首页|骨肉瘤预后相关致病基因的研究进展

骨肉瘤预后相关致病基因的研究进展

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Research progress on prognosis-related pathogenic genes of osteosarcoma
Osteosarcoma is a highly aggressive malignant tumor and its treatment remains a great challenge due to its high heterogeneity nature and complex pathogenesis.Over the past 20 years,there has been no improvement in prognosis with first-line chemotherapeutic agents and clinical outcomes.There is no effective anticancer drug for patients with drug-resistant,metastatic,and recurrent osteosarcoma,so new approaches are needed to improve prognosis.With the development of biotechnology and bioinformatics in recent years,research on osteosarcoma has made progress.Among them,the pathogenic genes and signaling pathways of osteosarcoma are the focus and hotspot of research.Understanding cancer biology helps to develop more effective detection and treatment methods,while the identification of pathogenic genes,especially driver genes,is one of the keys.The development of sequencing technology has promoted the identification of somatic mutations and copy number changes in osteosarcoma.Due to its high heterogeneity and low incidence,the research on the nature and quantity of driver genes related to the mechanism of osteosarcoma onset,invasion,metastasis,and prognosis is still in its early stages.This article reviews the pathogenic genes of osteosarcoma,biological functions,regulatory mechanisms,mutation characteristics,as well as the relevant signaling pathways and targeted therapies,hoping to provide hints of genes that classify patients into different therapeutic options.Among them,driver genes such as TP53,RB1,CDKN2A are considered to play an important role in the development of osteosarcoma,while genes such as ATRX,MDM2,PTEN,BRCA1/2,Rab22a have also been proven to be closely related to osteosarcoma development.

OsteosarcomaGenesMutationPrognosisDriver genesReview

刘璐、焦辰波、刘巍峰

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100035 北京,首都医科大学附属北京积水潭医院骨肿瘤科,北京积水潭医院骨科机器人工程研究中心有限公司

骨肉瘤 基因 突变 预后 驱动基因 综述

2024

中国骨与关节杂志
中国医疗保健国际交流促进会,北京中科康辰骨关节伤病研究所

中国骨与关节杂志

CSTPCD
影响因子:0.665
ISSN:2095-252X
年,卷(期):2024.13(5)
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