ReviewiScience2026
Research progress on precision targeted therapy strategies for breast cancer based on tumor microenvironment.
Review in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The tumor microenvironment (TME) plays a crucial role in the progression of BC, characterized by abnormal pH, aberrant enzyme expression, redox imbalance, etc. Nano-drug delivery systems (NDDSs) responsive to TME have emerged, including pH-responsive, enzyme-responsive, redox-responsive, and multi-responsive intelligent cascading systems. These systems effectively address tumor heterogeneity by improving intratumoral drug distribution and penetration, thereby enhancing therapeutic specificity and safety. In the future, the development of multi-modal intelligent NDDS, the design of programmable responsive systems, AI-driven personalized nano-drugs, and interdisciplinary collaboration to promote clinical translation will become key research focuses. This review not only systematically elucidates the response mechanism characteristics of TME in BC, but also focuses on analyzing the special requirements of the unique extracellular matrix and subtype specificity of BC for nanomedicine design. Furthermore, it summarizes the development directions of TME-responsive nano-delivery systems for BC, providing new insights to enhance the precise targeted therapy of BC.
Indexed as
Identifiers
What Socratic holds
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 Socratic graph.