Evidence map›Paper›PMID 32017467›Full record

ArticleCancer medicine2020

Characterization of the immune microenvironment in brain metastases from different solid tumors.

Jinling Jiang, Lihong Wu, Fei Yuan, Jun Ji, Xiaojing Lin, Wanning Yang, Junwei Wu, Min Shi, Hui Yang, Yanna Ma and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. 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
1.1field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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

14 authors at 3 institutions in 1 country.

Jinling JiangDepartment of Oncology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Lihong WuGenecast Precision Medicine Technology Institute, Beijing, China.
Fei YuanDepartment of Pathology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Jun JiShanghai Institute of Digestive Surgery, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Xiaojing LinGenecast Precision Medicine Technology Institute, Beijing, China.
Wanning YangGenecast Precision Medicine Technology Institute, Beijing, China.
Junwei WuDepartment of Oncology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Min ShiDepartment of Oncology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Hui YangDepartment of Oncology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Yanna MaGenecast Precision Medicine Technology Institute, Beijing, China.
Xue SongGenecast Precision Medicine Technology Institute, Beijing, China.
Zhenggang ZhuDepartment of Oncology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Henghui ZhangInstitute of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Jun ZhangDepartment of Oncology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.ORCID 0000-0002-7973-8416
Ruijin Hospital · CNGenecast (China) · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBrain metastases are one of the most common intracranial neoplasms. Increasing evidence have indicated that systemic immunotherapy may provide long-term benefits for brain metastases. Herein, we presented the results of an immune oncology panel RNA sequencing platform for patients with brain metastases from different primary sites.

methodsWe investigated 25 samples of human brain metastases from lung cancer (n = 12), breast cancer (n = 6), and colorectal cancer (n = 7). Besides, 13 paired samples of adjacent noncancerous brain tissue (10 from patients with lung cancer and 3 from patients with breast cancer) were collected as controls. By comparing the brain metastases and paired samples of adjacent noncancerous brain tissue from 13 patients, we detected three upregulated and six downregulated genes, representing the malignant properties of cancer cells and increased immune infiltration in the microenvironment. Next, we profiled the immune-related genes in brain metastases from three primary cancer types.

resultsA group of genes were significantly overexpressed in the microenvironment of brain metastases from lung cancer, covering the checkpoint pathways, lymphocyte infiltration, and TCR-coexpression. Especially, immune checkpoint molecules, PD-L1, PD-L2, and IDO1 were expressed at higher levels in brain metastases from lung cancer than those from the other two cancer types.

conclusionsThis study presents an immune landscape of brain metastases from different cancer types. With high RNA expression levels of PD-1/PD-L1 axis and immune infiltration in brain metastases, it would be worthwhile to explore the efficacy of immune checkpoint blockade for lung cancer patients with intracranial metastases.

Indexed as

Gene Expression Regulation, NeoplasticAgedBiomarkers, TumorBrain NeoplasmsCase-Control StudiesFemaleFollow-Up StudiesHumansLymphocytes, Tumor-InfiltratingMaleMiddle AgedNeoplasmsPrognosisRetrospective StudiesSurvival RateTumor MicroenvironmentBiomarkers, Tumorbrain metastasisimmune checkpointimmune systemlymphocytePD-L1

Identifiers

PMID32017467
PMCPMC7131856
OpenAlexW3005208566

What OpenQuestion holds

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LicenceCC BY
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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.