The OCT4 pseudogene POU5F1B is amplified and promotes an aggressive phenotype in gastric cancer
POU5F1B (POU domain class 5 transcription factor 1B), a processed pseudogene that is highly homologous to OCT4 , was recently shown to be transcribed in cancer cells, but its clinical relevance and biological function have remained unclear. We now show that POU5F1B , which is located adjacent to MYC...
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Veröffentlicht in: | Oncogene 2015-01, Vol.34 (2), p.199-208 |
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Sprache: | eng |
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Zusammenfassung: | POU5F1B
(POU domain class 5 transcription factor 1B), a processed pseudogene that is highly homologous to
OCT4
, was recently shown to be transcribed in cancer cells, but its clinical relevance and biological function have remained unclear. We now show that
POU5F1B
, which is located adjacent to
MYC
on human chromosome 8q24, is frequently amplified in gastric cancer (GC) cell lines.
POU5F1B
, but not
OCT4
, was also found to be expressed at a high level in GC cell lines and clinical specimens. In addition, the DNA copy number and mRNA abundance for
POU5F1B
showed a positive correlation in both cancer cell lines and GC specimens. Overexpression of
POU5F1B
in GC cells promoted colony formation
in vitro
as well as both tumorigenicity and tumor growth
in vivo
, and these effects were enhanced in the additional presence of
MYC
overexpression. Furthermore, knockdown of
POU5F1B
expression with a short hairpin RNA confirmed a role for the endogenous pseudogene in the promotion of cancer cell growth
in vitro
and tumor growth
in vivo
.
POU5F1B
overexpression induced upregulation of various growth factors in GC cells as well as exhibited mitogenic, angiogenic and antiapoptotic effects in GC xenografts. Finally, amplification of
POU5F1B
was detected in 17 (12%) of 145 cases of GC and was a significant predictor of poor prognosis in patients with stage IV disease. In conclusion, we found that the
POU5F1B
pseudogene is amplified and expressed at a high level in, as well as confers an aggressive phenotype on, GC, and that
POU5F1B
amplification is associated with a poor prognosis in GC patients. |
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ISSN: | 0950-9232 1476-5594 |
DOI: | 10.1038/onc.2013.547 |