BIRC5 is a target for molecular imaging and detection of human pancreatic cancer.
Animals
Biomarkers, Tumor
/ genetics
Carcinoma, Pancreatic Ductal
/ diagnostic imaging
Cell Line, Tumor
Feasibility Studies
Gene Expression Regulation, Neoplastic
Humans
Luciferases
/ genetics
Male
Mice, Nude
Molecular Imaging
Optical Imaging
Pancreatic Neoplasms
/ diagnostic imaging
Positron Emission Tomography Computed Tomography
Predictive Value of Tests
Promoter Regions, Genetic
Survivin
/ genetics
Thymidine Kinase
/ genetics
Tumor Burden
Up-Regulation
X-Ray Microtomography
BIRC5
Gaussia luciferase
Pancreatic cancer
Super promoter
Thymidine kinase, microPET/CT imaging
Journal
Cancer letters
ISSN: 1872-7980
Titre abrégé: Cancer Lett
Pays: Ireland
ID NLM: 7600053
Informations de publication
Date de publication:
10 08 2019
10 08 2019
Historique:
received:
13
02
2019
revised:
25
04
2019
accepted:
29
04
2019
pubmed:
7
5
2019
medline:
28
4
2020
entrez:
7
5
2019
Statut:
ppublish
Résumé
Pancreatic ductal adenocarcinoma (PDAC) is a major cause of cancer mortality with a dismal overall survival rate and an urgent need for detection of minute tumors. Current diagnostic modalities have high sensitivity and specificity for larger tumors, but not for minute PDAC. In this study, we test the feasibility of a precision diagnostic platform for detecting and localizing minute human PDAC in mice. This platform includes: 1) defining BIRC5 as an early PDAC-upregulated gene and utilizing an enhanced BIRC5 super-promoter to drive expression of dual Gaussia luciferase (GLuc) and sr39 thymidine kinase (sr39TK) reporter genes exponentially and specifically in PDAC; 2) utilizing a genetically-engineered AAV
Identifiants
pubmed: 31059751
pii: S0304-3835(19)30273-3
doi: 10.1016/j.canlet.2019.04.036
pii:
doi:
Substances chimiques
BIRC5 protein, human
0
Biomarkers, Tumor
0
Survivin
0
Luciferases
EC 1.13.12.-
Thymidine Kinase
EC 2.7.1.21
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Video-Audio Media
Langues
eng
Sous-ensembles de citation
IM
Pagination
10-19Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.