Evidence map›Paper›PMID 41130559›Full record

ReviewCancer letters2025

Regulated cell death in cancer: Mechanisms, crosstalk, and opportunities for therapy.

Yimei Meng, Qun Chen, Zhijun Zhou, Min Li

Abstract readReview
In one paragraph

Review in Cancer letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. The gasdermin family: from pyroptosis mechanisms to therapeutic targets.Signal transduction and targeted therapy · 2026
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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

4 authors.

Yimei MengDepartment of Medicine, The University of Oklahoma Health Campus, Oklahoma City, OK, 73104, USA.
Qun ChenDepartment of Medicine, The University of Oklahoma Health Campus, Oklahoma City, OK, 73104, USA.
Zhijun ZhouDepartment of Medicine, The University of Oklahoma Health Campus, Oklahoma City, OK, 73104, USA.
Min LiDepartment of Medicine, The University of Oklahoma Health Campus, Oklahoma City, OK, 73104, USA. Electronic address: Min-Li@ou.edu.

Funding

Prognostic Biomarkers for ZIP4-mediated Cachexia in Pancreatic CancerR01CA203108 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LI, MIN, LI, YI-PING · 2016 to 2020
$2.7M
ZIP4 is a Novel Molecular Target in Human Pancreatic CancerR01CA186338 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI FERNANDEZ-ZAPICO, MARTIN ERNESTO, LI, MIN · 2015 to 2019
$1.7M
Role of Zinc Dependent EMT-Transcription Factors (EMT-TF) in Pancreatic Cancer MetastasisR01CA247234 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LI, MIN · 2020 to 2024
$1.6M
NCI NIH HHS R01 CA186338NCI NIH HHS R01 CA203108NCI NIH HHS R01 CA247234
6 · The paper itself

Abstract

Regulated cell death (RCD) is a fundamental biological process essential for tissue homeostasis, and the elimination of damaged or malignant cells. In cancer, dysregulation of RCD is closely linked to tumor initiation, progression, therapeutic resistance, and remodeling of the tumor microenvironment (TME). In this review, we classify RCD in cancer into three broad groups. Classical cell death types include apoptosis, autophagy, necroptosis, and pyroptosis, which have well-established roles in controlling cell fate. Metal-dependent pathways, represented by ferroptosis, and cuproptosis, highlight vulnerabilities linked to iron and copper metabolism. Emerging modalities such as entosis, NETosis, disulfidptosis, and parthanatos, further expand the conceptual landscape of RCD, revealing diverse mechanisms by which cancer cells respond to stress. We synthesize the molecular mechanisms and signaling networks governing these processes, emphasizing their intricate crosstalk, shared regulators, and context-dependent dual roles in tumor suppression and promotion. Finally, we discuss translational strategies to exploit RCD, including pharmacologic modulators, nanomaterial-based approaches, and early clinical evidence, outlining future directions for precision oncology. Together, these insights establish RCD as a dynamic and targetable network that provides both mechanistic understanding and opportunities for novel therapeutic interventions in cancer.

Indexed as

NeoplasmsRegulated Cell DeathAnimalsAntineoplastic AgentsAutophagyFerroptosisHumansSignal TransductionTumor MicroenvironmentAntineoplastic AgentsDrug deliveryImmune evasionMetabolismPrecision oncologyProgrammed cell death

Identifiers

PMID41130559
PMCPMC12956738

What OpenQuestion 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 OpenQuestion graph.