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Isolation of ORCTL3 in a novel genetic screen for tumor-specific apoptosis inducers.

Abstract:
We have established a systematic high-throughput screen for genes that cause cell death specifically in transformed tumor cells. In a first round of screening, cDNAs that induce apoptosis in a transformed human cell line are detected. Positive genes are subsequently tested in a synthetic lethal screen in normal cells versus their isogenic counterparts that have been transformed by a particular oncogene. In this way, the organic cation transporter-like 3 (ORCTL3) gene was found to be inactive in normal rat kidney (NRK) cells, but to induce apoptosis in NRK cells transformed by oncogenic H-ras. ORCTL3 also causes cell death in v-src-transformed cells and in various human tumor cell lines but not in normal cells or untransformed cell lines. Although ORCTL3 is a member of the organic cation transporter gene family, our data indicate that this gene induces apoptosis independently of its putative transporter activity. Rather, various lines of evidence suggest that ORCTL3 brings about apoptosis by an endoplasmic reticulum stress-mediated mechanism. Finally, we detected ORCTL3 to be downregulated in human kidney tumors.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/cdd.2009.21

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Human Genetics Wt Centre
Role:
Author


Publisher:
Nature
Journal:
Cell death and differentiation More from this journal
Volume:
16
Issue:
6
Pages:
890-898
Publication date:
2009-06-01
DOI:
EISSN:
1476-5403
ISSN:
1350-9047


Language:
English
Keywords:
Pubs id:
pubs:548553
UUID:
uuid:9fa4558d-64cb-401d-9bba-f0167bf4d20e
Local pid:
pubs:548553
Source identifiers:
548553
Deposit date:
2015-12-13
ARK identifier:

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