Show simple item record

Identification of autophagic cell death and implications for therapy

dc.contributor.advisorBaehrecke, Eric Hen_US
dc.contributor.authorAlva, Ajjai Shivaramen_US
dc.date.accessioned2004-06-04T05:57:54Z
dc.date.available2004-06-04T05:57:54Z
dc.date.issued2004-05-04en_US
dc.identifier.urihttp://hdl.handle.net/1903/1516
dc.description.abstractAutophagy is an evolutionarily conserved mechanism of bulk protein and organelle degradation that requires the ATG class of genes. Although autophagy has been frequently observed in dying cells in several species, a causative role for autophagy in cell death has not been demonstrated. We show that inhibition of caspase-8 in mouse L929 fibroblast cells causes cell death with the morphology of autophagy. Autophagic cell death in L929 cells is dependent on ATG genes and involves the receptor interacting protein (RIP) and the activation of the MAP kinase kinase 7(MKK7) - Jun N-terminal kinase (JNK) - cJUN pathway. We also show that autophagy occurs in many primary human tumors including cancer of the breast, lung and pancreas. Our findings validate autophagic cell death and might explain the role of autophagy in development, viral infections, neurodegenerative diseases and cancer.en_US
dc.format.extent5394697 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoen_US
dc.titleIdentification of autophagic cell death and implications for therapyen_US
dc.typeThesisen_US
dc.relation.isAvailableAtDigital Repository at the University of Marylanden_US
dc.relation.isAvailableAtUniversity of Maryland (College Park, Md.)en_US
dc.contributor.departmentCell Biology & Molecular Geneticsen_US
dc.subject.pqcontrolledBiology, Cellen_US
dc.subject.pqcontrolledBiology, Molecularen_US
dc.subject.pquncontrolledAutophagyen_US
dc.subject.pquncontrolledCell Deathen_US
dc.subject.pquncontrolledTumorsen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record