Evidence map›Paper›PMID 37509334›Full record

ArticleCancers2023

Prediction of Prognosis, Immunotherapy and Chemotherapy with an Immune-Related Risk Score Model for Endometrial Cancer.

Wei Wei, Bo Ye, Zhenting Huang, Xiaoling Mu, Jing Qiao, Peng Zhao, Yuehang Jiang, Jingxian Wu, Xiaohui Zhan

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
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 3 institutions in 1 country.

Wei WeiDepartment of Bioinformatics, School of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Bo YeDepartment of Bioinformatics, School of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.ORCID 0000-0002-1267-8586
Zhenting HuangDepartment of Pathology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Xiaoling MuDepartment of Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Jing QiaoState Key Laboratory of Medical Genomics, Shanghai Institute of Hematology, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Peng ZhaoSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.ORCID 0000-0003-2361-6521
Yuehang JiangDepartment of Pathology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Jingxian WuDepartment of Pathology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Xiaohui ZhanDepartment of Bioinformatics, School of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.ORCID 0000-0003-1326-6601
Chongqing Medical University · CNThe Affiliated Yongchuan Hospital of Chongqing Medical University · CNShanghai Jiao Tong University · CN

Funding

2021 Chongqing Doctoral "Through Train" Scientific Research Project CSTB2022BSXM-JCX0065National Natural Science Foundation of China 32100530the Science and Technology Research Program of Chongqing Municipal Education Commission KJQN202200455
6 · The paper itself

Abstract

Endometrial cancer (EC) is the most common gynecologic cancer. The overall survival remains unsatisfying due to the lack of effective treatment screening approaches. Immunotherapy as a promising therapy has been applied for EC treatment, but still fails in many cases. Therefore, there is a strong need to optimize the screening approach for clinical treatment. In this study, we employed co-expression network (GCN) analysis to mine immune-related GCN modules and key genes and further constructed an immune-related risk score model (IRSM). The IRSM was proved effective as an independent predictor of poor prognosis. The roles of IRSM-related genes in EC were confirmed by IHC. The molecular basis, tumor immune microenvironment and clinical characteristics of the IRSM were revealed. Moreover, the IRSM effectiveness was associated with immunotherapy and chemotherapy. Patients in the low-risk group were more sensitive to immunotherapy and chemotherapy than those in the high-risk group. Interestingly, the patients responding to immunotherapy were also more sensitive to chemotherapy. Overall, we developed an IRSM which could be used to predict the prognosis, immunotherapy response and chemotherapy sensitivity of EC patients. Our analysis not only improves the treatment of EC but also offers targets for personalized therapeutic interventions.

Indexed as

chemotherapyco-expression network moduleendometrial cancerimmune-based risk score model (IRSM)immune-related key genesimmunotherapyprognosis

Identifiers

PMID37509334
PMCPMC10377799
OpenAlexW4384821049

What Socratic 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 Socratic graph.