Evidence map›Paper›PMID 30128738›Full record

ArticleCancer immunology, immunotherapy : CII2018

Expression of the inhibitory B7 family molecule VISTA in human colorectal carcinoma tumors.

Shan Xie, Jia Huang, Qin Qiao, Wenjuan Zang, Shanjuan Hong, Haidong Tan, Chen Dong, Zhiying Yang, Ling Ni

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
4.9field-weighted citation impact, top 3% 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

75 citing papers in PubMed, 108 citations in OpenAlex.

  1. Article
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  7. Expression of VISTA on T cells in patients with cancer colon.Journal of the Egyptian National Cancer Institute · 2025
    Article
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  12. VISTA-mediated immune evasion in cancer.Experimental & molecular medicine · 2024
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15 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 1 country.

Shan XieInstitute for Immunology and School of Medicine, Tsinghua University, Medical Research Building, No.30 Haidian Shuangqing Road, Beijing, 100084, China.
Jia HuangDepartment of General Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
Qin QiaoInstitute for Immunology and School of Medicine, Tsinghua University, Medical Research Building, No.30 Haidian Shuangqing Road, Beijing, 100084, China.
Wenjuan ZangInstitute for Immunology and School of Medicine, Tsinghua University, Medical Research Building, No.30 Haidian Shuangqing Road, Beijing, 100084, China.
Shanjuan HongInstitute for Immunology and School of Medicine, Tsinghua University, Medical Research Building, No.30 Haidian Shuangqing Road, Beijing, 100084, China.
Haidong TanDepartment of General Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
Chen DongInstitute for Immunology and School of Medicine, Tsinghua University, Medical Research Building, No.30 Haidian Shuangqing Road, Beijing, 100084, China.
Zhiying YangDepartment of General Surgery, China-Japan Friendship Hospital, Beijing, 100029, China. yangzhy@aliyun.com.
Ling NiInstitute for Immunology and School of Medicine, Tsinghua University, Medical Research Building, No.30 Haidian Shuangqing Road, Beijing, 100084, China. lingni@tsinghua.edu.cn.ORCID http://orcid.org/0000-0003-1569-882X
Tsinghua University · CNChina-Japan Friendship Hospital · CN

Funding

The National Natural Science Foundation of China 81502462
6 · The paper itself

Abstract

Colorectal carcinoma (CRC) is one of the most common malignancies in the world. PD-1/PD-L1 inhibitors have benefited cancer patients with multiple tumor types. However, their efficacy for CRC is low and this treatment in melanoma patients results in adaptive resistance through upregulation of VISTA, another checkpoint inhibitory pathway. Thus, there is an urgent need to explore additional co-inhibitory molecular pathways such as VISTA for CRC treatment. In this study, C10orf54 (encoding VISTA) expression was analyzed by RNA-seq data from 367 CRC patients in human cancer datasets. Moreover, 28 clinical CRC specimens were used to assess VISTA protein expression. Human cancer datasets showed that CRC tumors expressed higher levels of C10orf54 than CD274 (encoding PD-L1). Moreover, C10orf54 mRNA expression was significantly correlated with genes responsible for tumor immune evasion. VISTA protein expression was high in tumors compared with para-tumors and normal tissues, which is similar to PD-L1 expression. However, in contrast to PD-L1, VISTA was mainly expressed by tumor-infiltrating lymphocytes. This study is the first investigation of VISTA expression in human resected CRC tumors, and the results justify the need for future studies on the role of VISTA in anti-CRC immunity in clinical samples.

Indexed as

AgedAged, 80 and overB7 AntigensB7-H1 AntigenBiomarkers, TumorCase-Control StudiesColorectal NeoplasmsFemaleFollow-Up StudiesHumansLymphocytes, Tumor-InfiltratingMaleMiddle AgedPrognosisSurvival RateTumor EscapeB7 AntigensB7-H1 AntigenBiomarkers, TumorCD274 protein, humanVSIR protein, humanImmune checkpointImmunotherapyPD-L1Tumor immunityVISTA

Identifiers

PMID30128738
PMCPMC11028359
OpenAlexW2888302003

What OpenQuestion 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 OpenQuestion graph.