The flaxseed lignan secoisolariciresinol diglucoside decreases local inflammation, suppresses NFκB signaling, and inhibits mammary tumor growth.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 03 08 2018
accepted: 20 10 2018
pubmed: 28 10 2018
medline: 14 6 2019
entrez: 28 10 2018
Statut: ppublish

Résumé

Exposure to the polyphenolic plant lignan secoisolariciresinol diglucoside (SDG) and its metabolite enterolactone (ENL) has been associated with reduced breast cancer progression, particularly for estrogen receptor alpha (ERα)-negative disease, and decreased preclinical mammary tumor growth. However, while preclinical studies have established that SDG and ENL affect measures of progression in models of triple-negative breast cancer (TNBC, a subset of ERα-negative disease), the molecular mechanisms underlying these effects remain unclear. C57BL/6 mice were fed a control diet (control, 10% kcal from fat) or control diet + SDG (SDG, 100 mg/kg diet) for 8 weeks, then orthotopically injected with syngeneic E0771 mammary tumor cells (a model of TNBC); tumor growth was monitored for 3 weeks. The role of reduced NF-κB signaling in SDG's anti-tumor effects was explored in vitro via treatment with the bioactive SDG metabolite ENL. In addition to the murine E0771 cells, the in vitro studies utilized MDA-MB-231 and MCF-7 cells, two human cell lines which model the triple-negative and luminal A breast cancer subtypes, respectively. SDG supplementation in the mice significantly reduced tumor volume and expression of phospho-p65 and NF-κB target genes (P < 0.05). Markers of macrophage infiltration were decreased in the distal-to-tumor mammary fat pad of mice supplemented with SDG relative to control mice (P < 0.05). In vitro, ENL treatment inhibited viability, survival, and NF-κB activity and target gene expression in E0771, MDA-MB-231, and MCF-7 cells (P < 0.05). Overexpression of Rela attenuated ENL's inhibition of E0771 cell viability and survival. SDG reduces tumor growth in the E0771 model of TNBC, likely via a mechanism involving inhibition of NF-κB activity. SDG could serve as a practical and effective adjuvant treatment to reduce recurrence, but greater understanding of its effects is needed to inform the development of more targeted recommendations for its use.

Identifiants

pubmed: 30367332
doi: 10.1007/s10549-018-5021-6
pii: 10.1007/s10549-018-5021-6
pmc: PMC6394576
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Biomarkers 0
Butylene Glycols 0
Cytokines 0
Glucosides 0
Lignans 0
NF-kappa B 0
4-Butyrolactone OL659KIY4X
secoisolariciresinol diglucoside T9281L29MV
2,3-bis(3'-hydroxybenzyl)butyrolactone X01E7E1D6H

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

545-557

Subventions

Organisme : Susan G. Komen
ID : KG101039
Pays : United States
Organisme : Breast Cancer Research Foundation
ID : BCRF 16-075
Organisme : NCI NIH HHS
ID : R35CA197627
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK056350
Pays : United States
Organisme : NCI NIH HHS
ID : R25 CA057726
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM122741
Pays : United States
Organisme : NCI NIH HHS
ID : R35 CA197627
Pays : United States

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Auteurs

Laura W Bowers (LW)

Department of Nutrition, University of North Carolina, 135 Dauer Drive, CB #7461, Chapel Hill, NC, 27599, USA.
Lineberger Comprehensive Cancer Center, University of North Carolina, 450 West Drive, Chapel Hill, NC, 27514, USA.

Claire G Lineberger (CG)

Department of Nutrition, University of North Carolina, 135 Dauer Drive, CB #7461, Chapel Hill, NC, 27599, USA.

Nikki A Ford (NA)

Department of Nutritional Sciences, University of Texas at Austin, 1400 Barbara Jordan Blvd, R1800, Austin, TX, 78723, USA.

Emily L Rossi (EL)

Department of Nutrition, University of North Carolina, 135 Dauer Drive, CB #7461, Chapel Hill, NC, 27599, USA.
Lineberger Comprehensive Cancer Center, University of North Carolina, 450 West Drive, Chapel Hill, NC, 27514, USA.

Arunima Punjala (A)

Department of Nutrition, University of North Carolina, 135 Dauer Drive, CB #7461, Chapel Hill, NC, 27599, USA.

Kristina K Camp (KK)

Department of Nutrition, University of North Carolina, 135 Dauer Drive, CB #7461, Chapel Hill, NC, 27599, USA.

Bruce K Kimler (BK)

Department of Radiation Oncology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, KS, 66160, USA.

Carol J Fabian (CJ)

Department of Internal Medicine, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, KS, 66160, USA.

Stephen D Hursting (SD)

Department of Nutrition, University of North Carolina, 135 Dauer Drive, CB #7461, Chapel Hill, NC, 27599, USA. hursting@email.unc.edu.
Lineberger Comprehensive Cancer Center, University of North Carolina, 450 West Drive, Chapel Hill, NC, 27514, USA. hursting@email.unc.edu.
Nutrition Research Institute, University of North Carolina, 500 Laureate Way, Kannapolis, NC, 28081, USA. hursting@email.unc.edu.

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Classifications MeSH