Neuropilin 1

Source: Wikipedia, the free encyclopedia.
NRP1
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_008737
NM_001358959
NM_001358960

RefSeq (protein)

NP_032763
NP_001345888
NP_001345889

Location (UCSC)Chr 10: 33.18 – 33.34 MbChr 8: 129.09 – 129.23 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Neuropilin-1 is a protein that in humans is encoded by the NRP1 gene.[5][6][7] In humans, the neuropilin 1 gene is located at 10p11.22. This is one of two human neuropilins.

Function

NRP1 is a membrane-bound

SEMA3A) family members. NRP1 plays versatile roles in angiogenesis, axon guidance, cell survival, migration, and invasion.[supplied by OMIM][7]

Interactions

Neuropilin 1 has been shown to

Role in COVID-19

Research has shown that neuropilin 1 facilitates entry of

SARS-CoV-2 into cells, making it a possible target for future antiviral drugs.[9][10]

Implication in cancer

Neuropilin 1 has been implicated in the vascularization and progression of cancers. NRP1 expression has been shown to be elevated in a number of human patient tumor samples, including brain, prostate, breast, colon, and lung cancers and NRP1 levels are positively correlated with metastasis.[11][12][13][14][15][16]

In prostate cancer NRP1 has been demonstrated to be an androgen-suppressed gene, upregulated during the adaptive response of prostate tumors to androgen-targeted therapies and a prognostic biomarker of clinical metastasis and lethal PCa.[11] In vitro and in vivo mouse studies have shown membrane bound NRP1 to be proangiogenic and that NRP1 promotes the vascularization of prostate tumors.[17]

Elevated NRP1 expression is also correlated with the invasiveness of

non-small cell lung cancer both in vitro and in vivo.[16]

Target for cancer therapies

As a co-receptor for VEGF, NRP1 is a potential target for cancer therapies. A synthetic peptide, EG3287, was generated in 2005 and has been shown to block NRP1 activity.[18] EG3287 has been shown to induce apoptosis in tumor cells with elevated NRP1 expression.[18] A patent for EG3287 was filed in 2002 and approved in 2003.[19] As of 2015 there were no clinical trials ongoing or completed for EG3287 as a human cancer therapy.

Soluble NRP1 has the opposite effect of membrane bound NRP1 and has anti-VEGF activity. In vivo mouse studies have shown that injections of sNRP-1 inhibits progression of acute myeloid leukemia in mice.[20]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000099250Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025810Ensembl, 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. ^
    S2CID 547080
    .
  6. .
  7. ^ a b "Entrez Gene: NRP1 neuropilin 1".
  8. PMID 11986311
    .
  9. .
  10. ^ "Neuropilin-1 drives SARS-CoV-2 infectivity, finds breakthrough study". MedicalXpress.
  11. ^
    PMID 28092670
    .
  12. .
  13. .
  14. .
  15. .
  16. ^ .
  17. .
  18. ^ .
  19. ^ "Vegf peptides and their use (WO 2003082918 A1)" (patent). Oct 9, 2003.
  20. PMID 10688880
    .

Further reading