Department of Anatomy and Cell Biology, University of Florida, Gainesville, FL, 32610, USA.
Department of Pharmacology, Penn State University College of Medicine, Penn State Cancer Institute, Hershey, PA, 17033, USA.
Eur J Med Chem. 2019 Jan 1;161:456-467. doi: 10.1016/j.ejmech.2018.10.052. Epub 2018 Oct 23.
Despite new agent development and short-term benefits in patients with colorectal cancer (CRC), metastatic CRC cure rates have not improved due to high rates of 5-fluorouracil (5-FU)/leucovorin/oxaliplatin (FOLFOX)-resistance and a clinical therapeutic plateau. At the same time, this treatment regime leads to significant toxicity, cost, and patient inconvenience. Drug-resistance is linked to CRC stem cells, which are associated with the epidermal-to-mesenchymal transition (EMT) pathway. Thus, to optimally treat CRC, a therapy that can target the cell survival and EMT pathways in both CRC bulk and stem cell populations is critical. We recently identified a novel small molecule NSC30049 (7a) that is effective alone, and in combination potentiates 5-FU-mediated growth inhibition of CRC bulk, FOLFOX-resistant, and CRC stem cells both in vitro and in vivo models. In the present study, we report the synthesis and anti-CRC evaluation of several stable and effective 7a analogs. ASR352 (7b) was identified as one of the equipotent 7a analogs that inhibited the growth of CRC bulk cells, sensitized FOLFOX-resistant cells, and reduced the sphere formation capacity of CRC stem cells. It appears that the complex mechanism of cytotoxicity for 7b includes abrogation of 5-FU-induced the S phase, reduction of the phosphorylation of Chk1 at S317P, S345P and S296P, increased γH2AX staining, activation of caspase 3/PARP1 cleavage, and enhancement of Bax/Bcl2 ratio. Further 7b-mediated reduced phosphorylation of Chk1 was an indirect effect, since it did not inhibit Chk1 activity in an in vitro kinase assay. Our findings suggest that 7b as a single agent, or in combination with 5-FU can be developed as a therapeutic agent in CRC bulk, FOLFOX-resistant, and CRC stem cell populations for unmanageable metastatic CRC conditions.
尽管新的药物研发和在结直肠癌(CRC)患者中的短期获益,但转移性 CRC 的治愈率并未提高,这是因为氟尿嘧啶(5-FU)/亚叶酸/奥沙利铂(FOLFOX)耐药率高以及临床治疗平台期。同时,这种治疗方案会导致显著的毒性、成本和患者不便。耐药性与 CRC 干细胞有关,而后者与上皮-间质转化(EMT)途径有关。因此,为了优化 CRC 的治疗效果,一种能够针对 CRC 细胞群体和干细胞群体中的细胞存活和 EMT 途径的治疗方法至关重要。我们最近发现了一种新型小分子 NSC30049(7a),它单独使用有效,并且与 5-FU 联合使用能够增强 CRC 细胞群体、FOLFOX 耐药细胞和 CRC 干细胞的生长抑制作用,无论是在体外还是体内模型中。在本研究中,我们报告了几种稳定且有效的 7a 类似物的合成和抗 CRC 评估。ASR352(7b)被鉴定为与 7a 等效力的类似物之一,它抑制 CRC 细胞群体的生长,使 FOLFOX 耐药细胞敏感,并降低 CRC 干细胞的球体形成能力。似乎 7b 的细胞毒性复杂机制包括阻断 5-FU 诱导的 S 期、减少 Chk1 在 S317P、S345P 和 S296P 上的磷酸化、增加 γH2AX 染色、激活 caspase 3/PARP1 切割以及增强 Bax/Bcl2 比值。进一步的 7b 介导的 Chk1 磷酸化减少是一种间接作用,因为它不会在体外激酶测定中抑制 Chk1 活性。我们的研究结果表明,7b 作为单一药物,或与 5-FU 联合使用,可以作为 CRC 细胞群体、FOLFOX 耐药细胞和 CRC 干细胞群体中不可管理的转移性 CRC 条件下的治疗药物进行开发。