Evidence map›Paper›PMID 35869490›Full record

ArticleBMC cancer2022

Associations of IFT20 and GM130 protein expressions with clinicopathological features and survival of patients with lung adenocarcinoma.

Lianfeng Li, Yaobing Chen, Wei Liao, Qimei Yu, Hui Lin, Yuqin Shi, Ling Zhang, Guoqing Fu, Zhenyu Wang, Xi Li and 3 more

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Lianfeng Li *Department of Occupational and Environmental Health, School of Public Health, Wuhan University of Science and Technology, Wuhan, 430065, Hubei, China.
Yaobing Chen *Institute of Pathology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, Hubei, China.
Wei Liao *Department of Respiratory and Critical Care Medicine, Fifth Hospital in Wuhan, Wuhan, 430050, Hubei, China.
Qimei YuDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University of Science and Technology, Wuhan, 430065, Hubei, China.
Hui LinDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University of Science and Technology, Wuhan, 430065, Hubei, China.
Yuqin ShiDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University of Science and Technology, Wuhan, 430065, Hubei, China.
Ling ZhangDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University of Science and Technology, Wuhan, 430065, Hubei, China.
Guoqing FuDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University of Science and Technology, Wuhan, 430065, Hubei, China.
Zhenyu WangDepartment of Basic Medicine, Medical College, Wuhan University of Science and Technology, Wuhan, 430065, Hubei, China.
Xi LiDepartment of Basic Medicine, Medical College, Wuhan University of Science and Technology, Wuhan, 430065, Hubei, China.
Xianrong KongDepartment of Radiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, Hubei, China.
Ting ZhouDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University of Science and Technology, Wuhan, 430065, Hubei, China. zhouting84@wust.edu.cn.
Lingzhi QinInstitute of Pathology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, Hubei, China. qinlingzhi@163.com.
Wuhan University of Science and Technology · CNHuazhong University of Science and Technology · CNWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer is the leading cause of malignancy-related mortality and lung adenocarcinoma accounts for about 40% of lung malignancies. The aim of this study was to investigate the associations of intraflagellar transport protein 20 (IFT20) and Golgi matrix protein 130 (GM130) expression with clinicopathological features and survival in patients with lung adenocarcinoma.

methodsThe expressions of IFT20 and GM130 protein in cancerous and matched adjacent lung tissues of 235 patients with lung adenocarcinoma were assessed by tissue microarray and immunohistochemistry, which were indicated by the mean optical density (IOD/area), the rate of positive staining cells and staining intensity score. The correlation between IFT20 and GM130 protein was assessed by Spearman's rank correlation. Associations of IFT20 and GM130 protein expression with clinicopathological features of patients were analyzed by multivariate logistic regression models. The survival analysis of patients was performed by Cox proportional hazard regression models.

resultsWith adjustment for multiple potential confounders, each one-point increase in IFT20 protein staining intensity score was significantly associated with 32% and 29% reduced risk for TNM stage in II ~ IV and lymphatic metastasis of patients, respectively (P < 0.05). And each one-point increase in GM130 protein staining intensity score was associated with a significant reduction in the risk of poor differentiation and tumors size > 7 cm by 29% and 38% for lung adenocarcinoma patients, respectively (P < 0.05). In stratified Cox model analysis, enhanced IFT20 staining intensity score was significantly decreased the risk of death by 16% for patients without distant metastasis. And elevated the IOD/area of GM130 expression significantly decreased the death risk of lung adenocarcinoma patients with tumor size > 7 cm or distant metastasis by 54% and 65%, respectively (P < 0.05).

conclusionIFT20 and GM130 protein expressions were negatively associated with tumor differentiated types, size, TNM stage and lymphatic metastasis of lung adenocarcinoma. Both IFT20 and GM130 proteins have some protective effects on the survival of lung adenocarcinoma patients with specific clinicopathological features.

Indexed as

AdenocarcinomaAdenocarcinoma of LungLung NeoplasmsAutoantigensBiomarkers, TumorCarrier ProteinsHumansLymphatic MetastasisMembrane ProteinsNeoplasm StagingPrognosisAutoantigensBiomarkers, TumorCarrier ProteinsGolgin subfamily A member 2IFT20 protein, humanMembrane ProteinsClinicopathological featuresGM130IFT20Lung adenocarcinomaOverall survival

Identifiers

PMID35869490
PMCPMC9308367
OpenAlexW4286615495

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.