Evidence map›Paper›PMID 33850760›Full record

ArticleTranslational andrology and urology2021

Identification and validation of a five apoptosis-related genes signature for prediction of disease-free survival for testicular germ cell tumors.

Tengyue Zeng, Liangyu Yao, Kai Zhao, Rong Cong, Xianghu Meng, Ninghong Song

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In one paragraph

Article in Translational andrology and urology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Tengyue ZengDepartment of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Liangyu YaoDepartment of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Kai ZhaoDepartment of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Rong CongDepartment of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Xianghu MengDepartment of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Ninghong SongDepartment of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMore and more studies have paid attention to the role of apoptosis in tumorigenesis. A variety of apoptosis-related genes (ARGs) are related to tumor progression and resistance to chemotherapy drugs. Therefore, this study aims to establish a prognostic marker for ARG-based testicular germ cell tumors (TCGT).

methodsTCGT sequencing data and clinical information were downloaded from The Cancer Genome Atlas (TCGA) database and GEO database. The sequencing data of normal tissues came from the GTEx database. Through univariate COX, LASSO, and multiple COX regression analyses, we screened out key ARGs related to prognosis and constructed a risk signature and a prognostic nomogram. Finally, we performed internal and external verification to verify the signature we have established.

resultsFive ARGs, including CHGA, LPCAT1, PPP1CA, PSMB5, UBR2 were selected out and utilized to establish a novel signature. Based on this signature, TCGT patients were divided into high-risk groups and low-risk groups. The results showed that the disease-free survival (DFS) of patients in the high-risk group was lower than that in the low-risk group (P=0.02268). The subsequent univariate and multivariate Cox regression analysis further proved that the features we established are valuable independent prognostic factors (P<0.05). Also, a prognostic nomogram was created to visualize the relationship between various prognostic-related factors and the 1-, 3-, and 5-year DFS of TCGT in the TCGA cohort.

conclusionsWe constructed a new nomogram based on ARGs to predict the risk of testicular tumor recurrence. It can help clinicians better and more intuitively predict the survival of patients.

Indexed as

Apoptosisdisease-free survival (DFS)prognosissignaturetesticular germ cell tumor (TCGT)

Identifiers

PMID33850760
PMCPMC8039626

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