Complex prolactin crosstalk in breast cancer: new therapeutic implications.

Complex prolactin crosstalk in breast cancer: new therapeutic implications.
复制标题

DOI:
10.1016/j.mce.2009.03.014
复制
发表时间:
2009-08-13
影响因子:
4.1
通讯作者:
Schuler, Linda A.
Schuler, Linda A.
中科院分区:
医学2区
文献类型:
--
作者:
Carver, Kristopher C.;Arendt, Lisa M.;Schuler, Linda A.

文献摘要

参考文献

被引文献

相似文献

催乳素(PRL)对乳腺癌的贡献越来越被认识到。为了更好地了解PRL在这种疾病中的作用,必须表征其与其他致癌生长因子和激素的相互作用。在这里,我们回顾我们目前的了解PRL串扰与其他乳腺致癌因素,包括雌激素,表皮生长因子(EGF)家族成员,胰岛素样生长因子-I(IGF-I)。PRL增强这些非常成功的内分泌和分子疗法的靶点的作用的能力表明,PRL和/或其受体(PRLR)可能是有吸引力的治疗靶点。我们讨论了PRL/PRLR靶向治疗与现有治疗相结合的潜在益处,以及对新生和获得性耐药治疗的影响。
The contributions of prolactin (PRL) to breast cancer are becoming increasingly recognized. To better understand the role for PRL in this disease, its interactions with other oncogenic growth factors and hormones must be characterized. Here, we review our current understanding of PRL crosstalk with other mammary oncogenic factors, including estrogen, epidermal growth factor (EGF) family members, and insulin-like growth factor-I (IGF-I). The ability of PRL to potentiate the actions of these targets of highly successful endocrine and molecular therapies suggests that PRL and/or its receptor (PRLR) may be an attractive therapeutic target(s). We discuss the potential benefit of PRL/PRLR-targeted therapy in combination with established therapies and implications for de novo and acquired resistance to treatment.
DOI: 10.2353/ajpath.2009.080719
发表时间: 2009-03-01
影响因子: 6
作者:
Arendt, Lisa M.;Grafwallner-Huseth, Tara L.;Schuler, Linda A.
通讯作者: Schuler, Linda A.
DOI: 10.2353/ajpath.2008.070597
发表时间: 2008-01-01
影响因子: 6
作者:
Arendt, Lisa M.;Schuler, Linda A.
通讯作者: Schuler, Linda A.
DOI: 10.1016/s1534-5807(02)00365-9
发表时间: 2002-12-01
期刊: DEVELOPMENTAL CELL
影响因子: 11.8
作者:
Brisken, C;Ayyannan, A;Heineman, A
通讯作者: Heineman, A
DOI: 10.1007/s10549-005-9037-3
发表时间: 2005-01-01
影响因子: 3.8
作者:
Dowsett, M;Nicholson, RI;Pietras, RJ
通讯作者: Pietras, RJ