Mitola Giulia, Falvo Paolo, Bertolini Francesco
Laboratory of Hematology-Oncology, IEO European Institute of Oncology IRCCS, 16, 20139 Milan, Italy.
Life (Basel). 2021 Oct 24;11(11):1131. doi: 10.3390/life11111131.
Disease relapse caused by drug resistance still represents a major clinical hurdle in cancer treatments. Tumor cells may take advantage of different intracellular and genetic systems attenuating the drug effects. Resistant cells or minimal residual disease (MRD) cells have strong clinical relevance, as they might give rise to secondary tumors when the therapy is concluded. Thus, MRDs are crucial therapeutic targets in order to prevent tumor relapse. Therefore, several groups aim at understanding how MRDs are orginated, characterizing their molecular features, and eradicating them. In this review, we will describe MRD from a genetic, evolutionary, and molecular point of view. Moreover, we will focus on the new in vitro, in vivo, preclinical, and clinical studies that aim at eradicating tumor resistance.
耐药性导致的疾病复发仍是癌症治疗中的一个主要临床障碍。肿瘤细胞可能利用不同的细胞内和遗传系统来减弱药物作用。耐药细胞或微小残留病(MRD)细胞具有很强的临床相关性,因为在治疗结束后它们可能引发继发性肿瘤。因此,为了防止肿瘤复发,MRD是关键的治疗靶点。所以,有几个研究团队致力于了解MRD是如何产生的,描绘其分子特征,并根除它们。在这篇综述中,我们将从遗传学、进化和分子的角度来描述MRD。此外,我们将重点关注旨在根除肿瘤耐药性的新的体外、体内、临床前和临床研究。