TP53 in MDS and AML: Biological and clinical advances

被引:5
作者
Zhao, Yeqian [1 ,2 ,3 ,4 ]
Chen, Weihao [1 ]
Yu, Jing [5 ]
Pei, Shanshan [1 ,2 ,3 ,4 ]
Zhang, Qiang [6 ]
Shi, Jimin [1 ,2 ,3 ]
Huang, He [1 ,2 ,3 ]
Zhao, Yanmin [1 ,2 ,3 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Sch Med, Bone Marrow Transplantat Ctr, Hangzhou 310009, Peoples R China
[2] Zhejiang Univ, Med Ctr, Liangzhu Lab, Hangzhou 311121, Peoples R China
[3] Zhejiang Univ, Inst Hematol, Hangzhou, Peoples R China
[4] Zhejiang Prov Engn Lab Stem Cell & Immun Therapy, Hangzhou, Peoples R China
[5] Zhejiang Univ, Sch Med, Hangzhou, Peoples R China
[6] Zhejiang Jianfeng Grp Co Ltd, Jinhua, Peoples R China
基金
中国国家自然科学基金;
关键词
TP53; mutations; Malignant progression; Multi; -hit; VAF; Prognosis; Treatment; ACUTE MYELOID-LEUKEMIA; CLONAL HEMATOPOIESIS; MUTANT P53; MUTATIONS; EVOLUTION; ABNORMALITIES; AZACITIDINE; VENETOCLAX; FREQUENCY; DELETION;
D O I
10.1016/j.canlet.2024.216767
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recently, the WHO -5 and the ICC 2022 criteria have emphasized poor prognosis in AML/MDS patients with multi -hit TP53 mutations, whereas mutated TP53 plays a critical role in tumorigenesis, drawing substantial interest in exploring its biological behaviors. Diverse characteristics of TP53 mutations, including types, VAF, CNVs, allelic status, karyotypes, and concurrent mutations have been extensively studied. Novel potential targets and comprehensive treatment strategies nowadays are under swift development, owing to great advances in technology. However, accurately predicting prognosis of patients with TP53 -mutated myeloid neoplasms remains challenging. And there is still a lack of effective treatment for those patients.
引用
收藏
页数:10
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