(Q36554387)

English

Expression of the miR-302/367 cluster in glioblastoma cells suppresses tumorigenic gene expression patterns and abolishes transformation related phenotypes

scientific article published on 20 May 2015

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scholarly article

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Europe PubMed Central

14 August 2017

Expression of the miR-302/367 cluster in glioblastoma cells suppresses tumorigenic gene expression patterns and abolishes transformation related phenotypes (English)

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Europe PubMed Central

14 August 2017

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inferred from title

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11 June 2020

Vida Vafaizadeh

6

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11 June 2020

author name string

Tomohiro Chiba

2

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11 June 2020

Boris Brill

3

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11 June 2020

Natalia Delis

4

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11 June 2020

Viktoria von Manstein

5

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11 June 2020

Thomas Oellerich

7

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11 June 2020

Bernd Groner

8

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11 June 2020

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publication date

20 May 2015

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14 August 2017

International Journal of Cancer

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11 June 2020

137

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11 June 2020

10

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11 June 2020

2296-2309

1 reference

Europe PubMed Central

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11 June 2020

Drug resistance via feedback activation of Stat3 in oncogene-addicted cancer cells.

1 reference

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1 reference

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30 September 2017

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1 reference

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Premature termination of reprogramming in vivo leads to cancer development through altered epigenetic regulation

1 reference

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STAT3 induction of miR-146b forms a feedback loop to inhibit the NF-κB to IL-6 signaling axis and STAT3-driven cancer phenotypes

1 reference

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The use of small molecules in somatic-cell reprogramming

1 reference

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30 September 2017

Chromatin dynamics during cellular reprogramming

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Reprogramming in vivo produces teratomas and iPS cells with totipotency features.

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Epigenetics of cellular reprogramming

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Function of oncogenes in cancer development: a changing paradigm

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Epigenetic reprogramming in cancer

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Cancer genome landscapes

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Genome-wide chromatin state transitions associated with developmental and environmental cues

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Self-renewal and pluripotency acquired through somatic reprogramming to human cancer stem cells

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Reprogramming cancer cells: back to the future

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Terminal differentiation and loss of tumorigenicity of human cancers via pluripotency-based reprogramming

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Current trends in targeted therapies for glioblastoma multiforme

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30 September 2017

A novel role of miR-302/367 in reprogramming

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Embryonic stem cell-specific signatures in cancer: insights into genomic regulatory networks and implications for medicine

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Essential role of Stat3 in PI3K-induced oncogenic transformation

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Highly efficient miRNA-mediated reprogramming of mouse and human somatic cells to pluripotency

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30 September 2017

MicroRNA miR-302 inhibits the tumorigenecity of human pluripotent stem cells by coordinate suppression of the CDK2 and CDK4/6 cell cycle pathways

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STAT3 is required for proliferation and maintenance of multipotency in glioblastoma stem cells

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Embryonic stem cell-specific miR302-367 cluster: human gene structure and functional characterization of its core promoter

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12 December 2020

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10.1002/IJC.29606

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11 June 2020

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Europe PubMed Central

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11 June 2020

1 reference

Europe PubMed Central

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11 June 2020

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