Benz C C, Scott G K, Sarup J C, Johnson R M, Tripathy D, Coronado E, Shepard H M, Osborne C K
Cancer Research Institute, University of California, San Francisco 94143.
Breast Cancer Res Treat. 1992;24(2):85-95. doi: 10.1007/BF01961241.
Since the poor prognosis associated with HER2 amplified breast cancers might be explained by a mechanistic association between p185HER2 overexpression and therapeutic resistance, we assessed the chemo-endocrine sensitivity of estrogen receptor (ER) containing MCF-7 breast cancer cells transfected with full-length HER2 cDNA. Of the 36 isolated MCF/HER2 subclones, 7 were found to overexpress p185HER2 surface receptor at levels 3 to 45-fold greater than parental or control transfected cells (MCF/neo). The overexpressing transfectants possessed increased inositol-1,4,5-triphosphate-3'-kinase activity comparable to enzyme activity in the endogenously HER2 amplified breast cancer cell lines SK-Br-3 and BT-474. The anti-p185HER2 monoclonal antibody and receptor-specific partial agonist, muMAb4D5 (4D5), known to inhibit growth of SK-Br-3 and BT-474 cells, produced no significant growth inhibitory effect on any of the transfectants including the 45-fold overexpressing MCF/HER2-18 cells which were studied in greater detail. MCF/HER2-18 cells contained at least partially functioning exogenous receptor since 4D5 (3 micrograms/ml) specifically stimulated phosphorylation of p185HER2 and its co-precipitating ptyr56 substrate within 5 min, and this was followed at 1 h by a transient induction of c-myc but not c-fos mRNA. ER content and the in vitro sensitivity of MCF/HER2-18 cells to 5-fluorouracil and adriamycin were identical to those of control transfectants and parental cells. However, these highly overexpressing transfectants had acquired low level (2 to 4-fold) resistance to cisplatin and were no longer sensitive to the antiestrogen tamoxifen (TAM). To compare the hormone-dependent tumorigenicity of the HER2 transfectants, MCF/HER2-18 and control cells (MCF, MCF/neo-3) were implanted into ovariectomized athymic nude mice. No tumors were produced in the absence of estradiol (E2) administration. In E2 supplemented mice, MCF/HER2-18 tumors grew most rapidly. When E2 treatment was stopped and daily TAM injections were initiated, MCF-7 and MCF/neo-3 tumor growth ceased immediately, while MCF/HER2-18 tumors continued to show an accelerated growth rate lasting weeks. This pattern of hormone-dependent, TAM-resistant growth exhibited by the MCF/HER2-18 tumors in nude mice supports the possibility that p185HER2 overexpression in human breast cancers may be linked to therapeutic resistance.
由于HER2扩增型乳腺癌的不良预后可能是由p185HER2过表达与治疗耐药之间的机制关联所解释,我们评估了用全长HER2 cDNA转染的含雌激素受体(ER)的MCF-7乳腺癌细胞的化疗-内分泌敏感性。在36个分离的MCF/HER2亚克隆中,发现7个亚克隆过表达p185HER2表面受体,其水平比亲本或对照转染细胞(MCF/neo)高3至45倍。过表达的转染子具有增加的肌醇-1,4,5-三磷酸-3'-激酶活性,与内源性HER2扩增的乳腺癌细胞系SK-Br-3和BT-474中的酶活性相当。已知能抑制SK-Br-3和BT-474细胞生长的抗p185HER2单克隆抗体和受体特异性部分激动剂muMAb4D5(4D5),对任何转染子都没有产生显著的生长抑制作用,包括对过表达45倍的MCF/HER2-18细胞进行了更详细研究的情况。MCF/HER2-18细胞含有至少部分功能正常的外源性受体,因为4D5(3微克/毫升)在5分钟内特异性刺激p185HER2及其共沉淀的tyr56底物的磷酸化,随后在1小时时短暂诱导c-myc但不诱导c-fos mRNA。MCF/HER2-18细胞的ER含量以及对5-氟尿嘧啶和阿霉素的体外敏感性与对照转染子和亲本细胞相同。然而,这些高度过表达的转染子对顺铂获得了低水平(2至4倍)的耐药性,并且不再对抗雌激素他莫昔芬(TAM)敏感。为了比较HER2转染子的激素依赖性致瘤性,将MCF/HER2-18和对照细胞(MCF、MCF/neo-3)植入去卵巢的无胸腺裸鼠体内。在不给予雌二醇(E2)的情况下未产生肿瘤。在补充E2的小鼠中,MCF/HER2-18肿瘤生长最快。当停止E2治疗并开始每日注射TAM时,MCF-7和MCF/neo-3肿瘤生长立即停止,而MCF/HER2-18肿瘤继续显示加速生长率,持续数周。MCF/HER2-18肿瘤在裸鼠中表现出的这种激素依赖性、TAM耐药性生长模式支持了人类乳腺癌中p185HER2过表达可能与治疗耐药相关的可能性。