HCSGD entry for PRIMA1


1. General information

Official gene symbolPRIMA1
Entrez ID145270
Gene full nameproline rich membrane anchor 1
Other gene symbolsPRIMA
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:0016021Integral component of membraneIEAcellular_component
GO:0019899Enzyme bindingIEAmolecular_function
GO:0030054Cell junctionIEAcellular_component
GO:0031226Intrinsic component of plasma membraneIEAcellular_component
GO:0042135Neurotransmitter catabolic processIEAbiological_process
GO:0043495Protein anchorIEAmolecular_function
GO:0045202SynapseIEAcellular_component
GO:0051649Establishment of localization in cellIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.68703915500.81984015800.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.0302427814
GSE13712_SHEARUp0.1129334785
GSE13712_STATICUp0.0710921715
GSE19018Up0.0558097196
GSE19899_A1Up0.0099528591
GSE19899_A2Up0.1673373929
PubMed_21979375_A1Up0.0610793708
PubMed_21979375_A2Down-0.0185839612
GSE35957Up0.1754323174
GSE36640Down-0.0210557948
GSE54402Down-0.0544794976
GSE9593Down-0.0955706884
GSE43922Up0.0233788462
GSE24585Down-0.0600102763
GSE37065Down-0.0704653139
GSE28863_A1Down-0.1355557108
GSE28863_A2Down-0.0556986265
GSE28863_A3Up0.3878564010
GSE28863_A4Up0.0700784541
GSE48662Up0.0179717238

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-1MIMAT0000416MIRT023651MicroarrayFunctional MTI (Weak)18668037
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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: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

24804545PRIMA-1 selectively induces global DNA demethylation in p53 mutant-type thyroid cancer cells
24804545Recently, the identification of mutant p53-reactivating small molecules such as PRIMA-1 (p53 reactivation and induction of massive apoptosis) renders possibilities for the development of more efficient anticancer drugs
24804545Although PRIMA-1 has been widely used for cancer therapy and exhibits a promising anticancer activity, its biological effect, particularly the epigenetic aspect, remains to be well elucidated
24804545The present study attempts to explore the effect of PRIMA-1 on DNA methylation in a panel of thyroid cancer cell lines using luminometric methylation assay (LUMA)
24804545Our results showed that only p53 mutant-type cells were inhibited upon PRIMA-1 treatment
24804545Conversely, p53 wild-type cells were non-sensitive to PRIMA-1
24804545Moreover, our data demonstrated that PRIMA-1 selectively induced significant global DNA demethylation in p53 mutant-type cells
24804545Mechanically, PRIMA-1 induced global DNA demethylation in these cells mainly through inhibiting the expression of DNA methyltransferase (DNMT) 1, 3a and 3b, and upregulating the expression of GADD45a
24804545Notably, PRIMA-1 dramatically increased the expression of the ten-eleven translocation (TET) family of 5mC-hydroxylases, particularly TET1, in p53 mutant-type cells, further contributing to DNA demethylation
24804545Thus, this study uncovered a previously unrecognized and prominent biological effect of PRIMA-1 through which it can cause global DNA demethylation in p53 mutant-type cancer cells mainly by rescuing the function of mutant p53 protein
20498645The compound PRIMA-1 (p53 reactivation and induction of massive apoptosis) restores wild-type conformation to mutant p53 by binding to the core and induces apoptosis in human tumor cells
20498645The PRIMA-1 analog APR-246 is currently tested in a clinical trial
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