Evidence map›Paper›PMID 35116879›Full record

ArticleTranslational cancer research2019

Five tumor-associated autoantibodies expression levels in serum predict lung cancer and associate with poor outcome.

Shaolei Li, Yuanyuan Ma, Ying Xiong, Panpan Zhang, Xiao Wang, Yong Wang, Yue Yang

Open access · diamondAbstract read
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Article in Translational cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

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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, 16 citations in OpenAlex.

  1. The early diagnostic value of lung cancer autoantibodies and tumor markers in lung cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

7 authors at 2 institutions in 1 country.

Shaolei Li *Department of Thoracic Surgery II, Key Laboratory of Carcinogenesis and Translational Research, Peking University Cancer Hospital and Institute, Beijing 100142, China.
Yuanyuan Ma *Department of Thoracic Surgery II, Key Laboratory of Carcinogenesis and Translational Research, Peking University Cancer Hospital and Institute, Beijing 100142, China.
Ying Xiong *Department of Thoracic Surgery II, Key Laboratory of Carcinogenesis and Translational Research, Peking University Cancer Hospital and Institute, Beijing 100142, China.
Panpan ZhangDepartment of Thoracic Surgery II, Key Laboratory of Carcinogenesis and Translational Research, Peking University Cancer Hospital and Institute, Beijing 100142, China.
Xiao WangDepartment of Thoracic Surgery, Jilin Guowen Hospital, Gongzhulin City, Siping 136100, China.
Yong WangDepartment of Thoracic Surgery, Jilin Guowen Hospital, Gongzhulin City, Siping 136100, China.
Yue YangDepartment of Thoracic Surgery II, Key Laboratory of Carcinogenesis and Translational Research, Peking University Cancer Hospital and Institute, Beijing 100142, China.
Peking University · CNPeking University Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aims to evaluate diagnostic feasibility of the tumor-associated autoantibodies and their clinical significance in lung cancer.

methodsBlood samples were collected from 352 lung cancer patients and 226 healthy individuals. Immunohistochemical staining was used to evaluate the expression of autoantibodies in 69 cases of lung cancer tissues. Enzyme-linked immunosorbent assay (ELISA) was performed to measure the five autoantibodies levels in serum from lung cancer patients and healthy controls.

resultsHigher expression of GAGE7, MAGEA1, PGP9.5, CAGE and p53 were found in lung cancer tissues than normal tissues from the cancer genome atlas (TCGA) database. The expression levels of the five tumor-associated autoantibodies in lung cancer tissues were positively associated with those statuses in serum. There were significantly higher levels of each autoantibody in lung cancer patients than healthy individuals. The area under curve (AUC) for GAGE7, MAGEA1, PGP9.5, CAGE and p53 in diagnosis of lung cancer were 0.787, 0.641, 0.873, 0.825 and 0.749, respectively. With combination of these five autoantibodies by the logistic regression model, 0.891 of AUC was shown. In addition, the level of each autoantibody was increased in the advanced stage. Particularly, the level of PGP9.5 was significantly higher in the advanced T stage, N stage and TNM stage and CAGE was significantly elevated in the advanced N stage.

conclusionsSummarily, autoantibodies levels of GAGE7, MAGEA1, PGP9.5, CAGE and p53 in serum could be used for the diagnosis of lung cancer and PGP9.5 may predict poor prognosis for the patients with lung cancer.

Indexed as

diagnosislung cancerTumor-associated autoantibodies

Identifiers

PMID35116879
PMCPMC8798311
OpenAlexW4237714872

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LicenceCC BY-NC-ND
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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.