In work that could improve understanding of how cancer spreads, a team of engineers and medical researchers at the University of Michigan developed a new kind of microfluidic chip that can capture rare, aggressive cancer cells, grow them on the chip and release single cells on demand.

For the first time, they can easily compare two different "sister" cells – born of the same original cancer cell – to explore how different genes are activated and deactivated as cancer cells divide and spread. Studies with the new chip could also reveal why some cancer cells are resistant to drugs.

The ultimate goal of the project—led by Euisik Yoon, professor of electrical engineering and computer science – is to find out what drives the "self–renewal" processes that enable these aggressive cancer cells to behave like stem cells.

These cells are known as cancer stem cells. They are capable of dividing and turning into different kinds of cancer cells, with different genes turned on or off. Cancer researchers believe that if the stem–like properties can be switched off, the cancer will not be able to grow and spread.

"When a tumor forms, some cancer stem cells maintain stemness, while others are differentiated. By understanding this, we will know more about tumor formation and discover ways to inhibit it," said Yu–Chih Chen, a research scientist in electrical engineering and computer science and co–first–author on a paper newly published in the journal ACS Nano.

The base of the new chip is composed of carbon nanotubes covered in a plastic coating. When a cancer cell settles on the chip, it sticks itself to that coating. To release the cell, the researchers shone extremely short pulses of laser light near it. The light is readily absorbed by the carbon nanotubes, flash–heating them, while the plastic insulates the cell.

The heat causes trapped air between the nanotubes and plastic to expand, blowing a bubble under the cell. When the bubble bursts through the plastic, the cell detaches. Then, the cell can be flushed out of the chip and captured for genetic profiling.

Most existing methods for freeing individual captured cancer cells are either damaging to the cells or else cannot get them out of the chip reliably. The laser was precise enough that it could detach one side of a cell, leaving the other side anchored.

And the bubble detachment process was so gentle that even surface proteins on the cell membrane were unscathed. The surface proteins are an important nondestructive avenue for identifying cancer stem cells.

To begin exploring the differences in gene expression between sister cells, the team first looked at a gene called Notch, which is associated with both normal and cancerous stem cells. If Notch was expressed in the daughter cells, it was a rough indication that the division was self–renewing. A Notch–positive cell could go on to produce two cells expressing the same gene, one Notch–positive and one Notch–negative, or two Notch–negative cells.

Their analyses demonstrated that Notch does not serve as a sole indicator for a cancer cell's stem–like properties. Other genes associated with stem cells could be switched on or switched off in daughter cells with either Notch expression.

The task ahead of cancer researchers, with the help of the new chip, is to identify which of these genes are critical to a cancer stem cell's self–renewing capabilities. If these can be shut down, forcing all cancer stem cells to produce only nonstem cells when they divide, it may be possible to subvert a tumor's ability to grow and spread.

This work is reported in a paper titled "Selective photo–mechanical detachment and retrieval of divided sister cells from enclosed microfluidics for downstream analyses."