Evidence map›Paper›PMID 41310893›Full record

ArticleInternational journal of cancer2026

Reprogramming SREBP1-dependent lipogenesis and inflammation in high-risk breast with licochalcone A: A novel path to cancer prevention.

Atieh Hajirahimkhan, Elizabeth T Bartom, Carolina H Chung, Xingyu Guo, Kyli Berkley, Seyyedmohsen Hosseinibarkooie, Zahra Assadi, Shao Huan Samuel Weng, Raymond Moellering, Oukseub Lee and 5 more

Abstract read
In one paragraph

Article in International journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Atieh HajirahimkhanDepartment of Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0003-0585-5668
Elizabeth T BartomRobert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-5618-2582
Carolina H ChungDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0003-2490-1842
Xingyu GuoDepartment of Chemistry, University of Illinois Chicago, Chicago, Illinois, USA.
Kyli BerkleyDepartment of Chemistry, University of Illinois Chicago, Chicago, Illinois, USA.ORCID https://orcid.org/0009-0001-2435-5821
Seyyedmohsen HosseinibarkooieProteomics Platform, Office of Shared Research Facilities, University of Chicago, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-6121-8562
Zahra AssadiProteomics Platform, Office of Shared Research Facilities, University of Chicago, Chicago, Illinois, USA.
Shao Huan Samuel WengProteomics Platform, Office of Shared Research Facilities, University of Chicago, Chicago, Illinois, USA.ORCID https://orcid.org/0009-0003-0894-8517
Raymond MoelleringDepartment of Chemistry, The University of Chicago, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-2043-7838
Oukseub LeeDepartment of Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0003-0279-5460
Ruohui ChenRobert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-8746-5350
Wonhwa ChoDepartment of Chemistry, University of Illinois Chicago, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0003-1410-2481
Sriram ChandrasekaranDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0002-8405-5708
Susan E ClareDepartment of Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-9499-0855
Seema A KhanDepartment of Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-6307-2023

Funding

Supplement for Equipment for Lipid Regulation of Cellular Signaling and Protein-Protein InteractionsR35GM122530 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WONHWA CHO · 2017 to 2026
$6.1M
Bioinformatics Analysis of Next Generation Sequencing Data from Cancer CellsR50CA221848 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Elizabeth Thomas Bartom · 2017 to 2026
$1.8M
American Cancer Society 131667-PF-18-049-01NECBramsen-Hamill FoundationNational Cancer Institute T32 postdoctoral fellowship 5TfT32ActfCA247801NCI NIH HHS R50 CA221848NIGMS NIH HHS R35 GM122530NIH HHS R35GM122530Northwestern University Department of Surgery Seed fundingRobert H Lurie Comprehensive Cancer Center Translational Bridge Fellowship
6 · The paper itself

Abstract

Anti-estrogens have had a limited impact on breast cancer (BC) prevention. Novel agents with better tolerability, and efficacy beyond estrogen receptor (ER) positive BC are needed. We studied licochalcone A (LicA) for ER-agnostic BC prevention. We demonstrated that LicA significantly reduced proliferation in seven human breast cell lines and suppressed ER+ and ER- xenograft tumors in mice. We confirmed these observations ex vivo in the contralateral unaffected breast (CUB) of women with unilateral sporadic BC, and BC cell lines using RNA sequencing, metabolism flux modeling, confirmatory NanoString nCounter metabolic pathway panel analysis in independent sets of specimens, proteomics, and western blots. We found that LicA targets sterol regulatory element binding protein 1 (SREBP1) with subsequent metabolic-inflammatory changes, lowering spatiotemporally resolved cholesterol levels inside malignant cells to the levels in normal mammary cells. Mechanistically, in CUBs we observed that LicA downregulated PI3K-AKT-SREBP1-dependent lipogenesis, NF-kB-dependent inflammation, and de novo nucleotide biosynthesis, stalling proliferation. Studies in cell lines showed suppression of PI3K and AKT phosphorylation, SREBP1 protein expression, and the SREBP1-dependent enzymes such as ACAT2, ACLY, FASN, SCD, consistent with reduced NEDD8 required for SREBP1 stabilization. We found a significant reduction in NF-kB expression, its nuclear translocation mediator karyopherin β1, and prostaglandin E2 synthesis. We demonstrated a reduction in PRPS1-catalyzed de novo nucleotide biosynthesis, and downregulation of proliferative markers MKI67, RRM2, and the survival marker BCL2. LicA reduces pro-tumorigenic aberrations in lipid homeostasis and inflammation through SREBP1. It is a promising non-endocrine candidate for BC prevention. Future studies in immunocompetent BC prevention models are warranted.

Indexed as

Breast NeoplasmsChalconesInflammationLipogenesisSterol Regulatory Element Binding Protein 1AnimalsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMiceSignal TransductionXenograft Model Antitumor AssaysChalconeslicochalcone ASREBF1 protein, humanSterol Regulatory Element Binding Protein 1anti‐inflammationantiproliferationbreast cancer preventionlicochalcone aSREBP

Identifiers

PMID41310893
PMCPMC12875168

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.