| Literature DB >> 32702989 |
Hong Zheng1, Yinjie Zhu2, Xiaoguang Shao2, Aimin Cai1, Baijun Dong2, Wei Xue2, Hongchang Gao1.
Abstract
Tumor metabolic characteristics have been associated with the progression of prostate cancer (PCa), but little information is available regarding the metabolic alterations from hormone-sensitive (HSPC) to castration-resistant PCa (CRPC). In this study, therefore, we investigated the metabolic profiles in prostate tissues from patients with benign prostatic hyperplasia (BPH), HSPC, and CRPC using a 1H NMR-based metabolomics approach. The results show that clear separations in metabolic patterns were obtained in prostate tissues among BPH, HSPC, and CRPC; however, CRPC may induce a metabolic shift toward BPH, mainly involving amino acid metabolism, choline metabolism, and the Warburg effect. Based on these metabolic changes, we identified potential biomarker panels for the discrimination between BPH vs HSPC, BPH vs CRPC, and HSPC vs CRPC with the AUC values of 0.995, 0.972, and 0.937, respectively. Collectively, tissue-based metabolomics analysis not only identifies the altered metabolic pathways during PCa progression but also has the potential to help the classification and diagnosis of PCa in clinical practice.Entities:
Keywords: CRPC; citrate; diagnosis; metabolomics; prostate cancer
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Year: 2020 PMID: 32702989 DOI: 10.1021/acs.jproteome.0c00282
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466