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口服布西拉明、卡维地洛、二甲双胍或苯乙双胍不能预防无毛小鼠紫外线辐射诱导的鳞状细胞癌。

Oral intake of bucillamine, carvedilol, metformin, or phenformin does not protect against UVR-induced squamous cell carcinomas in hairless mice.

作者信息

Pihl Celina, Bjerring Peter, Andersen Flemming, Haedersdal Merete, Lerche Catharina M

机构信息

Department of Dermatology, Copenhagen University Hospital-Bispebjerg and Frederiksberg, Copenhagen, Denmark.

Department of Pharmacy, University of Copenhagen, 2400, Copenhagen, Denmark.

出版信息

Photochem Photobiol Sci. 2024 Mar;23(3):517-526. doi: 10.1007/s43630-024-00535-4. Epub 2024 Feb 9.

Abstract

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.

摘要

鳞状细胞癌是第二常见的角质形成细胞癌类型,紫外线辐射(UVR)是主要危险因素。口腔光保护旨在通过口服光保护化合物来降低发病率。最近,药物重新利用作为一种有趣的化学预防来源受到了关注。由于已报道的光保护特性,我们研究了布西拉明、卡维地洛、二甲双胍和苯乙双胍在紫外线照射的无毛小鼠口服后作为光保护化合物的潜力。所有组在紫外线照射后均观察到肿瘤发生,只有阳性对照(烟酰胺)显示肿瘤发生率降低(23.8%)。与紫外线对照组相比,四种重新利用药物组的肿瘤发生情况没有变化,而烟酰胺显著降低了致癌作用(P = 0.00012)。二甲双胍治疗显著降低了紫外线诱导的红斑(P = 0.012),布西拉明和苯乙双胍增加了背部色素沉着(P = 0.0013和P = 0.0005),但在重新利用药物组中未观察到其他光保护作用。这项研究表明,口服布西拉明、卡维地洛、二甲双胍或苯乙双胍不会影响无毛小鼠紫外线诱导的致癌作用。

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