Autocrine loops

Misregulation of autocrine signalling loops may contribute to cancer phenotypes. In November Nature Genetics, Thomas Graeber and David Eisenberg of the Howard Hughes Medical Institute and the University of California, Los Angeles describe a computer-based strategy to identify receptor-ligand pairs and autocrine loops in large datasets (Nat Gen 2001, 29:295-300).They compiled a Database of Ligand-Receptor Partners (DLRP) that is based on the published literature and contains 452 ligand-receptor p

Jonathan Weitzman(jonathanweitzman@hotmail.com)
Oct 31, 2001

Misregulation of autocrine signalling loops may contribute to cancer phenotypes. In November Nature Genetics, Thomas Graeber and David Eisenberg of the Howard Hughes Medical Institute and the University of California, Los Angeles describe a computer-based strategy to identify receptor-ligand pairs and autocrine loops in large datasets (Nat Gen 2001, 29:295-300).

They compiled a Database of Ligand-Receptor Partners (DLRP) that is based on the published literature and contains 452 ligand-receptor pairs. They then used this information to screen several published datasets of microarray expression profiling in cancer samples, and measured the correlation coefficient between ligand and receptor expression profiles.

Graeber and Eisenberg identified ligand-receptor partners previously implicated in autocrine signaling (for example, inerleukin 10 and its receptor and tumor necrosis factor and its receptors), and propose some new effectors (including several chemokines, such as CCL4 and the CCR5 receptor).

These results await experimental cofirmation that this strategy can...

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