Evidence map›Paper›PMID 35676688›Full record

ArticleBMC cancer2022

Semaphorin 4B promotes tumor progression and associates with immune infiltrates in lung adenocarcinoma.

Jun Jiang, Yuan Lu, Fang Zhang, Tao Pan, Zhipei Zhang, Yi Wan, Xinling Ren, Rui Zhang

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
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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 at 3 institutions in 1 country.

Jun Jiang *Department of Health Service, Base of Health Service, Fourth Military Medical University, Xi'an, China.
Yuan Lu *Department of Respiratory and Critical Care Medicine, Zhongda Hospital, Southeast University, Nanjing, China.
Fang ZhangDepartment of Respiratory and Critical Care Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Tao PanDepartment of Respiratory and Critical Care Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Zhipei ZhangDepartment of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Yi WanDepartment of Health Service, Base of Health Service, Fourth Military Medical University, Xi'an, China.
Xinling RenDepartment of Respiratory and Critical Care Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China. majrenxl@fmmu.edu.cn.
Rui ZhangState Key Laboratory of Cancer Biology, Department of Immunology, Fourth Military Medical University, Xi'an, 710032, Shaanxi, China. ruizhang@fmmu.edu.cn.
Air Force Medical University · CNXijing Hospital · CNZhongda Hospital Southeast University · CN

Funding

the Jiangsu basic research program No. BK20201484the Natural Science Foundation of China No. 81871880the Natural Science Foundation of China No.82100008the Shaanxi Provincial Research and Development Program Foundation No.2022SF-245
6 · The paper itself

Abstract

backgroundSemaphorins have been found to play important roles in multiple malignancy-related processes. However, the role of Semaphorin 4B (SEMA4B) in lung cancer remains unclear. Here, we aimed to explore the biological functions of SEMA4B in through bioinformatic analysis, in vitro and in vivo assays. In the present study, the possible mechanism by which SEMA4B affected the tumor growth and microenvironment of lung adenocarcinoma (LUAD) were investigated.

methodsThe expression of SEMA4B in LUAD was analyzed by bioinformatic analysis and verified by the immunohistochemistry staining. The prognostic value of SEMA4B in LUAD was investigated using the Kaplan-Meier survival and Cox's regression model. After silencing SEMA4B expression, the functions of SEMA4B in LUAD cells were investigated by in vitro experiments, including CCK-8 and plate clone formation. And the effect of SEMA4B on tumor growth and immune infiltration was explored in C57BL/6 mice tumor-bearing models.

resultsSEMA4B expression was upregulated in LUAD tissues and correlated with later pathological stages and poor prognosis of LUAD patients. Further study found that SEMA4B silencing suppressed the proliferation of lung cancer cells both in vitro and in vivo. Bioinformatic analysis showed that SEMA4B expression was correlated with the increased infiltration of myeloid-derived suppressor cells (MDSCs), T-regs and the decreased infiltration of CD8

conclusionsThese findings demonstrated SEMA4B might play an oncogenic role in LUAD progression, and be a promising therapeutic target for lung cancer.

Indexed as

Adenocarcinoma of LungLung NeoplasmsSemaphorinsAnimalsCell ProliferationHumansMiceMice, Inbred C57BLPrognosisTumor Microenvironmentsemaphorin 4B, humanSemaphorinsBioinformaticsImmune infiltrationLung adenocarcinomaPrognosisSEMA4B

Identifiers

PMID35676688
PMCPMC9178879
OpenAlexW4281644132

What OpenQuestion holds

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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.