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Links from GEO DataSets

Items: 20

1.

HDAC4 controls senescence and aging by safeguarding the epigenetic identity and  ensuring the genomic integrity

(Submitter supplied) Purpose: Define HDAC4 signature Outcome: HDAC4 is required for the repression of a senescence signature. HDAC4 KO promotes the expression of inflammatory genes, the derepression of ERVs and the accumulation of DNA damage. All together these signalling pathways lead to permanent cell-cycle arrest in low grade tumor cells and pre-transformation models, while they weaken the replicative potential of primary normal cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
12 Samples
Download data: TXT
Series
Accession:
GSE150427
ID:
200150427
2.

HDAC4 controls senescence and aging by safeguarding the epigenetic identity and  ensuring the genomic integrity

(Submitter supplied) Purpose: Define the epigenetic program of HDAC4 Outcome: HDAC4 controls the H3K27me3 of repetitive elements of retroviral origin (ERVs) and the H3K27 deacetylation of typical and super-enhancers found to be activated during senescence. The former response is due to the remodeling of the chromatin that sorrounds ERVs, while the latter is directly mediated by HDAC4 binding to the chromatin and the local deacetylation.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
7 Samples
Download data: BW
Series
Accession:
GSE149644
ID:
200149644
3.

Different class IIa HDACs repressive complexes regulate specific epigenetic responses related to cell survival in leiomyosarcoma cells.

(Submitter supplied) Purpose: Define the transcriptional networks supervising class IIa HDAC expression. Outcome: We demonstrate that MEF2D is the key factor controlling HDAC9 transcription. Comprehensive genome-wide studies demonstrate that HDAC4 and HDAC9 supervise different genetic programs and show both specific and common genomic bindings. Although the number of MEF2-target genes commonly regulated is similar, only HDAC4 represses many additional genes that are not MEF2D targets. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
9 Samples
Download data: NARROWPEAK
Series
Accession:
GSE132622
ID:
200132622
4.

Different class IIa HDACs repressive complexes regulate specific epigenetic responses related to cell survival in leiomyosarcoma cells

(Submitter supplied) Purpose: Define the transcriptional networks supervising class IIa HDAC expression. Outcome: We demonstrate that MEF2D is the key factor controlling HDAC9 transcription. Comprehensive genome-wide studies demonstrate that HDAC4 and HDAC9 supervise different genetic programs and show both specific and common genomic bindings. Although the number of MEF2-target genes commonly regulated is similar, only HDAC4 represses many additional genes that are not MEF2D targets. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
10 Samples
Download data: TXT
Series
Accession:
GSE132569
ID:
200132569
5.

BRD4 connects enhancer remodeling to senescence immune surveillance

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11154 GPL16791
94 Samples
Download data: BIGWIG
Series
Accession:
GSE74328
ID:
200074328
6.

BRD4 connects enhancer remodeling to senescence immune surveillance (RNA-seq)

(Submitter supplied) Cellular senescence is a homeostatic program associated with tumor suppression, wound healing, and certain age related pathologies. Senescent cells display a repressive chromatin configuration thought to stably silence proliferation-promoting genes, while at the same time activate an unusual form of immune surveillance involving a secretory program referred to as the senescence-associated secretory phenotype (SASP). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
72 Samples
Download data: TXT
7.

BRD4 connects enhancer remodeling to senescence immune surveillance (ChIP-Seq)

(Submitter supplied) Cellular senescence is a homeostatic program associated with tumor suppression, wound healing, and certain age related pathologies. Senescent cells display a repressive chromatin configuration thought to stably silence proliferation-promoting genes, while at the same time activate an unusual form of immune surveillance involving a secretory program referred to as the senescence-associated secretory phenotype (SASP). more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
22 Samples
Download data: BIGWIG
Series
Accession:
GSE74238
ID:
200074238
8.

Histone deacetylase 4 reverses cellular senescence via DDIT4 in dermal fibroblasts

(Submitter supplied) Histone deacetylases (HDACs) are known to be a class of enzymes that remove acetyl groups from lysine chains on histones or other proteins, and play a crucial role in epigenetic regulation and aging process. Previous studies have identified that HDAC4 is down-regulated in aged and UV-irradiated skin in vivo. Therefore, HDAC4 may be an important role in skin aging process. However, the role of HDAC4 in skin aging is rarely known. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: TAR
9.

AP-1 imprints a reversible transcriptional programme of senescent cells

(Submitter supplied) Senescent cells affect many physiological and pathophysiological processes. While select genetic and epigenetic elements for senescence induction have been identified, the dynamics, epigenetic mechanisms and regulatory networks defining senescence competence, induction and maintenance remain poorly understood, precluding the deliberate therapeutic targeting of senescence for health benefits. Here, we examined the possibility that the epigenetic state of enhancers determines senescent cell fate. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
96 Samples
Download data: CEL
Series
Accession:
GSE144397
ID:
200144397
10.

AP-1 Imprints a Reversible Transcriptional Programme of Senescent Cells

(Submitter supplied) Senescent cells affect many physiological and pathophysiological processes. While select genetic and epigenetic elements for senescence induction have been identified, the dynamics, epigenetic mechanisms and regulatory networks defining senescence competence, induction and maintenance remain poorly understood, precluding the deliberate therapeutic targeting of senescence for health benefits. Here, we examined the possibility that the epigenetic state of enhancers determines senescent cell fate. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
30 Samples
Download data: CEL
Series
Accession:
GSE143248
ID:
200143248
11.

Expression data from treatment-induced senescence in mouse Emu-myc B-cell lymphoma model.

(Submitter supplied) Treatment induced senescence (TIS) is a terminal cell cycle arrest program, increasingly recognized as a tumor suppressor mechanism complementing apoptosis in response to standard chemotherapy regimens. In particular cells with blocked apoptotic pathways rely on senescence as the only remaining failsafe mechanism to keep the neoplastic growth in check. However, little is known about biological properties, long-term fate of senescent tumor cells and their impact on the microenvironment. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
47 Samples
Download data: CEL
Series
Accession:
GSE134753
ID:
200134753
12.

Expression data from primary mouse Emu-myc B-cell lymphoma.

(Submitter supplied) We are interested in genetic programs and mutations which impact on tumor development and sensitivity to anticancer therapies. Utilizing Emu-myc transgenic mice, which spontaneously develop aggressive B-cell lymphomas, we aimed here to study the effects of drug responses in vivo. For that purpose, primary lymphomas from the Emu-myc transgenic mice were transplanted in several immunocompetent recipients and exposed to a single dose Cyclophosphamide (CTX), a standard component of chemotherapeutic regimens used to treat human B-cell lymphomas. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
109 Samples
Download data: CEL
Series
Accession:
GSE134751
ID:
200134751
13.

AP-1 Imprints a Reversible Transcriptional Programme of Senescent Cells

(Submitter supplied) Senescent cells affect many physiological and pathophysiological processes. While select genetic and epigenetic elements for senescence induction have been identified, the dynamics, epigenetic mechanisms and regulatory networks defining senescence competence, induction and maintenance remain poorly understood, precluding the deliberate therapeutic targeting of senescence for health benefits. Here, we examined the possibility that the epigenetic state of enhancers determines senescent cell fate. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
42 Samples
Download data: CEL
Series
Accession:
GSE122918
ID:
200122918
14.

AP-1 Imprints a Reversible Transcriptional Programme of Senescent Cells

(Submitter supplied) Senescent cells affect many physiological and pathophysiological processes. While select genetic and epigenetic elements for senescence induction have been identified, the dynamics, epigenetic mechanisms and regulatory networks defining senescence competence, induction and maintenance remain poorly understood, precluding the deliberate therapeutic targeting of senescence for health benefits. Here, we examined the possibility that the epigenetic state of enhancers determines senescent cell fate. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
24 Samples
Download data: CEL
Series
Accession:
GSE112084
ID:
200112084
15.

Histone acetyltransferase p300 induces de novo super-enhancers to drive cellular senescence [ChIP-seq]

(Submitter supplied) Cellular senescence is a state of stable proliferative arrest induced by stress and is associated with a pro-inflammatory program. Senescent cells have anti-tumorigenic properties, however, their accumulation during aging contributes to chronic inflammation and age-related diseases. While senescence is associated with profound alterations of the epigenome, a systematic view of epigenetic factors in regulating senescence is lacking. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
82 Samples
Download data: BIGWIG
Series
Accession:
GSE106146
ID:
200106146
16.

Histone acetyltransferase p300 induces de novo super-enhancers to drive cellular senescence [RNA-seq]

(Submitter supplied) Cellular senescence is a state of stable proliferative arrest induced by stress and is associated with a pro-inflammatory program. Senescent cells have anti-tumorigenic properties, however, their accumulation during aging contributes to chronic inflammation and age-related diseases. While senescence is associated with profound alterations of the epigenome, a systematic view of epigenetic factors in regulating senescence is lacking. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
16 Samples
Download data: TXT
17.

Histone acetyltransferase p300 induces de novo super-enhancers to drive cellular senescence

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Other; Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
150 Samples
Download data: BIGWIG, BW
Series
Accession:
GSE105937
ID:
200105937
18.

Histone acetyltransferase p300 induces de novo super-enhancers to drive cellular senescence [PRO-seq]

(Submitter supplied) Cellular senescence is a state of stable proliferative arrest induced by stress and is associated with a pro-inflammatory program. Senescent cells have anti-tumorigenic properties, however, their accumulation during aging contributes to chronic inflammation and age-related diseases. While senescence is associated with profound alterations of the epigenome, a systematic view of epigenetic factors in regulating senescence is lacking. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL18573
2 Samples
Download data: BW
Series
Accession:
GSE105936
ID:
200105936
19.

Histone acetyltransferase p300 induces de novo super-enhancers to drive cellular senescence [DNA-seq]

(Submitter supplied) Cellular senescence is a state of stable proliferative arrest induced by stress and is associated with a pro-inflammatory program. Senescent cells have anti-tumorigenic properties, however, their accumulation during aging contributes to chronic inflammation and age-related diseases. While senescence is associated with profound alterations of the epigenome, a systematic view of epigenetic factors in regulating senescence is lacking. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL18573
50 Samples
Download data: FA, TXT
Series
Accession:
GSE105935
ID:
200105935
20.

The transcription factor ERG regulates super-enhancers in endothelial cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18573 GPL11154
7 Samples
Download data: BEDGRAPH, BW
Series
Accession:
GSE124893
ID:
200124893
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