Evidence map›Paper›PMID 39448199›Full record

ArticleJournal for immunotherapy of cancer2024

AKAP12 positive fibroblast determines immunosuppressive contexture and immunotherapy response in patients with TNBC by promoting macrophage M2 polarization.

Zhenkun Liu, Siyuan Hu, Xinlei Zhao, Wenxin Xu, Feng Ju, Meiying Gu, Jialei Weng, Yabing Du

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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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

8 authors.

Zhenkun Liu *Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Siyuan Hu *Department of General Surgery, Zhongshan Hospital Fudan University, Shanghai, Shanghai, China.
Xinlei Zhao *Institute for Pathology, University Hospital of Cologne, Cologne, Germany.
Wenxin XuDepartment of Liver Surgery and Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University, Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shanghai, China.
Feng JuDepartment of General, Visceral, Tumor and Transplantation Surgery, University Hospital of Cologne, Cologne, Germany.
Meiying GuDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Jialei WengDepartment of Surgical Oncology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China fccduyb@zzu.edu.cn weng.jialei@zju.edu.cn.
Yabing DuDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China fccduyb@zzu.edu.cn weng.jialei@zju.edu.cn.ORCID http://orcid.org/0009-0008-1616-4305

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTriple-negative breast cancer (TNBC) is a molecular subtype of breast cancer with high aggressiveness and poor prognosis. Cancer-associated fibroblasts (CAFs) are major components of the TNBC microenvironment and play an important role in tumor progression and treatment responses. Our goal is to identify specific CAFs subpopulations contributing to TNBC development.

methodsMultiomics analyses were applied to identify the CAFs-specific genes related to immunotherapy response. The clinical significance of a CAFs subset with A-kinase anchoring protein 12 (AKAP12) positive was explored in 80 patients with TNBC through double-labeling immunofluorescence assay. Cytometry by time-of-flight and RNA sequencing were performed to elucidate the immune landscape of TNBC microenvironment and functional mechanism of AKAP12

resultsMultiomics analyses identified an AKAP12

conclusionsAKAP12 is mainly expressed in fibroblasts in TNBC. AKAP12

Indexed as

A Kinase Anchor ProteinsImmunotherapyMacrophagesTriple Negative Breast NeoplasmsTumor MicroenvironmentAnimalsCancer-Associated FibroblastsCell Cycle ProteinsCell Line, TumorFemaleHumansMiceAKAP12 protein, humanA Kinase Anchor ProteinsCell Cycle ProteinsBiomarkerBreast CancerImmunotherapy

Identifiers

PMID39448199
PMCPMC11499773

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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.