Losson Hélène, Schnekenburger Michael, Dicato Mario, Diederich Marc
Laboratoire de Biologie Moléculaire et Cellulaire du Cancer, Hôpital Kirchberg 9, rue Edward Steichen, L2540 Luxembourg, Luxembourg.
College of Pharmacy, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Korea.
Cancers (Basel). 2020 Jan 29;12(2):318. doi: 10.3390/cancers12020318.
Imatinib became the standard treatment for chronic myeloid leukemia (CML) about 20 years ago, which was a major breakthrough in stabilizing the pathology and improving the quality of life of patients. However, the emergence of resistance to imatinib and other tyrosine kinase inhibitors leads researchers to characterize new therapeutic targets. Several studies have highlighted the role of histone deacetylase 6 (HDAC6) in various pathologies, including cancer. This protein effectively intervenes in cellular activities by its primarily cytoplasmic localization. In this review, we will discuss the molecular characteristics of the HDAC6 protein, as well as its overexpression in CML leukemic stem cells, which make it a promising therapeutic target for the treatment of CML.
大约20年前,伊马替尼成为慢性粒细胞白血病(CML)的标准治疗方法,这是在稳定病情和改善患者生活质量方面的一项重大突破。然而,对伊马替尼和其他酪氨酸激酶抑制剂耐药性的出现促使研究人员寻找新的治疗靶点。多项研究强调了组蛋白去乙酰化酶6(HDAC6)在包括癌症在内的多种疾病中的作用。该蛋白主要定位于细胞质,从而有效地干预细胞活动。在本综述中,我们将讨论HDAC6蛋白的分子特征,以及它在CML白血病干细胞中的过表达情况,这些特性使其成为治疗CML的一个有前景的治疗靶点。