Evidence map›Paper›PMID 33614490›Full record

ArticleFrontiers in oncology2020

Autophagy Gene Panel-Based Prognostic Model in Myelodysplastic Syndrome.

Ming-Jing Wang, Wei-Yi Liu, Xue-Ying Wang, Yu-Meng Li, Hai-Yan Xiao, Ri-Cheng Quan, Gang Huang, Xiao-Mei Hu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. 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
0.3field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Immunologic Predictors for Clinical Responses during Immune Checkpoint Blockade in Patients with Myelodysplastic Syndromes.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  3. 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

8 authors at 3 institutions in 2 countries.

Ming-Jing WangDepartment of Hematology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Wei-Yi LiuDepartment of Hematology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Xue-Ying WangDepartment of Hematology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Yu-Meng LiDepartment of Hematology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Hai-Yan XiaoDepartment of Hematology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Ri-Cheng QuanDepartment of Hematology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Gang HuangDivisions of Pathology and Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Xiao-Mei HuDepartment of Hematology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Xiyuan Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNCincinnati Children's Hospital Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abnormal autophagy is related to the pathogenesis and clinical symptoms of myelodysplastic syndrome (MDS). However, the effect of autophagy-related genes (ARGs) on the prognosis of MDS remains unclear. Here, we examined the expression profile of 108 patients with MDS from the GSE58831 dataset, and identified 22 genes that were significantly associated with overall survival. Among them, seven ARGs were screened and APIs were calculated for all samples based on the expression of the seven ARGs, and then, MDS patients were categorized into high- and low-risk groups based on the median APIs. The overall survival of patients with high-risk scores based on these seven ARGs was shorter than patients with low-risk scores in both the training cohort (P = 2.851e-06) and the validation cohort (P = 9.265e-03). Additionally, API showed an independent prognostic indicator for survival in the training samples [hazard ratio (HR) = 1.322, 95% confidence interval (CI): 1.158-1.51; P < 0.001] and the validation cohort (HR = 1.05, 95% CI: 1-1.1; P < 0.01). The area under the receiver operating characteristic curve (AUROC) of API and IPSS were 43.0137 and 66.0274 in the training cohorts and the AUC of the validation cohorts were 41.5361 and 72.0219. Our data indicate these seven ARGs can predict prognosis in patients with MDS and could guide individualized treatment.

Indexed as

autophagyautophagy-related genesmyelodysplastic syndromeprognostic model

Identifiers

PMID33614490
PMCPMC7894207
OpenAlexW3128092581

What OpenQuestion holds

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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 OpenQuestion graph.