Loss of the polycomb protein Mel-18 enhances the epithelial-mesenchymal transition by ZEB1 and ZEB2 expression through the downregulation of miR-205 in breast cancer. (Q55057079)

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English	Loss of the polycomb protein Mel-18 enhances the epithelial-mesenchymal transition by ZEB1 and ZEB2 expression through the downregulation of miR-205 in breast cancer.	scientific article

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/23474752

Loss of the polycomb protein Mel-18 enhances the epithelial-mesenchymal transition by ZEB1 and ZEB2 expression through the downregulation of miR-205 in breast cancer. (English)

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/23474752

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J-Y Lee

1

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16 June 2018

http://europepmc.org/abstract/MED/23474752

M K Park

2

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16 June 2018

http://europepmc.org/abstract/MED/23474752

J-H Park

3

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16 June 2018

http://europepmc.org/abstract/MED/23474752

H J Lee

4

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16 June 2018

http://europepmc.org/abstract/MED/23474752

D H Shin

5

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16 June 2018

http://europepmc.org/abstract/MED/23474752

Y Kang

6

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16 June 2018

http://europepmc.org/abstract/MED/23474752

C H Lee

7

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16 June 2018

http://europepmc.org/abstract/MED/23474752

G Kong

8

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16 June 2018

http://europepmc.org/abstract/MED/23474752

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11 March 2013

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16 June 2018

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16 June 2018

http://europepmc.org/abstract/MED/23474752

33

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10

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16 June 2018

http://europepmc.org/abstract/MED/23474752

1325-1335

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16 June 2018

http://europepmc.org/abstract/MED/23474752

The basics of epithelial-mesenchymal transition

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Cancer stem cells: mirage or reality?

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The epithelial-mesenchymal transition generates cells with properties of stem cells

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Cancer stem cells and epithelial-mesenchymal transition: concepts and molecular links

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The polycomb group protein Bmi-1 represses the tumor suppressor PTEN and induces epithelial-mesenchymal transition in human nasopharyngeal epithelial cells

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Genome-scale epigenetic reprogramming during epithelial-to-mesenchymal transition

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The miR-200 family inhibits epithelial-mesenchymal transition and cancer cell migration by direct targeting of E-cadherin transcriptional repressors ZEB1 and ZEB2

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The microRNAs miR-373 and miR-520c promote tumour invasion and metastasis

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EMT and stem cell-like properties associated with miR-205 and miR-200 epigenetic silencing are early manifestations during carcinogen-induced transformation of human lung epithelial cells

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Interplay between microRNAs and the epigenetic machinery: an intricate network

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Stem cells and cancer; the polycomb connection

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Microarray analysis identifies a death-from-cancer signature predicting therapy failure in patients with multiple types of cancer

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Overexpression of Bmi-1 oncoprotein correlates with axillary lymph node metastases in invasive ductal breast cancer

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Bmi1 is essential in Twist1-induced epithelial–mesenchymal transition

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Regulation of stem cell pluripotency and differentiation involves a mutual regulatory circuit of the NANOG, OCT4, and SOX2 pluripotency transcription factors with polycomb repressive complexes and stem cell microRNAs.

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Identification of Bmi1-interacting proteins as constituents of a multimeric mammalian polycomb complex

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Epigenetic regulation of cellular memory by the Polycomb and Trithorax group proteins

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Mel-18, a polycomb group protein, regulates cell proliferation and senescence via transcriptional repression of Bmi-1 and c-Myc oncoproteins

1 reference

https://api.crossref.org/works/10.1038%2FONC.2013.53

31 March 2020

Mel-18 negatively regulates INK4a/ARF-independent cell cycle progression via Akt inactivation in breast cancer

1 reference

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31 March 2020

Loss of Mel-18 induces tumor angiogenesis through enhancing the activity and expression of HIF-1α mediated by the PTEN/PI3K/Akt pathway

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Coordinated regulation of polycomb group complexes through microRNAs in cancer.

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The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1

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Coordinated epigenetic repression of the miR-200 family and miR-205 in invasive bladder cancer.

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ERbeta impedes prostate cancer EMT by destabilizing HIF-1alpha and inhibiting VEGF-mediated snail nuclear localization: implications for Gleason grading

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Vascular endothelial growth factor-A stimulates Snail expression in breast tumor cells: implications for tumor progression

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Vascular endothelial growth factor receptor-1 activation mediates epithelial to mesenchymal transition in human pancreatic carcinoma cells

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Role of transforming growth factor beta in human disease

1 reference

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Critical and reciprocal regulation of KLF4 and SLUG in transforming growth factor β-initiated prostate cancer epithelial-mesenchymal transition

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Paracrine and autocrine signals induce and maintain mesenchymal and stem cell states in the breast

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Enhancer of zeste homolog 2 epigenetically silences multiple tumor suppressor microRNAs to promote liver cancer metastasis.

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Polycomb-mediated loss of miR-31 activates NIK-dependent NF-κB pathway in adult T cell leukemia and other cancers.

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Altered MicroRNA expression confined to specific epithelial cell subpopulations in breast cancer

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MicroRNAs and epigenetics

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Targeting of EZH2 to a defined genomic site is sufficient for recruitment of Dnmt3a but not de novo DNA methylation.

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The Polycomb group protein EZH2 directly controls DNA methylation

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Polycomb CBX7 promotes initiation of heritable repression of genes frequently silenced with cancer-specific DNA hypermethylation

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Bmi1 cooperates with Dnmt1-associated protein 1 in gene silencing

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Mel-18 acts as a tumor suppressor by repressing Bmi-1 expression and down-regulating Akt activity in breast cancer cells

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Id1 enhances RING1b E3 ubiquitin ligase activity through the Mel-18/Bmi-1 polycomb group complex

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Constitutive overexpression of Id‐1 in mammary glands of transgenic mice results in precocious and increased formation of terminal end buds, enhanced alveologenesis, delayed involution

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10.1038/ONC.2013.53

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/23474752

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/23474752

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