Publication

RANKL/RANK control Brca1 mutation-driven mammary tumors

Sigl, V., Owusu-Boaitey, K., Joshi, P. A., Kavirayani, A., Wirnsberger, G., Novatchkova, M., Kozieradzki, I., Schramek, D., Edokobi, N., Hersl, J., Sampson, A., Odai-Afotey, A., Lazaro, C., Gonzalez-Suarez, E., Pujana, M. A., Heyn, H., Vidal, E., Cruickshank, J., Berman, H., Sarao, R., Ticevic, M., Uribesalgo, I., Tortola, L., Rao, S., Tan, Y., Pfeiler, G., Lee, E. Y. H. P., Bago-Horvath, Z., Kenner, L., Popper, H., Singer, C., Khokha, R., Jones, L. P., Penninger, J. M. & CIMBA, Jul-2016, In : Cell research. 26, 7, p. 761-774 14 p.

Research output: Contribution to journalArticleAcademicpeer-review

  • Verena Sigl
  • Kwadwo Owusu-Boaitey
  • Purna A. Joshi
  • Anoop Kavirayani
  • Gerald Wirnsberger
  • Maria Novatchkova
  • Ivona Kozieradzki
  • Daniel Schramek
  • Nnamdi Edokobi
  • Jerome Hersl
  • Aishia Sampson
  • Ashley Odai-Afotey
  • Conxi Lazaro
  • Eva Gonzalez-Suarez
  • Miguel A. Pujana
  • Holger Heyn
  • Enrique Vidal
  • Jennifer Cruickshank
  • Hal Berman
  • Renu Sarao
  • Melita Ticevic
  • Iris Uribesalgo
  • Luigi Tortola
  • Shuan Rao
  • Yen Tan
  • Georg Pfeiler
  • Eva Y. H. P. Lee
  • Zsuzsanna Bago-Horvath
  • Lukas Kenner
  • Helmuth Popper
  • Christian Singer
  • Rama Khokha
  • Laundette P. Jones
  • Josef M. Penninger
  • CIMBA

Breast cancer is the most common female cancer, affecting approximately one in eight women during their lifetime. Besides environmental triggers and hormones, inherited mutations in the breast cancer 1 (BRCA1) or BRCA2 genes markedly increase the risk for the development of breast cancer. Here, using two different mouse models, we show that genetic inactivation of the key osteoclast differentiation factor RANK in the mammary epithelium markedly delayed onset, reduced incidence, and attenuated progression of Brca1; p53 mutation-driven mammary cancer. Long-term pharmacological inhibition of the RANK ligand RANKL in mice abolished the occurrence of Brca1 mutation-driven pre-neoplastic lesions. Mechanistically, genetic inactivation of Rank or RANKL/RANK blockade impaired proliferation and expansion of both murine Brca1; p53 mutant mammary stem cells and mammary progenitors from human BRCA1 mutation carriers. In addition, genome variations within the RANK locus were significantly associated with risk of developing breast cancer in women with BRCA1 mutations. Thus, RANKL/RANK control progenitor cell expansion and tumorigenesis in inherited breast cancer. These results present a viable strategy for the possible prevention of breast cancer in BRCA1 mutant patients.

Original languageEnglish
Pages (from-to)761-774
Number of pages14
JournalCell research
Volume26
Issue number7
Publication statusPublished - Jul-2016

    Keywords

  • BRCA1, RANK, RANKL, inherited breast cancer, mammary progenitor cells, SUSCEPTIBILITY GENE BRCA1, NEGATIVE BREAST-CANCER, BONE-MINERAL DENSITY, EPITHELIAL-CELLS, PROGESTERONE-RECEPTOR, POSTMENOPAUSAL WOMEN, PROSTATE-CANCER, MOUSE MAMMARY, MICE, DIFFERENTIATION

ID: 49401081