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Overview of Exosomes01:36

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Exosomes are stable, lipid bilayer-enclosed vesicles capable of crossing biological barriers. They can carry a wide range of molecules required for intercellular communication. Once exosomes are released from the cell where they originated, they enter a recipient cell through various pathways such as fusion, receptor-mediated endocytosis, macropinocytosis, and phagocytosis.
Stahl et al. discovered exosomes in 1983, but the exosomes were initially considered waste products released from the...
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Exosomal miRNA Analysis in Non-small Cell Lung Cancer NSCLC Patients' Plasma Through qPCR: A Feasible Liquid Biopsy Tool
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Chimeric RNA and Exosomes-Based Liquid Biopsy.

Xiurong Ke1,2, Xiao Xiong1, Yusheng Lin1,3

  • 1Cancer Research Center, Shantou University Medical College, Shantou, Guangdong, China.

Methods in Molecular Biology (Clifton, N.J.)
|November 16, 2019
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Chimeric RNA in exosomes from patient fluids can be detected using a novel RT-qPCR method. This approach offers a new strategy for disease diagnosis by analyzing exosome biomarkers.

Keywords:
Disease diagnosisExosomal chimeric RNAExosome extraction and purificationLiquid biopsyRT-qPCR

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Area of Science:

  • Biochemistry
  • Molecular Biology
  • Biotechnology

Background:

  • Exosomes are recognized as valuable sources of disease biomarkers due to their stability and cargo of genetic material and proteins.
  • Previous research has shown that chimeric RNA within exosomes from patient fluids can be detected and utilized for disease diagnosis.

Purpose of the Study:

  • To present a systematic methodology for isolating exosomes from various body fluids.
  • To establish a reliable RT-qPCR (reverse transcription quantitative polymerase chain reaction) strategy for detecting specific chimeric RNA expression within these exosomes.

Main Methods:

  • Isolation of exosomes from patient body fluids using a standardized protocol.
  • RNA extraction from the isolated exosomes.
  • Detection and quantification of specific chimeric RNA sequences via RT-qPCR.

Main Results:

  • Successful isolation of exosomes from diverse body fluid samples.
  • Demonstration of the RT-qPCR strategy's efficacy in detecting target chimeric RNA.
  • Validation of the method for potential diagnostic applications.

Conclusions:

  • The described systematic method enables efficient exosome isolation and chimeric RNA detection.
  • This approach provides a robust tool for disease diagnosis based on exosomal RNA biomarkers.
  • Further application of this method can advance non-invasive diagnostic strategies.