Evidence map›Paper›PMID 34685686›Full record

ReviewCells2021

Redox Control of the Dormant Cancer Cell Life Cycle.

Bowen Li, Yichun Huang, Hui Ming, Edouard C Nice, Rongrong Xuan, Canhua Huang

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 14% of its field
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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  13. Colorectal cancer and dormant metastases: Put to sleep or destroy?World journal of gastrointestinal oncology · 2024
    Article
  14. Review
  15. Review
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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

6 authors at 4 institutions in 2 countries.

Bowen LiThe Affiliated Hospital of Medical School of Ningbo University, Ningbo 315020, China.ORCID 0000-0001-8475-4800
Yichun HuangClinical Medical College, Hubei University of Science and Technology, Xianning 437000, China.
Hui MingState Key Laboratory of Biotherapy and Cancer Center, West China Hospital and West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University and Collaborative Innovation Center for Biotherapy, Chengdu 610041, China.
Edouard C NiceDepartment of Biochemistry and Molecular Biology, Monash University, Clayton, VIC 3800, Australia.ORCID 0000-0001-5480-4715
Rongrong XuanThe Affiliated Hospital of Medical School of Ningbo University, Ningbo 315020, China.
Canhua HuangThe Affiliated Hospital of Medical School of Ningbo University, Ningbo 315020, China.ORCID 0000-0003-2247-7750
Ningbo University · CNHubei University of Science and Technology · CNMonash University · AUSichuan University · CN

Funding

Guangdong Basic and Applied Basic Research Foundation 2019B030302012National Key Research and Development Program of China 2020YFA0509400National Natural Science Foundation of China 81790251National Natural Science Foundation of China 81821002National Natural Science Foundation of China 82130082Ningbo Health Young Talents Fund 2020SWSQNGGSichuan Applied Basic Research Project 2020YJ0107The Affiliated Hospital of Medical School of Ningbo University Qingmiao Talent Cultivation Fund FYQM-KY-202003
6 · The paper itself

Abstract

Following efficient tumor therapy, some cancer cells may survive through a dormancy process, contributing to tumor recurrence and worse outcomes. Dormancy is considered a process where most cancer cells in a tumor cell population are quiescent with no, or only slow, proliferation. Recent advances indicate that redox mechanisms control the dormant cancer cell life cycle, including dormancy entrance, long-term dormancy, and metastatic relapse. This regulatory network is orchestrated mainly through redox modification on key regulators or global change of reactive oxygen species (ROS) levels in dormant cancer cells. Encouragingly, several strategies targeting redox signaling, including sleeping, awaking, or killing dormant cancer cells are currently under early clinical evaluation. However, the molecular mechanisms underlying redox control of the dormant cancer cell cycle are poorly understood and need further exploration. In this review, we discuss the underlying molecular basis of redox signaling in the cell life cycle of dormant cancer and the potential redox-based targeting strategies for eliminating dormant cancer cells.

Indexed as

AnimalsClinical Trials as TopicHumansModels, BiologicalNeoplasm MetastasisNeoplasmsOxidation-ReductionTumor Microenvironmentcancer dormancycancer therapyredox signalingROS

Identifiers

PMID34685686
PMCPMC8535080
OpenAlexW3207634962

What Socratic holds

Textmetadata
LicenceCC BY
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.