Proteomic Profiling and Biomarker Discovery in Colorectal Liver Metastases

被引:14
作者
Wong, Geoffrey Yuet Mun [1 ,2 ]
Diakos, Connie [2 ,3 ]
Hugh, Thomas J. [1 ,2 ]
Molloy, Mark P. [4 ]
机构
[1] Royal North Shore Hosp, Dept Upper Gastrointestinal Surg, Sydney, NSW 2065, Australia
[2] Univ Sydney, Northern Clin Sch, Sydney, NSW 2065, Australia
[3] Royal North Shore Hosp, Dept Med Oncol, Sydney, NSW 2065, Australia
[4] Univ Sydney, Fac Med & Hlth, Sch Med Sci, Bowel Canc & Biomarker Res Lab, Sydney, NSW 2006, Australia
关键词
colorectal cancer; colorectal liver metastases; proteomics; prognosis; biomarkers; mass spectrometry; III COLON-CANCER; PROTEOGENOMIC CHARACTERIZATION; HEPATIC RESECTION; STAGE-III; ADJUVANT CHEMOTHERAPY; EXTRACELLULAR-MATRIX; MOLECULAR SUBTYPES; EARLY RECURRENCE; SURVIVAL; HETEROGENEITY;
D O I
10.3390/ijms23116091
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Colorectal liver metastases (CRLM) are the leading cause of death among patients with metastatic colorectal cancer (CRC). As part of multimodal therapy, liver resection is the mainstay of curative-intent treatment for select patients with CRLM. However, effective treatment of CRLM remains challenging as recurrence occurs in most patients after liver resection. Proposed clinicopathologic factors for predicting recurrence are inconsistent and lose prognostic significance over time. The rapid development of next-generation sequencing technologies and decreasing DNA sequencing costs have accelerated the genomic profiling of various cancers. The characterisation of genomic alterations in CRC has significantly improved our understanding of its carcinogenesis. However, the functional context at the protein level has not been established for most of this genomic information. Furthermore, genomic alterations do not always result in predicted changes in the corresponding proteins and cancer phenotype, while post-transcriptional and post-translational regulation may alter synthesised protein levels, affecting phenotypes. More recent advancements in mass spectrometry-based technology enable accurate protein quantitation and comprehensive proteomic profiling of cancers. Several studies have explored proteomic biomarkers for predicting CRLM after oncologic resection of primary CRC and recurrence after curative-intent resection of CRLM. The current review aims to rationalise the proteomic complexity of CRC and explore the potential applications of proteomic biomarkers in CRLM.
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页数:20
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