Faust Joshua R, Hamill Darcy, Kolb Edward Anders, Gopalakrishnapillai Anilkumar, Barwe Sonali P
Nemours Centers for Childhood Cancer Research & Cancer and Blood Disorders, Nemours Children's Hospital, Wilmington, DE 19803, USA.
Cancers (Basel). 2022 Mar 18;14(6):1550. doi: 10.3390/cancers14061550.
Modern targeted cancer therapies rely on the overexpression of tumor associated antigens with very little to no expression in normal cell types. Mesothelin is a glycosylphosphatidylinositol-anchored cell surface protein that has been identified in many different tumor types, including lung adenocarcinomas, ovarian carcinomas, and most recently in hematological malignancies, including acute myeloid leukemia (AML). Although the function of mesothelin is widely unknown, interactions with MUC16/CA125 indicate that mesothelin plays a role in the regulation of proliferation, growth, and adhesion signaling. Most research on mesothelin currently focuses on utilizing mesothelin to design targeted cancer therapies such as monoclonal antibodies, antibody-drug conjugates, chimeric antigen receptor T and NK cells, bispecific T cell engaging molecules, and targeted alpha therapies, amongst others. Both in vitro and in vivo studies using different immunotherapeutic modalities in mesothelin-positive AML models highlight the potential impact of this approach as a unique opportunity to treat hard-to-cure AML.
现代靶向癌症疗法依赖于肿瘤相关抗原的过表达,而这些抗原在正常细胞类型中很少或几乎不表达。间皮素是一种糖基磷脂酰肌醇锚定的细胞表面蛋白,已在许多不同的肿瘤类型中被发现,包括肺腺癌、卵巢癌,以及最近在血液系统恶性肿瘤中发现,包括急性髓系白血病(AML)。尽管间皮素的功能尚不清楚,但与MUC16/CA125的相互作用表明间皮素在增殖、生长和黏附信号调节中发挥作用。目前关于间皮素的大多数研究都集中在利用间皮素设计靶向癌症疗法,如单克隆抗体、抗体-药物偶联物、嵌合抗原受体T细胞和自然杀伤细胞、双特异性T细胞接合分子以及靶向α疗法等。在间皮素阳性AML模型中使用不同免疫治疗方式的体外和体内研究都凸显了这种方法作为治疗难治性AML的独特机会的潜在影响。