Evidence map›Paper›PMID 36284715›Full record

ArticleMolecular therapy oncolytics2022

ScRNA-seq and bulk RNA-seq reveal the characteristics of ferroptosis and establish a risk signature in cholangiocarcinoma.

Wenchao Yao, Xuxu Liu, Yuanhang He, Maolan Tian, Shixin Lu, Qiang Wang, Yi Zheng, Zhenyi Lv, Chenjun Hao, Dongbo Xue and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Emerging Roles of Ferroptosis in Skin Pathophysiology.The Journal of investigative dermatology · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Ferroptosis gene signature in cholangiocarcinoma.Molecular therapy oncolytics · 2022
    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

11 authors at 1 institution in 1 country.

Wenchao YaoDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Xuxu LiuDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Yuanhang HeDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Maolan TianDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Shixin LuDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Qiang WangDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Yi ZhengDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Zhenyi LvDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Chenjun HaoDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Dongbo XueDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Xianzhi MengDepartment of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, China.
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferroptosis is a recently discovered mode of cell death that inhibits tumor growth. Single-cell RNA sequencing (scRNA-seq) is a powerful tool for analyzing tumor heterogeneity and the immune microenvironment at the single-cell level. We used CIBERSORT to identify cellular immune scores and found that monocytes had significantly infiltrated and were correlated with prognosis in cholangiocarcinoma. scRNA-seq data were extracted from the Gene Expression Omnibus database, and the FindCluster() package was used for cell cluster analysis, which obtained 21 cell clusters, and there was increased TNFSF13B-TFRC intercellular communication between monocytes and cholangiocytes. A weighted correlation network analysis was performed with the WGCNA package to obtain monocyte-related gene modules. Univariate and multivariate Cox analyses were then performed to further establish the signature, and the reliability of the signature was assessed by receiver operating characteristic curve and decision curve analysis. A nomogram signature based on the Kaplan-Meier survival analysis was established. We found that the communication between monocytes and malignant cells in cholangiocarcinoma may be a regulatory factor of ferroptosis in cancer cells. The prognostic stratification system of the three-gene signature related to monocytes and ferroptosis can accurately assess the prognostic risk for cholangiocarcinoma.

Indexed as

cholangiocarcinomaferroptosismonocyteprognosissingle-cell sequencing

Identifiers

PMID36284715
PMCPMC9573880
OpenAlexW4297092790

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.