Evidence map›Paper›PMID 26097535›Full record

ArticleInternational journal of clinical and experimental pathology2015

Combined cancer testis antigens enhanced prediction accuracy for prognosis of patients with hepatocellular carcinoma.

Meng Wang, Jiansheng Li, Liping Wang, Xinfeng Chen, Zhen Zhang, Dongli Yue, Yu Ping, Xiaojuan Shi, Lan Huang, Tengfei Zhang and 10 more

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Cross-Species Upregulation ofCurrent issues in molecular biology · 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

20 authors.

Meng WangDepartment of Gastroenterology, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China ; Biotherapy Center, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Jiansheng LiDepartment of Gastroenterology, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Liping WangDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Xinfeng ChenBiotherapy Center, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Zhen ZhangBiotherapy Center, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Dongli YueDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Yu PingSchool of Life Sciences, Zhengzhou University Zhengzhou 450052, Henan, China.
Xiaojuan ShiBiotherapy Center, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Lan HuangBiotherapy Center, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Tengfei ZhangBiotherapy Center, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Li YangBiotherapy Center, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Yongfu ZhaoDepartment of Hepatobiliary Surgery, First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Xiuxian MaDepartment of Hepatobiliary Surgery, First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Dexu LiDepartment of Hepatobiliary Surgery, First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Zhengjun FanDepartment of Hepatobiliary Surgery, First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Longshuan ZhaoDepartment of Hepatobiliary Surgery, First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Zhe TangDepartment of Hepatobiliary Surgery, First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Wenlong ZhaiDepartment of Hepatobiliary Surgery, First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China.
Bin ZhangDepartment of Hematology/Oncology, School of Medicine, Northwestern University Chicago 60611, USA.
Yi ZhangBiotherapy Center, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China ; Department of Oncology, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, China ; School of Life Sciences, Zhengzhou University Zhengzhou 450052, Henan, China ; Engineering Key Laboratory for Cell Therapy of Henan Province Zhengzhou, Henan, 450052, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer testis antigens (CTAs) are selectively expressed in malignant cells and can serve as ideal targets for immunotherapy. We investigated the expressions of MAGE-A3, MAGE-A4, MAGE-C2 and NY-ESO-1 to determine if combinatorial expressions of CTAs might be as potential prognostic markers for patients with hepatocellular carcinoma (HCC). In tumor tissues of 142 HCC patients, the mRNA expressions of MAGE-A3, MAGE-A4, MAGE-C2 and NY-ESO-1 were 78.9%, 33.8%, 74.6% and 14.1% respectively. Furthermore, the expressions of MAGE-A3, MAGE-A4 and combination of MAGE-A3, MAGE-A4 and NY-ESO-1 (CTAs-A3/A4/NY) showed positive correlations with serum AFP, tumor stages and Ki-67 (P < 0.05). In addition, mRNA expressions of CTAs were significantly consistent with protein expressions of CTAs by immunohistochemistry (P > 0.05). Receiver operating characteristic curves (ROC) analysis showed that CTAs-A3/A4/NY had larger areas under ROC curve (0.768), specificity (99.1%), Youden's index (44.6), positive predictive value (90.9%) and negative predictive value (89.9%) for predicting HCC recurrence than other CTAs. Moreover, the combinatorial expression of CTAs-A3/A4/NY was significantly associated with HCC recurrence by Kaplan-Meier analysis (HR = 69.36, P < 0.01) and multivariate Cox analysis (RR = 17.11, P < 0.01). The combinatorial expression of CTAs-A3/A4/NY mRNA promotes the predictive accuracy of HCC recurrence and itself may be a potential target for immunotherapy of HCC as well.

Indexed as

Antigens, NeoplasmBiomarkers, TumorCarcinoma, HepatocellularCell Line, TumorFemaleHumansKaplan-Meier EstimateLiver NeoplasmsMaleMiddle AgedPrognosisROC CurveTesticular NeoplasmsTestisAntigens, NeoplasmBiomarkers, Tumorcancer testis antigenHepatocellular carcinomamarkerprognosis

Identifiers

PMID26097535
PMCPMC4466922

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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.