2014
DOI: 10.1016/j.bbrc.2014.03.086
|View full text |Cite
|
Sign up to set email alerts
|

RPS27a promotes proliferation, regulates cell cycle progression and inhibits apoptosis of leukemia cells

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

3
37
0

Year Published

2015
2015
2024
2024

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 55 publications
(40 citation statements)
references
References 25 publications
3
37
0
Order By: Relevance
“…Ubiquitin acts as a chaperone for its fusion partners and hence its presence is critical for proper ribosome biogenesis and thereof mRNA translation [37]. This is in line with the observation where exogenous expression of RPS27A has already been shown to induce cell proliferation whereas inhibition reduced the cell viability, induced cell cycle arrest at S and G2/M phases and increased cell apoptosis in the culture [38]. Whereas, inhibition of UBA52 didn't showed similar effects on cellular health as expression of only ~7% mRNAs was observed to be altered suggesting transcript-specific translation by the UBA52 [39].…”
Section: Functional Analysis Of Microvesicular Proteinssupporting
confidence: 75%
“…Ubiquitin acts as a chaperone for its fusion partners and hence its presence is critical for proper ribosome biogenesis and thereof mRNA translation [37]. This is in line with the observation where exogenous expression of RPS27A has already been shown to induce cell proliferation whereas inhibition reduced the cell viability, induced cell cycle arrest at S and G2/M phases and increased cell apoptosis in the culture [38]. Whereas, inhibition of UBA52 didn't showed similar effects on cellular health as expression of only ~7% mRNAs was observed to be altered suggesting transcript-specific translation by the UBA52 [39].…”
Section: Functional Analysis Of Microvesicular Proteinssupporting
confidence: 75%
“…As reported, the Uba80 encodes ubiquitin fused to ribosomal protein S27a, which promotes proliferation, inhibits cell apoptosis, and responses to ribosomal stress [49,50,51]. PPAR-α and PPAR-Îł agonist, a stress-induced transcription factor in response to reducing oxidative stress and others, benefit brain ischemia and injury recovery by protecting against neuron apoptosis [52,53].…”
Section: Discussionmentioning
confidence: 99%
“…However, the genes specifically controlling the size of DP and matrix remain elusive. In the present study, the up-regulated genes in the super fine wool group included 5 genes associated with the cell cycle and apoptosis: GSDMA3 [56], HSPA2 [57], RPS27A [58], PDCD6IP [59], DAP [60], CCNA2 [61] and FOS [62]; the down-regulated genes included 7 genes associated with promoting follicle cell proliferation and differentiation: KRT1 [63, 64], KRT7 [65, 66], HSD11B1 [67, 68], S100A8 [41, 69, 70], NT5C3 L [71] and DNAJC12 [72]. These genes may through promoting HF cell apoptosis, inhibiting follicle cell proliferation and differentiation, thereby reduce the WFD.…”
Section: Discussionmentioning
confidence: 99%