HCSGD entry for YPEL3


1. General information

Official gene symbolYPEL3
Entrez ID83719
Gene full nameyippee-like 3 (Drosophila)
Other gene symbols
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0005730NucleolusIEAcellular_component
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.21100425520.17362896550.88479698900.8070082995

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Down-0.1383307981
GSE13712_SHEARDown-0.1040892458
GSE13712_STATICDown-0.5555642984
GSE19018Up0.2614151367
GSE19899_A1Down-0.0599942880
GSE19899_A2Down-0.1639013999
PubMed_21979375_A1Down-0.5549779747
PubMed_21979375_A2Down-0.1247664681
GSE35957Up0.3092637700
GSE36640Up0.4690322152
GSE54402Down-0.0775393128
GSE9593Down-0.0224379561
GSE43922Down-0.3990219185
GSE24585Up1.4813320985
GSE37065Down-0.2429905037
GSE28863_A1Down-0.1203155840
GSE28863_A2Down-0.1764404959
GSE28863_A3Up0.2304595057
GSE28863_A4Down-0.0704646878
GSE48662Up0.8806367544

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

    • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-335-5pMIMAT0000765MIRT017916MicroarrayFunctional MTI (Weak)18185580
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    • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 4 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

21671470Novel senescence associated gene, YPEL3, is repressed by estrogen in ER+ mammary tumor cells and required for tamoxifen-induced cellular senescence
21671470Here, we identify YPEL3 as a growth suppressive protein downregulated by estrogen in estrogen receptor positive breast cancer cell lines
21671470Estrogen repression of YPEL3 expression was found to be independent of p53 but dependent on estrogen receptor alpha expression
21671470Importantly, YPEL3 expression, which is induced by the removal of estrogen or treatment with tamoxifen triggers cellular senescence in MCF-7 cells while loss of YPEL3 increases the growth rate of MCF-7 cells
21671470Taken together these findings suggest that YPEL3 may represent a potential target for directed hormonal therapy for estrogen receptor positive breast cancer patients
21267786Senescence-associated gene YPEL3 is downregulated in human colon tumors
21267786BACKGROUND: Previous work has demonstrated YPEL3 to be a growth-suppressive protein that acts through a pathway of cellular senescence
21267786We set out to determine whether human colon tumors demonstrated downregulation of YPEL3
21267786METHODS: We collected colon tumor samples with matched normal control samples and analyzed them for YPEL3 gene expression by reverse transcriptase-polymerase chain reaction and CpG hypermethylation of the YPEL3 promoter by base-specific polymerase chain reaction analysis
21267786Colon cancer cell lines (Caco-2 and HCT116(-/-) p53) were used to assess YPEL3 gene expression after treatment with 5-azadeoxycytidine or trichostatin A
21267786RESULTS: Reverse transcriptase-polymerase chain reaction analysis demonstrated a decrease in YPEL3 expression in tumor samples when compared to their patient-matched normal tissue
21267786We determined that DNA methylation of the YPEL3 promoter CpG island does not play a role in YPEL3 regulation in human colon tumors or colon cancer cells lines, consistent with the inability of 5-azadeoxycytidine treatment to induce YPEL3 expression in colon cancer cell lines
21267786In contrast, colon cell line results suggest that histone acetylation may play a role in YPEL3 regulation in colon cancer
21267786CONCLUSIONS: YPEL3 is preferentially downregulated in human colon adenocarcinomas
21267786DNA hypermethylation does not appear to be the mechanism of YPEL3 downregulation in this subset of collected patient samples or in colon cell lines
21267786Histone acetylation may be a relevant epigenetic modulator of YPEL3 in colon adenocarcinomas
21267786Future investigation of YPEL3 and its role in colon cancer signaling and development may lead to increased understanding and alternative treatment options for this disease
21196260Why YPEL3 represents a novel tumor suppressor
21196260Yippee-like 3 (YPEL3) was reported in 2004 as one of five family members of the Yippee protein with conservation in species down to slime molds
21196260While reports of other YPEL family members have surfaced our laboratory was the first to report that YPEL3 is induced by the p53 tumor suppressor
21196260Furthermore we demonstrated that YPEL3 is growth suppressive, triggering cellular senescence in human cell lines and is down-regulated in several human tumors
21196260Studies with mouse YPEL3, originally named small unstable apoptotic protein (SUAP), confirmed that the gene encodes a growth suppressive highly unstable protein
21196260While there are several reported YPEL3 transcripts and potentially 2 protein isoforms, no clear protein structure has been reported
21196260As evidence mounts that YPEL3 is a tumor suppressor gene, studies aimed at understanding its biological function, regulation of gene expression and impact on tumorigenesis will help
20388804YPEL3, a p53-regulated gene that induces cellular senescence
20388804In microarray studies in which p53 was reactivated in MCF7 cells, we discovered that Yippee-like-3 (YPEL3), a member of a recently discovered family of putative zinc finger motif coding genes consisting of YPEL1-5, is a p53-regulated gene
20388804YPEL3 expression induced by DNA damage leads to p53 recruitment to a cis-acting DNA response element located near the human YPEL3 promoter
20388804Physiologic induction of YPEL3 results in a substantial decrease in cell viability associated with an increase in cellular senescence
20388804Consistent with its growth suppressive activity, YPEL3 gene expression is repressed in ovarian tumor samples
20388804One mechanism of YPEL3 downregulation in ovarian tumor cell lines seems to be hypermethylation of a CpG island upstream of the YPEL3 promoter
20388804We believe these findings point to YPEL3 being a novel tumor suppressor, which upon induction triggers a permanent growth arrest in human tumor and normal cells
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