Evidence map›Paper›PMID 37381162›Full record

ArticleCancer biology & therapy2023

Targeting crosstalk of STAT3 between tumor-associated M2 macrophages and Tregs in colorectal cancer.

Lili Huang, Yu Zhao, Mengying Shan, Sitong Wang, Jianhua Chen, Zhuqing Liu, Qing Xu

Abstract read
In one paragraph

Article in Cancer biology & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

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  13. Exosomes in bridging macrophage-fibroblast polarity and cancer stemness.Medical oncology (Northwood, London, England) · 2025
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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

7 authors.

Lili HuangDepartment of Oncology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
Yu ZhaoDepartment of Oncology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
Mengying ShanDepartment of Oncology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
Sitong WangDepartment of Oncology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
Jianhua ChenDepartment of Oncology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
Zhuqing LiuDepartment of Oncology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.ORCID 0000-0003-3852-8807
Qing XuDepartment of Oncology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A comprehensive analysis of the molecular mechanism underlying colorectal tumor evaluated the development of colorectal cancer (CRC) and proposed targeting small molecular inhibitors. Nonetheless, the adoptive resistance of these therapies remains a challenge with respect to achieving an effective clinical response. Thus, identifying the molecular mechanisms guiding CRC growth is essential. The results of The Cancer Genome Atlas (TCGA) dataset analysis demonstrated a critical role of signal transducer and activator of transcription 3 (STAT3) pathway in tumor immune suppression via modulation of the recruitment of Treg cells and M2 type tumor-associated macrophages. The

Indexed as

Colorectal NeoplasmsTumor-Associated MacrophagesAnimalsDisease Models, AnimalMacrophagesMiceSTAT3 Transcription FactorSTAT3 Transcription FactorCRCCrosstalkM2 macrophagesSTAT3Tregs

Identifiers

PMID37381162
PMCPMC10312030

What OpenQuestion holds

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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.