Evidence map›Paper›PMID 37848444›Full record

ArticleNature communications2023

Phagocytosis-initiated tumor hybrid cells acquire a c-Myc-mediated quasi-polarization state for immunoevasion and distant dissemination.

Chih-Wei Chou, Chia-Nung Hung, Cheryl Hsiang-Ling Chiu, Xi Tan, Meizhen Chen, Chien-Chin Chen, Moawiz Saeed, Che-Wei Hsu, Michael A Liss, Chiou-Miin Wang and 15 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. ANXA2-mediated Phagocytosis Generates ARAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. The double-positive cells in the tumor microenvironment.Journal of translational internal medicine · 2026
    Article
  4. The authors respond to feedback onFrontiers in oncology · 2026
    Article
  5. Review
  6. Model Circulating Tumor Cells Induced by Mechanical Stress.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
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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

25 authors at 2 institutions in 2 countries.

Chih-Wei Chou *Department of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0001-5800-626X
Chia-Nung Hung *Department of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.
Cheryl Hsiang-Ling Chiu *Department of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0002-6946-9785
Xi TanDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0002-2511-9767
Meizhen ChenDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.
Chien-Chin ChenDepartment of Pathology, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi, Taiwan.ORCID http://orcid.org/0000-0001-9599-0884
Moawiz SaeedDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0002-3274-4739
Che-Wei HsuDepartment of Pathology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Michael A LissDepartment of Urology, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0001-6978-1026
Chiou-Miin WangDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0002-2681-725X
Zhao LaiDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.
Nathaniel AlvarezDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0002-6812-8591
Pawel A OsmulskiDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0002-5359-9200
Maria E GaczynskaDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0002-9033-5706
Li-Ling LinDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0001-9891-5900
Veronica OrtegaDepartment of Pathology and Laboratory Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.
Nameer B KirmaDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.
Kexin XuDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0002-2850-2083
Zhijie LiuDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0001-6956-7839
Addanki P KumarDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0001-5596-6265
Josephine A TavernaDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.
Gopalrao V N VelagaletiDepartment of Pathology and Laboratory Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0003-2811-8185
Chun-Liang ChenDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA. chenc4@uthscsa.edu.ORCID http://orcid.org/0000-0002-6774-9003
Zhao ZhangDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA. zhangz3@uthscsa.edu.ORCID http://orcid.org/0000-0002-3679-8945
Tim Hui-Ming HuangDepartment of Molecular Medicine, University of Texas Health Science Center, San Antonio, TX, 78229, USA. huangt3@uthscsa.edu.ORCID http://orcid.org/0000-0001-5985-9176
The University of Texas Health Science Center at San Antonio · USNational Cheng Kung University Hospital · TW

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
Systems Analysis of Epigenomic Architecture in Cancer ProgressionU54CA217297 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI WANG, QIANBEN · 2017 to 2021
$9.3M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthKL2TR001118 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, DOUGHERTY, DONALD M · 2013 to 2017
$3.4M
Advancing Cancer Research Through Next Generation Sequencing at Mays Cancer Center of UT Health San AntonioR50CA265339 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Zhao Lai · 2022 to 2026
$957k
NCATS NIH HHS KL2 TR001118NCI NIH HHS P30 CA054174NCI NIH HHS R50 CA265339NCI NIH HHS U54 CA217297
6 · The paper itself

Abstract

While macrophage phagocytosis is an immune defense mechanism against invading cellular organisms, cancer cells expressing the CD47 ligand send forward signals to repel this engulfment. Here we report that the reverse signaling using CD47 as a receptor additionally enhances a pro-survival function of prostate cancer cells under phagocytic attack. Although low CD47-expressing cancer cells still allow phagocytosis, the reverse signaling delays the process, leading to incomplete digestion of the entrapped cells and subsequent tumor hybrid cell (THC) formation. Viable THCs acquire c-Myc from parental cancer cells to upregulate both M1- and M2-like macrophage polarization genes. Consequently, THCs imitating dual macrophage features can confound immunosurveillance, gaining survival advantage in the host. Furthermore, these cells intrinsically express low levels of androgen receptor and its targets, resembling an adenocarcinoma-immune subtype of metastatic castration-resistant prostate cancer. Therefore, phagocytosis-generated THCs may represent a potential target for treating the disease.

Indexed as

CD47 AntigenMacrophagesNeoplasm MetastasisPhagocytosisProto-Oncogene Proteins c-mycTumor EscapeCarrier ProteinsHumansMaleProstatic NeoplasmsSignal TransductionTumor Cells, CulturedCarrier ProteinsCD47 AntigenProto-Oncogene Proteins c-myc

Identifiers

PMID37848444
PMCPMC10582093
OpenAlexW4387700062

What OpenQuestion holds

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Registered trials

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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.