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Glypican-1 as a Biomarker for Prostate Cancer: Isolation and Characterization.


ABSTRACT: Prostate cancer is the most frequently diagnosed male visceral cancer and the second leading cause of cancer death in the United States. Standard tests such as prostate-specific antigen (PSA) measurement have poor specificity (33%) resulting in a high number of false positive reports. Consequently there is a need for new biomarkers to address this problem. The MIL-38 antibody was first described nearly thirty years ago, however, until now, the identification of the target antigen remained elusive. By a series of molecular techniques and mass spectrometry, the MIL-38 antigen was identified to be the highly glycosylated proteoglycan Glypican-1 (GPC-1). This protein is present in two forms; a membrane bound core protein of 55-60 kDa and secreted soluble forms of 40 kDa and 52 kDa. GPC-1 identification was confirmed by immuno-precipitation, western blots and ELISA. An ELISA platform is currently being developed to assess the levels of GPC-1 in normal, benign prostatic hyperplasia (BPH) and prostate cancer patients to determine whether secreted GPC-1 may represent a clinically relevant biomarker for prostate cancer diagnosis.

SUBMITTER: Truong Q 

PROVIDER: S-EPMC4910593 | biostudies-literature | 2016

REPOSITORIES: biostudies-literature

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Glypican-1 as a Biomarker for Prostate Cancer: Isolation and Characterization.

Truong Quach Q   Justiniano Irene O IO   Nocon Aline L AL   Soon Julie T JT   Wissmueller Sandra S   Campbell Douglas H DH   Walsh Bradley J BJ  

Journal of Cancer 20160521 8


Prostate cancer is the most frequently diagnosed male visceral cancer and the second leading cause of cancer death in the United States. Standard tests such as prostate-specific antigen (PSA) measurement have poor specificity (33%) resulting in a high number of false positive reports. Consequently there is a need for new biomarkers to address this problem. The MIL-38 antibody was first described nearly thirty years ago, however, until now, the identification of the target antigen remained elusiv  ...[more]

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