A novel recombinant immunotoxin-based therapy targeting wild-type and mutant EGFR improves survival in murine models of glioblastoma.

dc.contributor.author

Chandramohan, Vidyalakshmi

dc.contributor.author

Bigner, Darell D

dc.date.accessioned

2022-09-01T13:32:24Z

dc.date.available

2022-09-01T13:32:24Z

dc.date.issued

2013-12

dc.date.updated

2022-09-01T13:32:24Z

dc.description.abstract

Both the amplification of the gene coding for wild-type (wt) epidermal growth factor receptor (EGFR) and the overexpression of the EGFR deletion mutant, commonly known as EGFRvIII, are hallmarks of glioblastoma. We have recently reported a novel, recombinant immunotoxin, D2C7-(scdsFv)-PE38KDEL, that targets both wt EGFR and EGFRvIII, exhibiting potent antineoplastic effects against established murine gliomas.

dc.identifier

2013ONCOIMM0299

dc.identifier.issn

2162-4011

dc.identifier.issn

2162-402X

dc.identifier.uri

https://hdl.handle.net/10161/25631

dc.language

eng

dc.publisher

Informa UK Limited

dc.relation.ispartof

Oncoimmunology

dc.relation.isversionof

10.4161/onci.26852

dc.subject

Pseudomonasexotoxin

dc.subject

bispecific antibody

dc.subject

brain tumors

dc.subject

convection-enhanced delivery

dc.subject

glioma-associated antigens

dc.title

A novel recombinant immunotoxin-based therapy targeting wild-type and mutant EGFR improves survival in murine models of glioblastoma.

dc.type

Journal article

duke.contributor.orcid

Chandramohan, Vidyalakshmi|0000-0002-0653-3014

duke.contributor.orcid

Bigner, Darell D|0000-0001-5548-4899

pubs.begin-page

e26852

pubs.issue

12

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Institutes and Centers

pubs.organisational-group

Pathology

pubs.organisational-group

Surgery

pubs.organisational-group

Duke Cancer Institute

pubs.organisational-group

Neurosurgery

pubs.organisational-group

Neurosurgery, Neuro-Oncology

pubs.publication-status

Published

pubs.volume

2

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