Evidence map›Paper›PMID 42374453›Full record

ReviewMolecular cancer2026

Dissecting oral premalignant carcinogenesis: spatial omics mechanisms and nanomedicine-driven therapeutic innovation.

Xinjia Cai, Yingying Cui, Chuanyang Ding, Yan Liu, Tiejun Li

Abstract readReview
In one paragraph

Review in Molecular cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Xinjia CaiCentral Laboratory, Peking University School and Hospital of Stomatology, Beijing, 100081, China. caixinjia1994@163.com.ORCID https://orcid.org/0000-0002-3212-7474
Yingying CuiCentral Laboratory, Peking University School and Hospital of Stomatology, Beijing, 100081, China.
Chuanyang DingCentral Laboratory, Peking University School and Hospital of Stomatology, Beijing, 100081, China.
Yan LiuCentral Laboratory, Peking University School and Hospital of Stomatology, Beijing, 100081, China. orthoyan@bjmu.edu.cn.
Tiejun LiNational Center for Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices & Beijing Key Laboratory of Digital Stomatology & Research Center of Engineering and Technology for Computerized Dentistry Ministry of Health & NMPA Key Laboratory for Dental Materials & Beijing Key Laboratory of Intelligent Biomanufacturing and Regeneration for Craniofacial Tissues, Beijing, 100081, China. litiejun22@vip.sina.com.

Funding

Beijing Municipal Natural Science Foundation L234017Beijing Nova Program 20240484655Beijing Science & Technology Development of Traditional Chinese Medicine BJZYQN-2025-11China Postdoctoral Science Foundation 2025M781685National Natural Science Foundation of China 82230030Peking University Medicine plus X Pilot Program-Key Technologies R&D Project 2024YXXLHGG004Talent development plan for the future in Medical-Engineering Integration by BRA-CDCHE and ZTA MBRC0012025013
6 · The paper itself

Abstract

Oral potentially malignant disorder (OPMD) remains a critical clinical challenge for cancer interception. However, the progression of OPMD toward oral squamous cell carcinoma (OSCC) is driven by profound cellular heterogeneity and dynamic microenvironmental remodeling. The mechanisms underlying these processes are not yet fully understood. Recent advancements in single-cell and spatial omics have facilitated high-resolution decoding of the precancerous landscape, unveiling multistep epithelial cell plasticity, fibroblast heterogeneity with extracellular matrix remodeling, immune suppression, and inflammatory reprogramming, as well as coupled metabolic and redox alterations that govern malignant transformation. These insights into the cellular mechanisms have led to a paradigm shift in the understanding of OPMD, reclassifying it as an ecosystem-level disease rather than a purely epithelial pathology. Nanomedicine is a potent platform for translating mechanistic knowledge into precision diagnostics and interventions at the precancerous stage. Nanomaterial-based strategies have been demonstrated to facilitate several critical processes, including enabling early lesion visualization and risk stratification, immune microenvironment reactivation, anti-fibrotic and anti-inflammatory remodeling, and targeted regulation of metabolic and oxidative stress pathways. A mounting body of evidence from preclinical and clinical studies lends support to the notion that nanotechnology-assisted early detection, microenvironmental reprogramming, and the interception of malignant transformation across oral and other precancerous conditions are indeed feasible. This review integrates single-cell-resolved mechanisms of OPMD progression with state-of-the-art nanomedicine-based diagnostic and therapeutic strategies, highlighting convergent biological axes and translational opportunities. By integrating single-cell biology with nanotechnology-driven precision medicine, this work is expected to improve the development of a nanomedicine framework for early cancer detection and treatment and outline future directions and challenges toward clinical implementation.

Indexed as

CarcinogenesisMouth NeoplasmsNanomedicinePrecancerous ConditionsAnimalsGenomicsHumansTumor MicroenvironmentCancerNanomedicineOral potentially malignant disorderPremalignancySingle-cell sequencing

Identifiers

PMID42374453
PMCPMC13587578

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.