DSE
O Epimerase de sulfato de dermatano é uma enzima que em humanos é codificada pelo gene DSE.[2][3][4][5][6] A proteína codificada por este gene é um antígeno de rejeição de tumor. Este antígeno possui epitopos tumorais capazes de induzir linfócitos T citotóxicos restritos a HLA-A24 e citotóxicos específicos para tumores em pacientes com câncer e podem ser úteis para imunoterapia específica. Este produto gênico está localizado no retículo endoplasmático. Duas variantes transcritas que codificam a mesma proteína foram encontradas para este gene.[4]
Referências
- ↑ «Human PubMed Reference:»
- ↑ Sasatomi T, Suefuji Y, Matsunaga K, Yamana H, Miyagi Y, Araki Y, Ogata Y, Itoh K, Shirouzu K (março de 2002). «Expression of tumor rejection antigens in colorectal carcinomas». Cancer. 94 (6): 1636–41. PMID 11920522. doi:10.1002/cncr.10421
- ↑ Maccarana M, Olander B, Malmstrom J, Tiedemann K, Aebersold R, Lindahl U, Li JP, Malmstrom A (abril de 2006). «Biosynthesis of dermatan sulfate: chondroitin-glucuronate C5-epimerase is identical to SART2». J Biol Chem. 281 (17): 11560–8. PMID 16505484. doi:10.1074/jbc.M513373200
- ↑ a b «Entrez Gene: DSE dermatan sulfate epimerase»
- ↑ Sasatomi T, Suefuji Y, Matsunaga K, Yamana H, Miyagi Y, Araki Y, Ogata Y, Itoh K, Shirouzu K (março de 2002). «Expression of tumor rejection antigens in colorectal carcinomas». Cancer. 94 (6): 1636–41. PMID 11920522. doi:10.1002/cncr.10421
- ↑ Maccarana M, Olander B, Malmström J, Tiedemann K, Aebersold R, Lindahl U, Li JP, Malmström A (abril de 2006). «Biosynthesis of dermatan sulfate: chondroitin-glucuronate C5-epimerase is identical to SART2». J. Biol. Chem. 281 (17): 11560–8. PMID 16505484. doi:10.1074/jbc.M513373200
Leitura adicional
- Nakao M, Shichijo S, Imaizumi T, et al. (2000). «Identification of a gene coding for a new squamous cell carcinoma antigen recognized by the CTL». J. Immunol. 164 (5): 2565–74. PMID 10679095. doi:10.4049/jimmunol.164.5.2565
- Tanaka S, Tsuda N, Kawano K, et al. (2001). «Expression of tumor-rejection antigens in gynecologic cancers». Jpn. J. Cancer Res. 91 (11): 1177–84. PMC 5926290
. PMID 11092984. doi:10.1111/j.1349-7006.2000.tb00902.x - Strausberg RL, Feingold EA, Grouse LH, et al. (2003). «Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences». Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. PMC 139241
. PMID 12477932. doi:10.1073/pnas.242603899 - Mungall AJ, Palmer SA, Sims SK, et al. (2003). «The DNA sequence and analysis of human chromosome 6». Nature. 425 (6960): 805–11. PMID 14574404. doi:10.1038/nature02055
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). «Complete sequencing and characterization of 21,243 full-length human cDNAs». Nat. Genet. 36 (1): 40–5. PMID 14702039. doi:10.1038/ng1285
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). «The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)». Genome Res. 14 (10B): 2121–7. PMC 528928
. PMID 15489334. doi:10.1101/gr.2596504 - Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). «Diversification of transcriptional modulation: Large-scale identification and characterization of putative alternative promoters of human genes». Genome Res. 16 (1): 55–65. PMC 1356129
. PMID 16344560. doi:10.1101/gr.4039406
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