Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Quantitative proteomic analysis identifies new effectors of FOXM1 involved in breast cancer cell migration.

International journal of clinical and experimental pathology - 1 Jan 2015

Ye Xiaojuan, Zhang Yi, He Bin, Meng Yuesheng, Li Yandong, Gao Yong

Abstract excerpt

The Forkhead Box M1 (FOXM1) transcription factor plays important roles in tumorigenesis and tumor metastasis in multiple human carcinomas. However, the underlying mechanisms for FOXM1 function remain to be classified. In the present study, we employed quantitative proteomic approach to search new downstream targets of FOXM1 in breast cancer MDA-MB-231 cells. A total of 4125 proteins were identified and quantified...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cell Movement
Share to Coenzyme A Ligases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Forkhead Transcription Factors

Share to Proteomics

Share to Receptors, Progesterone

Share to Reproducibility of Results

Share to RNA Interference

Share to Tandem Mass Spectrometry

Source

Open in PubMed Open full text

Identifiers

PMID: 26884854
PMCID: PMC4730067

Genes

FOXM1
ACSL4
PGRMC2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Quantitative proteomic analysis identifies new effectors of FOXM1 involved in breast cancer cell migration.PMID 26884854Read ↗

FOXM1 and Cancer: Faulty Cellular Signaling Derails HomeostasisSemantic proximity Read ↗

FOXM1 transcriptional regulationSemantic proximity Read ↗

Novel functions of FoxM1: from molecular mechanisms to cancer therapySemantic proximity Read ↗

Regulation of the master regulator FOXM1 in cancerSemantic proximity Read ↗

Quantitative Proteomic Profiling Analysis of Papillary Thyroid Cancer combined with Cervical Lymph Node Metastasis: Evidence from Cancer Tissue and SerumSemantic proximity Read ↗

Profilin-1 Overexpression in MDA-MB-231 Breast Cancer Cells Is Associated with Alterations in Proteomics Biomarkers of Cell Proliferation, Survival, and Motility as Revealed by Global Proteomics AnalysesSemantic proximity Read ↗

Quantitative proteome profiling of lymph node-positive vs. -negative colorectal carcinomas pinpoints MX1 as a marker for lymph node metastasis.Semantic proximity Read ↗

Small-molecule inhibitors targeting FOXM1: Current challenges and future perspectives in cancer treatmentsSemantic proximity Read ↗

Quantitative Proteomic and Genomic Profiling Reveals Metastasis-Related Protein Expression Patterns in Gastric Cancer CellsSemantic proximity Read ↗

Global identification of miR-373-regulated genes in breast cancer by quantitative proteomics.Semantic proximity Read ↗

Interactome Analysis Reveals that C1QBP (complement component 1, q subcomponent binding protein) Is Associated with Cancer Cell Chemotaxis and MetastasisSemantic proximity Read ↗

miR-342-3p suppresses proliferation, migration and invasion by targeting FOXM1 in human cervical cancer.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.