Key Genes Associated with Cancer Found in Circulating Blood Microvesicles
The research team also revealed that when tumors have amplification of certain oncogene sequences like c-Myc, this is reflected in the microvesicles isolated from the blood. "Increased levels of the oncogene c-Myc has been shown to play a role in cancer tumor progression and is typically associated with poor prognosis in medulloblastomas, the most common malignant brain tumor in children" says the first author Leonora Balaj at Massachusetts General Hospital.
Together, these findings expand the nucleic acid content of tumour microvesicles to include: elevated levels of certain coding and non-coding RNA and DNA, mutated and amplified oncogene sequences and transposable elements.
“This research could have significant implications for diagnosis and ongoing management of cancers,” said Dr. Skog, lead author on the paper and now Director of Research at Exosome Diagnostics. "The extensive variety of oncology biomarkers found in microvesicles can help enable diagnosis of disease, and provide insights to the precise mechanisms at play through disease progression in a particular patient.”
Exosome Diagnostics is developing a number of high-sensitivity blood and urine based molecular diagnostic tests from exosomes and other microvesicles with a focus on key gene expressions and mutations that can be targeted in therapeutic intervention and monitoring of disease recurrence. Detection of key genetic biomarkers in patient blood and urine samples is challenging because of the need for high sensitivity against a background of normal cellular DNA and RNA. Microvesicles contain DNA and RNA from the cell of origin, and because they efficiently store and protect their DNA and RNA, microvesicles released into the circulation can provide a window into the genetic profile of an individual’s tumour or other disease condition.
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