Unknown,Transcriptomics,Genomics,Proteomics

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PHH Chlorpromazine


ABSTRACT: Drug induced liver injury (DILI) is still a major reason for drug attrition during clinical trials and market-withdrawal of already approved drugs. DILI is difficult to predict in animal models, hence more suitable screening methods are needed to predict adverse effects in human. Here, transcriptomic data from short- and long-term cultured primary human hepatocytes exposed to the human hepatotoxin Chlorpromazine was analysed.

ORGANISM(S): Homo sapiens

SUBMITTER: Germaine Truisi 

PROVIDER: E-MTAB-1747 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Transcriptomic hepatotoxicity signature of chlorpromazine after short- and long-term exposure in primary human sandwich cultures.

Parmentier Céline C   Truisi Germaine L GL   Moenks Konrad K   Stanzel Sven S   Lukas Arno A   Kopp-Schneider Annette A   Alexandre Eliane E   Hewitt Philip G PG   Mueller Stefan O SO   Richert Lysiane L  

Drug metabolism and disposition: the biological fate of chemicals 20130802 10


Drug-induced liver injury is the most frequent reason for market withdrawal of approved drugs, and is difficult to predict in animal models. Here, we analyzed transcriptomic data derived from short- and long-term cultured primary human hepatocytes (PHH) exposed to the well known human hepatotoxin chlorpromazine (CPZ). Samples were collected from five PHH cultures after short-term (1 and 3 days) and long-term (14 days) repeat daily treatment with 0.1 or 0.2 µM CPZ, corresponding to C(max). Two PH  ...[more]

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