The C-Terminal Fragment of Prostate-Specific Antigen, a 2331 Da Peptide, as a New Urinary Pathognomonic Biomarker Candidate for Diagnosing Prostate Cancer

Autor: Junko Oosaga, Kenji Nakayama, Shinichi Iwamoto, Kuniko Ikawa, Shin-ichiro Kawabata, Hiroaki Tsuji, Sadanori Sekiya, Osamu Ogawa, Naoki Terada, Koichi Tanaka, Takahiro Inoue, Takayuki Goto, Yu Miyazaki, Shigeki Kajihara
Jazyk: angličtina
Rok vydání: 2014
Předmět:
Male
Proteomics
Aging
Pathology
lcsh:Medicine
Urine
urologic and male genital diseases
Biochemistry
Mass Spectrometry
Analytical Chemistry
Prostate cancer
Spectrum Analysis Techniques
Sequence Analysis
Protein

Pathognomonic
Medicine and Health Sciences
lcsh:Science
Matrix-Assisted Laser Desorption Ionization Time-of-Flight Mass Spectrometry
Digital Rectal Examination
Aged
80 and over

Clinical Chemistry
Multidisciplinary
Prostate Cancer
Middle Aged
Body Fluids
Chemistry
Prostate-specific antigen
Bioassays and Physiological Analysis
Oncology
Physical Sciences
Biomarker (medicine)
Anatomy
Research Article
PCA3
medicine.medical_specialty
Urology
Urinary system
Research and Analysis Methods
Antigen
Diagnostic Medicine
Biomarkers
Tumor

medicine
Humans
Amino Acid Sequence
Mass screening
Aged
business.industry
lcsh:R
Prostatic Neoplasms
Biology and Life Sciences
Cancers and Neoplasms
Prostate-Specific Antigen
medicine.disease
Peptide Fragments
Genitourinary Tract Tumors
Spectrometry
Mass
Matrix-Assisted Laser Desorption-Ionization

Cancer research
lcsh:Q
Clinical Medicine
Biochemical Analysis
business
Biomarkers
Zdroj: PLoS ONE
PLoS ONE, Vol 9, Iss 9, p e107234 (2014)
ISSN: 1932-6203
Popis: BACKGROUND AND OBJECTIVES: Prostate cancer (PCa) is one of the most common cancers and leading cause of cancer-related deaths in men. Mass screening has been carried out since the 1990s using prostate-specific antigen (PSA) levels in the serum as a PCa biomarker. However, although PSA is an excellent organ-specific marker, it is not a cancer-specific marker. Therefore, the aim of this study was to discover new biomarkers for the diagnosis of PCa. MATERIALS AND METHODS: We focused on urine samples voided following prostate massage (digital rectal examination [DRE]) and conducted a peptidomic analysis of these samples using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF/MS(n)). Urinary biomaterials were concentrated and desalted using CM-Sepharose prior to the following analyses being performed by MALDI-TOF/MS(n): 1) differential analyses of mass spectra; 2) determination of amino acid sequences; and 3) quantitative analyses using a stable isotope-labeled internal standard. RESULTS: Multivariate analysis of the MALDI-TOF/MS mass spectra of urinary extracts revealed a 2331 Da peptide in urine samples following DRE. This peptide was identified as a C-terminal PSA fragment composed of 19 amino acid residues. Moreover, quantitative analysis of the relationship between isotope-labeled synthetic and intact peptides using MALDI-TOF/MS revealed that this peptide may be a new pathognomonic biomarker candidate that can differentiate PCa patients from non-cancer subjects. CONCLUSION: The results of the present study indicate that the 2331 Da peptide fragment of PSA may become a new pathognomonic biomarker for the diagnosis of PCa. A further large-scale investigation is currently underway to assess the possibility of using this peptide in the early detection of PCa.
Databáze: OpenAIRE