ReviewCancer cell international2026
Transforming growth factor-β and integrins: key players in EMT and breast cancer progression.
Review in Cancer cell international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In advanced breast cancer, the integrin-TGF-β axis moves from a tumor-suppressive to a pro-metastatic state and is central to breast cancer metastasis. We review how integrins, especially αvβ3, αvβ6, and β1, serve as critical modulators of TGF-β signaling and play a key role in epithelial-to-mesenchymal transition (EMT), immune evasion, angiogenesis, and ECM remodeling. In addition to activating latent TGFβ, these integrins also function as downstream effectors that fuel EMT and tumor progression through a feedback loop. Integrins function mechanistically to promote cytoskeletal reorganization, ECM degradation, and tumor cell motility, and TGF-β signaling influences integrin expression and activity. Targeting this axis is explored as a therapeutic approach to reduce metastasis and improve patient outcomes, and the potential of integrin inhibitors, TGFβ pathway blockers, and combination therapies are discussed. This review highlights the need for novel interventions to disrupt this axis by elucidating the interplay between integrins and TGF-β.
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Registered trials
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.