ArticleBioactive materials2026
An immuno-chemotherapeutic bone scaffold for tumor eradication and bone regeneration in drug-resistant osteosarcoma.
Article in Bioactive materials, 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
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Postoperative management of osteosarcoma remains hindered by several critical challenges, including platinum-based chemoresistance, insufficient antitumor immune responses, and the difficulty of synchronously repairing large bone defects. Addressing these issues requires strategies capable of coordinating tumor eradication, immune modulation, and bone regeneration within the dynamic postoperative microenvironment. In this study, we developed a near-infrared (NIR)-responsive intelligent composite bone scaffold that integrates a reducible platinum (IV) prodrug (Pt (IV)) and cucurbitacin B (CuB) via hollow mesoporous silica and polydopamine interfacial engineering, enabling dual responsiveness to tumor-associated cues and exogenous photonic stimulation. Mechanistically, controlled CuB release suppresses DNA damage repair, amplifies Pt (IV)-induced DNA damage, and reverses platinum resistance, while the combined action of Pt (IV) and CuB induces immunogenic cell death and activates the cGAS-STING pathway, thereby remodeling an antitumor immune microenvironment. Concurrently, sustained Si
Indexed as
Identifiers
What OpenQuestion 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 OpenQuestion graph.