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Editorials |
From the Lillehei Heart Institute, University of Minnesota, Minneapolis.
Correspondence to Jennifer L. Hall, PhD, Lillehei Heart Institute, University of Minnesota, Minneapolis, MN 55455. E-mail jlhall@umn.edu
See related article, pages 472–479
Key Words: E2F-1 cell cycle DNA synthesis Bnip3 hypoxia retinoblastoma Rb myocyte
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
In this issue of Circulation Research, Yurkova et al1 present direct evidence that a cell cycle regulatory factor, E2F-1, binds to a proapoptotic gene in hypoxic cardiac myocytes, leading to apoptosis. Life embraces death.
The role of the cell cycle regulatory protein E2F-1 in a postmitotic cardiac myocyte has remained somewhat of a mystery. In 1997, while working in the laboratory of Schneider, Kirshenbaum and colleagues uncovered a critical clue. Cardiac myocytes overexpressing E2F-1 entered the cell cycle and headed for the grave.2,3 This work was among the first to lead a wave of evidence across disciplines to support a role for E2F-1 in the cell cycle and cell death.4 However, the mechanism(s) by which E2F-1 promotes apoptosis have remained unclear. Kirshenbaum has returned. This time with the discovery that E2F-1 binds to the promoter region of Bnip3, an apoptotic gene, promoting an intrinsic cell death signaling pathway under conditions of hypoxia (Figure).1 Thus, 10 years ago, Kirshenbaum and colleagues published findings causing us to reexamine the predefined 1-dimensional role of E2F-1 as a cell cycle regulatory factor and consider E2F-1 as a multidimensional protein with the ability to regulate both cell cycle and intrinsic cell death pathways. In this issue of Circulation Research, Yurkova et al have discovered that E2F-1 binds the promoter region of a cell death gene and promotes apoptosis.
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Related Article:
Circ. Res. 2008 102: 472-479.
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