髓样
免疫疗法
造血
髓系白血病
癌症研究
造血干细胞移植
表观遗传学
化疗
干细胞
免疫学
白血病
骨髓
生物
癌症
医学
免疫系统
基因
内科学
遗传学
作者
Raed Obaid Saleh,Ahmed Hjazi,Safia Obaidur Rab,Subasini Uthirapathy,S. Ganesan,Aman Shankhyan,Mohit Kumar,Girish Chandra Sharma,Muthena Kariem,Jawad Ahmed
摘要
ABSTRACT Acute myeloid leukemia (AML) is caused by altered maturation and differentiation of myeloid blasts, as well as transcriptional/epigenetic alterations and impaired apoptosis, all of which lead to excessive proliferation of malignant blood cells in the bone marrow. It is these mutations that cause tumor heterogeneity, which is linked to a higher risk of relapse and death and makes anti‐AML treatments like HSCT, chemotherapy, and immunotherapy (ICI, CAR T‐cell‐based therapies, and cancer vaccines) less effective. Single‐cell RNA sequencing (scRNA‐seq) also makes it possible to find cellular subclones and profile tumors, which opens up new diagnostic and therapeutic targets for better AML management. The HSCT process works better when genetic and transcriptional information about the patient and donor stem cells is collected. This saves time and lowers the risk of harmful side effects happening in the body.
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