Main Components of Liquid Biopsy are Greater than itSeems? by Seyed Mohammad Tavangar in OAJOM in Lupine Publishers.
Long time ago it was wrongly thought that tumor genes and cells
are only existence in the exact tumor site. In spite of the fact of the
hypothesis that circulating tumor cells (CTCs) are a fundamental
prerequisite to metastasis ( first projected in the 1896 by Thomas
Ashworth, an Australian pathologist, ) and the presence of cfDNA
report in human plasma by Mandel and Metals in 1948, liquid
biopsy were totally ignored till 1977. In 1977, researchers made
the novel observation that cancer patients carried cell-free DNA
in their peripheral blood which was Initial progress on further of
liquid biopsy. Without a doubt, significant progress was not made
until recent years with the advent of Next Generation Sequencing
(NGS) technology, which significantly improved the sensitivity and
specificity of ctDNA detection. Interestingly, research in this field of
liquid biopsy has entered a “golden age” in which the huge potential
of liquid biopsy main components including CTCs, cfDNA and
exosomes make tumor diagnosis and treatment much clearer than
before. Liquid biopsy tests are fast traction as a viable substitute
to traditional diagnostic tests for cancer. It has the potential to
facilitate detect cancer at earlier stages, present a less-expensive
and less-invasive way to monitor patients throughout treatment,
and can help doctors make better decisions about which drugs are
the best fit for personal patients.
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