TY - JOUR
T1 - Id proteins in development, cell cycle and cancer
AU - Ruzinova, Marianna B.
AU - Benezra, Robert
N1 - Funding Information:
We thank all of our colleagues who generously shared with us their results prior to publication. We also thank W. Forrester, A. Koff and members of the Benezra laboratory for valuable discussions. Our work was supported by grants from the NIH, the Breast Cancer Research Foundation and an MSTP grant to MR.
PY - 2003/8/1
Y1 - 2003/8/1
N2 - Id proteins are important parts of signaling pathways involved in development, cell cycle and tumorigenesis. They were first shown to act as dominant negative antagonists of the basic helix-loop-helix family of transcription factors, which positively regulate differentiation in many cell lineages. The Id proteins do this by associating with the ubiquitous E proteins and preventing them from binding DNA or other transcription factors. Id proteins also associate with Ets transcription factors and the Rb family of tumor suppressor proteins, and are downstream targets of transforming growth factor β and bone morphogenic protein signaling. Thus, the Id proteins have become important molecules for understanding basic biological processes as well as targets for potential therapeutic intervention in human disease.
AB - Id proteins are important parts of signaling pathways involved in development, cell cycle and tumorigenesis. They were first shown to act as dominant negative antagonists of the basic helix-loop-helix family of transcription factors, which positively regulate differentiation in many cell lineages. The Id proteins do this by associating with the ubiquitous E proteins and preventing them from binding DNA or other transcription factors. Id proteins also associate with Ets transcription factors and the Rb family of tumor suppressor proteins, and are downstream targets of transforming growth factor β and bone morphogenic protein signaling. Thus, the Id proteins have become important molecules for understanding basic biological processes as well as targets for potential therapeutic intervention in human disease.
UR - http://www.scopus.com/inward/record.url?scp=0042347689&partnerID=8YFLogxK
U2 - 10.1016/S0962-8924(03)00147-8
DO - 10.1016/S0962-8924(03)00147-8
M3 - Review article
C2 - 12888293
AN - SCOPUS:0042347689
SN - 0962-8924
VL - 13
SP - 410
EP - 418
JO - Trends in Cell Biology
JF - Trends in Cell Biology
IS - 8
ER -