首页> 外文期刊>Biochemical Pharmacology >LAV694, a new antiproliferative agent showing improved skin tolerability vs. clinical standards for the treatment of actinic keratosis.
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LAV694, a new antiproliferative agent showing improved skin tolerability vs. clinical standards for the treatment of actinic keratosis.

机译:LAV694是一种新型抗增殖剂,与光化性角化病的临床标准相比,具有更高的皮肤耐受性。

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摘要

The skin tolerability of the tubulin polymerisation inhibitor LAV694 was compared to that of 5% 5-fluorouracil (5-FU) and 0.5% podophyllotoxin in vitro using a human reconstructed epidermis (HRE), and in vivo using minipigs. Topical treatment of HRE for 1 or 3 days with a 0.2, 0.6 or 1% LAV694 cream or the placebo showed no signs of irritation in terms of morphology, cell viability (lactate dehydrogenase leakage) or interleukin-8 mRNA expression and release. 5-FU increased interleukin-8 production and induced morphological signs of irritation. The substances were also applied under occlusion to the back of two minipigs, twice daily, for 9 days to allow intraindividual comparison of skin effects and tolerability. Skin reactions were monitored by visual scoring, chromometry, pro-inflammatory activity, cell cycle and apoptosis by RT-PCR, laser scanning cytometry and histopathological examination of biopsies. Application of podophyllotoxin and 5-FU had to be stopped on days 4 and 8, respectively, due to severe skin lesions. LAV694 (1%) induced only moderate skin reddening after 9 days. 5-FU and podophyllotoxin, but not LAV694, increased mRNA expression of pro-inflammatory cytokines. LAV694 arrested keratinocytes in the M phase of the cell cycle and apoptosis was detected histologically in the basal layer. LAV694 increased the expression of pro-apoptotic genes in both experimental models. In conclusion, LAV694 selectively induced apoptosis, rather than necrosis, of growth-arrested keratinocytes, thus avoiding the occurrence of extensive inflammation. This resulted in an improved skin tolerability in comparison with 5-FU and podophyllotoxin.
机译:将微管蛋白聚合抑制剂LAV694的皮肤耐受性与体外使用人重建表皮(HRE)的5%5-氟尿嘧啶(5-FU)和0.5%鬼臼毒素的皮肤耐受性进行了比较,并在体内使用小型猪对皮肤耐受性进行了比较。用0.2%,0.6%或1%LAV694乳膏或安慰剂对HRE进行局部治疗1或3天,在形态,细胞活力(乳酸脱氢酶渗漏)或白介素8 mRNA表达和释放方面均无刺激迹象。 5-FU增加白介素8的产生并引起刺激的形态学征象。还在闭塞的情况下将这些物质应用到两只小型猪的背部,每天两次,持续9天,以进行皮肤效果和耐受性的个体比较。通过视觉评分,色度,促炎活性,细胞周期和细胞凋亡通过RT-PCR,激光扫描细胞术和活检组织病理学检查来监测皮肤反应。由于严重的皮肤病变,必须分别在第4天和第8天停止使用鬼臼毒素和5-FU。 9天后,LAV694(1%)仅引起中等程度的皮肤变红。 5-FU和鬼臼毒素,而不是LAV694,增加促炎细胞因子的mRNA表达。 LAV694在细胞周期的M期阻滞了角质形成细胞,并在组织学上检测了基底层的凋亡。 LAV694在两个实验模型中均增加了促凋亡基因的表达。总之,LAV694选择性诱导生长停滞的角质形成细胞凋亡而不是坏死,从而避免了广泛炎症的发生。与5-FU和鬼臼毒素相比,这提高了皮肤耐受性。

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