Evidence map›Paper›PMID 37925591›Full record

ArticleScientific reports2023

Comprehensive characterization of TGFB1 across hematological malignancies.

Cui-Zhu Wang, Zi-Qi Zhang, Yan Zhang, Liang-Feng Zheng, Yang Liu, Ai-Ting Yan, Yuan-Cui Zhang, Qing-Hua Chang, Suo Sha, Zi-Jun Xu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Oxidative Phosphorylation and Fatty Acid Oxidation Are Central to Mitochondrial Metabolism Rewiring in CML Stem/Progenitor Cell Survival.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Review
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  13. CD56Frontiers in immunology · 2024
    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

10 authors at 5 institutions in 1 country.

Cui-Zhu Wang *Department of Hematology and Oncology, Affiliated Haian Hospital of Nantong University, Nantong, China.
Zi-Qi Zhang *School of Medicine, Jiangsu University, Zhenjiang, China.
Yan Zhang *Department of Hematology and Oncology, Affiliated Haian Hospital of Nantong University, Nantong, China.
Liang-Feng ZhengLaboratory Center, Affiliated Haian Hospital of Nantong University, Nantong, China.
Yang LiuClinical Nutrition Department, Haian Hospital of Traditional Chinese Medicine, Nantong, China.
Ai-Ting YanDepartment of Hematology and Oncology, Affiliated Haian Hospital of Nantong University, Nantong, China.
Yuan-Cui ZhangDepartment of Respiratory Medicine, The Affiliated Zhenjiang Third Hospital of Jiangsu University, 1 Dingmao Bridge, Youth Square, Zhenjiang, 212002, China.
Qing-Hua ChangDepartment of Respiratory Medicine, The Affiliated Zhenjiang Third Hospital of Jiangsu University, 1 Dingmao Bridge, Youth Square, Zhenjiang, 212002, China. zjsycqh@163.com.
Suo ShaSurgery of Traditional Chinese Medicine, Haian Hospital of Traditional Chinese Medicine, Nantong, 226600, China. 790722530@qq.com.
Zi-Jun XuLaboratory Center, Affiliated People's Hospital of Jiangsu University, 8 Dianli Rd., Zhenjiang, 212002, China. xuzijun1989@hotmail.com.
Jiangsu University · CNNantong University · CNAffiliated Hospital of Jiangsu University · CNAffiliated Hospital of Nantong University · CNAnyang Hospital of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TGFB1, which encodes TGF-β1, a potent cytokine regulating varies cellular processes including immune responses. TGF-β1 plays context-dependent roles in cancers and is increasingly recognized as a therapeutic target to enhance immunotherapy responses. We comprehensively evaluated expression of TGFB1 and its clinical and biological effects across hematological malignancies. TGFB1 expression was first explored using data from the GTEx, CCLE, and TCGA databases. The expression and clinical significances of TGFB1 in hematological malignancies were analyzed using Hemap and our In Silico curated datasets. We also analyzed the relationship between TGFB1 with immune scores and immune cell infiltrations in Hemap. We further assessed the value of TGFB1 in predicting immunotherapy response using TIDE and real-world immunotherapy datasets. TGFB1 showed a hematologic-tissue-specific expression pattern both across normal tissues and cancer types. TGFB1 expression were broadly dysregulated in blood cancers and generally associated with adverse prognosis. TGFB1 expression were associated with distinct TME properties among different blood cancer types. In addition, TGFB1 expression was found to be a useful marker in predicting immunotherapy responses. Our results suggest that TGFB1 is broadly dysregulated in hematological malignancies. TGFB1 might regulate the immune microenvironment in a cancer-type-specific manner, which could be applied in the development of new targeted drugs for immunotherapy.

Indexed as

Hematologic NeoplasmsTransforming Growth Factor beta1CytokinesHumansImmunotherapyPrognosisTumor MicroenvironmentCytokinesTGFB1 protein, humanTransforming Growth Factor beta1

Identifiers

PMID37925591
PMCPMC10625629
OpenAlexW4388336577

What OpenQuestion holds

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LicenceCC BY
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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.