Bacterium actively drives colorectal cancer tumor cell growth

Scientists have known for some time that people infected with the S. gallolyticus subspecies gallolyticus (Sg) are more likely to have colorectal cancer (CRC), a leading cause of cancer death. However, it was unknown whether Sg actively promotes CRC or whether it simply grows comfortably in the environment provided by CRC tumor cells.

To investigate the precise role of Sg in CRC, Ritesh Kumar of Texas A&M Health Science Center and colleagues performed several experiments using cultured human colorectal cells, mice with CRC, and tissue from human tumors.

Experiments in which CRC cells and Sg were grown together showed that Sg promotes proliferation of CRC cells, and that this effect depends on what phase of growth the Sg bacteria are in. Sg¬-driven proliferation of CRC cells only occurred when the bacteria and CRC cells were in direct contact with each other; substances secreted by bacterial cells did not drive proliferation on their own.

The researchers also explored the effects of Sg on a human protein known as β-catenin, which plays a key role in the development of CRC. They found that Sg did not promote proliferation of CRC cells in which β-catenin production or activity were deliberately reduced, suggesting that Sg drives proliferation through the β-catenin cell signaling pathway.

In mice with CRC, those injected with Sg developed more tumors and had greater β-catenin production (as well as other signs of cancer severity) than did mice injected with a different type of bacteria as a control. The researchers also analyzed normal and tumor tissue samples from more than 100 human CRC patients and found that most were infected with Sg, which was previously unknown.

Overall, these findings strongly suggest that Sg plays an active role in CRC development in humans. In the future, the precise mechanisms of its tumor-promoting activity could potentially be exploited to develop new strategies to diagnose, prevent, and treat CRC. "A bacterium that has been well documented to have a strong clinical association with CRC is now found to also functionally promote the development of CRC."