logo

BET Proteins in Early Life Stress-induced Cardiovascular Disease

Sector: Education • Location: Switzerland

Source: EU Funding & Tenders Portal

Project
Forthcoming

Early life stress (ELS) in childhood due to physical or sexual violence, parental neglect, or trauma has been recently associated with an increased risk of cardiovascular disease in later life. However, the mechanisms linking ELS to cardiovascular impairment remain unexplored. Epigenetic regulation of gene expression is emerging as a pivotal process linking environmental exposure to disease phenot

Project Information FAQ

Project Information

3 Q
The project “BET Proteins in Early Life Stress-induced Cardiovascular Disease” is an infrastructure initiative in the Education sector, located in Switzerland. Taiyo aggregates data on it from EU Funding & Tenders Portal.

Want to explore the full details? View the full report

Participants

Sponsoring Agency

Obfuscated Data

Company

Obfuscated Data

Status

Original status

forthcoming

Taiyo status

Obfuscated Data

Taiyo last update

00-00-0000

Available timestamps

00-00-0000

Available timestamp type

Obfuscated Data

Contact

Contact name

Obfuscated Data

Phone

0000000000

Email

ObfuscatedData@email.com

Address

Obfuscated Data, Obfuscated data, obfuscated data, Obfuscated data

Description

Description

Early life stress (ELS) in childhood due to physical or sexual violence, parental neglect, or trauma has been recently associated with an increased risk of cardiovascular disease in later life. However, the mechanisms linking ELS to cardiovascular impairment remain unexplored. Epigenetic regulation of gene expression is emerging as a pivotal process linking environmental exposure to disease phenotypes. Among chromatin remodelers, BET (bromodomain and extra-terminal) proteins are key regulators of gene transcription through their binding to acetylated lysine residues on histone tails via tandem bromodomains. Own preliminary data suggest that BET proteins are heavily involved in transcriptional programs relevant to cardiovascular disease. In BETonSTRESS, I hypothesize that childhood adversities alter the epigenetic landscape thus leading to maladaptive transcriptional programs and cardiovascular disease development. Using a mouse model of ELS and longitudinal cohorts, I will: i) investigate the chromatin landscape, BET function and cell-specific transcriptional changes in the ELS mouse heart; ii) test the effects of BET editing on cardiovascular function in ELS mice; iii) study the impact of stress-mitigating strategies (environmental enrichment) in preventing chromatin remodeling, BET activation and cardiac dysfunction in ELS mice; iv) test the cardiovascular predictive value of BET-related circulating biomarkers in two longitudinal cohorts of ELS-exposed individuals. The preliminary data suggest a prominent role of BET proteins in epigenetic remodeling and cardiac dysfunction in ELS mice. BETonSTRESS will: i) unveil the role of BET proteins and chromatin remodeling in ELS-induced cardiovascular dysfunction; ii) set the stage for stress-mitigating approaches and epigenetic therapies in the setting of ELS; iii) identify epigenetic biomarkers of cardiovascular disease in ELS individuals; iv) increase the awareness on the negative role of ELS in the society.

Original sub-sector

Obfuscated

Original Currency

USD

Original budget

000000000000000

Procurement method

Obfuscated Data

Budget

000000000000000

Location

Region

Obfuscated

Country

Obfuscated

State

Obfuscated Data

County

Obfuscated

Location

Obfuscated Data, Obfuscated data, obfuscated data, Obfuscated data

Source

Source reliability

High

Data quality score

100%

Source

Obfuscated Data

URL

obfuscated_data,obfuscateddata.com

More Details

Project Type

Obfuscated Data

Article Published Date

Obfuscated Data