Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015 Oct 27;7(Suppl 1):13-9.
doi: 10.4137/BIC.S25250. eCollection 2015.

Biomarkers of Angiogenesis in Colorectal Cancer

Affiliations
Review

Biomarkers of Angiogenesis in Colorectal Cancer

Luay Mousa et al. Biomark Cancer. .

Abstract

Colorectal cancer (CRC) is the third most common cancer worldwide and accounts for 10% of all new cancer diagnoses. Angiogenesis is a tightly regulated process that is mediated by a group of angiogenic factors such as vascular endothelial growth factor and its receptors. Given the widespread use of antiangiogenic agents in CRC, there has been considerable interest in the development of methods to identify novel markers that can predict outcome in the treatment of this disease with angiogenesis inhibitors. Multiple biomarkers are in various phases of development and include tissue, serum, and imaging biomarkers. The complexity of the angiogenesis pathway and the overlap between the various angiogenic factors present a significant challenge to biomarker discovery. In our review, we discuss the angiogenesis pathway and the most promising evolving concepts in biomarker discovery, as well as highlight the landmark studies that identify subgroups of patients with CRC who may preferentially benefit from angiogenesis inhibitors.

Keywords: angiogenesis; circulating tumor cells; colorectal cancer; imaging biomarkers; microRNA.

PubMed Disclaimer

Figures

Figure 1
Figure 1
A schematic of the angiogenesis pathway, angiogenesis inhibitors, and the most promising biomarker techniques. Notes: A: Aflibercept; B: bevacizumab. Abbreviations: CTCs, circulating tumor cells; ctDNA, circulating tumor DNA; ctRNA, circulating tRNA; mRNA, microRNA; R, regorafenib; Ram, ramucirumab; VEGF, vascular endothelial growth factor.

References

    1. Global Burden of Disease Cancer Collaboration. Fitzmaurice C, Dicker D, et al. The global burden of cancer 2013. JAMA Oncol. 2015;1(4):505–527. - PMC - PubMed
    1. Schmoll HJ, Van Cutsem E, Stein A, et al. ESMO consensus guidelines for management of patients with colon and rectal cancer. A personalized approach to clinical decision making. Ann Oncol. 2012;23(10):2479–2516. - PubMed
    1. Böckelman C, Engelmann BE, Kaprio T, Hansen TF, Glimelius B. Risk of recurrence in patients with colon cancer stage II and III: a systematic review and meta-analysis of recent literature. Acta Oncol. 2015;54(1):5–16. - PubMed
    1. Heinemann V, von Weikersthal LF, Decker T, et al. FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment for patients with metastatic colorectal cancer (FIRE-3): a randomised, open-label, phase 3 trial. Lancet Oncol. 2014;15(10):1065–1075. - PubMed
    1. Simmonds PC, Primrose JN, Colquitt JL, Garden OJ, Poston GJ, Rees M. Surgical resection of hepatic metastases from colorectal cancer: a systematic review of published studies. Br J Cancer. 2006;94(7):982–999. - PMC - PubMed

LinkOut - more resources