Szumilak Marta, Wiktorowska-Owczarek Anna, Stanczak Andrzej
Department of Hospital Pharmacy, Faculty of Pharmacy, Medical University of Lodz, 1 Muszynskiego Street, 90-151 Lodz, Poland.
Department of Pharmacology and Toxicology, Medical University of Lodz, Zeligowskiego 7/9, 90-752 Lodz, Poland.
Molecules. 2021 Apr 29;26(9):2601. doi: 10.3390/molecules26092601.
Despite enormous progress in the treatment of many malignancies, the development of cancer resistance is still an important reason for cancer chemotherapy failure. Increasing knowledge of cancers' molecular complexity and mechanisms of their resistance to anticancer drugs, as well as extensive clinical experience, indicate that an effective fight against cancer requires a multidimensional approach. Multi-target chemotherapy may be achieved using drugs combination, co-delivery of medicines, or designing hybrid drugs. Hybrid drugs simultaneously targeting many points of signaling networks and various structures within a cancer cell have been extensively explored in recent years. The single hybrid agent can modulate multiple targets involved in cancer cell proliferation, possesses a simpler pharmacokinetic profile to reduce the possibility of drug interactions occurrence, and facilitates the process of drug development. Moreover, a single medication is expected to enhance patient compliance due to a less complicated treatment regimen, as well as a diminished number of adverse reactions and toxicity in comparison to a combination of drugs. As a consequence, many efforts have been made to design hybrid molecules of different chemical structures and functions as a means to circumvent drug resistance. The enormous number of studies in this field encouraged us to review the available literature and present selected research results highlighting the possible role of hybrid drugs in overcoming cancer drug resistance.
尽管在许多恶性肿瘤的治疗方面取得了巨大进展,但癌症耐药性的产生仍然是癌症化疗失败的一个重要原因。对癌症分子复杂性及其对抗癌药物耐药机制的了解不断增加,以及丰富的临床经验表明,有效对抗癌症需要采取多维度方法。多靶点化疗可以通过药物联合、药物共递送或设计杂合药物来实现。近年来,同时靶向信号网络多个节点和癌细胞内各种结构的杂合药物得到了广泛研究。单一杂合药物可以调节参与癌细胞增殖的多个靶点,具有更简单的药代动力学特征,以降低药物相互作用发生的可能性,并促进药物开发过程。此外,与联合用药相比,单一药物由于治疗方案更简单,不良反应和毒性数量减少,有望提高患者的依从性。因此,人们做出了许多努力来设计具有不同化学结构和功能的杂合分子,以规避耐药性。该领域大量的研究促使我们回顾现有文献,并呈现一些选定的研究结果,突出杂合药物在克服癌症耐药性方面可能发挥的作用。