Proceedings of the National Academy of Sciences - PNAS, 2019-06, Vol.116 (25), p.12452-12461
2019
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- Autor(en) / Beteiligte
- Titel
- Hypoxia-induced switch in SNAT2/SLC38A2 regulation generates endocrine resistance in breast cancer
- Ist Teil von
- Proceedings of the National Academy of Sciences - PNAS, 2019-06, Vol.116 (25), p.12452-12461
- Ort / Verlag
- United States: National Academy of Sciences
- Erscheinungsjahr
- 2019
- Quelle
- MEDLINE
- Beschreibungen/Notizen
- Tumor hypoxia is associated with poor patient outcomes in estrogen receptor-α–positive (ERα⁺) breast cancer. Hypoxia is known to affect tumor growth by reprogramming metabolism and regulating amino acid (AA) uptake. Here, we show that the glutamine transporter, SNAT2, is the AA transporter most frequently induced by hypoxia in breast cancer, and is regulated by hypoxia both in vitro and in vivo in xenografts. SNAT2 induction in MCF7 cells was also regulated by ERα, but it became predominantly a hypoxia-inducible factor 1α (HIF-1α)–dependent gene under hypoxia. Relevant to this, binding sites for both HIF-1α and ERα overlap in SNAT2’s cis-regulatory elements. In addition, the down-regulation of SNAT2 by the ER antagonist fulvestrant was reverted in hypoxia. Overexpression of SNAT2 in vitro to recapitulate the levels induced by hypoxia caused enhanced growth, particularly after ERα inhibition, in hypoxia, or when glutamine levels were low. SNAT2 up-regulation in vivo caused complete resistance to antiestrogen and, partially, anti-VEGF therapies. Finally, high SNAT2 expression levels correlated with hypoxia profiles and worse outcome in patients given antiestrogen therapies. Our findings show a switch in the regulation of SNAT2 between ERα and HIF-1α, leading to endocrine resistance in hypoxia. Development of drugs targeting SNAT2 may be of value for a subset of hormone-resistant breast cancer.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0027-8424eISSN: 1091-6490DOI: 10.1073/pnas.1818521116Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6589752
- Format
- –
- Schlagworte
- Amino Acid Transport System A - metabolism, Amino acids, Animals, Antiestrogens, Antineoplastic Agents, Hormonal - therapeutic use, Binding sites, Biological Sciences, Breast cancer, Breast Neoplasms - drug therapy, Breast Neoplasms - metabolism, Breast Neoplasms - pathology, Cell Hypoxia, Cell Line, Tumor, Down-regulation, Drug delivery, Drug development, Drug Resistance, Neoplasm, Estrogen Receptor alpha - metabolism, Estrogen Receptor Modulators - therapeutic use, Estrogen receptors, Estrogens, Female, Fulvestrant, Glutamine, Heterografts, Humans, Hypoxia, Hypoxia-inducible factors, Metabolism, Mice, PNAS Plus, Regulatory sequences, Tumor Microenvironment, Tumors, Vascular endothelial growth factor, Xenografts, Xenotransplantation