Deneka Alexander Y, Haber Leora, Kopp Meghan C, Gaponova Anna V, Nikonova Anna S, Golemis Erica A
Program in Molecular Therapeutics, Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States of America.
Department of Biochemistry, Kazan Federal University, Kazan, Russia.
PLoS One. 2017 Apr 28;12(4):e0176747. doi: 10.1371/journal.pone.0176747. eCollection 2017.
Non-small cell lung cancer (NSCLC) is the leading cause of cancer death worldwide, with a 5-year survival of only ~16%. Potential strategies to address NSCLC mortality include improvements in early detection and prevention, and development of new therapies suitable for use in patients with early and late stage diagnoses. Controlling the growth of early stage tumors could yield significant clinical benefits for patients with comorbidities that make them poor candidates for surgery: however, many drugs that limit cancer growth are not useful in the setting of long-term use or in comorbid patients, because of associated toxicities. In this study, we explored the use of a recently described small molecule agent, STA-8666, as a potential agent for controlling early stage tumor growth. STA-8666 uses a cleavable linker to merge a tumor-targeting moiety that binds heat shock protein 90 (HSP90) with the cytotoxic chemical SN38, and has been shown to have high efficacy and low toxicity, associated with efficient tumor targeting, in preclinical studies using patient-derived and other xenograft models for pancreatic, bladder, and small cell lung cancer. Using a genetically engineered model of NSCLC arising from induced mutation of KRas and knockout of Trp53, we continuously dosed mice with STA-8666 from immediately after tumor induction for 15 weeks. STA-8666 significantly slowed the rate of tumor growth, and was well tolerated over this extended dosing period. STA-8666 induced DNA damage and apoptosis, and reduced proliferation and phosphorylation of the proliferation-associated protein ERK1/2, selectively in tumor tissue. In contrast, STA-8666 did not affect tumor features, such as degree of vimentin staining, associated with epithelial-mesenchymal transition (EMT), or downregulate tumor expression of HSP90. These data suggest STA-8666 and other similar targeted compounds may be useful additions to control the growth of early stage NSCLC in patient populations.
非小细胞肺癌(NSCLC)是全球癌症死亡的主要原因,其5年生存率仅约为16%。应对NSCLC死亡率的潜在策略包括改善早期检测和预防,以及开发适用于早期和晚期诊断患者的新疗法。控制早期肿瘤的生长可为患有合并症而不适合手术的患者带来显著的临床益处:然而,许多限制癌症生长的药物由于相关毒性,在长期使用或合并症患者中并无用处。在本研究中,我们探索了一种最近描述的小分子药物STA-8666作为控制早期肿瘤生长的潜在药物。STA-8666使用可裂解连接子将与热休克蛋白90(HSP90)结合的肿瘤靶向部分与细胞毒性化学物质SN38融合,并且在使用患者来源的以及其他异种移植模型进行的胰腺癌、膀胱癌和小细胞肺癌的临床前研究中已显示出具有高效性和低毒性,且与有效的肿瘤靶向相关。使用由KRas诱导突变和Trp53基因敲除产生的NSCLC基因工程模型,我们在肿瘤诱导后立即开始连续15周给小鼠施用STA-8666。STA-8666显著减缓了肿瘤生长速度,并且在这个延长的给药期内耐受性良好。STA-8666诱导DNA损伤和凋亡,并选择性地在肿瘤组织中降低增殖相关蛋白ERK1/2的增殖和磷酸化。相比之下,STA-8666不影响与上皮-间质转化(EMT)相关的肿瘤特征,如波形蛋白染色程度,也不下调肿瘤中HSP90的表达。这些数据表明,STA-8666和其他类似的靶向化合物可能是控制患者群体中早期NSCLC生长的有用补充药物。