Gkikas Georgios, Katsiris Dimitrios, Vitsos Andreas, Gioran Anna, Ieronymaki Dimitra, Kostaki Maria, Ladopoulos Georgios, Ioannidou Vaya, Theodoraki Elisavet, Chondrogianni Niki, Sfiniadakis Ioannis, Papaioannou Georgios T, Rallis Michail Christou
Section of Pharmaceutical Technology, Department of Pharmacy, School of Health Sciences, National and Kapodistrian University of Athens, Panepistimiopolis Zografou, 15784 Athens, Greece.
National Hellenic Research Foundation, Institute of Chemical Biology, 48 Vassileos Constantinou Ave., 11635 Athens, Greece.
Cancers (Basel). 2024 Oct 21;16(20):3546. doi: 10.3390/cancers16203546.
: In recent decades, a significant global increase in the incidence of non-melanoma skin cancer has been observed. To explore the pathogenesis of and potential therapeutic approaches for squamous cell carcinoma, various in vivo studies using mouse models have been conducted. However, investigations comparing different hairless mouse models, with or without melanin, as well as models with hypercholesterolemia and immunosuppression, in terms of their ability to induce squamous cell carcinoma have yet to be undertaken. : Four mouse strains, namely SKH-hr1, SKH-hr2, SKH-hr2+ApoE, and immunodeficient Nude (Foxn1 knockout), were exposed to UVA and UVB radiation three times per week, initially to 1 Minimal Erythemal Dose (MED), incrementally increased weekly to a maximum dose of 3 MED. Clinical evaluation, photodocumentation, and biophysical parameters were monitored, along with proteasome protein activity and histopathological assessments. : The SKH-hr1 model primarily developed actinic keratosis without significant progression to invasive squamous cell carcinoma (SCC), while the SKH-hr2 and SKH-hr2+ApoE models exhibited a higher likelihood and intensity of papilloma and aggressive SCC formation, with the latter showing upregulated proteasome activity. Histopathological analysis confirmed the presence of poorly differentiated, invasive SCCs in the SKH-hr2 and SKH-hr2+ApoE models, contrasting with the less aggressive SCCs in the Nude mice and the mixed lesions observed in the SKH-hr1 mice. : The SKH-hr2+ApoE and SKH-hr2 mice were identified as the most suitable for further exploration of squamous cell carcinogenesis. In contrast, the SKH-hr1 mice were found to be the least suitable, even though they are albino. Notably, proteasome analysis revealed a potential role of proteasome activity in squamous cell carcinogenesis.
近几十年来,全球非黑色素瘤皮肤癌的发病率显著上升。为了探究鳞状细胞癌的发病机制和潜在治疗方法,已经开展了各种使用小鼠模型的体内研究。然而,尚未对不同的无毛小鼠模型(有无黑色素)以及高胆固醇血症和免疫抑制模型诱导鳞状细胞癌的能力进行比较研究。
四种小鼠品系,即SKH-hr1、SKH-hr2、SKH-hr2+ApoE和免疫缺陷裸鼠(Foxn1基因敲除),每周接受三次UVA和UVB辐射,初始剂量为1个最小红斑量(MED),每周逐渐增加至最大剂量3 MED。监测临床评估、照片记录、生物物理参数,以及蛋白酶体蛋白活性和组织病理学评估。
SKH-hr1模型主要发展为光化性角化病,未显著进展为侵袭性鳞状细胞癌(SCC),而SKH-hr2和SKH-hr2+ApoE模型出现乳头状瘤和侵袭性SCC形成的可能性和强度更高,后者蛋白酶体活性上调。组织病理学分析证实,SKH-hr2和SKH-hr2+ApoE模型中存在低分化侵袭性SCC,与裸鼠中侵袭性较弱的SCC以及SKH-hr1小鼠中观察到的混合病变形成对比。
SKH-hr2+ApoE和SKH-hr2小鼠被确定为最适合进一步探究鳞状细胞癌发生的模型。相比之下,SKH-hr1小鼠被发现最不适合,尽管它们是白化病小鼠。值得注意的是,蛋白酶体分析揭示了蛋白酶体活性在鳞状细胞癌发生中的潜在作用。