"Liquid biopsy” could one day inform decisions about the right therapy at the right time
Bethesda, MD - The ability to detect circulating tumor cells (CTCs) as they travel through the blood can play an important role in early diagnosis, characterization of cancer subtypes, treatment monitoring and metastasis. By measuring a patient’s CTC levels over time, clinicians can quickly determine if a particular cancer treatment is working.
CTCs can also be tested to identify genetic mutations associated with a tumor. Many newer cancer medications are designed to target specific genetic mutations, so they work best for limited types and stages of cancer. CTCs can provide a quick method to help physicians choose the most appropriate targeted therapy for a particular patient.
The potential benefits of CTCs abound. But with only one CTC for every one billion blood cells, finding any CTCs at all presents a significant challenge.
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With NIBIB funding, Mehmet Toner, Ph.D., and his research team at the Massachusetts General Hospital Cancer Center have been working to create a monitoring device centered on CTCs.
The researchers’ previously developed devices could reliably sort CTCs from the other types of cells in whole blood—namely, red blood cells, white blood cells, and platelets. But the CTCs could not be easily retrieved for further testing.
Seeking to improve their design, the researchers’ newest iteration of their “cancer lab on a chip,” the CTC-iChip, integrates several principles of magnetism and microfluidics to provide high-speed, automated sorting of the rare cells and can be applied to almost any type of cancer.
After collecting a blood sample, the researchers mixed the sample with tiny, magnetic beads coated with specific antibodies. In some cases, the researchers used antibodies that seek out and attach to CTCs, and in other cases they used antibodies that bind to white blood cells. This magnetic labeling would come into play later in the microfluidic sorting process.
In the first stage of the device, the whole blood (with magnetized cells) is sorted through an array of microposts that separates the various cells by size. Red blood cells, platelets, and other smaller particles are directed out of the device, while larger cells—including CTCs—flow into the next stage of the device.
A series of S-shaped curves aligns the remaining cells into a single file, a process known as inertial focusing. The cells then pass through a slight magnetic field, quickly and easily separating magnetically labeled cells from unlabeled cells.
While seemingly simple in concept, the inertial focusing mechanism is a significant advance in CTC isolation technology. Magnetic separation had been studied as a way to sort cells, but previous methods required relatively large magnetic beads or a large number of beads to be attached to cells. This often limited the yield or purity of the collected CTC sample. In Toner’s CTC-iChip, because the cells pass through the field one at a time, only a few small beads per cell are needed.
Toner and colleagues tested their device using positive and negative depletion methods.
Positive depletion identifies CTCs using antibodies that latch onto the protein EpCAM, commonly found on the surface of CTCs. Current commercially available CTC-sorting devices are based on positive depletion, and the CTC-iChip also successfully isolated magnetically labeled CTCs with this method. However, not all tumor cells produce EpCAM, and some studies suggest those that do may produce less EpCAM both in their earliest stages of growth and in later stages as they begin to metastasize; thus, the clinical usefulness of the positive depletion method is limited.
Negative depletion, in contrast, sorts out CTCs by eliminating all other “known” cells first. By magnetically labeling white blood cells rather than CTCs, the researchers were able to isolate a vast array of unlabeled tumor cells using CTC-iChip. Negative depletion allows for the detection of CTCs without having to know what type of tumor they came from beforehand and regardless of whether they produce EpCAM. Thus, negative depletion methods may be able to identify a greater variety of tumors across a broader range of development than positive depletion.
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