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Targeting glucose metabolism in cancer: a new class of agents for loco-regional and systemic therapy of liver cancer and beyond?
Author(s) -
Lynn Jeanette Savic,
Julius Chapiro,
Gregor Duwe,
Jean-François Geschwind
Publication year - 2016
Publication title -
hepatic oncology
Language(s) - English
Resource type - Journals
eISSN - 2045-0931
pISSN - 2045-0923
DOI - 10.2217/hep.15.36
Subject(s) - medicine , hepatocellular carcinoma , cancer , liver cancer , disease , tumor microenvironment , cancer research , bioinformatics , biology
Hepatocellular carcinoma (HCC) is one of the most prevalent cancers and the third leading cause of cancer-related deaths worldwide. In patients with unresectable disease, loco-regional catheter-based intra-arterial therapies (IAT) can achieve selective tumor control while minimizing systemic toxicity. As molecular features of tumor growth and microenvironment are better understood, new targets arise for selective anticancer therapy. Particularly, antiglycolytic drugs that exploit the hyperglycolytic cancer cell metabolism - also known as the 'Warburg effect' - have emerged as promising therapeutic options. Thus, future developments will combine the selective character of loco-regional drug delivery platforms with highly specific molecular targeted antiglycolytic agents. This review will exemplify literature on antiglycolytic approaches and particularly focus on intra-arterial delivery methods.

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