Department of Laboratory Medicine and Pathology, Division of Experimental Pathology, Mayo Clinic, Rochester, 55905 MN, USA.
Current address: Department of Preventive Medicine, John D. Bower School of Population Health, University of Mississippi Medical Center, Jackson, MS 39216, USA.
Aging (Albany NY). 2022 Feb 11;14(3):1200-1213. doi: 10.18632/aging.203882.
CCN1/CYR61 promotes angiogenesis, tumor growth and chemoresistance by binding to its integrin receptor αβ in endothelial and breast cancer (BC) cells. CCN1 controls also tissue regeneration by engaging its integrin receptor αβ to induce fibroblast senescence. Here, we explored if the ability of CCN1 to drive an endocrine resistance phenotype in estrogen receptor-positive BC cells relies on interactions with either αβ or αβ. First, we took advantage of site-specific mutagenesis abolishing the CCN1 receptor-binding sites to αβ and αβ to determine the integrin partner responsible for CCN1-driven endocrine resistance. Second, we explored a putative nuclear role of CCN1 in regulating ERα-driven transcriptional responses. Retroviral forced expression of a CCN1 derivative with a single amino acid change (D125A) that abrogates binding to αβ partially phenocopied the endocrine resistance phenotype induced upon overexpression of wild-type (WT) CCN1. Forced expression of the CCN1 mutant TM, which abrogates all the T1, H1, and H2 binding sites to αβ, failed to bypass the estrogen requirement for anchorage-independent growth or to promote resistance to tamoxifen. Wild-type CCN1 promoted estradiol-independent transcriptional activity of ERα and enhanced ERα agonist response to tamoxifen. The αβ-binding-defective TM-CCN1 mutant lost the ERα co-activator-like behavior of WT-CCN1. Co-immunoprecipitation assays revealed a direct interaction between endogenous CCN1 and ERα, and approaches confirmed the ability of recombinant CCN1 to bind ERα. CCN1 signaling via αβ, but not via αβ, drives an endocrine resistance phenotype that involves a direct binding of CCN1 to ERα to regulate its transcriptional activity in ER+ BC cells.
CCN1/CYR61 通过与内皮细胞和乳腺癌(BC)细胞中的整合素受体αβ结合,促进血管生成、肿瘤生长和化疗耐药性。CCN1 还通过与整合素受体αβ结合诱导成纤维细胞衰老来控制组织再生。在这里,我们探讨了 CCN1 驱动雌激素受体阳性 BC 细胞内分泌抵抗表型的能力是否依赖于与αβ或αβ的相互作用。首先,我们利用定点突变技术,消除了 CCN1 与αβ和αβ的受体结合位点,以确定负责 CCN1 驱动内分泌抵抗的整合素伴侣。其次,我们探讨了 CCN1 在调节 ERα 驱动的转录反应中的潜在核作用。逆转录病毒强制表达一种 CCN1 衍生物,该衍生物发生单一氨基酸改变(D125A),从而消除与αβ的结合,部分模拟了过表达野生型(WT)CCN1 诱导的内分泌抵抗表型。强制表达突变体 TM,该突变体消除了与αβ的所有 T1、H1 和 H2 结合位点,不能绕过雌激素对锚定非依赖性生长的要求,也不能促进对他莫昔芬的耐药性。野生型 CCN1 促进了 ERα 的雌二醇非依赖性转录活性,并增强了 ERα 激动剂对他莫昔芬的反应。缺乏与αβ结合能力的 TM-CCN1 突变体失去了 WT-CCN1 的 ERα 共激活子样行为。共免疫沉淀实验显示内源性 CCN1 与 ERα 之间存在直接相互作用,并且 方法证实了重组 CCN1 结合 ERα 的能力。CCN1 通过αβ而不是αβ的信号转导,驱动一种内分泌抵抗表型,该表型涉及 CCN1 与 ERα 的直接结合,以调节其在 ER+BC 细胞中的转录活性。