Amino acid aspartate helps make the lungs a common site for cancer metastasis, offering new insights for potential treatments.

Researchers from Prof. Sarah-Maria Fendt’s lab at VIB-KU Leuven have discovered that the availability of the amino acid aspartate contributes to the lung’s frequent role as a site of metastasis. Their findings, published in Nature, enhance our understanding of cancer biology and lay the groundwork for potential new therapies targeting metastatic diseases (1^✔ ✔Trusted Source
Aspartate signalling drives lung metastasis via alternative translation

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Lung Metastasis: A Common Challenge in Cancer

More than half of cancer patients in whom the cancer spreads beyond the primary site have lung metastases. What makes the lungs such a tempting place for cancer cells?

To find out, the team of Prof. Sarah-Maria Fendt and colleagues investigated the gene expression in cells from aggressive lung metastases. They found evidence for an alternative ‘translation program.’ What does this mean? Translation is the process that uses our genetic code as a blueprint to make proteins in cells. A change in the translational program results in a set of different proteins that allow cancer cells to grow easier in the lung environment.

But what starts this alternative translational program in aggressive metastases?

Ginevra Doglioni, Ph.D. student at the Fendt lab and first author of the study says “We found high levels of aspartate in the lungs of mice and patients with breast cancer compared to mice and patients without cancer, which suggests that aspartate may be important for lung metastasis”.

Aspartate is an amino acid (a protein building block) that has very low concentrations in blood plasma but, surprisingly, very high concentrations in the lungs of mice with metastatic breast cancer.

Hypusination: A Key Driver of Cancer Cell Aggressiveness

Many proteins in our bodies can affect the translation process, among them the so-called initiation factors. One such initiation factor is eIF5A, which kickstarts translation. In the cells of cancer cells within lung metastases, the researchers found an activating modification to eIF5A called ‘hypusination’, which was associated with higher cancer aggressiveness of lung metastases.

Does aspartate have something to do with this?

Yes, it does! The researchers discovered that aspartate triggered this modification on eIF5A through an unexpected mechanism. Surprisingly, aspartate was not taken up by the cancer cells. Instead, it activated a cell surface protein called an NMDA receptor in cancer cells, leading to a signaling cascade that, eventually, triggered eIF5A hypusination. This subsequently drives a translational program that enhances the ability of cancer cells to change their environment and make it more suitable for aggressive growth.

NMDA Receptor Subunit Expression in Lung Metastases

Looking at human lung tumor samples from patients with metastatic breast cancer, the scientists noted a similar translational program as in mice and an elevated expression of the NMDA receptor subunit that binds aspartate compared to metastases from other organs.

Potential for Targeted Therapies in Lung Metastasis

Prof. Fendt explains, “This correlation emphasizes the relevance of the findings in a clinical context and suggests that aspartate signaling may be a common feature of cancer cells growing in the lung. Moreover, there are drugs available to target the mechanism we identified and thus with further research a translation toward a clinical setting might be possible.”

Reference:

1. Aspartate signalling drives lung metastasis via alternative translation – (https://www.nature.com/articles/s41586-024-08335-7)

Source-Eurekalert