Semenchenko Kostyantyn, Wasylyk Christine, Cheung Henry, Tourrette Yves, Maas Peter, Schalken Jack A, van der Pluijm Gabri, Wasylyk Bohdan
Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
Centre National de la Recherche Scientifique, UMR7104, Illkirch, France.
PLoS One. 2016 Jul 18;11(7):e0159531. doi: 10.1371/journal.pone.0159531. eCollection 2016.
Transcription factors have an important role in cancer but are difficult targets for the development of tumour therapies. These factors include the Ets family, and in this study Elk3 that is activated by Ras oncogene /Erk signalling, and is involved in angiogenesis, malignant progression and epithelial-mesenchymal type processes. We previously described the identification and in-vitro characterisation of an inhibitor of Ras / Erk activation of Elk3 that also affects microtubules, XRP44X. We now report an initial characterisation of the effects of XRP44X in-vivo on tumour growth and metastasis in three preclinical models mouse models, subcutaneous xenografts, intra-cardiac injection-bone metastasis and the TRAMP transgenic mouse model of prostate cancer progression. XRP44X inhibits tumour growth and metastasis, with limited toxicity. Tumours from XRP44X-treated animals have decreased expression of genes containing Elk3-like binding motifs in their promoters, Elk3 protein and phosphorylated Elk3, suggesting that perhaps XRP44X acts in part by inhibiting the activity of Elk3. Further studies are now warranted to develop XRP44X for tumour therapy.
转录因子在癌症中发挥着重要作用,但却是肿瘤治疗开发的困难靶点。这些因子包括Ets家族,在本研究中,Elk3被Ras癌基因/Erk信号激活,并参与血管生成、恶性进展和上皮-间质转化过程。我们之前描述了一种抑制Ras/Erk激活Elk3且还影响微管的抑制剂XRP44X的鉴定及体外特性。我们现在报告XRP44X在三种临床前小鼠模型(皮下异种移植、心脏内注射-骨转移和前列腺癌进展的TRAMP转基因小鼠模型)中对肿瘤生长和转移影响的初步特性。XRP44X抑制肿瘤生长和转移,毒性有限。经XRP44X处理的动物的肿瘤在其启动子中含有Elk3样结合基序的基因、Elk3蛋白和磷酸化Elk3的表达降低,这表明XRP44X可能部分通过抑制Elk3的活性发挥作用。现在有必要进一步研究将XRP44X开发用于肿瘤治疗。