CD82 (Cluster of Differentiation 82), or KAI1, is a human protein encoded by the CD82gene.[5]
This metastasis suppressor gene product is a membrane glycoprotein that is a member of the tetraspanin/transmembrane 4 superfamily. Expression of this gene has been shown to be downregulated in tumor progression of human cancers and can be activated by p53 through a consensus binding sequence in the promoter. Its expression and that of p53 are strongly correlated, and the loss of expression of these two proteins is associated with poor survival for prostate cancer patients. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.[5]
^Imai T, Kakizaki M, Nishimura M, Yoshie O (August 1995). "Molecular analyses of the association of CD4 with two members of the transmembrane 4 superfamily, CD81 and CD82". Journal of Immunology. 155 (3): 1229–39. PMID7636191.
^Hammond C, Denzin LK, Pan M, Griffith JM, Geuze HJ, Cresswell P (October 1998). "The tetraspan protein CD82 is a resident of MHC class II compartments where it associates with HLA-DR, -DM, and -DO molecules". Journal of Immunology. 161 (7): 3282–91. PMID9759843.
Imai T, Fukudome K, Takagi S, Nagira M, Furuse M, Fukuhara N, et al. (November 1992). "C33 antigen recognized by monoclonal antibodies inhibitory to human T cell leukemia virus type 1-induced syncytium formation is a member of a new family of transmembrane proteins including CD9, CD37, CD53, and CD63". Journal of Immunology. 149 (9): 2879–86. PMID1401919.
Ichikawa T, Ichikawa Y, Dong J, Hawkins AL, Griffin CA, Isaacs WB, et al. (June 1992). "Localization of metastasis suppressor gene(s) for prostatic cancer to the short arm of human chromosome 11". Cancer Research. 52 (12): 3486–90. PMID1596907.
Gaugitsch HW, Hofer E, Huber NE, Schnabl E, Baumruker T (February 1991). "A new superfamily of lymphoid and melanoma cell proteins with extensive homology to Schistosoma mansoni antigen Sm23". European Journal of Immunology. 21 (2): 377–83. doi:10.1002/eji.1830210219. PMID1842498. S2CID423800.
Ichikawa T, Ichikawa Y, Isaacs JT (July 1991). "Genetic factors and suppression of metastatic ability of prostatic cancer". Cancer Research. 51 (14): 3788–92. PMID2065333.
Imai T, Kakizaki M, Nishimura M, Yoshie O (August 1995). "Molecular analyses of the association of CD4 with two members of the transmembrane 4 superfamily, CD81 and CD82". Journal of Immunology. 155 (3): 1229–39. PMID7636191.
Maruyama K, Sugano S (January 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID8125298.
Mannion BA, Berditchevski F, Kraeft SK, Chen LB, Hemler ME (September 1996). "Transmembrane-4 superfamily proteins CD81 (TAPA-1), CD82, CD63, and CD53 specifically associated with integrin alpha 4 beta 1 (CD49d/CD29)". Journal of Immunology. 157 (5): 2039–47. PMID8757325.
Szöllósi J, Horejsí V, Bene L, Angelisová P, Damjanovich S (October 1996). "Supramolecular complexes of MHC class I, MHC class II, CD20, and tetraspan molecules (CD53, CD81, and CD82) at the surface of a B cell line JY". Journal of Immunology. 157 (7): 2939–46. PMID8816400.
Dong JT, Isaacs WB, Barrett JC, Isaacs JT (April 1997). "Genomic organization of the human KAI1 metastasis-suppressor gene". Genomics. 41 (1): 25–32. doi:10.1006/geno.1997.4618. PMID9126478.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (October 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID9373149.
Hammond C, Denzin LK, Pan M, Griffith JM, Geuze HJ, Cresswell P (October 1998). "The tetraspan protein CD82 is a resident of MHC class II compartments where it associates with HLA-DR, -DM, and -DO molecules". Journal of Immunology. 161 (7): 3282–91. PMID9759843.
Odintsova E, Sugiura T, Berditchevski F (August 2000). "Attenuation of EGF receptor signaling by a metastasis suppressor, the tetraspanin CD82/KAI-1". Current Biology. 10 (16): 1009–12. doi:10.1016/S0960-9822(00)00652-7. PMID10985391. S2CID15731587.
Ono M, Handa K, Withers DA, Hakomori S (December 2000). "Glycosylation effect on membrane domain (GEM) involved in cell adhesion and motility: a preliminary note on functional alpha3, alpha5-CD82 glycosylation complex in ldlD 14 cells". Biochemical and Biophysical Research Communications. 279 (3): 744–50. doi:10.1006/bbrc.2000.4030. PMID11162423.