Evidence map›Paper›PMID 33584714›Full record

ArticleFrontiers in immunology2020

CU06-1004-Induced Vascular Normalization Improves Immunotherapy by Modulating Tumor Microenvironment

Songyi Park, Ji Hoon Oh, Dong Jin Park, Haiying Zhang, Minyoung Noh, Yeomyung Kim, Ye-Seul Kim, Hyejeong Kim, Young-Myeong Kim, Sang-Jun Ha and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  5. The MYC/TXNIP axis mediates NCL-Suppressed CD8Molecular medicine (Cambridge, Mass.) · 2025
    Article
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  7. The role and mechanisms of microvascular damage in the ischemic myocardium.Cellular and molecular life sciences : CMLS · 2023
    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

11 authors at 2 institutions in 1 country.

Songyi ParkDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Ji Hoon OhDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Dong Jin ParkDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Haiying ZhangR&D Department, Curacle Co. Ltd, Seongnam-si, South Korea.
Minyoung NohDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Yeomyung KimDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Ye-Seul KimDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Hyejeong KimDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Young-Myeong KimVascular System Research Center, Kangwon National University, Chuncheon, South Korea.
Sang-Jun HaDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Young-Guen KwonDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Yonsei University · KRKangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blocking the immune evasion mechanism of tumor cells has become an attractive means for treating cancers. However, the usage of a drug such as nivolumab (αPD-1), which blocks programmed cell death protein 1 (PD-1), turned out to be only effective against certain types of cancer. Especially, vascular abnormal structures of which deter delivery route by leakage and cause the poor perfusion were considered to be environment unfavorable to T cells and immune checkpoint blockade (ICB) delivery within the tumor microenvironment (TME). Herein, we report stabilization of tumor blood vessels by endothelial dysfunctional blocker CU06-1004, which modified the TME and showed synergistic effects with immunotherapy anti-PD-1 antibody. CU06-1004 combination therapy consistently prolonged the survival of tumor-bearing mice by decreasing tumor growth. T-cell infiltration increased in the tumors of the combination group, with cytotoxic CD8

Indexed as

AdenocarcinomaAnimalsAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsApoptosisCapillary PermeabilityCarcinoma, Lewis LungCell HypoxiaCell Line, TumorColonic NeoplasmsDrug Screening Assays, AntitumorDrug SynergismEndothelium, VascularImmune Checkpoint InhibitorsImmunotherapyLymphocytes, Tumor-InfiltratingAntineoplastic Agents, ImmunologicalCU06-1004Immune Checkpoint InhibitorsPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorSaponinsanti-PD-1combination therapyCU06-1004cytotoxic T lymphocytesdrug deliveryimmune checkpoint blockade (ICB)tumor microenvironment (TME)vascular leakage blocker

Identifiers

PMID33584714
PMCPMC7874050
OpenAlexW3122810489

What OpenQuestion 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 OpenQuestion graph.