Stiff stroma increases breast cancer risk by inducing the oncogene ZNF217.


Journal

The Journal of clinical investigation
ISSN: 1558-8238
Titre abrégé: J Clin Invest
Pays: United States
ID NLM: 7802877

Informations de publication

Date de publication:
02 11 2020
Historique:
received: 02 04 2019
accepted: 14 07 2020
pubmed: 30 7 2020
medline: 17 2 2021
entrez: 30 7 2020
Statut: ppublish

Résumé

Women with dense breasts have an increased lifetime risk of malignancy that has been attributed to a higher epithelial density. Quantitative proteomics, collagen analysis, and mechanical measurements in normal tissue revealed that stroma in the high-density breast contains more oriented, fibrillar collagen that is stiffer and correlates with higher epithelial cell density. microRNA (miR) profiling of breast tissue identified miR-203 as a matrix stiffness-repressed transcript that is downregulated by collagen density and reduced in the breast epithelium of women with high mammographic density. Culture studies demonstrated that ZNF217 mediates a matrix stiffness- and collagen density-induced increase in Akt activity and mammary epithelial cell proliferation. Manipulation of the epithelium in a mouse model of mammographic density supported a causal relationship between stromal stiffness, reduced miR-203, higher levels of the murine homolog Zfp217, and increased Akt activity and mammary epithelial proliferation. ZNF217 was also increased in the normal breast epithelium of women with high mammographic density, correlated positively with epithelial proliferation and density, and inversely with miR-203. The findings identify ZNF217 as a potential target toward which preexisting therapies, such as the Akt inhibitor triciribine, could be used as a chemopreventive agent to reduce cancer risk in women with high mammographic density.

Identifiants

pubmed: 32721948
pii: 129249
doi: 10.1172/JCI129249
pmc: PMC7598051
doi:
pii:

Substances chimiques

MIRN203 microRNA, human 0
MicroRNAs 0
Oncogene Proteins 0
RNA, Neoplasm 0
Trans-Activators 0
ZNF217 protein, human 0
Proto-Oncogene Proteins c-akt EC 2.7.11.1

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

5721-5737

Subventions

Organisme : NCI NIH HHS
ID : R01 CA192914
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA222508
Pays : United States
Organisme : NCI NIH HHS
ID : R33 CA206922
Pays : United States

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Auteurs

Jason J Northey (JJ)

Department of Surgery.
Center for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.

Alexander S Barrett (AS)

Department of Biochemistry and Molecular Genetics, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado, USA.

Irene Acerbi (I)

Department of Surgery.
Center for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.

Mary-Kate Hayward (MK)

Department of Surgery.
Center for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.

Stephanie Talamantes (S)

Department of Surgery.
Center for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.

Ivory S Dean (IS)

Department of Surgery.
Center for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.

Janna K Mouw (JK)

Department of Surgery.
Center for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.

Suzanne M Ponik (SM)

Department of Cell and Regenerative Biology, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Jonathon N Lakins (JN)

Department of Surgery.
Center for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.

Po-Jui Huang (PJ)

Department of Surgery.
Center for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.

Junmin Wu (J)

Harper Cancer Research Institute, Department of Chemistry and Biochemistry, University of Notre Dame, South Bend, Indiana, USA.

Quanming Shi (Q)

Department of Bioengineering, Stanford University, Palo Alto, California, USA.

Susan Samson (S)

Helen Diller Comprehensive Cancer Center, UCSF, San Francisco, California, USA.

Patricia J Keely (PJ)

Department of Cell and Regenerative Biology, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Rita A Mukhtar (RA)

Department of Surgery.

Jan T Liphardt (JT)

Department of Bioengineering, Stanford University, Palo Alto, California, USA.

John A Shepherd (JA)

Population Sciences in the Pacific Program (Cancer Epidemiology), University of Hawaii Cancer Center, University of Hawaii at Manoa, Manoa, Hawaii, USA.

E Shelley Hwang (ES)

Department of Surgery, Duke University Medical Center, Durham, North Carolina, USA.

Yunn-Yi Chen (YY)

Department of Pathology, UCSF, San Francisco, California, USA.

Kirk C Hansen (KC)

Department of Biochemistry and Molecular Genetics, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado, USA.
Division of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.

Laurie E Littlepage (LE)

Harper Cancer Research Institute, Department of Chemistry and Biochemistry, University of Notre Dame, South Bend, Indiana, USA.

Valerie M Weaver (VM)

Department of Surgery.
Center for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.
Helen Diller Comprehensive Cancer Center, UCSF, San Francisco, California, USA.
Population Sciences in the Pacific Program (Cancer Epidemiology), University of Hawaii Cancer Center, University of Hawaii at Manoa, Manoa, Hawaii, USA.
Radiation Oncology, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, UCSF, San Francisco, California, USA.

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