Publication:
Genetically engineered human cell-based microrobots for selective cancer cell death

dc.contributor.coauthorDogan, N. O.
dc.contributor.coauthorSuadiye, E.
dc.contributor.coauthorUnangst, J.
dc.contributor.coauthorDayan, C. B.
dc.contributor.coauthorRichter, G.
dc.contributor.departmentDepartment of Mechanical Engineering
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorSitti, Metin
dc.contributor.kuauthorÖnder, Tuğba Bağcı
dc.contributor.kuauthorCingöz, Ahmet
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.date.accessioned2026-07-07T08:49:27Z
dc.date.issued2026
dc.description.abstractMedical microrobots have strong potential for targeted therapeutic delivery; however, current systems achieve only physical targeting, and once at the target site, they are unable to distinguish healthy cells from cancerous ones because of the lack of biological selectivity. Here, we present a biohybrid microrobot system that combines magnetic targeting with biological selectivity. The microrobots are derived from human embryonic kidney cells genetically engineered to produce tumor necrosis factor–related apoptosis-inducing ligand (TRAIL), a molecule that induces cancer cell death in multiple tumor types without damaging healthy cells. Engineered cells are then conjugated to biocompatible magnetic Janus particles—silica beads half-coated with FePt nanofilms—to enable external magnetic control. With magnetic fields, the microrobots accumulate around the tumor spheroids and continuously release TRAIL for several days, leading to selective cancer cell death while avoiding damage to healthy cells. This study combines microrobotics with genetically engineered cell therapies to achieve a targeted, prolonged, and cancer-selective therapeutic delivery.
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipThis work was funded by the Max Planck Society. We also thank the Grassroots Program of the Max Planck Institute for Intelligent Systems for financial support.
dc.description.versionPublished Version
dc.identifier.WoSQuartileQ1
dc.identifier.doi10.1126/sciadv.aea9831
dc.identifier.embargoN/A
dc.identifier.issn2375-2548
dc.identifier.issue18
dc.identifier.pubmed42054463
dc.identifier.scopus2-s2.0-105037562563
dc.identifier.urihttp://doi.org/10.1126/sciadv.aea9831
dc.identifier.urihttps://hdl.handle.net/20.500.14288/33278
dc.identifier.volume12
dc.identifier.wos001788827500006
dc.keywordsGenetically engineered
dc.keywordsCancer cell
dc.keywordsEmbryonic stem cell
dc.keywordsCell
dc.keywordsCancer
dc.keywordsProgrammed cell death
dc.keywordsBiocompatible material
dc.keywordsHuman cell
dc.languageeng
dc.publisherAmerican Association for the Advancement of Science
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofScience Advances
dc.relation.openaccessN/A
dc.rightsN/A
dc.rights.uriN/A
dc.subjectMedicine
dc.subjectRobotics
dc.titleGenetically engineered human cell-based microrobots for selective cancer cell death
dc.typeJournal Article
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