CHK1 Inhibitor-Based Checkpoint Abrogation: A Classic, Yet New Therapeutic Approach in Advanced Cancer

K. Ando, A. Nakagawara, H. Nagase, S. Kobayashi, S. Wada
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Abstract

Recent advances in small molecule kinase inhibitors have markedly improved patient survival in various types of cancer. Most of these successes can be attributed to the concept of “targeting driver oncogenes,” as in the case of tyrosine kinase inhibitors (i.e., EGFR inhibitors), but not in serine/threonine kinase inhibitors including CHK1 inhibitor. Further investigation of the underlying mechanisms is needed to identify synergistic interactions of CHK1 that would help prolong patient survival and improve their quality of life.
基于CHK1抑制剂的检查点废除:晚期癌症的经典新治疗方法
小分子激酶抑制剂的最新进展显著提高了各种类型癌症患者的生存率。大多数这些成功可归因于“靶向驱动癌基因”的概念,如酪氨酸激酶抑制剂(即EGFR抑制剂),但不包括CHK1抑制剂在内的丝氨酸/苏氨酸激酶抑制剂。需要进一步研究潜在的机制,以确定CHK1的协同相互作用,这将有助于延长患者的生存期并改善他们的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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