Evidence map›Paper›PMID 41405822›Full record

ArticleMolecular biomedicine2025

Multi-omics factor analysis identifies the Tensin 1-Fermitin family homologue 2-Fibronectin 1-Integrin signaling axis as a prognostic determinant in colorectal cancer.

Tianwei Chen, Yebin Yang, Jing Shi, Fanhe Dong, Lesi Xie, Yuqiang Shan, Xiang Wang

Abstract read
In one paragraph

Article in Molecular biomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Tianwei Chen *Zhejiang Key Laboratory of Zero Magnetic Medicine, School of Medicine, Affiliated Hangzhou First People's Hospital, Westlake University, Hangzhou, China. chentianwei@sibs.ac.cn.ORCID 0009-0003-1600-6167
Yebin Yang *Department of Gastrointestinal Surgery, School of Medicine, Affiliated Hangzhou First People's Hospital, Westlake University, Hangzhou, China.
Jing Shi *Department of General Surgery, Zhejiang Hospital, Hangzhou, Zhejiang Province, China.
Fanhe DongDepartment of Gastrointestinal Surgery, School of Medicine, Affiliated Hangzhou First People's Hospital, Westlake University, Hangzhou, China.
Lesi XieDepartment of Pathology, School of Medicine, Affiliated Hangzhou First People's Hospital, Westlake University, Hangzhou, China.
Yuqiang ShanDepartment of Gastrointestinal Surgery, School of Medicine, Affiliated Hangzhou First People's Hospital, Westlake University, Hangzhou, China. shang110117@163.com.
Xiang WangZhejiang Key Laboratory of Zero Magnetic Medicine, School of Medicine, Affiliated Hangzhou First People's Hospital, Westlake University, Hangzhou, China. wangxiang2021@zju.edu.cn.

Funding

National Natural Science Foundation of China 82003076Natural Science Foundation of Zhejiang Province ZCLMS25H0302
6 · The paper itself

Abstract

Colorectal cancer (CRC) remains a leading cause of cancer-related mortality worldwide, with its heterogeneous molecular profiles complicating prognosis prediction. Multi-omics profiling of clinical CRC specimens is particularly valuable for uncovering prognostic variables; however, such integrated studies remain scarce. Here, we applied the Multi-Omics Factor Analysis v2 framework to multi-omics data (mutations, miRNA, RNA, proteomics, phospho-proteomics) from the CPTAC-2 cohort and constructed a comprehensive CRC model. This approach identified a survival-associated latent variable, which we term the CRC Prognostic Latent Factor (CPLF). The prognostic relevance of CPLF was then rigorously validated across three independent multi-omics cohorts, encompassing 579 patients with CRC. CPLF primarily reflects extracellular matrix deposition in the tumour microenvironment, with Tensin 1 (TNS1) and Fermitin family homologue 2 (FERMT2) as the highest-weighted features. Single-cell and spatial transcriptomic analyses, supplemented by immunohistochemistry, localized CPLF-associated gene expression predominantly to myofibroblasts. Functionally, knockdown of Tensin 1 or FERMT2 in fibroblasts attenuated tumour growth in vivo. Consistently, these top-weighted components of CPLF upregulated fibronectin 1 (FN1) expression in myofibroblasts, thereby activating integrin signaling in cancer cells and enhancing tumour progression. Altogether, our findings unveil CPLF as a data-inherent multi-omics prognostic factor and establish the CPLF/FN1/integrin axis as a key pathway mediating myofibroblast-cancer cell crosstalk in CRC progression.

Indexed as

Colorectal NeoplasmsFibronectinsIntegrinsMembrane ProteinsNeoplasm ProteinsSignal TransductionTensinsAnimalsBiomarkers, TumorCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMaleMiceMultiomicsBiomarkers, TumorFibronectinsFN1 protein, humanIntegrinsMembrane ProteinsNeoplasm ProteinsTensinsColorectal cancerExtracellular matrixFERMT2Multi-omics factor analysisMyofibroblastsTNS1

Identifiers

PMID41405822
PMCPMC12711624

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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.