Deborde chose to examine Schwann cells because it is one of the main components of the nerve and are in constant contact with the cancer cells in the peripheral nervous system, making them the perfect cells to study cancer invasion. Moreover, in response to a nerve injury, Schwann cells form tubes called “bands of hunger” to create a path for neurons and help direct them towards a specific target. Thus, Deborde hypothesized that Schwann cells would help guide cancer cells following the process of cancer invasion in a similar way to how Schwann cells help guide neurons during nerve repair. To test this hypothesis, Deborde injected cancer cells into the nerves of mice and found that there was a close association of a gene called GFAP (Glial fibrillary acidic protein) with Schwann cells and cancer cells. Moreover, after closely examining the dorsal root ganglion (DRG) explants from mice, Deborde was able to conclude that Schwann cells are responsible for recruiting cancer cells on DRG neurites. Deborde was also able discover that a regulator molecule called RA (retinoic acid) induces Schwann cell activation and increases Schwann cell migration. In contrast, Deborde
Deborde chose to examine Schwann cells because it is one of the main components of the nerve and are in constant contact with the cancer cells in the peripheral nervous system, making them the perfect cells to study cancer invasion. Moreover, in response to a nerve injury, Schwann cells form tubes called “bands of hunger” to create a path for neurons and help direct them towards a specific target. Thus, Deborde hypothesized that Schwann cells would help guide cancer cells following the process of cancer invasion in a similar way to how Schwann cells help guide neurons during nerve repair. To test this hypothesis, Deborde injected cancer cells into the nerves of mice and found that there was a close association of a gene called GFAP (Glial fibrillary acidic protein) with Schwann cells and cancer cells. Moreover, after closely examining the dorsal root ganglion (DRG) explants from mice, Deborde was able to conclude that Schwann cells are responsible for recruiting cancer cells on DRG neurites. Deborde was also able discover that a regulator molecule called RA (retinoic acid) induces Schwann cell activation and increases Schwann cell migration. In contrast, Deborde