Intrinsic apoptosis shapes the tumor spectrum linked to inactivation of the deubiquitinase BAP1

Author:

He Meng1ORCID,Chaurushiya Mira S.1ORCID,Webster Joshua D.2,Kummerfeld Sarah3ORCID,Reja Rohit3ORCID,Chaudhuri Subhra4,Chen Ying-Jiun4,Modrusan Zora4,Haley Benjamin4ORCID,Dugger Debra L.1ORCID,Eastham-Anderson Jeffrey2,Lau Shari2ORCID,Dey Anwesha5ORCID,Caothien Roger4ORCID,Roose-Girma Merone4ORCID,Newton Kim1ORCID,Dixit Vishva M.1ORCID

Affiliation:

1. Department of Physiological Chemistry, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.

2. Department of Pathology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.

3. Department of Bioinformatics, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.

4. Department of Molecular Biology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.

5. Department of Discovery Oncology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.

Abstract

Tissue specificity of tumor suppression It is well known that the loss of tumor suppressor genes leads to a limited subset of cancers in specific tissues. But why just those tissues? He et al. found a relatively simple explanation for how this tissue selectivity works for the tumor suppressor BAP1 using a mouse model of BAP1-induced cancer. In most cells, loss of BAP1 caused cell death or apoptosis. But in the tissues that formed tumors, differences in the regulation of genes with antiapoptotic effects allowed the cells to survive, even though BAP1 was lost. At least for this one tumor suppressor, its inactivation would normally cause a cell to die; however, this mechanism is absent in a subset of tissues, allowing the cells to proliferate and cause a tumor. Science , this issue p. 283

Funder

Genentech

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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