3,3-Diindolylmethane (DIM): a nutritional intervention and its impact on breast density in healthy BRCA carriers. A prospective clinical trial.


Journal

Carcinogenesis
ISSN: 1460-2180
Titre abrégé: Carcinogenesis
Pays: England
ID NLM: 8008055

Informations de publication

Date de publication:
15 10 2020
Historique:
received: 18 01 2020
revised: 10 04 2020
accepted: 23 05 2020
pubmed: 28 5 2020
medline: 9 7 2021
entrez: 28 5 2020
Statut: ppublish

Résumé

Women who carry the BRCA mutation are at high lifetime risk of breast cancer, but there is no consensus regarding an effective and safe chemoprevention strategy. A large body of evidence suggests that 3,3-diindolylmethane (DIM), a dimer of indole-3-carbinol found in cruciferous vegetables, can potentially prevent carcinogenesis and tumor development. The primary aim of this prospective single-arm study was to investigate the effect of DIM supplementation on breast density, a recognized predictive factor of breast cancer risk. Participants were 23 healthy female BRCA carriers (median age 47 years; 78% postmenopausal) who were treated with oral DIM 100 mg × 1/day for 1 year. The amount of fibroglandular tissue (FGT) and background parenchymal enhancement (BPE) on magnetic resonance imaging (MRI) performed before and after the intervention was scored by two independent expert radiologists using the Breast Imaging and Reporting Data System. The results showed a decrease in the average score for FGT amount from 2.8 ± 0.8 at the onset to 2.65 ± 0.84 after 1 year (P = 0.031), with no significant change in BPE (P = 0.429). A group of DIM-untreated age- and menopausal-status-matched women from the BRCA clinic did not show a significant change in FGT amount (P = 0.33) or BPE (P = 0.814) in a parallel year. Mean estradiol level decreased from 159 to 102 pmol/l (P = 0.01), and mean testosterone level decreased from 0.42 to 0.31 pmol/l (P = 0.007). Side effects were grade 1. In conclusion, 1 year's supplementation with DIM 100 mg × 1/day in BRCA carriers was associated with a significant decline in FGT amount on MRI. Larger randomized studies are warranted to corroborate these findings.

Identifiants

pubmed: 32458980
pii: 5847633
doi: 10.1093/carcin/bgaa050
pmc: PMC7566319
doi:

Substances chimiques

Anticarcinogenic Agents 0
BRCA1 Protein 0
BRCA2 Protein 0
Indoles 0
3,3'-diindolylmethane SSZ9HQT61Z

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1395-1401

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press.

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Auteurs

Rinat Yerushalmi (R)

Davidoff Cancer Center, Rabin Medical Center-Beilinson Campus, Petach Tikva, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Sharon Bargil (S)

Davidoff Cancer Center, Rabin Medical Center-Beilinson Campus, Petach Tikva, Israel.

Yaara Ber (Y)

Division of Urology, Petach Tikva, Israel.

Rachel Ozlavo (R)

Division of Urology, Petach Tikva, Israel.

Tuval Sivan (T)

Division of Urology, Petach Tikva, Israel.

Yael Rapson (Y)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Imaging Department, Petach Tikva, Israel.

Adi Pomerantz (A)

Davidoff Cancer Center, Rabin Medical Center-Beilinson Campus, Petach Tikva, Israel.

Daliah Tsoref (D)

Davidoff Cancer Center, Rabin Medical Center-Beilinson Campus, Petach Tikva, Israel.

Eran Sharon (E)

Division of Surgery, Hospital for Women, Rabin Medical Center-Beilinson Campus, Petach Tikva, Israel.

Opher Caspi (O)

Davidoff Cancer Center, Rabin Medical Center-Beilinson Campus, Petach Tikva, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Ahuvah Grubsrein (A)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Imaging Department, Petach Tikva, Israel.

David Margel (D)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Division of Urology, Petach Tikva, Israel.

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