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First published online September 15, 2004


Journal of Cell Science 117, 2005e (2004)
© The Company of Biologists Limited
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In this issue

NO takes the Myc


Nitric oxide (NO) is a negative regulator of proliferation in many cell types, including neural cell precursors, in which it promotes neuronal differentiation. By contrast, the protooncoprotein N-Myc promotes proliferation of neuronal precursors and is downregulated in neuroblastoma cells induced to differentiate by retinoic acid. This prompted Elisabetta Ciani and colleagues to ask whether the antiproliferative action of NO in neuronal precursors is mediated by negative regulation of N-Myc expression(see p. 4727). They show that increasing NO levels in retinoic-acid-treated neuroblastoma cells, by overexpressing neuronal NO synthase (nNOS) or exposing the cells to an exogenous NO source, slows down their proliferation, accelerates their differentiation, and decreases N-Myc expression. Conversely, nNOS inhibition in cerebellar granule cell cultures increases both neuronal precursor proliferation and N-Myc expression. The authors conclude that NO regulates a switch in neuronal precursor programming, from proliferation to differentiation, through N-Myc and suggest that this new function for NO could provide a therapeutic target for the treatment of aggressive N-Myc-expressing neuroblastomas.


Related articles in JCS:

Nitric oxide negatively regulates proliferation and promotes neuronal differentiation through N-Myc downregulation
Elisabetta Ciani, Sabina Severi, Andrea Contestabile, Renata Bartesaghi, and Antonio Contestabile
JCS 2004 117: 4727-4737. [Abstract] [Full Text]  




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