Cytochrome P450 1B1 (CYP1B1) is overexpressed in human colon adenocarcinomas relative to normal colon: implications for drug development

P Gibson, JH Gill, PA Khan, JM Seargent… - Molecular cancer …, 2003 - AACR
The cytochrome P450 family of enzymes is involved in the Phase I metabolism of a wide
variety of compounds. Although generally involved with detoxification, overexpression of …

Discovery and characterization of novel, potent, and selective cytochrome P450 2J2 inhibitors

S Ren, J Zeng, Y Mei, JZH Zhang, SF Yan, J Fei… - Drug Metabolism and …, 2013 - ASPET
Cytochrome P450 (CYP) 2J2 is one of the human CYPs involved in phase I xenobiotics
metabolism. It is mainly expressed in extrahepatic tissues, including intestine and …

CYP2B6: new insights into a historically overlooked cytochrome P450 isozyme

H Wang, LM Tompkins - Current drug metabolism, 2008 - ingentaconnect.com
Human CYP2B6 has been thought to account for a minor portion (< 1%) of total hepatic
cytochrome P450 (CYP) content and to have a minor function in human drug metabolism …

Human CYP1B1 and anticancer agent metabolism: mechanism for tumor-specific drug inactivation?

B Rochat, JM Morsman, GI Murray, WD Figg… - … of Pharmacology and …, 2001 - ASPET
The cytochrome P450 1B1 (CYP1B1) is involved in the metabolism of procarcinogens and
xenobiotics. Human CYP1B1 protein has been detected in a variety of tumors but is not …

Cytochrome P450 1B1: a novel anticancer therapeutic target

MCE McFadyen, GI Murray - Future oncology, 2005 - Taylor & Francis
Cytochrome P450 (CYP) 1B1 is overexpressed in tumor cells and is also recognized as a
biomarker of the tumor phenotype. This review highlights the tremendous potential of this …

[HTML][HTML] Evidence-based capacity of natural cytochrome enzyme inhibitors to increase the effectivity of antineoplastic drugs

L Manthalkar, Ajazuddin, S Bhattacharya - Discover Oncology, 2022 - Springer
Cytochrome (CYP) enzymes catalyze the metabolism of numerous exogenous and
endogenous substrates in cancer therapy leading to significant drug interactions due to their …

Cytochrome P450 interactions in human cancers: new aspects considering CYP1B1

PH Roos, HM Bolt - Expert opinion on drug metabolism & …, 2005 - Taylor & Francis
Molecular epidemiological studies are now a powerful tool to determine differential genetic
susceptibilities to cancer-causing agents, and to obtain information on potential …

Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development

SF Zhou, ZW Zhou, LP Yang… - Current medicinal …, 2009 - ingentaconnect.com
Cytochrome P450 2C9 (CYP2C9) is one of the most abundant CYP enzymes in the human
liver. CYP2C9 metabolizes more than 100 therapeutic drugs, including tolbutamide …

[PDF][PDF] Screening of potential anticancer compounds from marketed drugs: aripiprazole, haloperidol, miconazole, and terfenadine inhibit cytochrome P450 2J2

KH Liu - Journal of Life Science, 2011 - Citeseer
Cytochrome P450 2J2 (CYP2J2) plays important roles in the metabolism of endogenous
metabolites such as arachidonic acid as well as therapeutic drugs. CYP2J2 is …

Metabolism and mechanism of human cytochrome P450 enzyme 1A2

J Guo, X Zhu, S Badawy, A Ihsan, Z Liu… - Current drug …, 2021 - ingentaconnect.com
Human cytochrome P450 enzyme 1A2 (CYP1A2) is one of the most important cytochrome
P450 (CYP) enzymes in the liver, accounting for 13% to 15% of hepatic CYP enzymes …