Therapeutic potential of combating cancer by restoring wild-type p53 through mRNA nanodelivery

被引：8

作者：

Kamath, Divya ^{[1
]}

Iwakuma, Tomoo ^{[2
]}

Bossmann, Stefan H. ^{[1
]}

机构：

[1] Univ Kansas, Dept Canc Biol, Med Ctr, 3901 Rainbow Blvd,mailstop 1071, Kansas City, KS 66160 USA

[2] Childrens Mercy Hosp, 2401 Gillham Rd,Adele Hall Campus, Kansas City, MO 64108 USA

来源：

NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE | 2024年 / 56卷

关键词：

p53; mutant; cancer; Gene therapy; Nanotechnology; Restoring wild -type p53; GAIN-OF-FUNCTION; MUTANT P53; RESTORATION; MUTATION;

D O I：

10.1016/j.nano.2024.102732

中图分类号：

TB3 [工程材料学];

学科分类号：

0805 ; 080502 ;

摘要：

Among the tumor suppressor genes, TP53 is the most frequently mutated in human cancers, and most mutations are missense mutations causing production of mutant p53 (mutp53) proteins. TP53 mutations not only results in loss of function (LOH) as a transcription factor and a tumor suppressor, but also gain wild-type p53 (WTp53)independent oncogenic functions that enhance cancer metastasis and progression (Yamamoto and Iwakuma, 2018; Zhang et al., 2022). TP53 has extensively been studied as a therapeutic target as well as for drug development and therapies, however with limited success. Achieving targeted therapies for restoration of WTp53 function and depletion or repair of mutant p53 (mutp53) will have far reaching implication in cancer treatment and therapies. This review briefly discusses the role of p53 mutation in cancer and the therapeutic potential of restoring WTp53 through the advances in mRNA nanomedicine.

引用

页数：5

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