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Discovery of Drugs Targeting Mutant p53 and Progress in Nano-Enabled Therapeutic Strategy for p53-Mutated Cancers
by
Xu, Yuxue
, Wei, Pengfei
, Song, Jie
, Liang, Qiyue
, Wen, Longping
, Xu, Zhaowei
, Jing, Zhiyuan
, Zhang, Na
in
Animals
/ Antimitotic agents
/ Antineoplastic agents
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - pharmacology
/ Antineoplastic Agents - therapeutic use
/ Apoptosis
/ Cancer
/ Cancer therapies
/ Cell cycle
/ Cell death
/ Clinical trials
/ Development and progression
/ Drug delivery
/ Drug development
/ Drug Discovery
/ Enzymes
/ Genetic Therapy
/ Health aspects
/ Homeopathy
/ Humans
/ Materia medica and therapeutics
/ mutant p53
/ mutant p53 reactivation
/ Mutants
/ Mutation
/ nanodelivery
/ Nanotechnology
/ Neoplasms - drug therapy
/ Neoplasms - genetics
/ Neoplasms - metabolism
/ p53 Protein
/ protein stability
/ Proteins
/ Recovery of function
/ Review
/ Therapeutic targets
/ Therapeutics
/ Toxicity
/ Transcription factors
/ Tumor proteins
/ Tumor Suppressor Protein p53 - antagonists & inhibitors
/ Tumor Suppressor Protein p53 - genetics
/ Tumor Suppressor Protein p53 - metabolism
2025
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Discovery of Drugs Targeting Mutant p53 and Progress in Nano-Enabled Therapeutic Strategy for p53-Mutated Cancers
by
Xu, Yuxue
, Wei, Pengfei
, Song, Jie
, Liang, Qiyue
, Wen, Longping
, Xu, Zhaowei
, Jing, Zhiyuan
, Zhang, Na
in
Animals
/ Antimitotic agents
/ Antineoplastic agents
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - pharmacology
/ Antineoplastic Agents - therapeutic use
/ Apoptosis
/ Cancer
/ Cancer therapies
/ Cell cycle
/ Cell death
/ Clinical trials
/ Development and progression
/ Drug delivery
/ Drug development
/ Drug Discovery
/ Enzymes
/ Genetic Therapy
/ Health aspects
/ Homeopathy
/ Humans
/ Materia medica and therapeutics
/ mutant p53
/ mutant p53 reactivation
/ Mutants
/ Mutation
/ nanodelivery
/ Nanotechnology
/ Neoplasms - drug therapy
/ Neoplasms - genetics
/ Neoplasms - metabolism
/ p53 Protein
/ protein stability
/ Proteins
/ Recovery of function
/ Review
/ Therapeutic targets
/ Therapeutics
/ Toxicity
/ Transcription factors
/ Tumor proteins
/ Tumor Suppressor Protein p53 - antagonists & inhibitors
/ Tumor Suppressor Protein p53 - genetics
/ Tumor Suppressor Protein p53 - metabolism
2025
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Discovery of Drugs Targeting Mutant p53 and Progress in Nano-Enabled Therapeutic Strategy for p53-Mutated Cancers
by
Xu, Yuxue
, Wei, Pengfei
, Song, Jie
, Liang, Qiyue
, Wen, Longping
, Xu, Zhaowei
, Jing, Zhiyuan
, Zhang, Na
in
Animals
/ Antimitotic agents
/ Antineoplastic agents
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - pharmacology
/ Antineoplastic Agents - therapeutic use
/ Apoptosis
/ Cancer
/ Cancer therapies
/ Cell cycle
/ Cell death
/ Clinical trials
/ Development and progression
/ Drug delivery
/ Drug development
/ Drug Discovery
/ Enzymes
/ Genetic Therapy
/ Health aspects
/ Homeopathy
/ Humans
/ Materia medica and therapeutics
/ mutant p53
/ mutant p53 reactivation
/ Mutants
/ Mutation
/ nanodelivery
/ Nanotechnology
/ Neoplasms - drug therapy
/ Neoplasms - genetics
/ Neoplasms - metabolism
/ p53 Protein
/ protein stability
/ Proteins
/ Recovery of function
/ Review
/ Therapeutic targets
/ Therapeutics
/ Toxicity
/ Transcription factors
/ Tumor proteins
/ Tumor Suppressor Protein p53 - antagonists & inhibitors
/ Tumor Suppressor Protein p53 - genetics
/ Tumor Suppressor Protein p53 - metabolism
2025
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Discovery of Drugs Targeting Mutant p53 and Progress in Nano-Enabled Therapeutic Strategy for p53-Mutated Cancers
Journal Article
Discovery of Drugs Targeting Mutant p53 and Progress in Nano-Enabled Therapeutic Strategy for p53-Mutated Cancers
2025
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Overview
Mutations in the p53 gene are frequently observed in various cancers, prompting the initiation of efforts to restore p53 function as a therapeutic approach several decades ago. Nevertheless, only a limited number of drug development initiatives have progressed to late-stage clinical trials, and to date, no p53-targeted therapies have received approval in the USA or Europe. This situation can be attributed primarily to the characteristics of p53 as a nuclear transcription factor, which lacks the conventional features associated with drug targets and has historically been considered “undruggable”. In recent years, however, several promising strategies have emerged, including the enhanced iterations of previous approaches and novel techniques aimed at targeting proteins that have traditionally been considered undruggable. There is a growing interest in small molecules that can restore the tumor-suppressive functions of mutant p53 proteins, and the development of drugs specifically designed for particular p53 mutation types is currently underway. Other approaches aim to deplete mutant p53 or exploit vulnerabilities associated with its expression. Additionally, genetic therapy strategy and approaches have rekindled interest. Advances in mutant p53 biology, compound mechanisms, treatment modalities, and nanotechnology have opened up new avenues for p53-based therapies. However, significant challenges remain in clinical development. This review reassesses the progress in targeting p53-mutant cancers, discusses the obstacles in translating these approaches into effective therapies, and highlights p53-based therapies via nanotechnology.
Publisher
MDPI AG,MDPI
Subject
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - pharmacology
/ Antineoplastic Agents - therapeutic use
/ Cancer
/ Enzymes
/ Humans
/ Materia medica and therapeutics
/ Mutants
/ Mutation
/ Proteins
/ Review
/ Toxicity
/ Tumor Suppressor Protein p53 - antagonists & inhibitors
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