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抗肿瘤药Dabrafenib 被引量:1

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摘要 Ras/Raf/MEK/ERK信号转导通路是调控细胞生长、分化和增殖最重要的通路之一,其中信号蛋白的过度表达或突变可导致肿瘤的发生和发展。如Raf激酶家族共包括3个成员—A.Raf、B—Raf和C—Raf,B—Raf在这3个成员中的突变率最高,约有7%~8%的人类肿瘤发生B-Raf 基因突变,而4-Raf 和c-R妒基因则较少发生突变。最具致命性的皮肤癌——黑色素瘤中B-Raf的突变率最高,约有40%~68%的转移性黑色素瘤发生这种突变,因此,
作者 杨臻峥
出处 《药学进展》 CAS 2013年第2期93-94,共2页 Progress in Pharmaceutical Sciences
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  • 7FLAHERTY KT,INFANTE JR,DAUD AN,et al.Combined BRAF and MEK inhibition in melanoma with BRAF V600mutations[J].N Engl J Med,2012,367(18):1694-1703.
  • 8KING AJ,ARNONE MR,BLEAM MR,et al.Dabrafenib;preclinical characterization,increased efficacy when combined with trametinib,while BRAF/MEK tool combination reduced skin lesions[J].PLo S One,2013,8(7):e67583.
  • 9王尔兵,王肇炎.恶性黑色素瘤的分子靶向药物治疗研究进展[J].医药导报,2012,31(10):1333-1336. 被引量:12

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