Evidence map›Paper›PMID 37247083›Full record

ArticleJournal of cancer research and clinical oncology2023

A robust gene prognostic index composed of GZMB, IRF1, and TP63 can stratify the risk of two metastatic urothelial carcinoma cohorts based on immune checkpoint blockade therapy.

Jiaxing Lin, Mengting Ding, Caipeng Qin, Yuxuan Song, Wenbo Yang, Yiqing Du, Tao Xu

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 2 institutions in 1 country.

Jiaxing Lin *Department of Urology, Peking University People's Hospital, Beijing, 100044, China.
Mengting Ding *Department of Urology, Peking University People's Hospital, Beijing, 100044, China.
Caipeng Qin *Department of Urology, Peking University People's Hospital, Beijing, 100044, China.
Yuxuan SongDepartment of Urology, Peking University People's Hospital, Beijing, 100044, China.
Wenbo YangDepartment of Urology, Peking University People's Hospital, Beijing, 100044, China.
Yiqing DuDepartment of Urology, Peking University People's Hospital, Beijing, 100044, China. duyiqing@bjmu.edu.cn.
Tao XuDepartment of Urology, Peking University People's Hospital, Beijing, 100044, China. xutao@pkuph.edu.cn.
Peking University · CNPeking University People's Hospital · CN

Funding

National Key Research and Development Program of China 2018YFA0902802National Natural Science Foundation of China 81802533Natural science foundation of Beijing 7202219Natural Science Foundation of Beijing Municipality Z191100006619010
6 · The paper itself

Abstract

backgroundImmune checkpoint blockade (ICB) therapy has become a first-line treatment option for metastatic urothelial carcinoma (mUC) patients who do not meet the criteria of cisplatin. Still, only a few people can benefit from it, so useful predictive markers are needed.

methodsDownload the ICB-based mUC and chemotherapy-based bladder cancer cohorts, and extract the expression data of pyroptosis-related genes (PRG). The LASSO algorithm was used to construct the PRG prognostic index (PRGPI) in the mUC cohort, and we verified the prognostic ability of PRGPI in two mUC and two bladder cancer cohorts.

resultsMost of the PRG in the mUC cohort were immune-activated genes, and a few were immunosuppressive genes. The PRGPI composed of GZMB, IRF1, and TP63 can stratify the risk of mUC. In IMvigor210 and GSE176307 cohorts, the P-values of Kaplan Meier analysis was < 0.01 and 0.002, respectively. PRGPI could also predict ICB response, and the chi-square test of the two cohorts had P-values of 0.002 and 0.046, respectively. In addition, PRGPI can also predict the prognosis of two bladder cancer cohorts without ICB therapy. The PRGPI and the expression of PDCD1/CD274 had a high degree of synergistic correlation. The Low PRGPI group showed prominent characteristics of immune infiltration and was enriched in the immune signal activation pathway.

conclusionThe PRGPI we constructed can effectively predict the treatment response and overall survival rate of mUC patients treated with ICB. The PRGPI can help mUC patients achieve individualized and accurate treatment in the future.

Indexed as

Carcinoma, Transitional CellUrinary Bladder NeoplasmsCisplatinGranzymesHumansImmune Checkpoint InhibitorsInterferon Regulatory Factor-1PrognosisTranscription FactorsTumor Suppressor ProteinsCisplatinGranzymesGZMB protein, humanImmune Checkpoint InhibitorsInterferon Regulatory Factor-1IRF1 protein, humanTP63 protein, humanTranscription FactorsTumor Suppressor ProteinsICBmUCPRGPIPrognosisPyroptosis

Identifiers

PMID37247083
PMCPMC11797762
OpenAlexW4378640037

What OpenQuestion holds

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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.