Development of biomarkers of genitourinary cancer using mass spectrometry-based clinical proteomics

J Food Drug Anal. 2019 Apr;27(2):387-403. doi: 10.1016/j.jfda.2018.09.005. Epub 2018 Oct 27.

Abstract

Prostate, bladder and kidney cancer are the three most common types of genitourinary cancer in the world. Of these, prostate and bladder cancers are within the top 10 most common cancers in men. Notably, kidney cancer causes no obvious symptoms in the early stages. To satisfy clinical-management requirements, researchers have developed numerous biomarkers by applying proteomic approaches using clinical serum, urine and tissue specimens, as well as cell and animal models. Through application of biomarker pipeline protocols, including discovery, verification and validation phases, and mass-spectrometric based proteomic platforms coupled with multiplexed quantification assays, these studies have led to recent rapid progress in this area. With improvements in mass-spectrometric based proteomic techniques, numerous promising biomarker candidates and marker panels for various clinical purposes have been proposed. Verification of novel protein biomarker candidates is very resource demanding (e.g. on the clinical and laboratory sides). With the support of national consortia, it is now possible to investigate the future clinical use of such biomarker strategies and assess their cost-effectiveness in personalized medicine.

Keywords: Biomarker; Bladder cancer; Kidney cancer; Prostate cancer; Proteomics.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Biomarkers, Tumor / analysis*
  • Humans
  • Mass Spectrometry
  • Neoplasm Proteins / analysis*
  • Proteomics*
  • Urogenital Neoplasms / diagnosis*

Substances

  • Biomarkers, Tumor
  • Neoplasm Proteins

Grants and funding

This research was supported by grants from the Ministry of Science and Technology of Taiwan, Republic of China (106-2113-M-182-001-MY2, 104-2113-M-182-001-MY2), and Chang Gung Memorial Hospital (CMRPD1G0132, CMRPD3E0251, CMRPD3E0252, CMRPD3E0031, CMRPD3E0032, CMRPD3E0033 and BMRPD78).