Potential Diagnostic and Clinical Significance of Selected Genetic Alterations in Glioblastoma

. 2024 Apr 18 ; 25 (8) : . [epub] 20240418

Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/pmid38674026

Grantová podpora
MH CZ - DRO - FNOs/2023 Ministry of Health Czech Republic

Odkazy
PubMed 38674026
PubMed Central PMC11050250
DOI 10.3390/ijms25084438
PII: ijms25084438
Knihovny.cz E-zdroje

Glioblastoma is currently considered the most common and, unfortunately, also the most aggressive primary brain tumor, with the highest morbidity and mortality rates. The average survival of patients diagnosed with glioblastoma is 14 months, and only 2% of patients survive 3 years after surgery. Based on our clinical experience and knowledge from extensive clinical studies, survival is mainly related to the molecular biological properties of glioblastoma, which are of interest to the general medical community. Our study examined a total of 71 retrospective studies published from 2016 through 2022 and available on PubMed that deal with mutations of selected genes in the pathophysiology of GBM. In conclusion, we can find other mutations within a given gene group that have different effects on the prognosis and quality of survival of a patient with glioblastoma. These mutations, together with the associated mutations of other genes, as well as intratumoral heterogeneity itself, offer enormous potential for further clinical research and possible application in therapeutic practice.

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