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Schwann cells induce cancer cell dispersion and invasion
Sylvie Deborde, Tatiana Omelchenko, Anna Lyubchik, Yi Zhou, Shizhi He, William F. McNamara, Natalya Chernichenko, Sei-Young Lee, Fernando Barajas, Chun-Hao Chen, Richard L. Bakst, Efsevia Vakiani, Shuangba He, Alan Hall, Richard J. Wong
Sylvie Deborde, Tatiana Omelchenko, Anna Lyubchik, Yi Zhou, Shizhi He, William F. McNamara, Natalya Chernichenko, Sei-Young Lee, Fernando Barajas, Chun-Hao Chen, Richard L. Bakst, Efsevia Vakiani, Shuangba He, Alan Hall, Richard J. Wong
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Research Article Cell biology Oncology

Schwann cells induce cancer cell dispersion and invasion

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Abstract

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.

Authors

Sylvie Deborde, Tatiana Omelchenko, Anna Lyubchik, Yi Zhou, Shizhi He, William F. McNamara, Natalya Chernichenko, Sei-Young Lee, Fernando Barajas, Chun-Hao Chen, Richard L. Bakst, Efsevia Vakiani, Shuangba He, Alan Hall, Richard J. Wong

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Figure 6

Schwann cells induce cancer cell protrusions and intercalate between cancer cells.

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Schwann cells induce cancer cell protrusions and intercalate between can...
(A) Heterocellular contact induces protrusions in cancer cells. Time-lapse images of dynamic interactions of MiaPaCa-2 cells and a Schwann cell showing heterocellular contact and the formation of a cancer cell protrusion directed toward the Schwann cell (see Supplemental Video 3D). Quantification of cancer cell protrusion directionality measured on cancer cells with one site of contact with Schwann cells at a time. The images were rotated with the superior y axis representing the Schwann cell position on the image in which the Schwann cell and cancer cell were in contact before the formation of protrusion (n = 8 cells). (B) Schwann cells intercalate between cancer cells. Time-lapse images showing Schwann cell protrusions intercalating between cancer cells. The image at time 0:00 corresponds to the indicated boxed area in Figure 5C. White arrows show Schwann cell protrusions. Empty arrows show cancer cell–cancer cell contacts. Note weaker cancer cell–cancer cell contact at time 1:40 after Schwann cell intercalation and a stronger cancer cell–cancer cell contact at time 0:00 before intercalation (see Supplemental Video 3C). (C) The sequence of events — contact, protrusion, intercalation, and migration. Images show cancer cell (asterisk) dissociation after Schwann cell intercalation (see Supplemental Video 3E). The timeline of events after heterocellular contact and subsequent formation of cancer cell protrusion shows sequence and frequency of following events: contact, protrusion, intercalation, and migration (total n of events = 80). Although protrusions occur frequently after contact, migration mostly occurs after intercalation. Numbers along the y axis refer to events following Schwann cell–cancer cell contact and cancer cell protrusion. Scale bar: 50 μm. Times are shown as hours and minutes.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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