2026-09-20T19:57:14Zhttps://dspace.mit.edu/server/oai/request

oai:dspace.mit.edu:1721.1/844082026-06-16T18:17:11Zcom_1721.1_7582com_1721.1_7581col_1721.1_131022

Shiladitya Sengupta. Connor, Yamicia Doyasi Harvard--MIT Program in Health Sciences and Technology. Harvard University--MIT Division of Health Sciences and Technology 2014-01-23T18:42:12Z 2014-01-23T18:42:12Z 2013 http://hdl.handle.net/1721.1/84408 868020188 Thesis (Ph. D. in Medical Engineering and Medical Physics)--Harvard-MIT Program in Health Sciences and Technology, 2013. Cataloged from PDF version of thesis. Includes bibliographical references (pages 356-386). Elucidation of molecular mechanisms underlying metastasis is the final frontier in cancer biology research. Identifying individual pathways in the metastatic cascade could lead to development of metastasis-specific therapeutics; however, current in vivo metastasis model systems are not efficient tools for isolating a single molecular event from the network of complex biological pathways. In response to these needs, we have developed a 3D in vitro co-culture system that isolates molecular and physical interactions between metastatic cells and the endothelium, which are prerequisite for invasive spread. We have used this model to identify key mediators of epithelial-endothelial cell interactions, to screen metastasis specific therapeutics, and most significantly, to elucidate a novel form of intercellular communication through thin cytoskeletal projections called nanoChannels (nCs) that is involved in pathological angiogenesis and that may prime metastatic spread. Metastatic cells preferentially form nCs with the endothelium, enabling rapid and directed transfer of intracellular contents. Proteins, small cytoplasmic dyes, nanoparticles, and most interestingly, functional microRNAs (miRNAs) are transported through these structures. Communication of miRNAs through nCs presents a novel mechanism of pathological angiogenesis and the angiogenic switch. NanoChannel-mediated communication introduces a new paradigm of cancer progression in which tumor cells can directly transform surrounding cell populations in order to facilitate cancer pathogenesis. by Yamicia Doyasi Connor. Ph.D. in Medical Engineering and Medical Physics 386 pages eng Massachusetts Institute of Technology M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 Harvard--MIT Program in Health Sciences and Technology. Novel mechanisms of endothelial-epithelial interactions underlying cancer metastasis Thesis application/pdf false Publication unknown unknown <Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="794f0843-829f-4945-99ee-c97001b2203d"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>Novel mechanisms of endothelial-epithelial interactions underlying cancer metastasis</Title> <PublishedIn> <Publication> </Publication> </PublishedIn> <PublicationDate>2013</PublicationDate> <Authors> <Author> <DisplayName>Connor, Yamicia Doyasi</DisplayName> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>Massachusetts Institute of Technology</DisplayName> <OrgUnit /> </Publisher> </Publishers> <License>http://dspace.mit.edu/handle/1721.1/7582</License> <Keyword>Harvard--MIT Program in Health Sciences and Technology.</Keyword> <Abstract>Elucidation of molecular mechanisms underlying metastasis is the final frontier in cancer biology research. Identifying individual pathways in the metastatic cascade could lead to development of metastasis-specific therapeutics; however, current in vivo metastasis model systems are not efficient tools for isolating a single molecular event from the network of complex biological pathways. In response to these needs, we have developed a 3D in vitro co-culture system that isolates molecular and physical interactions between metastatic cells and the endothelium, which are prerequisite for invasive spread. We have used this model to identify key mediators of epithelial-endothelial cell interactions, to screen metastasis specific therapeutics, and most significantly, to elucidate a novel form of intercellular communication through thin cytoskeletal projections called nanoChannels (nCs) that is involved in pathological angiogenesis and that may prime metastatic spread. Metastatic cells preferentially form nCs with the endothelium, enabling rapid and directed transfer of intracellular contents. Proteins, small cytoplasmic dyes, nanoparticles, and most interestingly, functional microRNAs (miRNAs) are transported through these structures. Communication of miRNAs through nCs presents a novel mechanism of pathological angiogenesis and the angiogenic switch. NanoChannel-mediated communication introduces a new paradigm of cancer progression in which tumor cells can directly transform surrounding cell populations in order to facilitate cancer pathogenesis.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication>