Evidence map›Paper›PMID 37463926›Full record

ArticleSignal transduction and targeted therapy2023

Cancer cell employs a microenvironmental neural signal trans-activating nucleus-mitochondria coordination to acquire stemness.

Bin He, Rui Gao, Shasha Lv, Ailin Chen, Junxiu Huang, Luoxuan Wang, Yunxiu Feng, Jiesi Feng, Bing Liu, Jie Lei and 13 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Signal transduction and targeted therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 33 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 6 institutions in 2 countries.

Bin He *State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China.ORCID http://orcid.org/0000-0002-7690-4730
Rui Gao *State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China.
Shasha Lv *State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China.
Ailin ChenState Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China.
Junxiu HuangZhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, PR China.
Luoxuan WangInstitute of Cancer Stem Cell, Cancer Center, Dalian Medical University, Dalian, 116023, PR China.
Yunxiu FengInstitute of Cancer Stem Cell, Cancer Center, Dalian Medical University, Dalian, 116023, PR China.
Jiesi FengState Key Laboratory of Membrane Biology, Peking University School of Life Sciences, Beijing, 100871, PR China.
Bing LiuState Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China.
Jie LeiState Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China.
Bing DengState Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China.
Bin HeInstitute of Cancer Stem Cell, Cancer Center, Dalian Medical University, Dalian, 116023, PR China.
Bai CuiInstitute of Cancer Stem Cell, Cancer Center, Dalian Medical University, Dalian, 116023, PR China.
Fei PengInstitute of Cancer Stem Cell, Cancer Center, Dalian Medical University, Dalian, 116023, PR China.
Min YanState Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China.
Zifeng WangState Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China.
Eric W-F LamDepartment of Surgery and Cancer, Imperial College London, London, W12 0NN, UK.ORCID http://orcid.org/0000-0003-1274-3576
Bilian JinInstitute of Cancer Stem Cell, Cancer Center, Dalian Medical University, Dalian, 116023, PR China.
Zhiming ShaoDepartment of Breast Surgery, Precision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, 200032, PR China.
Yulong LiState Key Laboratory of Membrane Biology, Peking University School of Life Sciences, Beijing, 100871, PR China.ORCID http://orcid.org/0000-0002-9166-9919
Jianwei JiaoState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, PR China.ORCID http://orcid.org/0000-0002-7893-0721
Xi WangState Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China. wangxi@sysucc.org.cn.
Quentin LiuState Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, PR China. liuq9@mail.sysu.edu.cn.
Sun Yat-sen University · CNDalian Medical University · CNPeking University · CNChinese Academy of Sciences · CNFudan University Shanghai Cancer Center · CNImperial College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer cell receives extracellular signal inputs to obtain a stem-like status, yet how tumor microenvironmental (TME) neural signals steer cancer stemness to establish the hierarchical tumor architectures remains elusive. Here, a pan-cancer transcriptomic screening for 10852 samples of 33 TCGA cancer types reveals that cAMP-responsive element (CRE) transcription factors are convergent activators for cancer stemness. Deconvolution of transcriptomic profiles, specification of neural markers and illustration of norepinephrine dynamics uncover a bond between TME neural signals and cancer-cell CRE activity. Specifically, neural signal norepinephrine potentiates the stemness of proximal cancer cells by activating cAMP-CRE axis, where ATF1 serves as a conserved hub. Upon activation by norepinephrine, ATF1 potentiates cancer stemness by coordinated trans-activation of both nuclear pluripotency factors MYC/NANOG and mitochondrial biogenesis regulators NRF1/TFAM, thereby orchestrating nuclear reprograming and mitochondrial rejuvenating. Accordingly, single-cell transcriptomes confirm the coordinated activation of nuclear pluripotency with mitochondrial biogenesis in cancer stem-like cells. These findings elucidate that cancer cell acquires stemness via a norepinephrine-ATF1 driven nucleus-mitochondria collaborated program, suggesting a spatialized stemness acquisition by hijacking microenvironmental neural signals.

Indexed as

NeoplasmsTranscription FactorsCell NucleusMitochondriaNeoplastic Stem CellsNorepinephrineNorepinephrineTranscription Factors

Identifiers

PMID37463926
PMCPMC10354099
OpenAlexW4384661430

What OpenQuestion holds

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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 OpenQuestion graph.