Evidence map›Paper›PMID 42036506›Full record

ArticleClinical & experimental metastasis2026

FOXM1 expression is induced by the brain microenvironment and supports CRC brain metastatic adaptation.

Fayhaa Khair, Inbal Greenberg, Sivan Fuchs, Guy Shapira, Asia Zubkov, Noam Shomron, Michal Raz, Ido Wolf, Tami Rubinek

Abstract read
In one paragraph

Article in Clinical & experimental metastasis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Fayhaa Khair *Oncology Division, Tel Aviv Sourasky University Medical Center (Ichilov), Tel Aviv, Israel. fayhaa97@gmail.com.
Inbal Greenberg *Oncology Division, Tel Aviv Sourasky University Medical Center (Ichilov), Tel Aviv, Israel.
Sivan FuchsOncology Division, Tel Aviv Sourasky University Medical Center (Ichilov), Tel Aviv, Israel.
Guy ShapiraGray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Asia ZubkovInstitute of Pathology, Tel Aviv Sourasky University Medical Center (Ichilov), Tel Aviv, Israel.
Noam ShomronGray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Michal RazOncology Division, Tel Aviv Sourasky University Medical Center (Ichilov), Tel Aviv, Israel.
Ido WolfOncology Division, Tel Aviv Sourasky University Medical Center (Ichilov), Tel Aviv, Israel.
Tami RubinekOncology Division, Tel Aviv Sourasky University Medical Center (Ichilov), Tel Aviv, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is a leading cause of cancer-related mortality in the Western world. While brain metastasis (BMs) are relatively uncommon in CRC, they represent the fourth most frequent cause of BMs overall, and their occurrence is increasingly recognized as a complication in advanced CRC, associated with poor prognosis and limited treatment options. The brain microenvironment presents unique metabolic challenges, including low oxygen levels and restricted lipid availability. In order to survive in this hostile environment, CRC cells must acquire metabolic adaptations allowing them to survive and proliferate. To identify key drivers that enable CRC cells to metastasize to and survive within the brain, we conducted a transcriptomic screen of CRC BMs and compared it to liver metastasis (LMs). FOXM1, a transcription factor critical for tumor progression, was identified among the upregulated genes, and these results were validated by immunohistochemistry. To study the role of the brain microenvironment in mediating FOXM1 expression, we examined FOXM1 expression in CRC cell lines grown in either astrocyte-conditioned media (A-CM) or hepatocyte-conditioned media (H-CM). We observed a marked upregulation of FOXM1 following exposure to A-CM. Moreover, using an intracranial CRC BMs mouse model, a significant FOXM1 overexpression was observed. In accordance with the importance of fatty acid metabolism in BMs, our study revealed a significant correlation between FOXM1 and fatty acid synthase (FASN) in the CRC BMs, in agreement with public databases. These findings suggest that FOXM1 plays a key role in CRC BMs progression and may serve as a promising therapeutic target in this challenging disease setting.

Indexed as

Brain NeoplasmsColorectal NeoplasmsForkhead Box Protein M1Tumor MicroenvironmentAdaptation, PhysiologicalAnimalsAstrocytesBrainCell Line, TumorCulture Media, ConditionedFemaleGene Expression Regulation, NeoplasticHumansLiver NeoplasmsMiceCulture Media, ConditionedForkhead Box Protein M1FOXM1 protein, humanBMsColorectal cancerFOXM1Lipid metabolismMetabolic adaptation

Identifiers

PMID42036506
PMCPMC13111526

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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.