GC-MS-Based Endometabolome Analysis Differentiates Prostate Cancer from Normal Prostate Cells

• Type: Article in International Scientific Journal
• Date: 2018

Authors

Lima, AR (Author) Other; Araujo, AM (Author) Other; Pinto, J (Author) Other; Carmen Jeronimo (Author) ICBAS; henrique, rmf (Author) ICBAS; Maria de Lourdes Bastos (Author) FFUP; Carvalho, M (Author) Other; de Pinho, PG (Author) FFUP

Journal

Title: Metabolites

Vol. 8

Final page: 23

ISSN: 2218-1989

Publisher: MDPI

Indexing

ISI Web of Knowledge - 22 Citations

Scopus - 22 Citations

Other information

Authenticus ID: P-00N-SXK

DOI: 10.3390/metabo8010023

Abstract (EN): Prostate cancer (PCa) is an important health problem worldwide. Diagnosis and management of PCa is very complex because the detection of serum prostate specific antigen (PSA) has several drawbacks. Metabolomics brings promise for cancer biomarker discovery and for better understanding PCa biochemistry. In this study, a gas chromatography-mass spectrometry (GC-MS) based metabolomic profiling of PCa cell lines was performed. The cell lines include 22RV1 and LNCaP from PCa with androgen receptor (AR) expression, DU145 and PC3 (which lack AR expression), and one normal prostate cell line (PNT2). Regarding the metastatic potential, PC3 is from an adenocarcinoma grade IV with high metastatic potential, DU145 has a moderate metastatic potential, and LNCaP has a low metastatic potential. Using multivariate analysis, alterations in levels of several intracellular metabolites were detected, disclosing the capability of the endometabolome to discriminate all PCa cell lines from the normal prostate cell line. Discriminant metabolites included amino acids, fatty acids, steroids, and sugars. Six stood out for the separation of all the studied PCa cell lines from the normal prostate cell line: ethanolamine, lactic acid, beta-Alanine, L-valine, L-leucine, and L-tyrosine.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 15