Glypican 2

Glypican 2 (GPC2), also known cerebroglycan, is a protein which in humans is encoded by the GPC2 gene.[5][6] The GPC2 gene is at locus 7q22.1 and encodes for a 579 amino acid protein.[7] The C-terminus of GPC2 has the GPI attachment site, at G554, and the N-terminus encodes a signal peptide, from M1 to S24. Multiple GPC2 mRNA transcripts have been identified.[8] GPC2-201 is the isoform overexpressed in pediatric cancers. Tumor-associated exon 3 of GPC2 shows the lowest expression in normal tissues compared with other exons.[8]

GPC2
Identifiers
AliasesGPC2, Glypican 2
External IDsOMIM: 618446 MGI: 1919201 HomoloGene: 17657 GeneCards: GPC2
Orthologs
SpeciesHumanMouse
Entrez

221914

71951

Ensembl

ENSG00000213420

ENSMUSG00000029510

UniProt

Q8N158

Q8BKV1

RefSeq (mRNA)

NM_152742

NM_172412

RefSeq (protein)

NP_689955

NP_766000

Location (UCSC)Chr 7: 100.17 – 100.18 MbChr 5: 138.27 – 138.28 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

Cerebroglycan is a glycophosphatidylinositol-linked integral membrane heparan sulfate proteoglycan found in the developing nervous system. Cerebroglycan participates in cell adhesion and is thought to regulate the growth and guidance of axons.[9] Cerebroglycan has especially high affinity for laminin-1.[10]

Implications in cancer

GPC2 has been identified as a therapeutic target in neuroblastoma in two independent studies published by Dr. Mitchell Ho's lab at the NCI and Dr. John Maris's lab at the University of Pennsylvania in 2017.[11][12] GPC2 is highly expressed in about half of neuroblastoma cases and that high GPC2 expression correlates with poor overall survival.[11][13] GPC2 silencing inactivates Wnt/β-catenin signaling and reduces the expression of N-Myc, an oncogenic driver of neuroblastoma tumorigenesis.[11] Chimeric antigen receptor (CAR) T cells and Immunotoxins (antibody-cytotoxin fusion proteins) targeting GPC2 inhibit neuroblastoma growth in mouse models.[11] The Ho lab at the National Cancer Institute generated a mouse monoclonal antibody called CT3 targeting human GPC2.[8] The CT3 antibody has been shown to recognize a tumor-associated isoform (isoform 201) of GPC2 with high affinity.[8] Immunohistochemistry using CT3 shows that the antibody has high binding signals on neuroblastoma, medulloblastoma, and retinoblastoma.[8] CT3 does not bind human normal tissues except the testis.[8] CT3-derived CAR T cells regress neuroblastoma in mice.[8][14] The CT3 mAb is commercially available for Western blot, flow cytometry, immunohistochemistry, and immunofluorescence. A GPC2 specific antibody-drug conjugate (ADC) can inhibit neuroblastoma and small-cell lung cancer cell proliferation and tumor growth in mice.[12][15]

See also

References

  1. GRCh38: Ensembl release 89: ENSG00000213420 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000029510 - Ensembl, 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. Stipp CS, Litwack ED, Lander AD (January 1994). "Cerebroglycan: an integral membrane heparan sulfate proteoglycan that is unique to the developing nervous system and expressed specifically during neuronal differentiation". The Journal of Cell Biology. 124 (1–2): 149–160. doi:10.1083/jcb.124.1.149. PMC 2119891. PMID 8294498.
  6. "Entrez Gene: GPC2 glypican 2".
  7. Li N, Spetz MR, Li D, Ho M (July 2021). "Advances in immunotherapeutic targets for childhood cancers: A focus on glypican-2 and B7-H3". Pharmacology & Therapeutics. 223: 107892. doi:10.1016/j.pharmthera.2021.107892. PMC 8202769. PMID 33992682.
  8. Li N, Torres MB, Spetz MR, Wang R, Peng L, Tian M, et al. (June 2021). "CAR T cells targeting tumor-associated exons of glypican 2 regress neuroblastoma in mice". Cell Reports. Medicine. 2 (6): 100297. doi:10.1016/j.xcrm.2021.100297. PMC 8233664. PMID 34195677.
  9. Ivins JK, Litwack ED, Kumbasar A, Stipp CS, Lander AD (April 1997). "Cerebroglycan, a developmentally regulated cell-surface heparan sulfate proteoglycan, is expressed on developing axons and growth cones". Developmental Biology. 184 (2): 320–332. doi:10.1006/dbio.1997.8532. PMID 9133438. S2CID 23283933.
  10. Herndon ME, Stipp CS, Lander AD (February 1999). "Interactions of neural glycosaminoglycans and proteoglycans with protein ligands: assessment of selectivity, heterogeneity and the participation of core proteins in binding". Glycobiology. 9 (2): 143–155. doi:10.1093/glycob/9.2.143. PMID 9949192.
  11. Li N, Fu H, Hewitt SM, Dimitrov DS, Ho M (August 2017). "Therapeutically targeting glypican-2 via single-domain antibody-based chimeric antigen receptors and immunotoxins in neuroblastoma". Proceedings of the National Academy of Sciences of the United States of America. 114 (32): E6623–E6631. doi:10.1073/pnas.1706055114. PMC 5559039. PMID 28739923.
  12. Bosse KR, Raman P, Zhu Z, Lane M, Martinez D, Heitzeneder S, et al. (September 2017). "Identification of GPC2 as an Oncoprotein and Candidate Immunotherapeutic Target in High-Risk Neuroblastoma". Cancer Cell. 32 (3): 295–309.e12. doi:10.1016/j.ccell.2017.08.003. PMC 5600520. PMID 28898695.
  13. Li N, Spetz MR, Ho M (December 2020). "The Role of Glypicans in Cancer Progression and Therapy". The Journal of Histochemistry and Cytochemistry. 68 (12): 841–862. doi:10.1369/0022155420933709. PMC 7711243. PMID 32623934.
  14. Sun M, Cao Y, Okada R, Reyes-González JM, Stack HG, Qin H, et al. (January 2023). "Preclinical optimization of a GPC2-targeting CAR T-cell therapy for neuroblastoma". Journal for Immunotherapy of Cancer. 11 (1): e005881. doi:10.1136/jitc-2022-005881. PMC 9835961. PMID 36631162.
  15. Raman S, Buongervino SN, Lane MV, Zhelev DV, Zhu Z, Cui H, et al. (July 2021). "A GPC2 antibody-drug conjugate is efficacious against neuroblastoma and small-cell lung cancer via binding a conformational epitope". Cell Reports. Medicine. 2 (7): 100344. doi:10.1016/j.xcrm.2021.100344. PMC 8324494. PMID 34337560.
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