Use of microRNAs as Diagnostic, Prognostic, and Therapeutic Tools for Glioblastoma.
David Valle-GarciaVerónica Pérez de la CruzItamar FloresAleli SalazarBenjamín PinedaKarla F Meza-SosaPublished in: International journal of molecular sciences (2024)
Glioblastoma (GB) is the most aggressive and common type of cancer within the central nervous system (CNS). Despite the vast knowledge of its physiopathology and histology, its etiology at the molecular level has not been completely understood. Thus, attaining a cure has not been possible yet and it remains one of the deadliest types of cancer. Usually, GB is diagnosed when some symptoms have already been presented by the patient. This diagnosis is commonly based on a physical exam and imaging studies, such as computed tomography (CT) and magnetic resonance imaging (MRI), together with or followed by a surgical biopsy. As these diagnostic procedures are very invasive and often result only in the confirmation of GB presence, it is necessary to develop less invasive diagnostic and prognostic tools that lead to earlier treatment to increase GB patients' quality of life. Therefore, blood-based biomarkers (BBBs) represent excellent candidates in this context. microRNAs (miRNAs) are small, non-coding RNAs that have been demonstrated to be very stable in almost all body fluids, including saliva, serum, plasma, urine, cerebrospinal fluid (CFS), semen, and breast milk. In addition, serum-circulating and exosome-contained miRNAs have been successfully used to better classify subtypes of cancer at the molecular level and make better choices regarding the best treatment for specific cases. Moreover, as miRNAs regulate multiple target genes and can also act as tumor suppressors and oncogenes, they are involved in the appearance, progression, and even chemoresistance of most tumors. Thus, in this review, we discuss how dysregulated miRNAs in GB can be used as early diagnosis and prognosis biomarkers as well as molecular markers to subclassify GB cases and provide more personalized treatments, which may have a better response against GB. In addition, we discuss the therapeutic potential of miRNAs, the current challenges to their clinical application, and future directions in the field.
Keyphrases
- magnetic resonance imaging
- computed tomography
- papillary thyroid
- contrast enhanced
- cerebrospinal fluid
- squamous cell
- end stage renal disease
- chronic kidney disease
- positron emission tomography
- lymph node metastasis
- newly diagnosed
- physical activity
- childhood cancer
- genome wide
- combination therapy
- sleep quality
- dna methylation
- blood brain barrier
- dual energy
- case report
- young adults
- replacement therapy
- patient reported
- cancer stem cells
- genome wide identification
- bioinformatics analysis