Arteaga C L, Kitten L J, Coronado E B, Jacobs S, Kull F C, Allred D C, Osborne C K
Division of Medical Oncology, University of Texas Health Science Center, San Antonio 78284.
J Clin Invest. 1989 Nov;84(5):1418-23. doi: 10.1172/JCI114315.
Insulin and insulin-like growth factors (IGIs) stimulate the growth of human breast cancer cells in vitro. The type I somatomedin receptor (SR) expressed in these cells may mediate the growth effects of these peptides. We have examined the role of this receptor on human breast cancer growth with a monoclonal antibody (alpha-IR-3) that blocks the receptor binding domain and inhibits IGF-I-induced growth. alpha-IR-3 inhibited clonal growth in vitro and blocked the mitogenic effect of exogenous IGF-I in both MCF-7 and MDA-231 breast cancer cell lines. Antibody-induced blockade of the type I SR also inhibited the estrogen-independent MDA-231 cells growing in vivo in nude mice, but growth of the estrogen-dependent MCF-7 cells was unaffected. IGIs are important growth regulators of MDA-231 breast cancer cells. Blockade of this growth stimulatory pathway may provide a new treatment strategy.
胰岛素和胰岛素样生长因子(IGFs)在体外可刺激人乳腺癌细胞的生长。这些细胞中表达的I型生长调节素受体(SR)可能介导这些肽的生长效应。我们用一种能阻断受体结合域并抑制IGF-I诱导生长的单克隆抗体(α-IR-3)研究了该受体在人乳腺癌生长中的作用。α-IR-3在体外抑制克隆生长,并阻断外源性IGF-I对MCF-7和MDA-231两种乳腺癌细胞系的促有丝分裂作用。抗体诱导的I型SR阻断也抑制了裸鼠体内雌激素非依赖性MDA-231细胞的生长,但雌激素依赖性MCF-7细胞的生长未受影响。IGFs是MDA-231乳腺癌细胞重要的生长调节因子。阻断这种生长刺激途径可能提供一种新的治疗策略。