Evidence map›Paper›PMID 39456028›Full record

ArticleBreast cancer research : BCR2024

Effect of genistein supplementation on microenvironment regulation of breast tumors in obese mice.

Shengzi Jin, Yingce Zheng, Ding Li, Xingyao Liu, Tingting Zhu, Shuang Wang, Zhonghua Liu, Yun Liu

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
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  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Shengzi Jin *College of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China.
Yingce Zheng *College of Life Sciences, Northeast Agricultural University, No. 600 Changjiang Road, Harbin, 150030, PR China.
Ding LiCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China.
Xingyao LiuCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China.
Tingting ZhuCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China.
Shuang WangCollege of Veterinary Medicine, Zhejiang A&F University, Hangzhou, 311300, PR China.
Zhonghua LiuCollege of Life Sciences, Northeast Agricultural University, No. 600 Changjiang Road, Harbin, 150030, PR China. liuzhonghua@neau.edu.cn.
Yun LiuCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China. liuyun@neau.edu.cn.

Funding

Earmarked Fund for China Agriculture Research System earmarked fundNational Natural Resources Foundation of China 31872527
6 · The paper itself

Abstract

Obesity is an important risk factor for breast cancer in women before and after menopause. Adipocytes, key mediators in the tumor microenvironment, play a pivotal role in the relationship between obesity with cancer. However, the potential of dietary components in modulating this relationship remains underexplored. Genistein, a soy-derived isoflavone, has shown promise in reducing breast cancer risk, attenuating obesity-associated inflammation, and improving insulin resistance. However, there are no reports examining whether genistein has the ability to reduce the effects of obesity on breast tumor development. In this study, we constructed a mammary tumor model in ovariectomized obese mice and examined the effects of genistein on body condition and tumor growth. Moreover, the effects of genistein on the tumor microenvironment were examined via experimental observation of peritumoral adipocytes and macrophages. In addition, we further investigated the effect of genistein on adipocyte and breast cancer cell crosstalk via coculture experiments. Our findings indicate that dietary genistein significantly alleviates obesity, systemic inflammation, and metabolic disorders induced by a high-fat diet in ovariectomized mice. Notably, it also inhibits tumor growth in vivo. The impact of genistein extends to the tumor microenvironment, where it reduces the production of cancer-associated adipocytes (CAAs) and the recruitment of M2d-subtype macrophages. In vitro, genistein mitigates the transition of adipocytes into CAAs and inhibits the expression of inflammatory factors by activating PPAR-γ pathway and degrading nuclear NF-κB. Furthermore, it impedes the acquisition of invasive properties and epithelial‒mesenchymal transition in breast cancer cells under CAA-induced inflammation, disrupting the Wnt3a/β-catenin pathway. Intriguingly, the PPAR-γ inhibitor T0070907 counteracted the effects of genistein in the coculture system, underscoring the specificity of its action. Our study revealed that genistein can mitigate the adverse effects of obesity on breast cancer by modulating the tumor microenvironment. These findings provide new insights into how genistein intake and a soy-based diet can reduce breast cancer risk.

Indexed as

AdipocytesBreast NeoplasmsGenisteinObesityTumor MicroenvironmentAnimalsCell Line, TumorCell ProliferationDietary SupplementsDiet, High-FatDisease Models, AnimalFemaleHumansMacrophagesMiceMice, ObeseGenisteinPPAR gammaBreast cancerCancer associated adipocyteGenisteinObesityPPAR-γTumor microenvironment

Identifiers

PMID39456028
PMCPMC11515845

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.