Bailey Charvann K, Budina-Kolomets Anna, Murphy Maureen E, Nefedova Yulia
a Tumor Microenvironment and Metastasis; The Wistar Institute ; Philadelphia , PA USA.
b Molecular and Cellular Oncogenesis; The Wistar Institute ; Philadelphia , PA USA.
Cancer Biol Ther. 2015;16(9):1422-6. doi: 10.1080/15384047.2015.1071743. Epub 2015 Jul 15.
Multiple myeloma (MM) is a common and largely incurable blood cancer for which new treatment options are needed, as resistance to current modalities is an issue. Additionally, because this tumor type often resides in a hypoxic niche of the bone marrow, new therapeutics that remain effective even under hypoxic conditions are sought. Because of the secretory nature of MM cells they are uniquely under proteotoxic stress, and we hypothesized that these tumor cells may alleviate this stress by upregulating the major stress-induced cytosolic form of the chaperone HSP70. In this work we test the efficacy of the HSP70 inhibitor PET-16 for MM. We show that MM cell lines express significant levels of HSP70, and further that inhibition of HSP70 causes decreased viability and apoptosis, along with proteotoxic stress, as assessed by the accumulation of poly-ubiquitylated proteins. Importantly, we show that growth of these tumor cells under hypoxic conditions has no effect on the ability of PET-16 to be cytotoxic. The HSP70 inhibitor PET-16 should thus be considered further for pre-clinical analyses of efficacy in MM.
多发性骨髓瘤(MM)是一种常见且大多无法治愈的血液癌症,由于对当前治疗方式产生耐药性是一个问题,因此需要新的治疗选择。此外,由于这种肿瘤类型通常存在于骨髓的低氧微环境中,所以人们在寻找即使在低氧条件下仍有效的新疗法。由于MM细胞的分泌特性,它们独特地处于蛋白质毒性应激之下,我们推测这些肿瘤细胞可能通过上调伴侣蛋白HSP70的主要应激诱导胞质形式来减轻这种应激。在这项研究中,我们测试了HSP70抑制剂PET-16对MM的疗效。我们发现MM细胞系表达显著水平的HSP70,并且进一步发现抑制HSP70会导致活力下降和凋亡,同时伴随着蛋白质毒性应激,这可通过多泛素化蛋白的积累来评估。重要的是,我们表明这些肿瘤细胞在低氧条件下的生长对PET-16的细胞毒性能力没有影响。因此,HSP70抑制剂PET-16应进一步考虑用于MM疗效的临床前分析。