Binding of the angiogenic/senescence inducer CCN1/CYR61 to integrin α6β1 drives endocrine resistance in breast cancer cells
| Autor: | Ingrid Espinoza, Lin Yang, Travis Vander Steen, Luciano Vellon, Elisabet Cuyàs, Sara Verdura, Lester Lau, Javier A. Menendez, Ruth Lupu |
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| Rok vydání: | 2022 |
| Předmět: | |
| Zdroj: | Aging-Us, 2022, vol. 14, núm. 3, p. 1200-1213 Articles publicats (IdIBGi) Espinoza, Ingrid Yang, Lin Steen, Travis Vander Vellon, Luciano Cuyàs, Elisabet Verdura, Sara Lau, Lester Menéndez Menéndez, Javier Abel Lupu, Rut 2022 Binding of the angiogenic/senescence inducer CCN1/CYR61 to integrin α6β1 drives endocrine resistance in breast cancer cells Aging-Us 14 3 1200 1213 DUGiDocs – Universitat de Girona instname |
| ISSN: | 1945-4589 |
| DOI: | 10.18632/aging.203882 |
| Popis: | CCN1/CYR61 promotes angiogenesis, tumor growth and chemoresistance by binding to its integrin receptor αvβ3 in endothelial and breast cancer (BC) cells. CCN1 controls also tissue regeneration by engaging its integrin receptor α6β1 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 αvβ3 or α6β1. First, we took advantage of site-specific mutagenesis abolishing the CCN1 receptor-binding sites to αvβ3 and α6β1 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 αvβ3 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 α6β1, failed to bypass the estrogen requirement for anchorage-independent growth or to promote resistance to tamoxifen. Wild-type CCN1 promoted estradiolindependent transcriptional activity of ERα and enhanced ERα agonist response to tamoxifen. The α6β1-bindingdefective 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 in vitro approaches confirmed the ability of recombinant CCN1 to bind ERα. CCN1 signaling via α6β1, but not via αvβ3, drives an endocrine resistance phenotype that involves a direct binding of CCN1 to ERα to regulate itstranscriptional activity in ER+ BC cells |
| Databáze: | OpenAIRE |
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