Recommend Cell Cycle to your librarian for 2008. Download form here.

Sign up for Table of Contents Alerts.

home subscribe search archive forthcoming

Email this page Print this page

Review

Deciphering AP-1 Function in Tumorigenesis: Fra-ternizing on Target Promoters

Pasquale Verde, Laura Casalino, Francesco Talotta, Moshe Yaniv and Jonathan B. Weitzman

volume 6 | issue 21

1 November 2007
Pages: 2633 - 2639

Purchase article for $19

Subscribe to this journal for $129/year

Multi-gene families of transcription factors pose a formidable challenge to molecular and functional analysis. Dissecting distinct functions for individual family members requires a combination of approaches in different cellular and animal models. The AP-1 transcription factor complex serves as a paradigm for understanding the dynamics of transcriptional regulation. Knockout, knockdown and transgenic strategies, inducible alleles, mutational analysis, chemical genetics, etc.; researchers have applied all the tricks of the trade to understand how AP-1 works. AP-1 refers to a mixture of dimers formed between members of the Jun, Fos and ATF families. The complexity of the AP-1 biological functions reflects the wide combinatorial diversity of its components.1 AP-1 has been linked to cancer and neoplastic transformation ever since the first jun and fos genes were cloned as cellular homologues of viral oncogenes twenty years ago. Because of the oncogenic or tumor suppressive activity exhibited by distinct Jun and Fos nuclear proteins depending on the cell context and the genetic background of the tumor, the AP-1 complex has been called a “double-edged sword” in tumorigenesis.2 The cumulating results over the last decade are finally leading to the identification of specific functions for individual AP-1 components and their contribution to neoplastic disease. Here, we focus on the Fra-1 protein in tumorigenesis, which offers an illustrative example of this helter-skelter voyage.

Authors

Pasquale Verde

Institute of Genetics and Biophysics 𠇊. Buzzati Traverso” CNR; Naples, Italy

Laura Casalino

Institute of Genetics and Biophysics 𠇊. Buzzati Traverso” CNR; Naples, Italy

Francesco Talotta

Institute of Genetics and Biophysics 𠇊. Buzzati Traverso” CNR; Naples, Italy

Moshe Yaniv

Pasteur Institute; Paris, France

Jonathan B. Weitzman

Université Paris; Paris, France


Purchase article for $19

Subscribe to this journal for $129/year