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{{Ficha de proteína}}

'''La proteína 3 de resistencia a los antiestrógenos del cáncer de mama''' es una [[proteína]] que en los humanos está codificada por el [[gen]] ''BCAR3''. <ref name="pmid9582273">{{Cita publicación|título=Identification of BCAR3 by a random search for genes involved in antiestrogen resistance of human breast cancer cells|apellidos=van Agthoven T, van Agthoven TL, Dekker A, van der Spek PJ, Vreede L, Dorssers LC|fecha=Jul 1998|publicación=EMBO J|volumen=17|número=10|páginas=2799–808|doi=10.1093/emboj/17.10.2799|pmc=1170620|pmid=9582273}}</ref> <ref name="entrez">{{Cita web|url=https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8412|título=Entrez Gene: BCAR3 breast cancer anti-estrogen resistance 3}}</ref>
La '''proteína 3 de resistencia a los antiestrógenos del cáncer de mama''' es una [[proteína]] que en los humanos está codificada por el [[gen]] ''BCAR3''. <ref name="pmid9582273">{{Cita publicación|título=Identification of BCAR3 by a random search for genes involved in antiestrogen resistance of human breast cancer cells|apellidos=van Agthoven T, van Agthoven TL, Dekker A, van der Spek PJ, Vreede L, Dorssers LC|fecha=Jul 1998|publicación=EMBO J|volumen=17|número=10|páginas=2799–808|doi=10.1093/emboj/17.10.2799|pmc=1170620|pmid=9582273}}</ref> <ref name="entrez">{{Cita web|url=https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8412|título=Entrez Gene: BCAR3 breast cancer anti-estrogen resistance 3}}</ref>


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== Referencias ==
== Referencias ==

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== Otras lecturas ==
== Otras lecturas ==
*{{cite journal | authors=Dorssers LC, van Agthoven T |title=Genetic mechanisms of estrogen-independence in breast cancer. |journal=Pathol. Res. Pract. |volume=192 |issue= 7 |pages= 743–51 |year= 1997 |pmid= 8880875 |doi= 10.1016/S0344-0338(96)80096-3}}

*{{cite journal | author=Johnston SR |title=Acquired tamoxifen resistance in human breast cancer--potential mechanisms and clinical implications. |journal=Anticancer Drugs |volume=8 |issue= 10 |pages= 911–30 |year= 1998 |pmid= 9436634 |doi=10.1097/00001813-199711000-00002 }}
*{{cite journal | authors=Lu Y, Brush J, Stewart TA |title=NSP1 defines a novel family of adaptor proteins linking integrin and tyrosine kinase receptors to the c-Jun N-terminal kinase/stress-activated protein kinase signaling pathway. |journal=J. Biol. Chem. |volume=274 |issue= 15 |pages= 10047–52 |year= 1999 |pmid= 10187783 |doi=10.1074/jbc.274.15.10047 }}
*{{cite journal | authors=Strausberg RL, Feingold EA, Grouse LH |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |bibcode=2002PNAS...9916899M |display-authors=etal}}
*{{cite journal | authors=Cai D, Felekkis KN, Near RI |title=The GDP exchange factor AND-34 is expressed in B cells, associates with HEF1, and activates Cdc42. |journal=J. Immunol. |volume=170 |issue= 2 |pages= 969–78 |year= 2003 |pmid= 12517963 |doi= 10.4049/jimmunol.170.2.969|display-authors=etal}}
*{{cite journal | authors=Clark HF, Gurney AL, Abaya E |title=The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. |journal=Genome Res. |volume=13 |issue= 10 |pages= 2265–70 |year= 2003 |pmid= 12975309 |doi= 10.1101/gr.1293003 | pmc=403697 |display-authors=etal}}
*{{cite journal | authors=Ota T, Suzuki Y, Nishikawa T |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285}}
*{{cite journal | authors=Gerhard DS, Wagner L, Feingold EA |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 |display-authors=etal}}
*{{cite journal | authors=Dorssers LC, van Agthoven T, Brinkman A |title=Breast cancer oestrogen independence mediated by BCAR1 or BCAR3 genes is transmitted through mechanisms distinct from the oestrogen receptor signalling pathway or the epidermal growth factor receptor signalling pathway. |journal=Breast Cancer Res. |volume=7 |issue= 1 |pages= R82–92 |year= 2006 |pmid= 15642172 |doi= 10.1186/bcr954 | pmc=1064102 |display-authors=etal}}
*{{cite journal | authors=Felekkis KN, Narsimhan RP, Near R |title=AND-34 activates phosphatidylinositol 3-kinase and induces anti-estrogen resistance in a SH2 and GDP exchange factor-like domain-dependent manner. |journal=Mol. Cancer Res. |volume=3 |issue= 1 |pages= 32–41 |year= 2005 |doi=10.1158/1541-7786.32.3.1 |pmid= 15671247 |s2cid=2758592 |display-authors=etal}}
*{{cite journal | authors=Gregory SG, Barlow KF, McLay KE |title=The DNA sequence and biological annotation of human chromosome 1. |journal=Nature |volume=441 |issue= 7091 |pages= 315–21 |year= 2006 |pmid= 16710414 |doi= 10.1038/nature04727 |bibcode=2006Natur.441..315G |display-authors=etal}}
*{{cite journal | authors=Beausoleil SA, Villén J, Gerber SA |title=A probability-based approach for high-throughput protein phosphorylation analysis and site localization. |journal=Nat. Biotechnol. |volume=24 |issue= 10 |pages= 1285–92 |year= 2006 |pmid= 16964243 |doi= 10.1038/nbt1240 |s2cid=14294292 |display-authors=etal}}
*{{cite journal | authors=Olsen JV, Blagoev B, Gnad F |title=Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. |journal=Cell |volume=127 |issue= 3 |pages= 635–48 |year= 2006 |pmid= 17081983 |doi= 10.1016/j.cell.2006.09.026 |display-authors=etal}}
*{{cite journal | authors=Vervoort VS, Roselli S, Oshima RG, Pasquale EB |title=Splice variants and expression patterns of SHEP1, BCAR3 and NSP1, a gene family involved in integrin and receptor tyrosine kinase signaling. |journal=Gene |volume=391 |issue= 1–2 |pages= 161–70 |year= 2007 |pmid= 17270363 |doi= 10.1016/j.gene.2006.12.016 | pmc=1876674 }}
*{{cite journal | authors=Ewing RM, Chu P, Elisma F |title=Large-scale mapping of human protein-protein interactions by mass spectrometry. |journal=Mol. Syst. Biol. |volume=3 |issue= 1|pages= 89 |year= 2007 |pmid= 17353931 |doi= 10.1038/msb4100134 | pmc=1847948 |display-authors=etal}}
*{{cite journal | authors=Near RI, Zhang Y, Makkinje A |title=AND-34/BCAR3 differs from other NSP homologs in induction of anti-estrogen resistance, cyclin D1 promoter activation and altered breast cancer cell morphology. |journal=J. Cell. Physiol. |volume=212 |issue= 3 |pages= 655–65 |year= 2007 |pmid= 17427198 |doi= 10.1002/jcp.21059 | pmc=2640322 |display-authors=etal}}
*{{cite journal | authors=Schrecengost RS, Riggins RB, Thomas KS |title=Breast cancer antiestrogen resistance-3 expression regulates breast cancer cell migration through promotion of p130Cas membrane localization and membrane ruffling. |journal=Cancer Res. |volume=67 |issue= 13 |pages= 6174–82 |year= 2007 |pmid= 17616674 |doi= 10.1158/0008-5472.CAN-06-3455 |display-authors=etal|pmc=4109708 }}
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[[Categoría:Genes del cromosoma 1]]
[[Categoría:Genes del cromosoma 1]]

Revisión actual - 03:25 24 abr 2024

BCAR3
Identificadores

La proteína 3 de resistencia a los antiestrógenos del cáncer de mama es una proteína que en los humanos está codificada por el gen BCAR3. [1][2]

Función[editar]

Los tumores de mama dependen inicialmente de los estrógenos para su crecimiento y progresión y pueden ser inhibidos por antiestrógenos como el tamoxifeno. Sin embargo, los cánceres de mama progresan hasta volverse resistentes a los antiestrógenos. El gen 3 de resistencia a los estrógenos del cáncer de mama se identificó en la búsqueda de genes implicados en el desarrollo de la resistencia a los estrógenos. El gen codifica un componente de la transducción de señales intracelulares que provoca la proliferación independiente de estrógenos en las células de cáncer de mama humano. La proteína contiene un dominio putativo de homología src 2 (SH2), un sello distintivo de las moléculas de señalización de tirosina quinasa celular, y es parcialmente homólogo a la proteína del ciclo de división celular CDC48. [2]

Referencias[editar]

Otras lecturas[editar]