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About:
Angiotensin-converting enzyme 2 is a potential therapeutic target for EGFR-mutant lung adenocarcinoma
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
wasabi.inria.fr
associated with source
document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Angiotensin-converting enzyme 2 is a potential therapeutic target for EGFR-mutant lung adenocarcinoma
Creator
Takahashi, Hiroki
Uchida, Hiroaki
Hasegawa, Tadashi
Hirai, Sachie
Nishii, Yukari
Sakuma, Yuji
Sumi, Toshiyuki
Tada, Makoto
Tanaka, Yusuke
Watanabe, Atsushi
Yamada, Gen
Yamaguchi, Miki
Source
Elsevier; Medline; PMC
abstract
Abstract EGFR-mutant lung adenocarcinomas contain a subpopulation of cells that have undergone epithelial-to-mesenchymal transition and can grow independently of EGFR. To kill these cancer cells, we need a novel therapeutic approach other than EGFR inhibitors. If a molecule is specifically expressed on the cell surface of such EGFR-independent EGFR-mutant cancer cells, it can be a therapeutic target. We found that a mesenchymal EGFR-independent subline derived from HCC827 cells, an EGFR-mutant lung adenocarcinoma cell line, expressed angiotensin-converting enzyme 2 (ACE2) to a greater extent than its parental cells. ACE2 was also expressed at least partially in most of the primary EGFR-mutant lung adenocarcinomas examined, and the ACE2 expression level in the cancer cells was much higher than that in normal lung epithelial cells. In addition, we developed an anti-ACE2 mouse monoclonal antibody (mAb), termed H8R64, that was internalized by ACE2-expressing cells. If an antibody-drug conjugate consisting of a humanized mAb based on H8R64 and a potent anticancer drug were produced, it could be effective for the treatment of EGFR-mutant lung adenocarcinomas.
has issue date
2017-06-03
(
xsd:dateTime
)
bibo:doi
10.1016/j.bbrc.2017.04.102
bibo:pmid
28433633
has license
els-covid
sha1sum (hex)
3d4106215f4d9cc9189f90d1beac917bdf3d9b09
schema:url
https://doi.org/10.1016/j.bbrc.2017.04.102
resource representing a document's title
Angiotensin-converting enzyme 2 is a potential therapeutic target for EGFR-mutant lung adenocarcinoma
has PubMed Central identifier
PMC7092918
has PubMed identifier
28433633
schema:publication
Biochemical and Biophysical Research Communications
resource representing a document's body
covid:3d4106215f4d9cc9189f90d1beac917bdf3d9b09#body_text
is
schema:about
of
named entity 'MUTANT'
named entity 'expressed'
named entity 'EGFR inhibitors'
named entity 'target'
named entity 'lung adenocarcinoma'
named entity 'CONJUGATE'
named entity 'APPROACH'
named entity 'THERAPEUTIC TARGET'
named entity 'MOLECULE'
named entity 'THESE'
named entity 'MUCH'
named entity 'EGFR INHIBITORS'
named entity 'ITS'
named entity 'CELLS'
named entity 'MAB'
covid:arg/3d4106215f4d9cc9189f90d1beac917bdf3d9b09
named entity 'HIGHER'
named entity 'MUTANT'
named entity 'POTENTIAL'
named entity 'EPITHELIAL CELLS'
named entity 'HCC827'
named entity 'PRIMARY'
named entity 'PARENTAL'
named entity 'ACE2'
named entity 'HAVE'
named entity 'IS A'
named entity 'THERAPEUTIC TARGET'
named entity 'LUNG ADENOCARCINOMA'
named entity 'TRANSITION'
named entity 'COULD BE'
named entity 'EFFECTIVE'
named entity 'ANGIOTENSIN-CONVERTING ENZYME 2'
named entity 'FOUND'
named entity 'PARTIALLY'
named entity 'EGFR'
named entity 'GREATER'
named entity 'EPITHELIAL'
named entity 'EXPRESSED'
named entity 'CONTAIN'
named entity 'CANCER CELLS'
named entity 'HUMANIZED'
named entity 'EGFR'
named entity 'ANGIOTENSIN-CONVERTING ENZYME 2'
named entity 'BASED'
named entity 'GROW'
named entity 'S T'
named entity 'ANTIBODY'
named entity 'EXPRESSION LEVEL'
named entity 'THERAPEUTIC'
named entity 'LUNG ADENOCARCINOMA CELL LINE'
named entity 'ADDITION'
named entity 'EXAMINED'
named entity 'TREATMENT'
named entity 'INDEPENDENT'
named entity 'NEED'
named entity 'DRUG'
named entity 'KILL'
named entity 'MOUSE MONOCLONAL ANTIBODY'
named entity 'DERIVED'
named entity 'CELL SURFACE'
named entity 'OTHER THAN'
named entity 'EXTENT'
named entity 'NOVEL'
named entity 'SUBPOPULATION'
named entity 'MESENCHYMAL'
named entity 'ADENOCARCINOMAS'
named entity 'LUNG'
named entity 'MOST OF'
named entity 'kill'
named entity 'mAb'
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