4.8 Article

Histone deacetylase 11 inhibition promotes breast cancer metastasis from lymph nodes

Journal

NATURE COMMUNICATIONS
Volume 10, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-12222-5

Keywords

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Funding

  1. NCI Center Core Support Grant [CA016086]
  2. North Carolina Biotech Center Institutional Support Grant [2012-IDG-1006]
  3. Susan G. Komen Scholar Award
  4. UNC Specialized Program of Research Excellence (SPORE) [P50-CA58223]
  5. National Cancer Institute of the National Institute of Health [T32CA196589]
  6. National Institutes of Health [R01CA215075]
  7. Mentored Research Scholar Grants in Applied and Clinical Research from the American Cancer Society [MRSG-14-222-01-RMC]
  8. Jimmy V. Foundation Scholar award
  9. UCRF Innovator Award
  10. Stuart Scott V. Foundation/Lung Cancer Initiative Award for Clinical Research
  11. University Cancer Research Fund
  12. Lung Cancer Research Foundation
  13. Free to Breathe Metastasis Research Award
  14. Susan G. Komen Career Catalyst Award
  15. NCBC translational research grant

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Lymph node (LN) metastases correspond with a worse prognosis in nearly all cancers, yet the occurrence of cancer spreading from LNs remains controversial. Additionally, the mechanisms explaining how cancers survive and exit LNs are largely unknown. Here, we show that breast cancer patients frequently have LN metastases that closely resemble distant metastases. In addition, using a microsurgical model, we show how LN metastasis development and dissemination is regulated by the expression of a chromatin modifier, histone deacetylase 11 (HDAC11). Genetic and pharmacologic blockade of HDAC11 decreases LN tumor growth, yet substantially increases migration and distant metastasis formation. Collectively, we reveal a mechanism explaining how HDAC11 plasticity promotes breast cancer growth as well as dissemination from LNs and suggest caution with the use of HDAC inhibitors.

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