Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/54413
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dc.contributor.authorLiu, Linanen
dc.contributor.authorZhang, Shirley Xen
dc.contributor.authorLiao, Wenbinen
dc.contributor.authorFarhoodi, Henry Pen
dc.contributor.authorWong, Chi Wen
dc.contributor.authorChen, Claire Cen
dc.contributor.authorSégaliny, Aude Ien
dc.contributor.authorChacko, Jenu Ven
dc.contributor.authorNguyen, Lily Pen
dc.contributor.authorLu, Mengrouen
dc.contributor.authorPolovin, Georgeen
dc.contributor.authorPone, Egest Jen
dc.contributor.authorDowning, Timothy Len
dc.contributor.authorLawson, Devon Aen
dc.contributor.authorDigman, Michelle Aen
dc.contributor.authorZhao, Weianen
dc.date.accessioned2023-03-27T23:57:00Z-
dc.date.available2023-03-27T23:57:00Z-
dc.date.issued2017-07-26-
dc.identifier.citationScience Translational Medicine, 9(400), p. 1-12en
dc.identifier.issn1946-6242en
dc.identifier.issn1946-6234en
dc.identifier.urihttps://hdl.handle.net/1959.11/54413-
dc.description.abstract<p>Despite decades of effort, little progress has been made to improve the treatment of cancer metastases. To leverage the central role of the mechanoenvironment in cancer metastasis, we present a mechanoresponsive cell system (MRCS) to selectively identify and treat cancer metastases by targeting the specific biophysical cues in the tumor niche in vivo. Our MRCS uses mechanosensitive promoter-driven mesenchymal stem cell (MSC-based vectors, which selectively home to and target cancer metastases in response to specific mechanical cues to deliver therapeutics to effectively kill cancer cells, as demonstrated in a metastatic breast cancer mouse model. Our data suggest a strong correlation between collagen cross-linking and increased tissue stiffness at the metastatic sites, where our MRCS is specifically activated by the specific cancer-associated mechano-cues. MRCS has markedly reduced deleterious effects compared to MSCs constitutively expressing therapeutics. MRCS indicates that biophysical cues, specifically matrix stiffness, are appealing targets for cancer treatment due to their long persistence in the body (measured in years), making them refractory to the development of resistance to treatment. Our MRCS can serve as a platform for future diagnostics and therapies targeting aberrant tissue stiffness in conditions such as cancer and fibrotic diseases, and it should help to elucidate mechanobiology and reveal what cells "feel" in the microenvironment in vivo.</p>en
dc.languageenen
dc.publisherAmerican Association for the Advancement of Science (AAAS)en
dc.relation.ispartofScience Translational Medicineen
dc.titleMechanoresponsive stem cells to target cancer metastases through biophysical cuesen
dc.typeJournal Articleen
dc.identifier.doi10.1126/scitranslmed.aan2966en
dc.identifier.pmid28747514en
dc.subject.keywordsCell Biologyen
dc.subject.keywordsResearch & Experimental Medicineen
dc.subject.keywordsMedicine, Research & Experimentalen
local.contributor.firstnameLinanen
local.contributor.firstnameShirley Xen
local.contributor.firstnameWenbinen
local.contributor.firstnameHenry Pen
local.contributor.firstnameChi Wen
local.contributor.firstnameClaire Cen
local.contributor.firstnameAude Ien
local.contributor.firstnameJenu Ven
local.contributor.firstnameLily Pen
local.contributor.firstnameMengrouen
local.contributor.firstnameGeorgeen
local.contributor.firstnameEgest Jen
local.contributor.firstnameTimothy Len
local.contributor.firstnameDevon Aen
local.contributor.firstnameMichelle Aen
local.contributor.firstnameWeianen
local.profile.schoolSchool of Science and Technologyen
local.profile.emailmdigman@une.edu.auen
local.output.categoryC1en
local.record.placeauen
local.record.institutionUniversity of New Englanden
local.publisher.placeUnited States of Americaen
local.identifier.runningnumbereaan2966en
local.format.startpage1en
local.format.endpage12en
local.peerreviewedYesen
local.identifier.volume9en
local.identifier.issue400en
local.contributor.lastnameLiuen
local.contributor.lastnameZhangen
local.contributor.lastnameLiaoen
local.contributor.lastnameFarhoodien
local.contributor.lastnameWongen
local.contributor.lastnameChenen
local.contributor.lastnameSégalinyen
local.contributor.lastnameChackoen
local.contributor.lastnameNguyenen
local.contributor.lastnameLuen
local.contributor.lastnamePolovinen
local.contributor.lastnamePoneen
local.contributor.lastnameDowningen
local.contributor.lastnameLawsonen
local.contributor.lastnameDigmanen
local.contributor.lastnameZhaoen
dc.identifier.staffune-id:mdigmanen
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local.identifier.unepublicationidune:1959.11/54413en
dc.identifier.academiclevelAcademicen
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local.title.maintitleMechanoresponsive stem cells to target cancer metastases through biophysical cuesen
local.relation.fundingsourcenoteThis work was supported by the NIH (1DP2CA195763-01) and the Department of Defense (W81XWH-13-1-0326 to W.Z.), NIH (2P41GM103540 to M.A.D.), and American Cancer Society (IRG-98-279-10) and NIH/ National Cancer Institute (1K22CA190511-01A1 to D.A.L.) S.X.Z. was supported by a Cardiovascular Applied Research and Entrepreneurship fellowship [NIH/National Heart, Lung, and Blood Institute (T32)]. W.L. was supported by a California Institute for Regenerative Medicine (CIRM) fellowship (TG2-01152). C.C.C. was supported by NSF Graduate Research Fellowship. A.I.S. received a fellowship from the Fondation ARC pour la recherche sur le cancer (SAE20150602901). G.P. was supported by a CIRM training grant (TB1-01182).en
local.output.categorydescriptionC1 Refereed Article in a Scholarly Journalen
local.search.authorLiu, Linanen
local.search.authorZhang, Shirley Xen
local.search.authorLiao, Wenbinen
local.search.authorFarhoodi, Henry Pen
local.search.authorWong, Chi Wen
local.search.authorChen, Claire Cen
local.search.authorSégaliny, Aude Ien
local.search.authorChacko, Jenu Ven
local.search.authorNguyen, Lily Pen
local.search.authorLu, Mengrouen
local.search.authorPolovin, Georgeen
local.search.authorPone, Egest Jen
local.search.authorDowning, Timothy Len
local.search.authorLawson, Devon Aen
local.search.authorDigman, Michelle Aen
local.search.authorZhao, Weianen
local.uneassociationYesen
local.atsiresearchNoen
local.sensitive.culturalNoen
local.identifier.wosid000406302800005en
local.year.published2017en
local.fileurl.closedpublishedhttps://rune.une.edu.au/web/retrieve/db34842b-6a9e-421f-b405-f5c434037f44en
local.subject.for2020321101 Cancer cell biologyen
local.subject.seo2020280102 Expanding knowledge in the biological sciencesen
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