Metastatic bladder cancer cells distinctively sense and respond to physical cues of collagen fibril-mimetic nanotopography

Tumor metastasis is characterized by enhanced invasiveness and migration of tumor cells through the extracellular matrix (ECM), resulting in extravasation into the blood and lymph and colonization at secondary sites. The ECM provides a physical scaffold consisting of components such as collagen fibr...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Experimental biology and medicine (Maywood, N.J.) N.J.), 2015-05, Vol.240 (5), p.601-610
Hauptverfasser: Iuliano, James N, Kutscha, Paul D, Biderman, NJ, Subbaram, Sita, Groves, Timothy R, Tenenbaum, Scott A, Hempel, Nadine
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 610
container_issue 5
container_start_page 601
container_title Experimental biology and medicine (Maywood, N.J.)
container_volume 240
creator Iuliano, James N
Kutscha, Paul D
Biderman, NJ
Subbaram, Sita
Groves, Timothy R
Tenenbaum, Scott A
Hempel, Nadine
description Tumor metastasis is characterized by enhanced invasiveness and migration of tumor cells through the extracellular matrix (ECM), resulting in extravasation into the blood and lymph and colonization at secondary sites. The ECM provides a physical scaffold consisting of components such as collagen fibrils, which have distinct dimensions at the nanoscale. In addition to the interaction of peptide moieties with tumor cell integrin clusters, the ECM provides a physical guide for tumor cell migration. Using nanolithography we set out to mimic the physical dimensions of collagen fibrils using lined nanotopographical silicon surfaces and to explore whether metastatic tumor cells are uniquely able to respond to these physical dimensions. Etched silicon surfaces containing nanoscale lined patterns with varying trench and ridge sizes (65–500 nm) were evaluated for their ability to distinguish between a non-metastatic (253J) and a highly metastatic (253J-BV) derivative bladder cancer cell line. Enhanced alignment was distinctively observed for the metastatic cell lines on feature sizes that mimic the dimensions of collagen fibrils (65–100 nm lines, 1:1–1:1.5 pitch). Further, these sub-100 nm lines acted as guides for migration of metastatic cancer cells. Interestingly, even at this subcellular scale, metastatic cell migration was abrogated when cells were forced to move perpendicular to these lines. Compared to flat surfaces, 65 nm lines enhanced the formation of actin stress fibers and filopodia of metastatic cells. This was accompanied by increased formation of focal contacts, visualized by immunofluorescent staining of phospho-focal adhesion kinase along the protruding lamellipodia. Simple lined nanotopography appears to be an informative platform for studying the physical cues of the ECM in a pseudo-3D format and likely mimics physical aspects of collagen fibrils. Metastatic cancer cells appear distinctively well adapted to sense these features using filopodia protrusions to enhance their alignment and migration.
doi_str_mv 10.1177/1535370214560973
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4615689</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_1535370214560973</sage_id><sourcerecordid>1680755158</sourcerecordid><originalsourceid>FETCH-LOGICAL-c500t-bdaeebde5af6ead7f0c8b57e3f7bf2f175bed3e85aed3d8ae133fb60965aaad43</originalsourceid><addsrcrecordid>eNp1UU2PFCEU7BiNu67ePRmOXlqhu4Gei4nZ-JWs8aJn8oDHLBsaWmA2GX-9dGZ3oyaeivCq6kFV171k9A1jUr5lfOSjpAObuKA7OT7qzrerfhS73eP7c5ufdc9KuaGUcTmIp93ZwCfBBzqdd7--YoVSoXpDdABrMRMD0WyAIRRifak-mupvMRxJwViQQLQkY1lTw5rIen0s3kAg5oCFJEdMCgH2GInzOvvQL37BbUGEmGpa0z5D0zzvnjgIBV_c4UX34-OH75ef-6tvn75cvr_qDae09toCorbIwQkEKx01s-YSRye1GxyTXKMdcebQwM6AbBydbnEIDgB2Gi-6dyff9aAXtAZjzRDUmv0C-agSePX3JPprtU-3ahKMi3nXDF7fGeT0s32xqsWXLR2ImA5FMTFTyTnjc6PSE9XkVEpG97CGUbVVpv6trEle_fm8B8F9R43QnwilZapu0iHHFtf_DX8DrZmkYg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1680755158</pqid></control><display><type>article</type><title>Metastatic bladder cancer cells distinctively sense and respond to physical cues of collagen fibril-mimetic nanotopography</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>SAGE Complete</source><source>PubMed Central</source><creator>Iuliano, James N ; Kutscha, Paul D ; Biderman, NJ ; Subbaram, Sita ; Groves, Timothy R ; Tenenbaum, Scott A ; Hempel, Nadine</creator><creatorcontrib>Iuliano, James N ; Kutscha, Paul D ; Biderman, NJ ; Subbaram, Sita ; Groves, Timothy R ; Tenenbaum, Scott A ; Hempel, Nadine</creatorcontrib><description>Tumor metastasis is characterized by enhanced invasiveness and migration of tumor cells through the extracellular matrix (ECM), resulting in extravasation into the blood and lymph and colonization at secondary sites. The ECM provides a physical scaffold consisting of components such as collagen fibrils, which have distinct dimensions at the nanoscale. In addition to the interaction of peptide moieties with tumor cell integrin clusters, the ECM provides a physical guide for tumor cell migration. Using nanolithography we set out to mimic the physical dimensions of collagen fibrils using lined nanotopographical silicon surfaces and to explore whether metastatic tumor cells are uniquely able to respond to these physical dimensions. Etched silicon surfaces containing nanoscale lined patterns with varying trench and ridge sizes (65–500 nm) were evaluated for their ability to distinguish between a non-metastatic (253J) and a highly metastatic (253J-BV) derivative bladder cancer cell line. Enhanced alignment was distinctively observed for the metastatic cell lines on feature sizes that mimic the dimensions of collagen fibrils (65–100 nm lines, 1:1–1:1.5 pitch). Further, these sub-100 nm lines acted as guides for migration of metastatic cancer cells. Interestingly, even at this subcellular scale, metastatic cell migration was abrogated when cells were forced to move perpendicular to these lines. Compared to flat surfaces, 65 nm lines enhanced the formation of actin stress fibers and filopodia of metastatic cells. This was accompanied by increased formation of focal contacts, visualized by immunofluorescent staining of phospho-focal adhesion kinase along the protruding lamellipodia. Simple lined nanotopography appears to be an informative platform for studying the physical cues of the ECM in a pseudo-3D format and likely mimics physical aspects of collagen fibrils. Metastatic cancer cells appear distinctively well adapted to sense these features using filopodia protrusions to enhance their alignment and migration.</description><identifier>ISSN: 1535-3702</identifier><identifier>EISSN: 1535-3699</identifier><identifier>DOI: 10.1177/1535370214560973</identifier><identifier>PMID: 25465204</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Cell Line, Tumor ; Collagen - metabolism ; Fluorescent Antibody Technique ; Humans ; Microscopy, Electron, Scanning ; Nanotechnology ; Neoplasm Metastasis ; Original Research ; Surface Properties ; Urinary Bladder Neoplasms - metabolism ; Urinary Bladder Neoplasms - pathology</subject><ispartof>Experimental biology and medicine (Maywood, N.J.), 2015-05, Vol.240 (5), p.601-610</ispartof><rights>2014 by the Society for Experimental Biology and Medicine</rights><rights>2014 by the Society for Experimental Biology and Medicine.</rights><rights>2014 by the Society for Experimental Biology and Medicine 2014 The Society for Experimental Biology and Medicine</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c500t-bdaeebde5af6ead7f0c8b57e3f7bf2f175bed3e85aed3d8ae133fb60965aaad43</citedby><cites>FETCH-LOGICAL-c500t-bdaeebde5af6ead7f0c8b57e3f7bf2f175bed3e85aed3d8ae133fb60965aaad43</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/PMC4615689/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615689/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,21798,27901,27902,43597,43598,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25465204$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iuliano, James N</creatorcontrib><creatorcontrib>Kutscha, Paul D</creatorcontrib><creatorcontrib>Biderman, NJ</creatorcontrib><creatorcontrib>Subbaram, Sita</creatorcontrib><creatorcontrib>Groves, Timothy R</creatorcontrib><creatorcontrib>Tenenbaum, Scott A</creatorcontrib><creatorcontrib>Hempel, Nadine</creatorcontrib><title>Metastatic bladder cancer cells distinctively sense and respond to physical cues of collagen fibril-mimetic nanotopography</title><title>Experimental biology and medicine (Maywood, N.J.)</title><addtitle>Exp Biol Med (Maywood)</addtitle><description>Tumor metastasis is characterized by enhanced invasiveness and migration of tumor cells through the extracellular matrix (ECM), resulting in extravasation into the blood and lymph and colonization at secondary sites. The ECM provides a physical scaffold consisting of components such as collagen fibrils, which have distinct dimensions at the nanoscale. In addition to the interaction of peptide moieties with tumor cell integrin clusters, the ECM provides a physical guide for tumor cell migration. Using nanolithography we set out to mimic the physical dimensions of collagen fibrils using lined nanotopographical silicon surfaces and to explore whether metastatic tumor cells are uniquely able to respond to these physical dimensions. Etched silicon surfaces containing nanoscale lined patterns with varying trench and ridge sizes (65–500 nm) were evaluated for their ability to distinguish between a non-metastatic (253J) and a highly metastatic (253J-BV) derivative bladder cancer cell line. Enhanced alignment was distinctively observed for the metastatic cell lines on feature sizes that mimic the dimensions of collagen fibrils (65–100 nm lines, 1:1–1:1.5 pitch). Further, these sub-100 nm lines acted as guides for migration of metastatic cancer cells. Interestingly, even at this subcellular scale, metastatic cell migration was abrogated when cells were forced to move perpendicular to these lines. Compared to flat surfaces, 65 nm lines enhanced the formation of actin stress fibers and filopodia of metastatic cells. This was accompanied by increased formation of focal contacts, visualized by immunofluorescent staining of phospho-focal adhesion kinase along the protruding lamellipodia. Simple lined nanotopography appears to be an informative platform for studying the physical cues of the ECM in a pseudo-3D format and likely mimics physical aspects of collagen fibrils. Metastatic cancer cells appear distinctively well adapted to sense these features using filopodia protrusions to enhance their alignment and migration.</description><subject>Cell Line, Tumor</subject><subject>Collagen - metabolism</subject><subject>Fluorescent Antibody Technique</subject><subject>Humans</subject><subject>Microscopy, Electron, Scanning</subject><subject>Nanotechnology</subject><subject>Neoplasm Metastasis</subject><subject>Original Research</subject><subject>Surface Properties</subject><subject>Urinary Bladder Neoplasms - metabolism</subject><subject>Urinary Bladder Neoplasms - pathology</subject><issn>1535-3702</issn><issn>1535-3699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1UU2PFCEU7BiNu67ePRmOXlqhu4Gei4nZ-JWs8aJn8oDHLBsaWmA2GX-9dGZ3oyaeivCq6kFV171k9A1jUr5lfOSjpAObuKA7OT7qzrerfhS73eP7c5ufdc9KuaGUcTmIp93ZwCfBBzqdd7--YoVSoXpDdABrMRMD0WyAIRRifak-mupvMRxJwViQQLQkY1lTw5rIen0s3kAg5oCFJEdMCgH2GInzOvvQL37BbUGEmGpa0z5D0zzvnjgIBV_c4UX34-OH75ef-6tvn75cvr_qDae09toCorbIwQkEKx01s-YSRye1GxyTXKMdcebQwM6AbBydbnEIDgB2Gi-6dyff9aAXtAZjzRDUmv0C-agSePX3JPprtU-3ahKMi3nXDF7fGeT0s32xqsWXLR2ImA5FMTFTyTnjc6PSE9XkVEpG97CGUbVVpv6trEle_fm8B8F9R43QnwilZapu0iHHFtf_DX8DrZmkYg</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Iuliano, James N</creator><creator>Kutscha, Paul D</creator><creator>Biderman, NJ</creator><creator>Subbaram, Sita</creator><creator>Groves, Timothy R</creator><creator>Tenenbaum, Scott A</creator><creator>Hempel, Nadine</creator><general>SAGE Publications</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150501</creationdate><title>Metastatic bladder cancer cells distinctively sense and respond to physical cues of collagen fibril-mimetic nanotopography</title><author>Iuliano, James N ; Kutscha, Paul D ; Biderman, NJ ; Subbaram, Sita ; Groves, Timothy R ; Tenenbaum, Scott A ; Hempel, Nadine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c500t-bdaeebde5af6ead7f0c8b57e3f7bf2f175bed3e85aed3d8ae133fb60965aaad43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Cell Line, Tumor</topic><topic>Collagen - metabolism</topic><topic>Fluorescent Antibody Technique</topic><topic>Humans</topic><topic>Microscopy, Electron, Scanning</topic><topic>Nanotechnology</topic><topic>Neoplasm Metastasis</topic><topic>Original Research</topic><topic>Surface Properties</topic><topic>Urinary Bladder Neoplasms - metabolism</topic><topic>Urinary Bladder Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iuliano, James N</creatorcontrib><creatorcontrib>Kutscha, Paul D</creatorcontrib><creatorcontrib>Biderman, NJ</creatorcontrib><creatorcontrib>Subbaram, Sita</creatorcontrib><creatorcontrib>Groves, Timothy R</creatorcontrib><creatorcontrib>Tenenbaum, Scott A</creatorcontrib><creatorcontrib>Hempel, Nadine</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iuliano, James N</au><au>Kutscha, Paul D</au><au>Biderman, NJ</au><au>Subbaram, Sita</au><au>Groves, Timothy R</au><au>Tenenbaum, Scott A</au><au>Hempel, Nadine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metastatic bladder cancer cells distinctively sense and respond to physical cues of collagen fibril-mimetic nanotopography</atitle><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle><addtitle>Exp Biol Med (Maywood)</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>240</volume><issue>5</issue><spage>601</spage><epage>610</epage><pages>601-610</pages><issn>1535-3702</issn><eissn>1535-3699</eissn><abstract>Tumor metastasis is characterized by enhanced invasiveness and migration of tumor cells through the extracellular matrix (ECM), resulting in extravasation into the blood and lymph and colonization at secondary sites. The ECM provides a physical scaffold consisting of components such as collagen fibrils, which have distinct dimensions at the nanoscale. In addition to the interaction of peptide moieties with tumor cell integrin clusters, the ECM provides a physical guide for tumor cell migration. Using nanolithography we set out to mimic the physical dimensions of collagen fibrils using lined nanotopographical silicon surfaces and to explore whether metastatic tumor cells are uniquely able to respond to these physical dimensions. Etched silicon surfaces containing nanoscale lined patterns with varying trench and ridge sizes (65–500 nm) were evaluated for their ability to distinguish between a non-metastatic (253J) and a highly metastatic (253J-BV) derivative bladder cancer cell line. Enhanced alignment was distinctively observed for the metastatic cell lines on feature sizes that mimic the dimensions of collagen fibrils (65–100 nm lines, 1:1–1:1.5 pitch). Further, these sub-100 nm lines acted as guides for migration of metastatic cancer cells. Interestingly, even at this subcellular scale, metastatic cell migration was abrogated when cells were forced to move perpendicular to these lines. Compared to flat surfaces, 65 nm lines enhanced the formation of actin stress fibers and filopodia of metastatic cells. This was accompanied by increased formation of focal contacts, visualized by immunofluorescent staining of phospho-focal adhesion kinase along the protruding lamellipodia. Simple lined nanotopography appears to be an informative platform for studying the physical cues of the ECM in a pseudo-3D format and likely mimics physical aspects of collagen fibrils. Metastatic cancer cells appear distinctively well adapted to sense these features using filopodia protrusions to enhance their alignment and migration.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>25465204</pmid><doi>10.1177/1535370214560973</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1535-3702
ispartof Experimental biology and medicine (Maywood, N.J.), 2015-05, Vol.240 (5), p.601-610
issn 1535-3702
1535-3699
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4615689
source MEDLINE; EZB-FREE-00999 freely available EZB journals; SAGE Complete; PubMed Central
subjects Cell Line, Tumor
Collagen - metabolism
Fluorescent Antibody Technique
Humans
Microscopy, Electron, Scanning
Nanotechnology
Neoplasm Metastasis
Original Research
Surface Properties
Urinary Bladder Neoplasms - metabolism
Urinary Bladder Neoplasms - pathology
title Metastatic bladder cancer cells distinctively sense and respond to physical cues of collagen fibril-mimetic nanotopography
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T04%3A26%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Metastatic%20bladder%20cancer%20cells%20distinctively%20sense%20and%20respond%20to%20physical%20cues%20of%20collagen%20fibril-mimetic%20nanotopography&rft.jtitle=Experimental%20biology%20and%20medicine%20(Maywood,%20N.J.)&rft.au=Iuliano,%20James%20N&rft.date=2015-05-01&rft.volume=240&rft.issue=5&rft.spage=601&rft.epage=610&rft.pages=601-610&rft.issn=1535-3702&rft.eissn=1535-3699&rft_id=info:doi/10.1177/1535370214560973&rft_dat=%3Cproquest_pubme%3E1680755158%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1680755158&rft_id=info:pmid/25465204&rft_sage_id=10.1177_1535370214560973&rfr_iscdi=true