Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:1.6.5.2 (
NQO1
)
6,196
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
NAD(P)H:quinone oxidoreductase
(
NQO1
) is a flavoenzyme that catalyzes the two-electron reduction of quinones and related compounds. With the use of biochemical assays,
NQO1
has been shown to be overexpressed in many types of cancer, including non-small cell lung cancer (NSCLC).
NQO1
can bioactivate antitumor quinones such as mitomycin C, and new quinone-based drugs are currently being developed to target this enzyme in tumors such as NSCLC. Because there is no information on the cell-specific expression of
NQO1
in lung, the purpose of this study was to examine the expression of
NQO1
in human NSCLC, small cell lung cancer,
carcinoid
lung tumors, and normal lung using immunohistochemistry. A high level of NQO1 protein expression was detected by immunohistochemistry in NSCLC (adenocarcinoma, squamous cell carcinoma, and bronchoalveolar carcinoma), but no NQO1 protein could be detected in small cell lung cancer or
carcinoid
lung tumors. In addition, NQO1 protein expression was examined by immunohistochemistry in normal lung tissue. A high level of NQO1 protein expression was detected by immunohistochemistry in normal lung respiratory epithelium, with the highest levels of expression observed in ciliated columnar epithelial cells. Significant amounts of NQO1 protein were also detected in the vascular endothelium and adipocytes. These data demonstrate that
NQO1
is overexpressed in NSCLC. Cells in normal lung also contain marked NQO1 protein and may be damaged by drugs activated by
NQO1
. These data validate NSCLC as a target for
NQO1
-directed agents and suggest that the potential for lung toxicity be considered in the preclinical development of quinone-based antitumor drugs.
...
PMID:Immunohistochemical detection of NAD(P)H:quinone oxidoreductase in human lung and lung tumors. 974 20