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Exosomal PTEN as a Predictive Marker of Aggressive Gliomas
Sreekanth Patnam1, Rasmita Samal2, Rajeswari Koyyada3
1Apollo Hospitals Educational and Research Foundation (AHERF), Hyderabad; Indian Institute of Technology Hyderabad (IITH), Sangareddy, Telangana, India.
Liquid biopsies can detect Phosphatase and tensin homolog deleted in chromosome 10 (PTEN) and its downstream genes in glioma patient serum exosomes. This non-invasive method aids in identifying aggressive gliomas and assessing patient survival.
Area of Science:
- Oncology
- Molecular Biology
- Biomarkers
Background:
- Liquid biopsies offer a non-invasive alternative to traditional biopsies for disease detection and monitoring.
- Phosphatase and tensin homolog deleted in chromosome 10 (PTEN) is a critical tumor suppressor frequently altered in gliomas.
Purpose of the Study:
- To assess the feasibility of detecting PTEN and its downstream genes non-invasively in serum exosomes from glioma patients.
- To correlate exosomal PTEN expression with tumor tissue expression and patient survival.
Main Methods:
- PTEN, Yes-associated-protein 1 (YAP1), and lysyl oxidase (LOX) transcript expression were analyzed using polymerase chain reaction (PCR) in serum exosomes and paired tumor tissues.
- Sanger sequencing was employed to identify PTEN mutations.
- Overall survival (OS) was monitored in relation to PTEN and its axis genes expression.
Main Results:
- PTEN loss was observed in 32.9% of tumor samples and 32.9% of paired exosomal fractions.
- Upregulation of YAP1 and LOX was noted in PTEN-deficient samples.
- PTEN loss correlated with poorer patient survival, and exosomal PTEN levels mirrored tumor tissue PTEN status.
Conclusions:
- PTEN and its responsive genes YAP1 and LOX are detectable in serum exosomes.
- Serum exosomal PTEN and its axis genes serve as valuable non-invasive biomarkers for identifying aggressive gliomas.
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