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- Publisher Website: 10.1007/s00109-011-0855-y
- Scopus: eid_2-s2.0-84865149277
- PMID: 22231744
- WOS: WOS:000305734700009
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Article: Inhibitors Of Hypoxia-inducible Factor 1 Block Breast Cancer Metastatic Niche Formation And Lung Metastasis
Title | Inhibitors Of Hypoxia-inducible Factor 1 Block Breast Cancer Metastatic Niche Formation And Lung Metastasis |
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Authors | |
Keywords | Cardiac glycosides Extracellular matrix HIF-1 Individualized therapy Targeted therapy Triple-negative breast cancer |
Issue Date | 2012 |
Publisher | Springer. The Journal's web site is located at http://www.springer.com/biomed/molecular/journal/109 |
Citation | Journal of Molecular Medicine, 2012, v. 90 n. 7, p. 803-15 How to Cite? |
Abstract | Intratumoral hypoxia, a frequent finding in metastatic cancer, results in the activation of hypoxia-inducible factors (HIFs). HIFs are implicated in many steps of breast cancer metastasis, including metastatic niche formation through increased expression of lysyl oxidase (LOX) and lysyl oxidase-like (LOXL) proteins, enzymes that remodel collagen at the metastatic site and recruit bone marrow-derived cells (BMDCs) to the metastatic niche. We investigated the effect of two chemically and mechanistically distinct HIF inhibitors, digoxin and acriflavine, on breast cancer metastatic niche formation. Both drugs blocked the hypoxia-induced expression of LOX and LOXL proteins, collagen cross-linking, CD11b(+) BMDC recruitment, and lung metastasis in an orthotopic breast cancer model. Patients with HIF-1 alpha-overexpressing breast cancers are at increased risk of metastasis and mortality and our results suggest that such patients may benefit from aggressive therapy that includes a HIF inhibitor. |
Persistent Identifier | http://hdl.handle.net/10722/186456 |
ISSN | 2023 Impact Factor: 4.8 2023 SCImago Journal Rankings: 1.422 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Wong, CCL | en_US |
dc.contributor.author | Zhang, H | en_US |
dc.contributor.author | Gilkes, DM | en_US |
dc.contributor.author | Chen, J | en_US |
dc.contributor.author | Wei, H | en_US |
dc.contributor.author | Chaturvedi, P | en_US |
dc.contributor.author | Hubbi, ME | en_US |
dc.contributor.author | Semenza, GL | en_US |
dc.date.accessioned | 2013-08-20T12:09:09Z | - |
dc.date.available | 2013-08-20T12:09:09Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Journal of Molecular Medicine, 2012, v. 90 n. 7, p. 803-15 | en_US |
dc.identifier.issn | 0946-2716 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/186456 | - |
dc.description.abstract | Intratumoral hypoxia, a frequent finding in metastatic cancer, results in the activation of hypoxia-inducible factors (HIFs). HIFs are implicated in many steps of breast cancer metastasis, including metastatic niche formation through increased expression of lysyl oxidase (LOX) and lysyl oxidase-like (LOXL) proteins, enzymes that remodel collagen at the metastatic site and recruit bone marrow-derived cells (BMDCs) to the metastatic niche. We investigated the effect of two chemically and mechanistically distinct HIF inhibitors, digoxin and acriflavine, on breast cancer metastatic niche formation. Both drugs blocked the hypoxia-induced expression of LOX and LOXL proteins, collagen cross-linking, CD11b(+) BMDC recruitment, and lung metastasis in an orthotopic breast cancer model. Patients with HIF-1 alpha-overexpressing breast cancers are at increased risk of metastasis and mortality and our results suggest that such patients may benefit from aggressive therapy that includes a HIF inhibitor. | en_US |
dc.language | eng | en_US |
dc.publisher | Springer. The Journal's web site is located at http://www.springer.com/biomed/molecular/journal/109 | en_US |
dc.relation.ispartof | Journal of Molecular Medicine | en_US |
dc.rights | The original publication is available at www.springerlink.com | en_US |
dc.subject | Cardiac glycosides | - |
dc.subject | Extracellular matrix | - |
dc.subject | HIF-1 | - |
dc.subject | Individualized therapy | - |
dc.subject | Targeted therapy | - |
dc.subject | Triple-negative breast cancer | - |
dc.subject.mesh | Bone Marrow Cells - drug effects - metabolism - pathology | en_US |
dc.subject.mesh | Breast Neoplasms - genetics - metabolism - pathology | en_US |
dc.subject.mesh | Hypoxia-Inducible Factor 1 - antagonists and inhibitors - metabolism | en_US |
dc.subject.mesh | Lung Neoplasms - genetics - metabolism - secondary | en_US |
dc.subject.mesh | Neoplasm Metastasis | en_US |
dc.title | Inhibitors Of Hypoxia-inducible Factor 1 Block Breast Cancer Metastatic Niche Formation And Lung Metastasis | en_US |
dc.type | Article | en_US |
dc.identifier.email | Wong, CCL: carmencl@pathology.hku.hk | en_US |
dc.identifier.authority | Wong, CCL=rp01602 | en_US |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1007/s00109-011-0855-y | en_US |
dc.identifier.pmid | 22231744 | en_US |
dc.identifier.pmcid | PMC3437551 | en_US |
dc.identifier.scopus | eid_2-s2.0-84865149277 | - |
dc.identifier.hkuros | 219800 | en_US |
dc.identifier.hkuros | 219799 | - |
dc.identifier.volume | 90 | en_US |
dc.identifier.issue | 7 | en_US |
dc.identifier.spage | 803 | en_US |
dc.identifier.epage | 15 | en_US |
dc.identifier.isi | WOS:000305734700009 | - |
dc.publisher.place | Germany | en_US |
dc.identifier.issnl | 0946-2716 | - |