Open Access
The BET inhibitor JQ1 targets fat metabolism and counteracts obesity
Claudia Fornelli
1
,
Alessia Sofia Cento
1
,
Cento AS
1
,
Lorenzo Nevi
2
,
Raffaella Mastrocola
1
,
Gustavo Ferreira Alves
3
,
Giuseppina Caretti
2
,
Massimo Collino
3
,
FABIO PENNA
1
Тип публикации: Journal Article
Дата публикации: 2025-02-01
scimago Q1
wos Q1
БС1
SJR: 2.576
CiteScore: 22.1
Impact factor: 13.0
ISSN: 20901232, 20901224
PubMed ID:
38365172
Multidisciplinary
Краткое описание
Obesity, one of the most frequent health problems in the adult population, is a condition characterized by excessive white adipose tissue accumulation and accompanied by the increased risk to develop other disorders such as type II diabetes, cardiovascular disorders, physical disability, frailty and sarcopenia. Total fat mass frequently increases during aging, often coexisting with sarcopenia, thus resulting in an emerging condition defined sarcopenic obesity (SO). Our previous data demonstrated the relevant role of the bromo and extra-terminal domain (BET) proteins inhibitor JQ1 in attenuating inflammation and fibrosis in sarcopenic mice. Moreover, we preliminarily observed that JQ1 administration markedly reduces white adipose tissue mass, suggesting a potential role of BET proteins on visceral fat deposition during aging. Starting from those observations, the aim of this study was to investigate the ability of JQ1 to reduce adiposity in a chronic diet-induced obesity (DIO) mouse model mimicking the human metabolic syndrome. Male C57BL/6J mice were divided in subgroups, either fed a standard diet or a high fat diet for 22 or 12 weeks, treated over the last 14 days with JQ1 or with vehicle. The results showed that JQ1 administration reduces fat mass, preserving skeletal muscle mass and function. A direct JQ1 lipolytic effect was demonstrated on mature adipocyte cultures. JQ1-mediated loss of adipose tissue mass was not associated with systemic inflammation or with lipid accumulation in muscle and liver. JQ1 administration did not impinge on skeletal muscle metabolism and oxidative capability, as shown by the lack of significant impact on mitochondrial mass and biogenesis. In conclusion, the current data highlight a potential benefit of JQ1 administration to counteract obesity, suggesting epigenetic modulation as a prospective target in the treatment of obesity and sarcopenic obesity, despite the underlying multiorgan molecular mechanism is still not completely elucidated.
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Fornelli C. et al. The BET inhibitor JQ1 targets fat metabolism and counteracts obesity // Journal of Advanced Research. 2025. Vol. 68. pp. 403-413.
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Fornelli C., Sofia Cento A., AS C., Nevi L., Mastrocola R., Ferreira Alves G., Caretti G., Collino M., PENNA F. The BET inhibitor JQ1 targets fat metabolism and counteracts obesity // Journal of Advanced Research. 2025. Vol. 68. pp. 403-413.
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TY - JOUR
DO - 10.1016/j.jare.2024.02.001
UR - https://linkinghub.elsevier.com/retrieve/pii/S2090123224000511
TI - The BET inhibitor JQ1 targets fat metabolism and counteracts obesity
T2 - Journal of Advanced Research
AU - Fornelli, Claudia
AU - Sofia Cento, Alessia
AU - AS, Cento
AU - Nevi, Lorenzo
AU - Mastrocola, Raffaella
AU - Ferreira Alves, Gustavo
AU - Caretti, Giuseppina
AU - Collino, Massimo
AU - PENNA, FABIO
PY - 2025
DA - 2025/02/01
PB - Elsevier
SP - 403-413
VL - 68
PMID - 38365172
SN - 2090-1232
SN - 2090-1224
ER -
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@article{2025_Fornelli,
author = {Claudia Fornelli and Alessia Sofia Cento and Cento AS and Lorenzo Nevi and Raffaella Mastrocola and Gustavo Ferreira Alves and Giuseppina Caretti and Massimo Collino and FABIO PENNA},
title = {The BET inhibitor JQ1 targets fat metabolism and counteracts obesity},
journal = {Journal of Advanced Research},
year = {2025},
volume = {68},
publisher = {Elsevier},
month = {feb},
url = {https://linkinghub.elsevier.com/retrieve/pii/S2090123224000511},
pages = {403--413},
doi = {10.1016/j.jare.2024.02.001}
}