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Suppressing Cancer With A Master Control Gene

Date:
February 23, 2009
Source:
Public Library of Science
Summary:
Starting with the tiny fruit fly and then moving into mice and humans, researchers have shown that expression of the same gene suppresses cancer in all three organisms. Reciprocally, switching off the gene -- called Ato in flies and ATOH1 in mammals -- leads to cancer. The authors show there is a good chance that the gene can be switched on again with a drug.
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Starting with the tiny fruit fly and then moving into mice and humans, researchers at VIB and K. U. Leuven show that expression of the same gene suppresses cancer in all three organisms. Reciprocally, switching off the gene – called Ato in flies and ATOH1 in mammals – leads to cancer. The authors show there is a good chance that the gene can be switched on again with a drug. 

All of us begin our lives as a single cell (made when an egg and sperm fuse) which repeatedly divides into the few billion cells that constitute an adult human. During these divisions cells become increasingly differentiated from each other, until in an adult almost all cells are highly specialized to perform a specific function – skin cells, liver cells, eye lens cells, nerve cells, etc. Cancer is a collection of cells without a function, which grow when normal genetic controls of cell division are interrupted. Cancer cells are less differentiated than normal cells – leading to the hypothesis that the final steps of differentiation prevent cells from becoming cancerous.

New work conducted by Wouter Bossuyt, Bassem Hassan, and colleagues at VIB and K. U. Leuven has tested this theory. They demonstrate that in the fruit fly, master control genes steering the specialization step inhibit tumor formation.

In collaboration with colleagues from the United States, they show that loss of one of those genes, Atonal homolog 1 (ATOH1), causes colon cancer in mice. The gene regulates the last step in the specialization to epithelial cells of the colon. Humans with colon cancer frequently have an inactivated ATOH1 gene, the researchers show.

The researchers could reactivate the gene in human colon cancer cells grown in culture. This caused the tumor cells to stop growing and commit suicide. This exciting, but preliminary, result suggests that it may be possible to switch the gene back on in living patients to target their cancers. Taking this work in the test tube and using it to develop a therapy is an exciting but complicated challenge. Therefore, more work will be required to further understand the role of ATOH1 in suppressing cancer formation.


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The above post is reprinted from materials provided by Public Library of Science. Note: Materials may be edited for content and length.


Journal References:

  1. Bossuyt et al. The Atonal Proneural Transcription Factor Links Differentiation and Tumor Formation in Drosophila. PLoS Biology, 2009; 7 (2): e40 DOI: 10.1371/journal.pbio.1000040
  2. Bossuyt et al. Atonal homolog 1 Is a Tumor Suppressor Gene. PLoS Biology, 2009; 7 (2): e39 DOI: 10.1371/journal.pbio.1000039

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Public Library of Science. "Suppressing Cancer With A Master Control Gene." ScienceDaily. ScienceDaily, 23 February 2009. <www.sciencedaily.com/releases/2009/02/090223094702.htm>.
Public Library of Science. (2009, February 23). Suppressing Cancer With A Master Control Gene. ScienceDaily. Retrieved July 29, 2015 from www.sciencedaily.com/releases/2009/02/090223094702.htm
Public Library of Science. "Suppressing Cancer With A Master Control Gene." ScienceDaily. www.sciencedaily.com/releases/2009/02/090223094702.htm (accessed July 29, 2015).

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