Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Glucocorticoid (GC) steroid hormone signalling via the glucocorticoid receptor (GR) underlies most daily physiological rhythms in mammals by synchronising cellular circadian rhythms throughout the body. Impaired circadian synchrony is associated with many non-communicable diseases such as cardiovascular disease, diabetes and cancer. The functions and daily regulation of systemic GC levels are relatively well understood, yet a clearly defined mechanism for GC/GR-mediated circadian synchronisation is lacking. Historically, mechanistic studies of GR action have focused on its role as a transcription factor, sufficient to explain many, but not all, consequences of GC/GR signalling. Recently, several non-canonical modes of GR action have been described and proposed as a basis for understanding rapid cellular response to GCs, that cannot be explained by relatively slow changes in transcription. Here we review the current state of knowledge on the cellular mechanism of GR-signalling in the context of GR-mediated circadian synchronisation, outline gaps in current understanding and suggest new avenues for investigation.

More information Original publication

DOI

10.1530/joe-25-0340

Type

Journal article

Publication Date

2026-03-01T00:00:00+00:00

Addresses

1, M, R, C, , L, a, b, o, r, a, t, o, r, y, , o, f, , M, o, l, e, c, u, l, a, r, , B, i, o, l, o, g, y, ,, , C, a, m, b, r, i, d, g, e, ,, , C, B, 2, , 0, Q, H, ,, , 0, 1, 2, 2, 3, , 2, 6, 7, 0, 0, 0, ,, , U, n, i, t, e, d, , K, i, n, g, d, o, m, .