Evidence map›Paper›PMID 39932384›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

Ribonuclease 1 Induces T-Cell Dysfunction and Impairs CD8

Wen-Hao Yang, Bao-Yue Huang, Hsing-Yu Rao, Peng Ye, Bi Chen, Hao-Ching Wang, Chih-Hung Chung, Heng-Hsiung Wu, Hung-Rong Yen, Shao-Chun Wang and 4 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  9. Ribonuclease 1 Induces T-Cell Dysfunction and Impairs CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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

14 authors.

Wen-Hao YangGraduate Institute of Cell Biology and Cancer Biology and Precision Therapeutics Center, China Medical University, Taichung, 406040, Taiwan.ORCID https://orcid.org/0000-0002-6292-9048
Bao-Yue HuangGraduate Institute of Cell Biology and Cancer Biology and Precision Therapeutics Center, China Medical University, Taichung, 406040, Taiwan.ORCID https://orcid.org/0009-0003-8438-0468
Hsing-Yu RaoGraduate Institute of Cell Biology and Cancer Biology and Precision Therapeutics Center, China Medical University, Taichung, 406040, Taiwan.ORCID https://orcid.org/0009-0000-7673-3858
Peng YeAffiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, Guangdong, 910095, China.ORCID https://orcid.org/0000-0002-8327-2241
Bi ChenAffiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, Guangdong, 910095, China.ORCID https://orcid.org/0009-0005-6827-5224
Hao-Ching WangThe PhD Program for Translational Medicine, and Graduate Institute of Translational Medicine, College of Medical Science and Technology, Taipei Medical University, Taipei, 110301, Taiwan.ORCID https://orcid.org/0000-0003-2396-717X
Chih-Hung ChungCancer and Immunology Research Center, National Yang Ming Chiao Tung University, Taipei, 112304, Taiwan.
Heng-Hsiung WuGraduate Institute of Biomedical Sciences, China Medical University, Taichung, 404328, Taiwan.ORCID https://orcid.org/0000-0002-7220-8519
Hung-Rong YenSchool of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, 404328, Taiwan.ORCID https://orcid.org/0000-0002-0131-1658
Shao-Chun WangGraduate Institute of Biomedical Sciences, China Medical University, Taichung, 404328, Taiwan.ORCID https://orcid.org/0000-0002-5477-1682
Jong-Ho ChaDepartment of Biomedical Science and Engineering, Graduate School, Inha University, Incheon, 22212, Republic of Korea.ORCID https://orcid.org/0000-0003-2181-7768
Xiuwen YanAffiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, Guangdong, 910095, China.ORCID https://orcid.org/0000-0003-1785-7783
Muh-Hwa YangInstitute of Clinical Medicine and Cancer and Immunology Research Center, National Yang Ming Chiao Tung University, Taipei, 112304, Taiwan.ORCID https://orcid.org/0000-0002-8918-1244
Mien-Chie HungGraduate Institute of Biomedical Sciences, Institute of Biochemistry and Molecular Biology, Research Center for Cancer Biology, Cancer Biology and Precision Therapeutics Center and Center for Molecular Medicine, China Medical University, Taichung, 406040, Taiwan.ORCID https://orcid.org/0000-0003-4317-4740

Funding

China Medical University, Taiwan CMU108-YTY-04China Medical University, Taiwan CMU113-MF-12Ministry of EducationMinistry of Health and Welfare MOHW114-TDU-B-222-144016National Health Research Institutes NHRI-EX112-11010BINational Health Research Institutes NHRI-EX112-11215BINational Natural Science Foundation of China 82172789National Science and Technology Council NSTC 111-2314-B-A49-030-MY3National Science and Technology Council NSTC 111-2320-B-039-061National Science and Technology Council NSTC 112-2320-B-039-024National Science and Technology Council NSTC 112-2320-B-A49-006National Science and Technology Council NSTC 113-2320-B-039-017National Science and Technology Council NSTC113-2639-B-039-001-ASPNational Science and Technology Council T-StarCenterNSTC113-2634-F-039-001Project of Educational Commission of Guangdong Province of China 2021KCXTD023Science and Technology Project of Guangzhou Health Commission 20241A011117
6 · The paper itself

Abstract

T-cell-based immunotherapy holds promise for eliminating cancer through T-cell activation. However, prolonged interaction between T cells and tumors and the presence of immunosuppressive factors can diminish T-cell cytotoxicity, leading to treatment failure. Here, ribonuclease 1 (RNase1), which degrades RNA, reduced the expression of effector cytokines and increases immune checkpoint protein levels, inducing T-cell dysfunction. RNase1 expression is positively associated with exhausted T-cell gene signatures and immune checkpoint proteins across several cancer types. Cancer cells expressing RNase1 are resistant to CD8

Indexed as

CD8-Positive T-LymphocytesNeoplasmsSTAT1 Transcription FactorAnimalsCell Line, TumorFemaleHumansImmunotherapyMiceSTAT1 protein, humanSTAT1 Transcription Factoreffector cytokineimmune checkpoint proteinribonuclease 1STAT1T‐cell dysfunction

Identifiers

PMID39932384
PMCPMC11967817

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.