Schwann cells induce cancer cell dispersion and invasion
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 contrib...
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Veröffentlicht in: | The Journal of clinical investigation 2016-04, Vol.126 (4), p.1538-1554 |
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creator | Deborde, Sylvie Omelchenko, Tatiana Lyubchik, Anna Zhou, Yi He, Shizhi McNamara, William F Chernichenko, Natalya Lee, Sei-Young Barajas, Fernando Chen, Chun-Hao Bakst, Richard L Vakiani, Efsevia He, Shuangba Hall, Alan Wong, Richard J |
description | 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. |
doi_str_mv | 10.1172/JCI82658 |
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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.</description><identifier>ISSN: 0021-9738</identifier><identifier>EISSN: 1558-8238</identifier><identifier>DOI: 10.1172/JCI82658</identifier><identifier>PMID: 26999607</identifier><language>eng</language><publisher>United States: American Society for Clinical Investigation</publisher><subject>Animals ; Biomedical research ; Cancer cells ; CD56 Antigen - metabolism ; Cell Line, Tumor ; Cell proliferation ; Coculture Techniques ; Experiments ; Growth ; Health aspects ; Humans ; Mice ; Mice, Nude ; Neoplasm Invasiveness ; Neoplasms, Experimental - metabolism ; Neoplasms, Experimental - pathology ; NIH 3T3 Cells ; Proteins ; Schwann cells ; Schwann Cells - metabolism ; Schwann Cells - pathology ; Software ; Studies ; Thyroid cancer</subject><ispartof>The Journal of clinical investigation, 2016-04, Vol.126 (4), p.1538-1554</ispartof><rights>COPYRIGHT 2016 American Society for Clinical Investigation</rights><rights>Copyright American Society for Clinical Investigation Apr 2016</rights><rights>Copyright © 2016, American Society for Clinical Investigation 2016 American Society for Clinical Investigation</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-1aba89ed8a289e729dfd9616483d7cd0fc5d7cbb922501b3cf54db74d0998bf3</citedby><cites>FETCH-LOGICAL-c503t-1aba89ed8a289e729dfd9616483d7cd0fc5d7cbb922501b3cf54db74d0998bf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811155/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811155/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26999607$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Deborde, Sylvie</creatorcontrib><creatorcontrib>Omelchenko, Tatiana</creatorcontrib><creatorcontrib>Lyubchik, Anna</creatorcontrib><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>He, Shizhi</creatorcontrib><creatorcontrib>McNamara, William F</creatorcontrib><creatorcontrib>Chernichenko, Natalya</creatorcontrib><creatorcontrib>Lee, Sei-Young</creatorcontrib><creatorcontrib>Barajas, Fernando</creatorcontrib><creatorcontrib>Chen, Chun-Hao</creatorcontrib><creatorcontrib>Bakst, Richard L</creatorcontrib><creatorcontrib>Vakiani, Efsevia</creatorcontrib><creatorcontrib>He, Shuangba</creatorcontrib><creatorcontrib>Hall, Alan</creatorcontrib><creatorcontrib>Wong, Richard J</creatorcontrib><title>Schwann cells induce cancer cell dispersion and invasion</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>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.</description><subject>Animals</subject><subject>Biomedical research</subject><subject>Cancer cells</subject><subject>CD56 Antigen - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Cell proliferation</subject><subject>Coculture Techniques</subject><subject>Experiments</subject><subject>Growth</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasms, Experimental - metabolism</subject><subject>Neoplasms, Experimental - pathology</subject><subject>NIH 3T3 Cells</subject><subject>Proteins</subject><subject>Schwann cells</subject><subject>Schwann Cells - metabolism</subject><subject>Schwann Cells - pathology</subject><subject>Software</subject><subject>Studies</subject><subject>Thyroid cancer</subject><issn>0021-9738</issn><issn>1558-8238</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkUtrGzEUhUVpqB230F9QBgolm0mvXiNpEwgmTwxd1HuhkTT2mLHGkWYS8u8rx0maZtPVQdLH0b3nIPQVwynGgvy8nd9IUnH5AU0x57KUhMqPaApAcKkElRN0nNIGADPG2Sc0IZVSqgIxRfK3XT-YEArruy4VbXCj9YU1wfr4dFe4Nu18TG0fChNcJu7N_vAZHTWmS_7Ls87Q8vJiOb8uF7-ububni9JyoEOJTW2k8k4akkUQ5RqnKlwxSZ2wDhrLs9a1IoQDrqltOHO1YA6UknVDZ-jsYLsb66131ochmk7vYrs18VH3ptX_voR2rVf9vWYS45xFNjh5Noj93ejToLdt2i9mgu_HpLGQnBABeaD_o0IoSRngjH5_h276MYYcxN4QABjNuc_QjwO1Mp3Xa2-6YZ36bhxyfkmfMw5EcCLE359t7FOKvnldEIPeN6xfGs7ot7eBvIIvldI_f7afVg</recordid><startdate>20160401</startdate><enddate>20160401</enddate><creator>Deborde, Sylvie</creator><creator>Omelchenko, Tatiana</creator><creator>Lyubchik, Anna</creator><creator>Zhou, Yi</creator><creator>He, Shizhi</creator><creator>McNamara, William F</creator><creator>Chernichenko, Natalya</creator><creator>Lee, Sei-Young</creator><creator>Barajas, Fernando</creator><creator>Chen, Chun-Hao</creator><creator>Bakst, Richard L</creator><creator>Vakiani, Efsevia</creator><creator>He, Shuangba</creator><creator>Hall, Alan</creator><creator>Wong, Richard J</creator><general>American Society for Clinical Investigation</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>S0X</scope><scope>7X8</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20160401</creationdate><title>Schwann cells induce cancer cell dispersion and invasion</title><author>Deborde, Sylvie ; Omelchenko, Tatiana ; Lyubchik, Anna ; Zhou, Yi ; He, Shizhi ; McNamara, William F ; Chernichenko, Natalya ; Lee, Sei-Young ; Barajas, Fernando ; Chen, Chun-Hao ; Bakst, Richard L ; Vakiani, Efsevia ; He, Shuangba ; Hall, Alan ; Wong, Richard J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-1aba89ed8a289e729dfd9616483d7cd0fc5d7cbb922501b3cf54db74d0998bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Biomedical research</topic><topic>Cancer cells</topic><topic>CD56 Antigen - 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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. 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subjects | Animals Biomedical research Cancer cells CD56 Antigen - metabolism Cell Line, Tumor Cell proliferation Coculture Techniques Experiments Growth Health aspects Humans Mice Mice, Nude Neoplasm Invasiveness Neoplasms, Experimental - metabolism Neoplasms, Experimental - pathology NIH 3T3 Cells Proteins Schwann cells Schwann Cells - metabolism Schwann Cells - pathology Software Studies Thyroid cancer |
title | Schwann cells induce cancer cell dispersion and invasion |
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