Department of Dermatology, National Cheng Kung University College of Medicine and Hospital, 138 Sheng-Li Road, Tainan, Taiwan.
J Dermatol Sci. 2011 Aug;63(2):83-92. doi: 10.1016/j.jdermsci.2011.04.003. Epub 2011 Apr 21.
The Solanum species herbs have been used to treat cancer for centuries; however, the underlying mechanisms and effectiveness in vivo remain unclear.
SR-T100, extracted from the Solanum incanum, contains solamargine alkaloid as the main active ingredient. Here, we investigated the apoptosis-inducing effects of SR-T100 for targeting squamous cell carcinoma (SCC) in vitro and in vivo.
We elucidated the mechanism by which SR-T100 induces apoptosis of human SCCs (A431, SCC4, SCC9, and SCC25) cells. The efficacy and safety issues were addressed regarding topical treatment of SR-T100 on UVB-induced cutaneous SCC of hairless mice and actinic keratoses (AKs) of human.
SR-T100 induces apoptosis in human SCCs cell lines by up-regulating the expressions of tumor necrosis factor receptors (TNFRs) and Fas, and downstream adaptors FADD/TRADD of the TNF-α and Fas ligand signaling cascades. SR-T100 also triggered the mitochondrial apoptotic pathway, as up-regulated cytochrome c and Bax, down-regulated Bcl-X(L). Animal experiments showed that all papillomas (35/35) and 27 of 30 UVB-induced microinvasive SCCs in hairless mice disappeared within 10 weeks after once-daily application of topical SR-T100. Furthermore, 13 patients, who suffered with 14 AKs, were treated with once-daily topical SR-T100 gel and 10 AKs cured after 16 weeks, showing negligible discomforts.
Our studies indicate that SR-T100 induces apoptosis of SCC cells via death receptors and the mitochondrial death pathway. The high efficacy of SR-T100 in our preclinical trial suggests that SR-T100 is a highly promising herb for AKs and related disorders.
茄属植物草药已被用于治疗癌症数百年;然而,其体内的潜在机制和有效性仍不清楚。
从茄属颠茄中提取的 SR-T100 含有茄碱生物碱作为主要活性成分。在这里,我们研究了 SR-T100 诱导体外和体内鳞状细胞癌(SCC)细胞凋亡的作用。
我们阐明了 SR-T100 诱导人 SCC(A431、SCC4、SCC9 和 SCC25)细胞凋亡的机制。我们研究了 SR-T100 对 UVB 诱导的无毛小鼠皮肤 SCC 和人类光化性角化病(AK)的局部治疗的疗效和安全性问题。
SR-T100 通过上调肿瘤坏死因子受体(TNFRs)和 Fas 及其下游 TNF-α和 Fas 配体信号级联的 Fas 衔接蛋白 FADD/TRADD 的表达,诱导人 SCC 细胞系凋亡。SR-T100 还触发了线粒体凋亡途径,上调细胞色素 c 和 Bax,下调 Bcl-X(L)。动物实验表明,所有 35/35 个乳头状瘤和 30 个 UVB 诱导的无毛小鼠微侵袭性 SCC 中的 27 个在每日一次应用局部 SR-T100 后 10 周内消失。此外,13 名患有 14 个 AK 的患者每天接受一次局部 SR-T100 凝胶治疗,10 个 AK 在 16 周后治愈,几乎没有不适感。
我们的研究表明,SR-T100 通过死亡受体和线粒体死亡途径诱导 SCC 细胞凋亡。SR-T100 在我们的临床前试验中的高疗效表明,SR-T100 是 AK 及其相关疾病的一种很有前途的草药。