Evidence mapPaperPMID 41415713Full record

ReviewMedComm2025

Tumor Cell Plasticity in Cancer: Signaling Pathways and Pharmaceutical Interventions.

Shangwei Sun, Yunwei Sun, Ling Lan, Siyuan Luan, Jin Zhou, Jiehui Deng, Yong Yuan, Zhong Wu

Abstract readReview
In one paragraph

Review in MedComm, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

8 authors.

Shangwei SunDepartment of Thoracic Surgery West China Hospital, Sichuan University Chengdu Sichuan China.ORCID https://orcid.org/0009-0002-3450-2941
Yunwei SunDivision of Pancreatic Surgery, Department of General Surgery West China Hospital, Sichuan University Chengdu Sichuan China.
Ling LanDepartment of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy West China Hospital of Sichuan University Chengdu Sichuan China.
Siyuan LuanDepartment of Thoracic Surgery West China Hospital, Sichuan University Chengdu Sichuan China.
Jin ZhouDivision of Liver Surgery, Department of General Surgery West China Hospital, Sichuan University Chengdu Sichuan China.
Jiehui DengLaura and Isaac Perlmutter Cancer Center New York University Grossman School of Medicine New York New York USA.
Yong YuanDepartment of Thoracic Surgery West China Hospital, Sichuan University Chengdu Sichuan China.
Zhong WuDivision of Pancreatic Surgery, Department of General Surgery West China Hospital, Sichuan University Chengdu Sichuan China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular plasticity, the ability of cells to dynamically alter their phenotypes, is a key driver of tumor evolution. This process is a hallmark of cancer which enables the acquisition of malignant traits, leading to metastasis, progression, and therapy resistance. It is governed by cell-intrinsic factors, such as genomic instability and epigenetic reprogramming, and extrinsic stimuli from the tumor microenvironment. However, a unified framework is still needed to position plasticity as the central process that links these drivers to diverse cancer hallmarks. In this review, we first explore how plasticity enables key steps of tumor evolution, including tumorigenesis, metastasis driven by epithelial-mesenchymal plasticity (EMP), therapy resistance, and cancer stem cell (CSC) dynamics. We then summarize the intrinsic and extrinsic mechanisms that govern this adaptability. Finally, we discuss clinical advances in monitoring and targeting plasticity and highlight how new spatiotemporal technologies can address current research challenges. This review provides a framework positioning cellular plasticity as a central mechanism in cancer evolution, connecting its fundamental drivers to clinical translation. By synthesizing the latest advances, we offer perspectives for developing therapies that integrate prediction, monitoring, and targeting of plasticity to proactively guide cancer evolution toward manageable outcomes.

Indexed as

differentiation therapyepigenetic reprogrammingspatiotemporal omicstherapy resistancetumor cell plasticitytumor evolutiontumor microenvironment

Identifiers

PMID41415713
PMCPMC12710448

What Socratic holds

Textmetadata
LicenceCC BY
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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.