作者
Mahboubeh S Noori, John D O’Brien, Zachary J Champa, Sudhir P Deosarkar, Olivia L Lanier, Chunyan Qi, Monica M Burdick, Frank L Schwartz, Stephen C Bergmeier, Kelly D McCall, Douglas J Goetz
发表日期
2017/5/15
期刊
European journal of pharmacology
卷号
803
页码范围
130-137
出版商
Elsevier
简介
Inhibition of interleukin–6 (IL-6) holds significant promise as a therapeutic approach for triple negative breast cancer (TNBC). We previously reported that phenylmethimazole (C10) reduces IL-6 expression in several cancer cell lines. We have identified a more potent derivative of C10 termed COB-141. In the present work, we tested the hypothesis that C10 and COB-141 inhibit TNBC cell expressed IL-6 and investigated the potential for classical IL-6 pathway induced signaling within TNBC cells. A panel of TNBC cell lines (MDA-MB-231, Hs578T, MDA-MB-468) was used. Enzyme linked immunosorbent assays (ELISA) revealed that C10 and COB-141 inhibit MDA-MB-231 cell IL-6 secretion, with COB-141 being ~6.5 times more potent than C10. Therefore, the remainder of the study focused on COB-141 which inhibited IL-6 secretion, and was found, via quantitative real time polymerase chain reaction (QRT-PCR), to …
引用总数
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