Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P42345 (
mTOR
)
26,049
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Translationally controlled tumour protein
TCTP
(gene symbol: TPT1) is a highly-conserved, cyto-protective protein implicated in many physiological and disease processes, in particular cancer, where it is associated with poor patient outcomes. To understand the mechanisms underlying the accumulation of high
TCTP
levels in cancer cells, we studied the signalling pathways that control translation of
TCTP
mRNA, which contains a 5'-terminal oligopyrimidine tract (5'-TOP). In HT29 colon cancer cells and in HeLa cells, serum increases the expression of
TCTP
two- and four-fold, respectively, and this is inhibited by rapamycin or
mTOR
kinase inhibitors. Polysome profiling and mRNA quantification indicate that these effects occur at the level of mRNA translation. Blocking this pathway upstream of
mTOR
complex 1 (mTORC1) by inhibiting Akt also prevented increases in
TCTP
levels in both HeLa and HT29 colon cancer cells, whereas knockout of TSC2, a negative regulator of mTORC1, led to derepression of
TCTP
synthesis under serum starvation. Overexpression of eIF4E enhanced the polysomal association of the
TCTP
mRNA, although it did not protect its translation from inhibition by rapamycin. Conversely, expression of a constitutively-active mutant of the eIF4E inhibitor 4E-BP1, which is normally inactivated by mTORC1, inhibited
TCTP
mRNA translation in HEK293 cells. Our results demonstrate that
TCTP
mRNA translation is regulated by signalling through the PI3-K/Akt/mTORC1 pathway. This explains why
TCTP
levels are frequently increased in cancers, since mTORC1 signalling is hyperactive in ~80% of tumours.
...
PMID:Growth-factor dependent expression of the translationally controlled tumour protein TCTP is regulated through the PI3-K/Akt/mTORC1 signalling pathway. 2593 23