Publication: Genetically engineered human cell-based microrobots for selective cancer cell death
| dc.contributor.coauthor | Dogan, N. O. | |
| dc.contributor.coauthor | Suadiye, E. | |
| dc.contributor.coauthor | Unangst, J. | |
| dc.contributor.coauthor | Dayan, C. B. | |
| dc.contributor.coauthor | Richter, G. | |
| dc.contributor.department | Department of Mechanical Engineering | |
| dc.contributor.department | School of Medicine | |
| dc.contributor.kuauthor | Sitti, Metin | |
| dc.contributor.kuauthor | Önder, Tuğba Bağcı | |
| dc.contributor.kuauthor | Cingöz, Ahmet | |
| dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
| dc.contributor.schoolcollegeinstitute | College of Engineering | |
| dc.date.accessioned | 2026-07-07T08:49:27Z | |
| dc.date.issued | 2026 | |
| dc.description.abstract | Medical 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.harvestedfrom | Manual | |
| dc.description.indexedby | WOS | |
| dc.description.indexedby | Scopus | |
| dc.description.indexedby | PubMed | |
| dc.description.publisherscope | International | |
| dc.description.readpublish | N/A | |
| dc.description.sponsoredbyTubitakEu | N/A | |
| dc.description.sponsorship | This 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.version | Published Version | |
| dc.identifier.WoSQuartile | Q1 | |
| dc.identifier.doi | 10.1126/sciadv.aea9831 | |
| dc.identifier.embargo | N/A | |
| dc.identifier.issn | 2375-2548 | |
| dc.identifier.issue | 18 | |
| dc.identifier.pubmed | 42054463 | |
| dc.identifier.scopus | 2-s2.0-105037562563 | |
| dc.identifier.uri | http://doi.org/10.1126/sciadv.aea9831 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14288/33278 | |
| dc.identifier.volume | 12 | |
| dc.identifier.wos | 001788827500006 | |
| dc.keywords | Genetically engineered | |
| dc.keywords | Cancer cell | |
| dc.keywords | Embryonic stem cell | |
| dc.keywords | Cell | |
| dc.keywords | Cancer | |
| dc.keywords | Programmed cell death | |
| dc.keywords | Biocompatible material | |
| dc.keywords | Human cell | |
| dc.language | eng | |
| dc.publisher | American Association for the Advancement of Science | |
| dc.relation.affiliation | Koç University | |
| dc.relation.collection | Koç University Institutional Repository | |
| dc.relation.ispartof | Science Advances | |
| dc.relation.openaccess | N/A | |
| dc.rights | N/A | |
| dc.rights.uri | N/A | |
| dc.subject | Medicine | |
| dc.subject | Robotics | |
| dc.title | Genetically engineered human cell-based microrobots for selective cancer cell death | |
| dc.type | Journal Article | |
| dspace.entity.type | Publication | |
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