HCSGD entry for MARCKS


1. General information

Official gene symbolMARCKS
Entrez ID4082
Gene full namemyristoylated alanine-rich protein kinase C substrate
Other gene symbols80K-L MACS PKCSL PRKCSL
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0005080Protein kinase C bindingIEAmolecular_function
GO:0005516Calmodulin bindingIEAmolecular_function
GO:0005813CentrosomeIEAcellular_component
GO:0005886Plasma membraneTAScellular_component
GO:0005938Cell cortexIEAcellular_component
GO:0006112Energy reserve metabolic processTASbiological_process
GO:0015629Actin cytoskeletonTAScellular_component
GO:0042585Germinal vesicleIEAcellular_component
GO:0044281Small molecule metabolic processTASbiological_process
GO:0050796Regulation of insulin secretionTASbiological_process
GO:0051015Actin filament bindingTASmolecular_function
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.97551654570.00127750470.99999024730.0683439024

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

Data sourceUp or downLog fold change
GSE11954Down-0.6369258994
GSE13712_SHEARUp0.1285307909
GSE13712_STATICDown-0.2579403604
GSE19018Down-0.1087661319
GSE19899_A1Down-1.1686247623
GSE19899_A2Down-1.0160364231
PubMed_21979375_A1Down-2.1243511023
PubMed_21979375_A2Down-2.2096661145
GSE35957Down-0.7458958724
GSE36640Down-1.0024534688
GSE54402Down-0.6828632410
GSE9593Down-0.2234892877
GSE43922Down-0.5893231811
GSE24585Down-0.1560904298
GSE37065Down-0.3717750432
GSE28863_A1Up0.8870329889
GSE28863_A2Up0.3082624182
GSE28863_A3Up0.0996125663
GSE28863_A4Down-0.4772317330
GSE48662Down-0.1928320893

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-21-5pMIMAT0000076MIRT001221Luciferase reporter assay//Western blotFunctional MTI19302977
hsa-miR-155-5pMIMAT0000646MIRT020762ProteomicsFunctional MTI (Weak)18668040
hsa-miR-122-5pMIMAT0000421MIRT023285MicroarrayFunctional MTI (Weak)17612493
hsa-miR-1MIMAT0000416MIRT023806MicroarrayFunctional MTI (Weak)18668037
hsa-miR-877-5pMIMAT0004949MIRT037313CLASHFunctional MTI (Weak)23622248
hsa-miR-15b-5pMIMAT0000417MIRT046418CLASHFunctional MTI (Weak)23622248
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  • mirRecord

MicroRNA name

mirBase ID

Target site number

MiRNA mature ID

Test method inter

MiRNA regulation site

Reporter target site

Pubmed ID

hsa-miR-21-5pMIMAT00000761hsa-miR-21{Western blot}{downregulation by anti-miRNA oligonucleotide}19302977
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6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 8 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

27081703MARCKS contributes to stromal cancer-associated fibroblast activation and facilitates ovarian cancer metastasis
27081703Here, we determined that myristoylated alanine-rich C-kinase substrate (MARCKS) was highly expressed in ovarian stroma, and was required for the differentiation and tumor promoting function of CAFs
27081703Suppression of MARCKS resulted in the loss of CAF features, and diminished role of CAFs in supporting tumor cell growth in 3D organotypic cultures and in murine xenograft model
27081703Mechanistically, we found that MARCKS maintained CAF activation through suppression of cellular senescence and activation of the AKT/Twist1 signaling
27081703Moreover, high MARCKS expression was associated with poor patient survival in EOC
27081703Collectively, our findings identify the potential of MARCKS inhibition as a novel stroma-oriented therapy in EOC
26084179METHOD: Sca-1 + HSC/HPC was isolated by magnetic cell sorting (MACS) and divided into five groups: the normal control group, the aging group, the positive control group, the Rg1 anti-senescence group, and the Rg1-treated group
25993799METHOD: Acute myelogenous leukemia stem cells were isolated by magnetic activated cell sorting (MACS)
25688074Demographic, clinical and laboratory parameters were collected in all patients and we isolated naive (CD45RA(+)) and memory (CD45RO(+)) CD4(+) and CD8(+) T-cell subsets by MACS technology
24335839Sca-1(+) HSC/HPCs were isolated and purified from their bone marrow using MACS
23643076Thereafter, Sca-1(+);HSC/HPC were isolated by magnetic-activated cell sorting (MACS) from bone marrow of all the mice
23643076RESULTS: The purity of Sca-1(+);HSC/HPC reached 94% after MACS
21657082METHOD: Sca-1 + HSC was isolated by magnetic cell sorting (MACS) and divided into five groups
8536797The life span of the biotin-conjugated cells was found to be normal (approximately 110 days), and the stability of the biotin ligand was adequate for efficient retrieval of cells using avidin-coated magnetic beads (magnetic cell sorting [MACS])
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