Researchers at Hokkaido University in Japan have demonstrated that a molecule, called biglycan, plays an intrinsic role in attracting tumour cells toward the inner wall of tumour blood vessels.
Biglycan is a normal component of the supportive matrix outside cells and appears to modulate the biological activities of a number of growth factors. It is also released by immune cells in inflamed tissues.
The team conducted investigations by grafting low-metastatic (LM) and high-metastatic (HM) melanoma tumour cells under the skin of mice.
They found the “endothelial” cells forming the inner lining of blood vessels in the HM tumours secrete increased levels of biglycan, which then binds to specific receptors on the tumour cells, attracting them to the endothelium.
When they neutralised the biglycan receptors with antibodies, tumour cell migration toward the endothelium was inhibited.
They speculate that the tumour cells created a micro-environment that could induce abnormal gene expression in the neighbouring tissue.
The team analysed a large database that contains gene expression data in cancer patients.
They found that high biglycan expression was associated with poor prognosis in patients with breast, lung and colorectal cancer.
Further investigation on a specific metastatic cancer case showed high levels of biglycan in the blood of patients with metastatic cancer, while it was barely detected in another non-metastatic case.
Blood vessel endothelial cells act as “gatekeepers”, the researchers write in their study published in the journal Scientific Reports.
In highly metastatic tumours, these cells give tumour cells the “key” molecule, biglycan, which allows them to break through the gate and proceed into the blood stream, resulting in metastases.
“The present observations, together with unravelling certain remaining issues, may contribute to establishing accurate diagnostics or potent anti-metastatic strategies that target the communications between tumour cells and endothelial cells,” the researchers conclude.
[hr] Source: Hokkaido University