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SDPR

From Wikipedia, the free encyclopedia
CAVIN2
Identifiers
AliasesCAVIN2, PS-p68, SDR, cavin-2, SDPR, serum deprivation response, caveolae associated protein 2
External IDsOMIM: 606728; MGI: 99513; HomoloGene: 3422; GeneCards: CAVIN2; OMA:CAVIN2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004657

NM_138741

RefSeq (protein)

NP_004648

NP_620080

Location (UCSC)Chr 2: 191.83 – 191.85 MbChr 1: 51.33 – 51.34 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Cavin-2 or Serum deprivation-response protein (SDPR) is a protein that in humans is encoded by the SDPR gene.[5][6][7] Cavin-2 is highly expressed in a variety of human endothelial cells.[8]

This gene has a calcium-independent phospholipid-binding protein whose expression increases in serum-starved cells. This protein has also been shown to be a substrate for protein kinase C (PKC) phosphorylation.[7]

Function

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Cavin-2 is required for blood vessel formation (angiogenesis) in humans and zebrafish and required also for the endothelial cell proliferation, migration and invasion in humans.[8] Cavin-2 plays an important role in endothelial cell maintenance by regulating eNOS activity.[8] Cavin-2 controls the generation of nitric oxide (NO) in human endothelial cells by controlling the activity and stability of the protein endothelial nitric-oxide synthase (eNOS).[8]

Secretion

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Cavin-2 is highly secreted from human endothelial cells (HUVEC), they are secreted through endothelial microparticles (EMPs) but not exosomes and is required for EMP biogenesis.[8]

Clinical significance

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SDPR is shown to act as a metastasis suppressor by xenograft studies utilizing breast cancer cell lines.[9] SDPR may elicit its metastasis suppressor function by directly interacting with ERK and limiting its pro-survival role.[9] Moreover, it is suggested that SDPR is silenced during breast cancer progression by promoter DNA methylation.[9] Metastasis suppressor role of SDPR may go beyond breast cancer since tumor samples from bladder, colorectal, lung, pancreatic, and ovarian cancers as well as sarcomas also exhibited loss of SDPR expression.[9]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000168497Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000045954Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Gustincich S, Vatta P, Goruppi S, Wolf M, Saccone S, Della Valle G, et al. (April 1999). "The human serum deprivation response gene (SDPR) maps to 2q32-q33 and codes for a phosphatidylserine-binding protein". Genomics. 57 (1): 120–9. doi:10.1006/geno.1998.5733. PMID 10191091.
  6. ^ Gustincich S, Schneider C (September 1993). "Serum deprivation response gene is induced by serum starvation but not by contact inhibition". Cell Growth & Differentiation. 4 (9): 753–60. PMID 8241023.
  7. ^ a b "Entrez Gene: SDPR serum deprivation response (phosphatidylserine binding protein)".
  8. ^ a b c d e Boopathy GT, Kulkarni M, Ho SY, Boey A, Chua EW, Barathi VA, et al. (October 2017). "Cavin-2 regulates the activity and stability of endothelial nitric-oxide synthase (eNOS) in angiogenesis". The Journal of Biological Chemistry. 292 (43): 17760–17776. doi:10.1074/jbc.M117.794743. PMC 5663877. PMID 28912276.
  9. ^ a b c d Ozturk S, Papageorgis P, Wong CK, Lambert AW, Abdolmaleky HM, Thiagalingam A, et al. (January 2016). "SDPR functions as a metastasis suppressor in breast cancer by promoting apoptosis". Proceedings of the National Academy of Sciences of the United States of America. 113 (3): 638–43. Bibcode:2016PNAS..113..638O. doi:10.1073/pnas.1514663113. PMC 4725521. PMID 26739564.

Further reading

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