Trastuzumab-induced HER Reprogramming in "Resistant" Breast Carcinoma Cells

被引:179
作者
Narayan, Murli [4 ]
Wilken, Jason A. [1 ,2 ,3 ]
Harris, Lyndsay N. [4 ,5 ,6 ]
Baron, Andre T. [9 ,10 ]
Kimbler, Kimberly D. [9 ]
Maihle, Nita J. [1 ,2 ,3 ,7 ,8 ]
机构
[1] Yale Univ, Dept Obstet, New Haven, CT USA
[2] Yale Univ, Dept Gynecol, New Haven, CT USA
[3] Yale Univ, Dept Reprod Sci, New Haven, CT USA
[4] Yale Univ, Div Med Oncol, Yale Canc Ctr, New Haven, CT USA
[5] Yale Univ, Dept Internal Med, New Haven, CT USA
[6] Yale Univ, Sch Nursing, New Haven, CT 06536 USA
[7] Yale Univ, Dept Pathol, New Haven, CT USA
[8] Yale Univ, Dept Pharmacol, New Haven, CT USA
[9] Univ Kentucky, Dept Internal Med, Div Hematol Oncol & Blood & Bone Marrow Transplan, Lexington, KY USA
[10] Univ Kentucky, Dept Epidemiol, Lexington, KY USA
关键词
GROWTH-FACTOR RECEPTOR; CANCER CELLS; SUSCEPTIBILITY; CONTRIBUTES; ACTIVATION; MECHANISMS; EXPRESSION; HERCEPTIN; ERBB3;
D O I
10.1158/0008-5472.CAN-08-1056
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although trastuzumab (Herceptin) is an important advance in the treatment of breast cancer, a significant proportion of patients do not respond to trastuzumab either alone or in combination with chemotherapy. In this study, we observe that epidermal growth factor receptor (EGFR) and HER3 expression is substantially increased after long-term trastuzumab exposure of HER2-positive breast carcinoma-derived cell lines that show primary resistance to trastuzumab. Furthermore, long-term trastuzumab exposure of trastuzumab-resistant cell lines induces de novo sensitivity to the EGFR-targeted agents gefitinib or cetuximab in two of three cell lines accompanied by increased EGFR expression. Together, these results indicate that primary trastuzumab resistance is not synonymous with lack of responsiveness to trastuzumab and, importantly, suggest that trastuzumab priming may sensitize trastuzumab-resistant tumors to other HER family-directed therapeutics. [Cancer Res 2009;69(6):2191-4]
引用
收藏
页码:2191 / 2194
页数:4
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