Evidence map›Paper›PMID 39948553›Full record

ArticleBMC medicine2025

Cryoablation-induced modulation of Treg cells and the TGF-β pathway in lung adenocarcinoma: implications for increased antitumor immunity.

Shicheng Lin, Dianna Liu, Tianyu Liang, Yaoxue Zhuang, Xiaofan Wang, Shengmao Ma, Quanwang Li, Kaiwen Hu

Abstract read
In one paragraph

Article in BMC medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 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.

Shicheng Lin *Graduate School, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Dianna Liu *Oncology Department, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Tianyu Liang *Graduate School, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Yaoxue ZhuangGraduate School, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Xiaofan WangGraduate School, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Shengmao MaDepartment of Thoracic Surgery, People's Hospital of Ningxia Hui Autonomous Region, Yinchuan, People's Republic of China.
Quanwang LiOncology Department, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, People's Republic of China. quanwangli@126.com.
Kaiwen HuOncology Department, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, People's Republic of China. kaiwenh@163.com.

Funding

Fundamental Research Funds for the Central Universities No. 2020-JYB-ZDGG-127
6 · The paper itself

Abstract

backgroundCryoablation plays a key role in the comprehensive management of lung adenocarcinoma, characterized by its ability to activate antitumor immunity. This study aimed to explore the impact of cryoablation on the local immune microenvironment, focusing on regulatory T cells (Tregs) and the TGF-β pathway.

methodsSingle-cell sequencing was employed to identify differences in immune cell populations and related pathway expression between lung adenocarcinoma tissues and adjacent noncancerous tissues. Prospective observations of changes in Tregs in the peripheral blood pre- and post-cryoablation for lung adenocarcinoma were conducted at Dongfang Hospital, Beijing University of Chinese Medicine. Bulk RNA-seq analysis of mouse tumor tissues was performed to predict the potential mechanisms underlying cryoablation-induced antitumor immunity. Finally, these predictions were validated through in vitro and in vivo experiments employing cell cryoablation and mouse subcutaneous tumor transplantation models.

resultsSingle-cell RNA sequencing analysis revealed intricate interactions between Tregs subpopulations and the regulation of the immune response in lung adenocarcinoma, highlighting the involvement of the TGF-β pathway. A significant decrease in the level of Tregs was noted at 30 days post-cryoablation compared to pre-surgical and 3-day post-surgery levels. The cellular and murine cryoablation models validated the inhibitory effect of cryoablation on Tregs and its potential to stimulate antitumor immunity. Additionally, the results of bulk RNA-seq demonstrated the role of cryoablation in regulating postoperative immunity via the TGF-β pathway. Cryoablation decreased the expression levels of TGF-β1, suppressed the phosphorylation of Smad2 and Smad3, and downregulated the expression of FOXP3, thereby inhibiting the conversion of CD4 + T cell precursors into Tregs. Moreover, cryoablation enhanced the expression of interferon-gamma (IFN-γ), thereby promoting its antitumor activity.

conclusionsThis study revealed the effective modification of the lung adenocarcinoma microenvironment by cryoablation through the suppression of Tregs and activation of antitumor immunity via the TGF-β pathway. These findings hold implications for optimizing cryoablation-based therapies and guiding future clinical trials on lung adenocarcinoma treatment.

trial registrationThis trial was registered with the Chinese Clinical Trial Registry (Chictr.org.cn, ChiCTR2000038580, Sep 24, 2020).

Indexed as

Adenocarcinoma of LungCryosurgeryLung NeoplasmsT-Lymphocytes, RegulatoryTransforming Growth Factor betaAnimalsFemaleHumansMaleMiceSignal TransductionTumor MicroenvironmentTransforming Growth Factor betaCryoablationImmune responsesSingle-cell sequencingTGF-β pathwayTregs

Identifiers

PMID39948553
PMCPMC11827211

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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.