Abstract 5088: Silibinin inhibits UVB-induced promotion and progression of microscopic basal cell carcinoma formation via targeting bone morphogenic protein 2

Cynthia M. Rigby, G. Deep, A. Jain, D. Orlicky, C. Agarwal, K. Raina, R. Agarwal
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Abstract

Non-melanoma skin cancers (NMSCs) account for about half of all malignancies diagnosed annually in the United States. Around 80% of NMSCs are basal cell carcinoma (BCC) and 20% are squamous cell carcinoma (SCC). Whereas the efficacy of several chemopreventive agents has been examined and reported against both BCC and SCC, a majority of these studies have focused on the test agent’s activity in a long-term setting to determine the amount of tumors formed. Notably, the studies evaluating the efficacy of chemopreventive agents during early stage/s of BCC development are lacking. Accordingly, utilizing the well-established patched (Ptch)+/- mouse model of UVB-induced BCC formation, we excised skin samples from UVB exposed mice prior to tumor formation to study the promotion/progression of BCC and to determine the target/s of silibinin, a well-known skin cancer (SCC) chemopreventive agent, in tumor growth inhibition. Ptch+/- and Ptch+/+ mice were irradiated with UVB 240mJ/cm2 3 times per week with or without topically applied silibinin 5 times per week. As early as one month, we found that UVB exposure significantly increased the number of mast cells in Ptch+/- mice by about 48% (P Citation Format: Cynthia M. Rigby, Gagan Deep, Anil K. Jain, David J. Orlicky, Chapla Agarwal, Komal Raina, Rajesh Agarwal. Silibinin inhibits UVB-induced promotion and progression of microscopic basal cell carcinoma formation via targeting bone morphogenic protein 2 [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA. Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr 5088.
摘要5088:水飞蓟宾通过靶向骨形态发生蛋白2抑制uvb诱导的显微基底细胞癌的形成和进展
非黑色素瘤皮肤癌(NMSCs)约占美国每年诊断的所有恶性肿瘤的一半。约80%的NMSCs为基底细胞癌(BCC), 20%为鳞状细胞癌(SCC)。虽然已经对几种化学预防剂对BCC和SCC的疗效进行了检查和报道,但这些研究中的大多数都集中在测试剂在长期环境中的活性上,以确定肿瘤形成的数量。值得注意的是,在BCC发展的早期阶段,评估化学预防药物疗效的研究是缺乏的。因此,我们利用已建立的UVB诱导BCC形成的补丁(Ptch)+/-小鼠模型,在肿瘤形成之前切除UVB暴露小鼠的皮肤样本,研究BCC的促进/进展,并确定水飞蓟宾(一种著名的皮肤癌(SCC)化学预防剂)在肿瘤生长抑制中的靶标/s。Ptch+/-和Ptch+/+小鼠以240mJ/cm2的UVB照射,每周3次,外加或不外加水飞蓟宾,每周5次。早在一个月前,我们就发现UVB暴露使Ptch+/-小鼠肥大细胞数量显著增加约48% (P引文格式:Cynthia M. Rigby, Gagan Deep, Anil K. Jain, David J. Orlicky, Chapla Agarwal, Komal Raina, Rajesh Agarwal)。水飞蓟宾通过靶向骨形态发生蛋白2抑制uvb诱导的显微基底细胞癌形成的促进和进展[摘要]。摘自:2019年美国癌症研究协会年会论文集;2019年3月29日至4月3日;亚特兰大,乔治亚州。费城(PA): AACR;癌症杂志,2019;79(13增刊):5088。
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