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肺癌新靶点药物研究进展 被引量:2

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摘要 肺癌的新靶点药物是近几年临床研究和关注的热点 ,主要有表皮生长因子受体 (EGFR)阻断剂、单克隆抗体、诱导分化剂、抗肿瘤血管生成药物、肿瘤耐药逆转剂以及抗肿瘤疫苗等 。
出处 《国外医学(肿瘤学分册)》 2004年第3期211-214,共4页 Foreign Medical Sciences (Cancer Section)
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参考文献14

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同被引文献16

  • 1申文江.表皮生长因子受体与肿瘤治疗[J].癌症进展,2004,2(1):60-63. 被引量:6
  • 2钱军,秦叔逵.针对表皮生长因子受体的靶向治疗研究进展[J].中国药科大学学报,2004,35(3):285-288. 被引量:14
  • 3顾岩,王立红,李国华.非小细胞肺癌的多药耐药[J].中国肿瘤临床与康复,2005,12(2):184-186. 被引量:6
  • 4王立红,顾岩,孙勤暖.非小细胞肺癌肿瘤血管生成研究进展[J].中国肿瘤临床与康复,2005,12(3):280-282. 被引量:1
  • 5管忠震,张力,李龙芸,蒋国梁,刘叙仪,储大同,赵洪云,李玮.吉非替尼治疗局部晚期或转移性非小细胞肺癌在中国的临床研究[J].癌症,2005,24(8):980-984. 被引量:114
  • 6Jemal A, Murray T, Samuels A, et al. Cancer statistics 2003 [ J ]. CA Cancer J Clin, 2003, 53( 1 ): 5-26.
  • 7Giordano A, Rustum YM, Wenner CE. Cell cycle: molecular targets for diagnesis and therapy : tumor suppressor genes and cell cycle progression in cancer [J]. J Cell Biochem, 1998, 70(1): 1-7.
  • 8Judit A, Pablo M, Joan AI, et al. ZD1839, a Specific epidermal growth factor receptor(EGFR) tyrosine kinase inhibitor, induces the formation of inactive EGFR/HER2 and EGFR/HER3 heterodimers and prevents heregulin Signaling in HER2 - overexpressing breast cancer cells [ J ]. Clinical Cancer Research,2003, 9:1274-1283.
  • 9Wakeling AE, Guy SP, Woodburn JR, et al. ZD1839 (Iressa) : an orally active inhibitor of epidermal growth factor signaling with potential for cancer therapy[J]. Cancer Res, 2002, 62:5749-5754.
  • 10Moulder SL, Yakes FM, Muthuswamy SK, et al. Epidermal growth factor receptor ( HER1 ) tyrosine kinase inhibitor ZD1839 (Iressa) inhibits HER2/neu (erbB2)-overexpressing breast cancer cells in vitro and in vivo [J]. Cancer Res, 2001, 61:8887-8895.

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