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CD30

From Wikipedia, the free encyclopedia

Mammalian protein found in humans
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This article'slead sectionmay be too short to adequatelysummarize the key points. Please consider expanding the lead toprovide an accessible overview of all important aspects of the article.(November 2016)
TNFRSF8
Available structures
PDBOrtholog search:PDBeRCSB
List of PDB id codes

1D01

Identifiers
AliasesTNFRSF8, CD30, D1S166E, Ki-1, tumor necrosis factor receptor superfamily member 8, TNF receptor superfamily member 8
External IDsOMIM:153243;MGI:99908;HomoloGene:949;GeneCards:TNFRSF8;OMA:TNFRSF8 - orthologs
Gene location (Human)
Chromosome 1 (human)
Chr.Chromosome 1 (human)[1]
Chromosome 1 (human)
Genomic location for TNFRSF8
Genomic location for TNFRSF8
Band1p36.22Start12,063,303bp[1]
End12,144,207bp[1]
Gene location (Mouse)
Chromosome 4 (mouse)
Chr.Chromosome 4 (mouse)[2]
Chromosome 4 (mouse)
Genomic location for TNFRSF8
Genomic location for TNFRSF8
Band4 E1|4 78.17 cMStart144,993,707bp[2]
End145,041,734bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • granulocyte

  • monocyte

  • testicle

  • blood

  • pancreatic ductal cell

  • decidua

  • subcutaneous adipose tissue

  • periodontal fiber

  • appendix

  • right auricle of heart
Top expressed in
  • neural layer of retina

  • blastocyst

  • secondary oocyte

  • embryo

  • zygote

  • morula

  • embryo

  • thymus

  • dentate gyrus of hippocampal formation granule cell

  • primary oocyte
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo /QuickGO
Orthologs
SpeciesHumanMouse
Entrez

943

21941

Ensembl

ENSG00000120949

ENSMUSG00000028602

UniProt

P28908

Q60846

RefSeq (mRNA)

NM_001243
NM_001281430
NM_152942

NM_009401

RefSeq (protein)

NP_001234
NP_001268359

NP_033427

Location (UCSC)Chr 1: 12.06 – 12.14 MbChr 4: 144.99 – 145.04 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

CD30, also known asTNFRSF8 (TNF receptor superfamily member 8),[5] is a cell membraneprotein of thetumor necrosis factor receptor family and atumor marker foranaplastic large cell lymphoma.

Function

[edit]

This receptor is expressed by activated, but not by resting,T andB cells.TRAF2 andTRAF5 can interact with this receptor, and mediate the signal transduction that leads to the activation ofNF-kappaB.[6] It is a positive regulator ofapoptosis,[7] and also has been shown to limit the proliferative potential of autoreactive CD8 effector T cells and protect the body against autoimmunity.[citation needed] Twoalternatively spliced transcript variants of this gene encoding distinct isoforms have been reported.[5]

Clinical significance

[edit]

CD30 is associated withanaplastic large cell lymphoma. It is expressed inembryonal carcinoma but not inseminoma and is thus a useful marker in distinguishing between thesegerm cell tumors.[8] CD30 andCD15 are also expressed onReed-Sternberg cells typical forHodgkin's lymphoma.[9]

Cancer treatment

[edit]

CD30 is the target of the FDA approved therapeuticbrentuximab vedotin (Adcetris). It is approved for use in:

  1. Hodgkin lymphoma (HL) (brentuximab vedotin) after failure of autologous stem cell transplant (ASCT)
  2. HL in patients who are not ASCT candidates after failure of at least 2 multiagent chemotherapy regimens
  3. Systemic anaplastic large cell lymphoma (sALCL) after failure of at least 1 multiagent chemotherapy regimen[10]
  4. Primary cutaneous anaplastic large cell lymphoma (pcALCL) or CD30-expressingmycosis fungoides (MF) who have received prior systemic therapy[11]
  5. Various types of CD30-positiveT cell lymphomas[12]

Brentuximab vedotin is also currently being studied in and recommended for treating:

  1. Various types of CD30-positive B cell lymphomas[13]
  2. CD30-positive cases of theNK cell lymphoma,extranodal NK/T-cell lymphoma, nasal type[14]

Interactions

[edit]

CD30 has been shown tointeract withTRAF5,[6] andTRAF2.[6][7]

References

[edit]
  1. ^abcGRCh38: Ensembl release 89: ENSG00000120949Ensembl, May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000028602Ensembl, 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. ^ab"Entrez Gene: TNFRSF8 tumor necrosis factor receptor superfamily member 8".National Library of Medicine, National Center for Biotechnology Information. 22 September 2022. Retrieved6 November 2022.
  6. ^abcAizawa S, Nakano H, Ishida T, Horie R, Nagai M, Ito K, et al. (January 1997)."Tumor necrosis factor receptor-associated factor (TRAF) 5 and TRAF2 are involved in CD30-mediated NFkappaB activation".The Journal of Biological Chemistry.272 (4):2042–2045.doi:10.1074/jbc.272.4.2042.PMID 8999898.
  7. ^abDuckett CS, Thompson CB (November 1997)."CD30-dependent degradation of TRAF2: implications for negative regulation of TRAF signaling and the control of cell survival".Genes & Development.11 (21):2810–2821.doi:10.1101/gad.11.21.2810.PMC 316646.PMID 9353251.
  8. ^Teng LH, Lu DH, Xu QZ, Fu YJ, Yang H, He ZL (Nov 2005). "[Expression and diagnostic significance of OCT4, CD117 and CD30 in germ cell tumors]".Zhonghua Bing Li Xue Za Zhi Chinese Journal of Pathology (in Chinese).34 (11):711–5.PMID 16536313.
  9. ^Gorczyca W, Tsang P, Liu Z, Wu CD, Dong HY, Goldstein M, Cohen P, Gangi M, Weisberger J (Feb 2003). "CD30-positive T-cell lymphomas co-expressing CD15: an immunohistochemical analysis".International Journal of Oncology.22 (2):319–24.doi:10.3892/ijo.22.2.319.PMID 12527929.
  10. ^Deng C, Pan B, O'Connor OA (Jan 2013)."Brentuximab vedotin".Clinical Cancer Research.19 (1):22–7.doi:10.1158/1078-0432.CCR-12-0290.PMID 23155186.
  11. ^"FDA approves Brentuximab vedotin for the treatment of adult patients with primary cutaneous anaplastic large cell lymphoma".FDA.gov. Archived fromthe original on November 14, 2017. RetrievedMarch 2, 2018.
  12. ^"FDA approves first-line treatment for peripheral T-cell lymphoma under new review pilot".FDA.gov. 24 March 2020. Archived fromthe original on December 15, 2019. RetrievedDecember 13, 2023.
  13. ^Berger GK, McBride A, Lawson S, Royball K, Yun S, Gee K, Bin Riaz I, Saleh AA, Puvvada S, Anwer F (January 2017)."Brentuximab vedotin for treatment of non-Hodgkin lymphomas: A systematic review".Critical Reviews in Oncology/Hematology.109:42–50.doi:10.1016/j.critrevonc.2016.11.009.PMC 5218629.PMID 28010897.
  14. ^Hu B, Oki Y (2018)."Novel Immunotherapy Options for Extranodal NK/T-Cell Lymphoma".Frontiers in Oncology.8: 139.doi:10.3389/fonc.2018.00139.PMC 5937056.PMID 29761078.

Further reading

[edit]

External links

[edit]

This article incorporates text from theUnited States National Library of Medicine, which is in thepublic domain.


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