Steinkamp Anne-Dorothee, Schmitt Laurenz, Chen Xiaoyun, Fietkau Katharina, Heise Ruth, Baron Jens M, Bolm Carsten
Institute of Organic Chemistry, RWTH Aachen University, Aachen, Germany.
Skin Pharmacol Physiol. 2016;29(6):281-290. doi: 10.1159/000453042. Epub 2016 Dec 24.
Tasisulam is a promising antitumor agent with complex pharmacology, which is used as an antiproliferative agent in patients with metastatic melanoma and other solid tumors. Phase 2 melanoma studies showed promising results but had to be stopped because of insufficient tasisulam clearance leading to toxic side effects. To reduce the negative effects of tasisulam, we synthesized a novel sulfonimidamide-based analog to evaluate its antiproliferative effects in comparison to the original compound by performing a cell proliferation assay in melanoma cell lines SKMel23 and A375. The results revealed that the analog had inhibitory effects on the proliferation comparable to tasisulam in both investigated cell lines. These results could contribute to a reduced toxicity of tasisulam and lead to further clinical trials in metastatic melanoma.
他西硫胺是一种具有复杂药理学的有前景的抗肿瘤药物,在转移性黑色素瘤和其他实体瘤患者中用作抗增殖剂。2期黑色素瘤研究显示出有前景的结果,但由于他西硫胺清除不足导致毒性副作用而不得不停止。为了减少他西硫胺的负面影响,我们合成了一种新型的基于磺酰亚胺酰胺的类似物,通过在黑色素瘤细胞系SKMel23和A375中进行细胞增殖试验来评估其与原始化合物相比的抗增殖作用。结果显示,该类似物在两种研究的细胞系中对增殖的抑制作用与他西硫胺相当。这些结果可能有助于降低他西硫胺的毒性,并导致在转移性黑色素瘤中进行进一步的临床试验。