Evidence map›Paper›PMID 36781833›Full record

ArticleCell death & disease2023

Dynamic differentiation of F4/80+ tumor-associated macrophage and its role in tumor vascularization in a syngeneic mouse model of colorectal liver metastasis.

Ting Qiao, Wanli Yang, Xiangchuan He, Ping Song, Xiao Chen, Ruijie Liu, Jian Xiao, Xiaoli Yang, Mingqi Li, Yudan Gao and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Reprogramming macrophages to treat liver diseases.Hepatology (Baltimore, Md.) · 2026
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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

15 authors at 4 institutions in 1 country.

Ting Qiao *School of Medicine, Southern University of Science and Technology, 518055, Shenzhen, China.ORCID 0000-0002-3083-4028
Wanli Yang *Department of Immunology, Harbin Medical University, Harbin, China.
Xiangchuan He *Department of Immunology, Harbin Medical University, Harbin, China.
Ping Song *Department of Immunology, Harbin Medical University, Harbin, China.
Xiao ChenSchool of Medicine, Southern University of Science and Technology, 518055, Shenzhen, China.
Ruijie LiuDepartment of Immunology, Harbin Medical University, Harbin, China.
Jian XiaoDepartment of Microbiology & Immunology, Guangxi Chinese Medicine University, Nanning, China.
Xiaoli YangSchool of Medicine, Southern University of Science and Technology, 518055, Shenzhen, China.
Mingqi LiDepartment of Colorectal Surgery, the 3rd Hospital Affiliated to Harbin Medical University, Harbin, China.
Yudan GaoSchool of Medicine, Southern University of Science and Technology, 518055, Shenzhen, China.
Guoan ChenSchool of Medicine, Southern University of Science and Technology, 518055, Shenzhen, China.ORCID 0000-0001-5608-6761
Yi LuSchool of Medicine, Southern University of Science and Technology, 518055, Shenzhen, China.
Jian ZhangSchool of Medicine, Southern University of Science and Technology, 518055, Shenzhen, China. zhangjian@sustech.edu.cn.ORCID 0000-0002-3702-2946
Jing LengDepartment of Microbiology & Immunology, Guangxi Chinese Medicine University, Nanning, China. lj986771558@163.com.ORCID 0000-0001-6115-2153
Huan RenSchool of Medicine, Southern University of Science and Technology, 518055, Shenzhen, China. renh@sustech.edu.cn.ORCID 0000-0001-7114-2012
Southern University of Science and Technology · CNHarbin Medical University · CNGuangxi University · CNHarbin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-associated macrophages (TAMs) are highly heterogeneous and play vital roles in tumor progression. Here we adopted a C57BL/6 mouse model imitating the late-stage colorectal liver metastasis (CRLM) by Mc38 colorectal cancer cell injection via the portal vein. With serial sections of CRLM biopsies, we defined 7-9 days post-injection as the critical period for tumor neovascularization, which was initiated from the innate liver vessels via vessel cooption and extended by vascular mimicry and thereof growth of CD34

Indexed as

Colorectal NeoplasmsLiver NeoplasmsTumor-Associated MacrophagesAnimalsCell DifferentiationDisease Models, AnimalEndothelial CellsMiceMice, Inbred C57BLNeovascularization, PathologicTumor Microenvironment

Identifiers

PMID36781833
PMCPMC9925731
OpenAlexW4320482471

What OpenQuestion 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 OpenQuestion graph.