Evidence map›Paper›PMID 39395905›Full record

ArticleGenes & genomics2024

Integrated analysis of single-cell RNA-seq and bulk RNA-seq revealed key genes for bone metastasis and chemoresistance in prostate cancer.

Hongai Bai, Zhenyue Li, Yueyue Weng, Facai Cui, Wenpu Chen

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Article in Genes & genomics, 2024. 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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1 · What the graph read from it

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3 · Its place in the literature

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2 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.

Hongai BaiClinical Trial Department, Wenzhou Central Hospital, Wenzhou, People's Republic of China.
Zhenyue LiPharmacy Department, Wenzhou Central Hospital, Wenzhou, People's Republic of China.
Yueyue WengPharmacy Department, Wenzhou Central Hospital, Wenzhou, People's Republic of China.
Facai CuiDepartment of Clinical Laboratory, Henan provincial people's hospital, The people's hospital of Zhengzhou University, Zhengzhou, People's Republic of China.
Wenpu ChenUrology Surgery, Jinshan Branch of Shanghai Sixth People's Hospital, Shanghai, People's Republic of China. cwp305@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate cancer (PCa) is a serious malignancy. The main causes of PCa aggravation and death are unexplained resistance to chemotherapy and bone metastases.

objectiveThis study aimed to investigate the molecular mechanisms associated with the dynamic processes of progression, bone metastasis, and chemoresistance in PCa.

methodsThrough comprehensive analysis of single-cell RNA sequencing (scRNA-seq) data, Gene Expression Omnibus (GEO) tumor progression and metastasis-related genes were identified. These genes were subjected to lasso regression modeling using the Cancer Genome Atlas (TCGA) database. Tartrate-resistant acid phosphatase (TRAP) staining and real-time quantitative PCR (RT-qPCR) were used to evaluate osteoclast differentiation. CellMiner was used to confirm the effect of LDHA on chemoresistance. Finally, the relationship between LDHA and chemoresistance was verified using doxorubicin-resistant PCa cell lines.

results7928 genes were identified as genes related to tumor progression and metastasis. Of these, 7 genes were found to be associated with PCa prognosis. The scRNA-seq and TCGA data showed that the expression of LDHA was higher in tumors and associated with poor prognosis of PCa. In addition, upregulation of LDHA in PCa cells induces osteoclast differentiation. Additionally, high LDHA expression was associated with resistance to Epirubicin, Elliptinium acetate, and doxorubicin. Cellular experiments demonstrated that LDHA knockdown inhibited doxorubicin resistance in PCa cells.

conclusionsLDHA may play a potential contributory role in PCa initiation and development, bone metastasis, and chemoresistance. LDHA is a key target for the treatment of PCa.

Indexed as

Bone NeoplasmsDrug Resistance, NeoplasmProstatic NeoplasmsSingle-Cell AnalysisCell Line, TumorDoxorubicinGene Expression Regulation, NeoplasticHumansL-Lactate DehydrogenaseMaleOsteoclastsPrognosisRNA-SeqSingle-Cell Gene Expression AnalysisDoxorubicinLDHA protein, humanL-Lactate DehydrogenaseBone metastasisChemoresistanceLDHAProstate cancerSingle-cell RNA sequencing

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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.