Regardless of the intrusive and exhaustive diagnosis being followed, a new and simple blood test can diagnose, monitor and tailor appropriate treatment plans for different cancer types.
A simple blood test can diagnose, monitor and tailor appropriate therapies for different cancers, a breakthrough research by Professor Ryan Kelly of Brigham Young University. Monitoring cancer through biopsy and spinal taps is an intrusive and exhaustive process for patients.// Creating therapies for cancer patients is greatly enhanced when doctors know about the biochemical makeup of tumors, including what proteins are present and at what levels. For this project, recently published in top-ranked journal Analytical Chemistry, Kelly collaborated with researchers from the Pacific Northwest National Laboratory and Oregon Health & Science University to isolate circulating tumor cells (CTCs) from blood and determine which proteins were present.
‘‘The blood test comprises of isolating circulating tumor cells (CTC) from blood and measuring the proteins present in it, which further helps the physicians to continue or modify the treatment accordingly’.’
Their technique uses a new technology, called nanopots, to capture more protein information from a single cell than ever before. CTCs are extremely rare cells that have shed from a tumor and are carried around the body, acting as seeds for the growth of additional tumors in distant organs. Traditionally, learning about the protein makeup of a blood or tissue sample has required thousands or millions of cells. Because CTCs are so rare, their proteins could not be studied.
"It used to be that the only thing you could do with CTCs is count them, which would usually correlate with cancer," said Kelly. "But it's not always effective. We want to get beyond that."
By measuring the proteins in CTCs, physicians will be better equipped to know what is working with a therapy regimen and continue or modify treatment accordingly.
"Targeted approaches for studying proteins from single cells have been around for a while, but the problem is you have to know exactly what you're looking for," Kelly said. "What we are doing is cataloging as many proteins as possible from single cells, without having to pick what we're looking for beforehand. Nobody's done that before with small numbers of CTCs."
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"We would like to know how a therapy is impacting a cancer without having to do an invasive biopsy every time," Kelly said. "We're excited about the implications this could have in the long run for cancer diagnosis, treatment and the development of new therapeutic approaches."
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Source-Eurekalert