TY - JOUR
T1 - Schwann cells induce cancer cell dispersion and invasion
AU - Deborde, Sylvie
AU - Omelchenko, Tatiana
AU - Lyubchik, Anna
AU - Zhou, Yi
AU - He, Shizhi
AU - McNamara, William F.
AU - Chernichenko, Natalya
AU - Lee, Sei Young
AU - Barajas, Fernando
AU - Chen, Chun Hao
AU - Bakst, Richard L.
AU - Vakiani, Efsevia
AU - He, Shuangba
AU - Hall, Alan
AU - Wong, Richard J.
N1 - Funding Information:
This work was supported by NIH grants CA157686 (to R.J. Wong) and P30 CA008748 (Memorial Sloan Kettering Cancer Center support grant). The authors dedicate this work to the memory of Alan Hall.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Nerves enable cancer progression, as cancers have been shown to extend along nerves through the process of perineural invasion, which carries a poor prognosis. Furthermore, the innervation of some cancers promotes growth and metastases. It remains unclear, however, how nerves mechanistically contribute to cancer progression. Here, we demonstrated that Schwann cells promote cancer invasion through direct cancer cell contact. Histological evaluation of murine and human cancer specimens with perineural invasion uncovered a subpopulation of Schwann cells that associates with cancer cells. Coculture of cancer cells with dorsal root ganglion extracts revealed that Schwann cells direct cancer cells to migrate toward nerves and promote invasion in a contact-dependent manner. Upon contact, Schwann cells induced the formation of cancer cell protrusions in their direction and intercalated between the cancer cells, leading to cancer cell dispersion. The formation of these processes was dependent on Schwann cell expression of neural cell adhesion molecule 1 (NCAM1) and ultimately promoted perineural invasion. Moreover, NCAM1-deficient mice showed decreased neural invasion and less paralysis. Such Schwann cell behavior reflects normal Schwann cell programs that are typically activated in nerve repair but are instead exploited by cancer cells to promote perineural invasion and cancer progression.
AB - Nerves enable cancer progression, as cancers have been shown to extend along nerves through the process of perineural invasion, which carries a poor prognosis. Furthermore, the innervation of some cancers promotes growth and metastases. It remains unclear, however, how nerves mechanistically contribute to cancer progression. Here, we demonstrated that Schwann cells promote cancer invasion through direct cancer cell contact. Histological evaluation of murine and human cancer specimens with perineural invasion uncovered a subpopulation of Schwann cells that associates with cancer cells. Coculture of cancer cells with dorsal root ganglion extracts revealed that Schwann cells direct cancer cells to migrate toward nerves and promote invasion in a contact-dependent manner. Upon contact, Schwann cells induced the formation of cancer cell protrusions in their direction and intercalated between the cancer cells, leading to cancer cell dispersion. The formation of these processes was dependent on Schwann cell expression of neural cell adhesion molecule 1 (NCAM1) and ultimately promoted perineural invasion. Moreover, NCAM1-deficient mice showed decreased neural invasion and less paralysis. Such Schwann cell behavior reflects normal Schwann cell programs that are typically activated in nerve repair but are instead exploited by cancer cells to promote perineural invasion and cancer progression.
UR - http://www.scopus.com/inward/record.url?scp=84964608177&partnerID=8YFLogxK
U2 - 10.1172/JCI82658
DO - 10.1172/JCI82658
M3 - Article
C2 - 26999607
AN - SCOPUS:84964608177
SN - 0021-9738
VL - 126
SP - 1538
EP - 1554
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
IS - 4
ER -