Department of Pathology and Massey Cancer Center, Virginia Commonwealth University Health System, Richmond, Virginia.
Department of Pathology, Northwestern University, Chicago, Illinois.
Cancer Res. 2018 Jul 15;78(14):3877-3887. doi: 10.1158/0008-5472.CAN-17-2892. Epub 2018 Jun 29.
The prolyl isomerase cyclophilin A (CypA) regulates the Jak2/Stat5 pathway, which is necessary for mammary differentiation and the pathogenesis of breast cancer. In this study, we assessed the role of this isomerase during mammary gland development and erbB2-driven tumorigenesis. Genetic deletion of CypA resulted in delayed mammary gland morphogenesis and differentiation with corresponding decrease in Jak2/Stat5 activation; mammary gland cross-transplantation confirmed this defect was epithelial in nature. Analysis of mammary stem and progenitor populations revealed significant disruption of epithelial maturation. Loss of CypA in the erbB2 transgenic mouse model revealed a marked increase in mammary tumor latency that correlated with decreased Stat5 activation, associated gene expression, and reduced epithelial cell proliferation. These results demonstrate an important role for CypA in the regulation of Jak2/Stat5-mediated biology in mammary epithelium, identifying this isomerase as a novel target for therapeutic intervention. These findings reveal cyclophilin A functions in normal mammary epithelial development and ErbB2-driven mammary tumorigenesis and suggest therapies targeting cyclophilin A may be efficacious for breast cancer treatment. http://cancerres.aacrjournals.org/content/canres/78/14/3877/F1.large.jpg .
脯氨酰异构酶亲环素 A(CypA)调节 Jak2/Stat5 通路,该通路对于乳腺分化和乳腺癌的发病机制是必要的。在这项研究中,我们评估了这种异构酶在乳腺发育和 erbB2 驱动的肿瘤发生过程中的作用。CypA 的基因缺失导致乳腺形态发生和分化延迟,Jak2/Stat5 激活相应减少;乳腺交叉移植证实了这种缺陷是上皮性的。对乳腺干细胞和祖细胞群体的分析显示上皮成熟严重受损。在 erbB2 转基因小鼠模型中缺失 CypA 导致乳腺肿瘤潜伏期明显延长,与 Stat5 激活减少、相关基因表达降低和上皮细胞增殖减少相关。这些结果表明 CypA 在调节乳腺上皮细胞中的 Jak2/Stat5 介导的生物学中起着重要作用,将这种异构酶鉴定为治疗干预的新靶标。这些发现揭示了亲环素 A 在正常乳腺上皮发育和 erbB2 驱动的乳腺肿瘤发生中的功能,并表明针对亲环素 A 的治疗可能对乳腺癌治疗有效。