AI Article Synopsis

  • Glioblastoma multiforme is a highly aggressive brain tumor with a poor prognosis and low survival rates, primarily due to ineffective treatment options and invasive diagnostic methods.
  • The article emphasizes the need for novel, less invasive biomarkers, including genetic mutations (like IDH, MGMT, and EGFR) and microRNAs, to improve diagnosis and treatment outcomes for glioblastoma patients.
  • Recent advancements in clinical approaches to treating glioblastoma and preventing its relapse are also discussed, aiming to enhance patient care and therapeutic effectiveness.

Article Abstract

Glioblastoma multiforme is a serious and life-threatening tumor of central nervous system, characterized by aggressive behavior, poor prognosis, and low survival rate. Despite of the availability of aggressive antitumor therapeutic regimen for glioblastoma (radiotherapy followed by chemotherapeutic dose), recovery rate, and patients' survival ratio is attributed to the lack of selectivity of therapeutic drugs and less advancement in cancer therapeutics over last decade. Moreover, tools employed in conventional diagnosis of glioblastoma are more invasive and painful, making the process excruciating for the patients. These challenges urge for the need of novel biomarkers for diagnosis, prognosis, and prediction purpose with less invasiveness and more patient compliance. This article will explore the genetic biomarkers isocitrate dehydrogenase mutation, MGMT mutations, and EGFR that can be deployed as an analytical tool in diagnosis of disease and prognosis of a therapeutic course. The review also highlights the importance of employing novel microRNAs as prognostic biomarkers. Recent clinical advancements to treat GBM and to prevent relapse of the disease are also discussed in this article in the hope of finding a robust and effective method to treat GBM.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519330PMC
http://dx.doi.org/10.1155/2022/4022960DOI Listing

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