Wang Si Chun, Yan Xing Yi, Yang Chang, Naranmandura Hua
Department of Toxicology, School of Medicine and Public Health, Zhejiang University, Hangzhou 310058, China.
Department of Hematology, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310058, China.
Bioengineering (Basel). 2022 Nov 2;9(11):635. doi: 10.3390/bioengineering9110635.
Hematologic malignancies, including leukemia, lymphoma, myeloproliferative disorder and plasma cell neoplasia, are genetically heterogeneous and characterized by an uncontrolled proliferation of their corresponding cell lineages in the bone marrow, peripheral blood, tissues or plasma. Although there are many types of therapeutic drugs (e.g., TKIs, chemotherapy drugs) available for treatment of different malignancies, the relapse, drug resistance and severe side effects due to the lack of selectivity seriously limit their clinical application. Currently, although antibody-drug conjugates have been well established as able to target and deliver highly potent chemotherapy agents into cancer cells for the reduction of damage to healthy cells and have achieved success in leukemia treatment, they still also have shortcomings such as high cost, high immunogenicity and low stability. Aptamers are ssDNA or RNA oligonucleotides that can also precisely deliver therapeutic agents into cancer cells through specifically recognizing the membrane protein on cancer cells, which is similar to the capabilities of monoclonal antibodies. Aptamers exhibit higher binding affinity, lower immunogenicity and higher thermal stability than antibodies. Therefore, in this review we comprehensively describe recent advances in the development of aptamer-drug conjugates (ApDCs) with cytotoxic payload through chemical linkers or direct incorporation, as well as further introduce the latest promising aptamers-based therapeutic strategies such as aptamer-T cell therapy and aptamer-PROTAC, clarifying their bright application, development direction and challenges in the treatment of hematologic malignancies.
血液系统恶性肿瘤,包括白血病、淋巴瘤、骨髓增殖性疾病和浆细胞肿瘤,具有遗传异质性,其特征是相应细胞谱系在骨髓、外周血、组织或血浆中不受控制地增殖。尽管有多种治疗药物(如酪氨酸激酶抑制剂、化疗药物)可用于治疗不同的恶性肿瘤,但由于缺乏选择性导致的复发、耐药和严重副作用严重限制了它们的临床应用。目前,尽管抗体药物偶联物已被充分证实能够将高效化疗药物靶向递送至癌细胞中,以减少对健康细胞的损伤,并且在白血病治疗中取得了成功,但它们仍然存在成本高、免疫原性高和稳定性低等缺点。适体是单链DNA或RNA寡核苷酸,其也能够通过特异性识别癌细胞上的膜蛋白将治疗剂精确递送至癌细胞中,这与单克隆抗体的功能类似。适体表现出比抗体更高的结合亲和力、更低的免疫原性和更高的热稳定性。因此,在本综述中,我们全面描述了通过化学连接物或直接掺入具有细胞毒性载荷的适体-药物偶联物(ApDCs)开发的最新进展,并进一步介绍了最新的有前景的基于适体的治疗策略,如适体-T细胞疗法和适体-蛋白酶体靶向嵌合体,阐明它们在血液系统恶性肿瘤治疗中的光明应用、发展方向和挑战。