摘要P5-05-05:一类新化合物对FOXM1活性和乳腺癌生长的体外和体内抑制作用

B. Katzenellenbogen, Y. Ziegler, M. Laws, V. S. Guillen, Sung-Hoon Kim, Parama Dey, B. Smith, P. Gong, Noah A. Bindman, Yuechao Zhao, K. Carlson, Mayuri A. Yasuda, Divya Singh, Zhong Li, D. El-Ashry, Zeynep Madak-Erdogan, J. Katzenellenbogen
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引用次数: 2

摘要

转录因子FOXM1在激素受体阳性和三阴性乳腺癌的侵袭性、治疗耐药形式中上调和过度表达,并与较差的患者生存率相关。FOXM1信号也是许多其他癌症的关键驱动因素。在这里,我们发现了一类新的化合物,可以有效地抑制乳腺癌中FOXM1的活性,并显示出良好的抗肿瘤功效。这些化合物直接与FOXM1结合并改变其蛋白水解敏感性,通过蛋白酶体依赖过程降低FOXM1蛋白的细胞水平,抑制乳腺癌细胞增殖和细胞周期进程,增加凋亡。RNA-seq和基因集富集分析表明,化合物降低FOXM1调控基因的表达,抑制FOXM1调控下的基因本体。几种化合物具有良好的药代动力学性质,在临床前乳腺肿瘤模型中表现出良好的肿瘤抑制作用。这些化合物可能适合用于针对FOXM1驱动的侵袭性乳腺癌的进一步临床评估。(由乳腺癌研究基金会资助(BCRF-083到BSK),朱利叶斯和玛丽兰德菲尔德癌症研究基金(BSK), NIH资助R01 DK015556 (JAK), NIH T32 GM070421奖学金(VSG), Bankhead-Coley基金会资助09BW04 (DEA), USDA奖illuu -698-909和国家超级计算应用中心教师奖学金(ZME), UIUC环境毒理学奖学金(BPS))。)引文格式:Benita S. Katzenellenbogen, Yvonne Ziegler, Mary J Laws, Valeria S. Guillen, SungHoon Kim, Parama Dey, Brandi P. Smith, Gong Ping, Noah Bindman, yuecchao Zhao, Kathryn Carlson, Mayuri A. Yasuda, Divya Singh, Zhong Li, Dorraya El-Ashry, Zeynep Madak-Erdogan, John A. Katzenellenbogen。一类新化合物在体外和体内抑制FOXM1活性和乳腺癌生长[摘要]。摘自:2019年圣安东尼奥乳腺癌研讨会论文集;2019年12月10日至14日;费城(PA): AACR;中国癌症杂志,2020;31(增刊):P5-05-05。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract P5-05-05: Suppression of FOXM1 activities and breast cancer growth in vitro and in vivo by a new class of compounds
The transcription factor FOXM1 is up-regulated and overexpressed in aggressive, therapy-resistant forms of hormone receptor-positive and triple negative breast cancers, and is associated with less good patient survival. FOXM1 signaling is also a key driver in many other cancers. Here, we identify a new class of compounds effective in suppressing FOXM1 activity in breast cancers, and displaying good potency for antitumor efficacy. The compounds bind directly to FOXM1 and alter its proteolytic sensitivity, reduce the cellular level of FOXM1 protein by a proteasome-dependent process, and suppress breast cancer cell proliferation and cell cycle progression and increase apoptosis. RNA-seq and gene set enrichment analyses indicate that the compounds decrease expression of FOXM1-regulated genes and suppress gene ontologies under FOXM1 regulation. Several compounds have favorable pharmacokinetic properties and show good tumor suppression in preclinical breast tumor models. These compounds may be suitable for further clinical evaluation in targeting aggressive breast cancers driven by FOXM1. (Supported by Breast Cancer Research Foundation grant (BCRF-083 to BSK), The Julius and Mary Landfield Cancer Research Fund (to BSK), NIH grant R01 DK015556 (to JAK), NIH T32 GM070421 Fellowship (to VSG), Bankhead-Coley Foundation grant 09BW04 (to DEA), USDA award ILLU-698-909 and National Center for Supercomputing Applications Faculty Fellowship (to ZME), and UIUC Environmental Toxicology Scholarship (to BPS)). Citation Format: Benita S. Katzenellenbogen, Yvonne Ziegler, Mary J Laws, Valeria S. Guillen, SungHoon Kim, Parama Dey, Brandi P. Smith, Ping Gong, Noah Bindman, Yuechao Zhao, Kathryn Carlson, Mayuri A. Yasuda, Divya Singh, Zhong Li, Dorraya El-Ashry, Zeynep Madak-Erdogan, John A. Katzenellenbogen. Suppression of FOXM1 activities and breast cancer growth in vitro and in vivo by a new class of compounds [abstract]. In: Proceedings of the 2019 San Antonio Breast Cancer Symposium; 2019 Dec 10-14; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2020;80(4 Suppl):Abstract nr P5-05-05.
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