Evidence map›Paper›PMID 35528180›Full record

ArticleBioMed research international2022

The Significance of Tumor Microenvironment Score for Breast Cancer Patients.

Yuan Tian, Jingnan Wang, Qing Wen, Aiqin Gao, Alan Huang, Ran Li, Ye Zhang, Guohai Su, Yuping Sun

Abstract read
In one paragraph

Article in BioMed research international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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.

Yuan TianDepartment of Oncology, Jinan Central Hospital Affiliated to Shandong University, Jinan, 250013 Shandong, China.ORCID https://orcid.org/0000-0002-2296-1246
Jingnan WangDepartment of Oncology, Jinan Central Hospital Affiliated to Shandong University, Jinan, 250013 Shandong, China.ORCID https://orcid.org/0000-0003-0651-3379
Qing WenJinan Clinical Research Center of Shandong First Medical University, Jinan, China.ORCID https://orcid.org/0000-0002-6408-2370
Aiqin GaoDepartment of Oncology, Jinan Central Hospital Affiliated to Shandong University, Jinan, 250013 Shandong, China.ORCID https://orcid.org/0000-0003-1157-6104
Alan HuangDepartment of Oncology, Jinan Central Hospital, The Hospital Affiliated with Shandong First Medical University, Jinan, Shandong 250013, China.ORCID https://orcid.org/0000-0002-6587-3000
Ran LiDepartment of Oncology, Jinan Central Hospital, Weifang Medical University, Weifang, 261053 Shandong, China.ORCID https://orcid.org/0000-0003-3287-3757
Ye ZhangDepartment of Oncology, Jinan Central Hospital, Weifang Medical University, Weifang, 261053 Shandong, China.ORCID https://orcid.org/0000-0001-8507-0718
Guohai SuDepartment of Cardiovascular Diseases, Jinan Central Hospital Affiliated to Shandong University, Jinan, 250013 Shandong, China.ORCID https://orcid.org/0000-0003-3403-1692
Yuping SunDepartment of Oncology, Jinan Central Hospital Affiliated to Shandong University, Jinan, 250013 Shandong, China.ORCID https://orcid.org/0000-0002-0804-6850

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: This study was designed to clarify the prognostic value of tumor microenvironment score and abnormal genomic alterations in TME for breast cancer patients. Method: The TCGA-BRCA data were downloaded from TCGA and analyzed with R software. The results from analyses were further validated using the dataset from GSE96058, GSE124647, and GSE25066. Results: After analyzing the TCGA data and verifying it with the GEO data, we developed a TMEscore model based on the TME infiltration pattern and validated it in 3273 breast cancer patients. The results suggested that our TMEscore model has high prognostic value. TME features with the TMEscore model can help to predict breast cancer patients' response to immunotherapy and provide new strategies for breast cancer treatment. Signature 24 was first found in breast cancer. In focal SCNAs, a total of 95 amplified genes and 169 deletion genes in the TMEscore high group were found to be significantly related to the prognosis of breast cancer patients, while 61 amplified genes and 174 deletion genes in the TMEscore low group were identified. LRRC48, CFAP69, and cg25726128 were first discovered and reported to be related to the survival of breast cancer patients. We identified specific mutation signatures that correlate with TMEscore and prognosis. Conclusion: TMEscore model has high predictive value regarding prognosis and patients' response to immunotherapy. Signature 24 was first found in breast cancer. Specific mutation signatures that correlate with TMEscore and prognosis might be used for providing additional indicators for disease evaluation.

Indexed as

Breast NeoplasmsTumor MicroenvironmentFemaleHumansImmunotherapyMutationPrognosis

Identifiers

PMID35528180
PMCPMC9071896

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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.