When the blood supply is low cancer cells use lipid molecules as fuel instead of blood glucose to grow. This mechanism has been shown in animal tumor models by researchers at Karolinska Institutet in Sweden in a study published in Cell Metabolism.
The process may help explain why tumors often develop resistance to cancer drugs that inhibit the formation of blood vessels.
Tumor growth and spread rely on angiogenesis, a process of growing new blood vessels that supply the cancer cells with nutrients and hormones, including glucose (sugar). Treatment with antiangiogenic drugs reduces the number of blood vessels in the tumor as well as the blood glucose supply. Many such drugs have been developed and are now used in human patients for treating various cancer types.
In collaboration with Japanese and Chinese scientists, a research group at Karolinska Institutet in Sweden has discovered a new mechanism by which cancers can evade antiangiogenic treatment and become resistant.
The reduction of tumor blood vessels results in low oxygenation in tumor tissues - a process called hypoxia. In the current study, the researchers show that hypoxia acts as a trigger to tell fat cells surrounding or within tumor tissues to break down the stored excessive lipid energy molecules. These lipid energy molecules can when the blood supply is low be used for cancer tissue expansion.
"Based on this mechanism, we propose that a combination therapy consisting of antiangiogenic drugs and drugs blocking lipid energy pathways would be more effective for treating cancers. In animal tumor models, we have validated this very important concept, showing that combination therapy is superior to monotherapy," says Yihai Cao, Professor at the Department of Microbiology, Tumor and Cell Biology at Karolinska Institutet, who led the study.
Professor Cao's group now plans to work with drug companies and clinical oncologists to explore whether such a new combination therapy would improve the quality of life and lifespan in human cancer patients.