NOTCH1 directly regulates c-MYC and activates a feed-forward-loop transcriptional network promoting leukemic cell growth

Teresa Palomero, Keat Lim Wei, Duncan T. Odom, Maria Luisa Sulis, Pedro J. Real, Adam Margolin, Kelly C. Barnes, Jennifer O'Neil, Donna Neuberg, Andrew P. Weng, Jon C. Aster, Francois Sigaux, Jean Soulier, A. Thomas Look, Richard A. Young, Andrea Califano, Adolfo A. Ferrando

Research output: Contribution to journalArticlepeer-review

640 Scopus citations


The NOTCH1 signaling pathway directly links extracellular signals with transcriptional responses in the cell nucleus and plays a critical role during T cell development and in the pathogenesis over 50% of human T cell lymphoblastic leukemia (T-ALL) cases. However, little is known about the transcriptional programs activated by NOTCH1. Using an integrative systems biology approach we show that NOTCH1 controls a feed-forward-loop transcriptional network that promotes cell growth. Inhibition of NOTCH1 signaling in T-ALL cells led to a reduction in cell size and elicited a gene expression signature dominated by down-regulated biosynthetic pathway genes. By integrating gene expression array and ChIP-on-chip data, we show that NOTCH1 directly activates multiple biosynthetic routes and induces c-MYC gene expression. Reverse engineering of regulatory networks from expression profiles showed that NOTCH1 and c-MYC govern two directly interconnected transcriptional programs containing common target genes that together regulate the growth of primary T-ALL cells. These results identify c-MYC as an essential mediator of NOTCH1 signaling and integrate NOTCH1 activation with oncogenic signaling pathways upstream of c-MYC.

Original languageEnglish (US)
Pages (from-to)18261-18266
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Issue number48
StatePublished - Nov 28 2006
Externally publishedYes


  • T cell lymphoblastic leukemia

ASJC Scopus subject areas

  • General


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