Evidence map›Paper›PMID 36881132›Full record

ArticleCancer immunology, immunotherapy : CII2023

Targeting CD73 increases therapeutic response to immunogenic chemotherapy by promoting dendritic cell maturation.

Yun-Shan Lin, Shu-Fen Chiang, Chia-Yi Chen, Wei-Ze Hong, Tsung-Wei Chen, William Tzu-Liang Chen, Tao-Wei Ke, Pei-Chen Yang, Ji-An Liang, An-Cheng Shiau and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
7.0field-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

19 citing papers in PubMed, 27 citations in OpenAlex.

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  18. The Immune Regulatory Role of Adenosine in the Tumor Microenvironment.International journal of molecular sciences · 2023
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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

12 authors at 3 institutions in 1 country.

Yun-Shan LinDepartment of Pathology, China Medical University Hospital, China Medical University, Taichung, 40402, Taiwan, ROC.
Shu-Fen ChiangLab of Precision Medicine, Feng-Yuan Hospital, Ministry of Health and Welfare, Taichung, 42055, Taiwan, ROC.
Chia-Yi ChenProton Therapy and Science Center, China Medical University Hospital, China Medical University, Taichung, 40402, Taiwan, ROC.
Wei-Ze HongProton Therapy and Science Center, China Medical University Hospital, China Medical University, Taichung, 40402, Taiwan, ROC.
Tsung-Wei ChenGraduate Institute of Biomedical Science, China Medical University, Taichung, 40402, Taiwan, ROC.
William Tzu-Liang ChenDepartment of Colorectal Surgery, China Medical University HsinChu Hospital, China Medical University, HsinChu, 302, Taiwan, ROC.
Tao-Wei KeDepartment of Colorectal Surgery, China Medical University Hospital, China Medical University, Taichung, 40402, Taiwan, ROC.
Pei-Chen YangProton Therapy and Science Center, China Medical University Hospital, China Medical University, Taichung, 40402, Taiwan, ROC.
Ji-An LiangDepartment of Radiation Oncology, China Medical University Hospital, China Medical University, Taichung, Taiwan, ROC.
An-Cheng ShiauProton Therapy and Science Center, China Medical University Hospital, China Medical University, Taichung, 40402, Taiwan, ROC.
K S Clifford Chao *Proton Therapy and Science Center, China Medical University Hospital, China Medical University, Taichung, 40402, Taiwan, ROC. d94032@mail.cmuh.org.tw.ORCID http://orcid.org/0000-0002-7162-2566
Kevin Chih-Yang Huang *Department of Biomedical Imaging and Radiological Science, China Medical University, Taichung, 40402, Taiwan, ROC. chihyang0425@mail.cmu.edu.tw.ORCID http://orcid.org/0000-0002-0266-3233
China Medical University · TWAsia University · TWMinistry of Health and Welfare · TW

Funding

China Medical University Hospital DMR-111-045China Medical University Hospital DMR-CELL-2102China Medical University Hospital DMR-CELL-2103Ministry of Science and Technology, Taiwan MOST110-2314-B-039-032Ministry of Science and Technology, Taiwan MOST110-2628-B-039-005
6 · The paper itself

Abstract

The CD39-CD73-adenosinergic pathway converts adenosine triphosphate (ATP) to adenosine for inhibiting anti-tumor immune responses. Therefore, targeting CD73 to reinvigorate anti-tumor immunity is considered the novel cancer immunotherapy to eradicate tumor cells. To fully understand the critical role of CD39/CD73 in colon adenocarcinoma (COAD), this study aims to comprehensive investigate the prognostic significance of CD39 and CD73 in stage I-IV COAD. Our data demonstrated that CD73 staining strongly marked malignant epithelial cells and CD39 was highly expressed in stromal cells. Attractively, tumor CD73 expression was significantly associated with tumor stage and the risk of distant metastasis, which suggested CD73 was as an independent factor for colon adenocarcinoma patients in univariate COX analysis [HR = 1.465, 95%CI = 1.084-1.978, p = 0.013]; however, high stromal CD39 in COAD patients was more likely to have favorable survival outcome [HR = 1.458, p = 1.103-1.927, p = 0.008]. Notably, high CD73 expression in COAD patients showed poor response to adjuvant chemotherapy and high risk of distant metastasis. High CD73 expression was inversely associated with less infiltration of CD45

Indexed as

AdenocarcinomaColonic NeoplasmsLung NeoplasmsAdenosine TriphosphateDendritic CellsHumansOxaliplatinAdenosine TriphosphateOxaliplatinAnti-tumor immunityATPCD73Colon adenocarcinomaDistant metastasis

Identifiers

PMID36881132
PMCPMC10991491
OpenAlexW4323348738

What Socratic 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 Socratic graph.