotarget. 2015 Apr 20;6(11):9457-66.
REF 17 MiR-204/miR-211 downregulation contributes to candidemia-induced kidney injuries via derepression of Hmx1 expression.Life Sci. 2014 May 2;102(2):139-44.
REF 18 Genome-wide identification of target genes for miR-204 and miR-211 identifies their proliferation stimulatory role in breast cancer cells. Sci Rep. 2016 Apr 28;6:25287.
REF 19 IL-10R expression is post-transcriptionally regulated by miR-15a, miR-185, and miR-211 in melanoma.BMC Med Genomics. 2015 Dec 3;8:81.
REF 20 MiR-211 inhibits invasion and epithelial-to-mesenchymal transition (EMT) of cervical cancer cells via targeting MUC4.Biochem Biophys Res Commun. 2017 Apr 1;485(2):556-562.
REF 21 Melanoma cell invasiveness is regulated by miR-211 suppression of the BRN2 transcription factor.Pigment Cell Melanoma Res. 2011 Jun;24(3):525-37.
REF 22 MiR-211 inhibits cell proliferation and invasion of gastric cancer by down-regulating SOX4. Int J Clin Exp Pathol. 2015 Nov 1;8(11):14013-20.
REF 23 miR-211-5p Suppresses Metastatic Behavior by Targeting SNAI1 in Renal Cancer.Mol Cancer Res. 2017 Apr;15(4):448-456.

If You Find Any Error in Data or Bug in Web Service, Please Kindly Report It to Dr. Zhou and Dr. Zhang.