Evidence map›Paper›PMID 37517087›Full record

ArticleAging2023

The integration of machine learning and multi-omics analysis provides a powerful approach to screen aging-related genes and predict prognosis and immunotherapy efficacy in hepatocellular carcinoma.

Jiahui Shen, Han Gao, Bowen Li, Yan Huang, Yinfang Shi

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Article in Aging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jiahui ShenDepartment of Pharmacy, Huzhou Maternity and Child Health Care Hospital, Huzhou, China.
Han GaoDepartment of Stomatology, First Affiliated Hospital of Huzhou University, Huzhou, China.
Bowen LiSchool of Pharmacy, Anhui Medical University, Hefei, China.
Yan HuangSchool of Pharmacy, Anhui Medical University, Hefei, China.
Yinfang ShiDepartment of Stomatology, First Affiliated Hospital of Huzhou University, Huzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is a highly malignant tumor with high incidence and mortality rates. Aging-related genes are closely related to the occurrence and development of cancer. Therefore, it is of great significance to evaluate the prognosis of HCC patients by constructing a model based on aging-related genes.

methodNon-negative matrix factorization (NMF) clustering analysis was used to cluster the samples. The correlation between the risk score and immune cells, immune checkpoints, and Mismatch Repair (MMR) was evaluated through Spearman correlation test. Real Time Quantitative PCR (RT-qPCR) and immunohistochemistry were used to validate the expression levels of key genes in tissue and cells for the constructed model.

resultBy performing NMF clustering, we were able to effectively group the liver cancer samples into two distinct clusters. Considering the potential correlation between aging-related genes and the prognosis of liver cancer patients, we used aging-related genes to construct a prognostic model. Spearman correlation analysis showed that the model risk score was closely related to MMR and immune checkpoint expression. Drug sensitivity analysis also provided guidance for the clinical use of chemotherapy drugs. RT-qPCR showed that TFDP1, NDRG1, and FXR1 were expressed at higher levels in different liver cancer cell lines compared to normal liver cells.

conclusionIn summary, we have developed an aging-related model to predict the prognosis of hepatocellular carcinoma and guide clinical drug treatment for different patients.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAgingHumansImmunotherapyMachine LearningMultiomicsPrognosisRNA-Binding ProteinsTumor MicroenvironmentFXR1 protein, humanRNA-Binding Proteinsaginghepatocellular carcinomaimmunotherapymachine learningprognostic model

Identifiers

PMID37517087
PMCPMC10415564

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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.