| Literature DB >> 27847095 |
Shyh-Horng Chiou1, King-Teh Lee2.
Abstract
Hepatocellular carcinoma (HCC) has been ranked as the third leading cause of cancer-related mortality worldwide. Typically, patients are already in advanced stages of liver cirrhosis at the time of HCC diagnosis. Because HCC is often detected at a late stage and is highly aggressive, noninvasive biomarkers are urgently needed for early diagnosis. Recent advances in gene-expression profiling technologies have enabled molecular classification of HCC into defined subclasses that provide a firm basis for further study of potential mechanisms and biomarkers underlying the development of HCC. This study applied an integrated onco-proteogenomics approach to identify and characterize HCC biomarkers. Specifically, this study integrated proteomic, genomic, and transcriptomic methods to obtain protein expression profiles of urine and tissue samples from HCC patients and from normal controls. Two mediators of inflammation were positively identified: S100A9 and granulin protein markers, which belong to the cytoplasmic alarmin family of the host innate immune system. These HCC-associated cancer-specific biomarkers may have contributing roles not only in the dysregulated processes associated with various inflammatory and autoimmune conditions, but also in tumorigenesis and cancer metastasis.Entities:
Keywords: Hepatocellular carcinoma; Onco-proteogenomics; Proteogenomics; Urine proteomics
Mesh:
Substances:
Year: 2016 PMID: 27847095 DOI: 10.1016/j.kjms.2016.09.002
Source DB: PubMed Journal: Kaohsiung J Med Sci ISSN: 1607-551X Impact factor: 2.744