TY - JOUR
T1 - Oral intake of bucillamine, carvedilol, metformin, or phenformin does not protect against UVR-induced squamous cell carcinomas in hairless mice
AU - Pihl, Celina
AU - Bjerring, Peter
AU - Andersen, Flemming
AU - Haedersdal, Merete
AU - Lerche, Catharina M
N1 - © 2024. The Author(s).
PY - 2024/3
Y1 - 2024/3
N2 - Squamous cell carcinoma represents the second most common type of keratinocyte carcinoma with ultraviolet radiation (UVR) making up the primary risk factor. Oral photoprotection aims to reduce incidence rates through oral intake of photoprotective compounds. Recently, drug repurposing has gained traction as an interesting source of chemoprevention. Because of their reported photoprotective properties, we investigated the potential of bucillamine, carvedilol, metformin, and phenformin as photoprotective compounds following oral intake in UVR-exposed hairless mice. Tumour development was observed in all groups in response to UVR, with only the positive control (Nicotinamide) demonstrating a reduction in tumour incidence (23.8%). No change in tumour development was observed in the four repurposed drug groups compared to the UV control group, whereas nicotinamide significantly reduced carcinogenesis (P = 0.00012). Metformin treatment significantly reduced UVR-induced erythema (P = 0.012), bucillamine and phenformin increased dorsal pigmentation (P = 0.0013, and P = 0.0005), but no other photoprotective effect was observed across the repurposed groups. This study demonstrates that oral supplementation with bucillamine, carvedilol, metformin, or phenformin does not affect UVR-induced carcinogenesis in hairless mice.
AB - Squamous cell carcinoma represents the second most common type of keratinocyte carcinoma with ultraviolet radiation (UVR) making up the primary risk factor. Oral photoprotection aims to reduce incidence rates through oral intake of photoprotective compounds. Recently, drug repurposing has gained traction as an interesting source of chemoprevention. Because of their reported photoprotective properties, we investigated the potential of bucillamine, carvedilol, metformin, and phenformin as photoprotective compounds following oral intake in UVR-exposed hairless mice. Tumour development was observed in all groups in response to UVR, with only the positive control (Nicotinamide) demonstrating a reduction in tumour incidence (23.8%). No change in tumour development was observed in the four repurposed drug groups compared to the UV control group, whereas nicotinamide significantly reduced carcinogenesis (P = 0.00012). Metformin treatment significantly reduced UVR-induced erythema (P = 0.012), bucillamine and phenformin increased dorsal pigmentation (P = 0.0013, and P = 0.0005), but no other photoprotective effect was observed across the repurposed groups. This study demonstrates that oral supplementation with bucillamine, carvedilol, metformin, or phenformin does not affect UVR-induced carcinogenesis in hairless mice.
KW - Mice
KW - Animals
KW - Ultraviolet Rays
KW - Carvedilol/pharmacology
KW - Mice, Hairless
KW - Phenformin/pharmacology
KW - Carcinoma, Squamous Cell/prevention & control
KW - Carcinogenesis/radiation effects
KW - Niacinamide/pharmacology
KW - Skin Neoplasms/etiology
KW - Skin/radiation effects
KW - Cysteine/analogs & derivatives
UR - http://www.scopus.com/inward/record.url?scp=85184514676&partnerID=8YFLogxK
U2 - 10.1007/s43630-024-00535-4
DO - 10.1007/s43630-024-00535-4
M3 - Journal article
C2 - 38337129
SN - 1474-905X
VL - 23
SP - 517
EP - 526
JO - Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
JF - Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
IS - 3
ER -