Intracellular bacteria in tumors help cancer cells metastasize
Cell Press | 04-07-2022
Intracellular bacteria promote cancer metastasis by enhancing the resistance of circulating tumor cells to mechanical stress in the bloodstream, promoting cell survival during tumor progression. The findings appear in the journal Cell.
“Our study reveals that the cancer cell’s behavior is also controlled by the microbes hiding inside tumors, the majority of which were originally thought to be sterile,” says senior author Shang Cai of the Westlake Laboratory of Life Sciences and Biomedicine. “This microbial involvement is distinct from the genetic, epigenetic, and metabolic components that most cancer drugs target.”
“However, our study does not mean that using antibiotics during cancer treatment will benefit patients,” he says. “Therefore, it is still an important scientific question of how to manage the intratumor bacteria to improve cancer treatment in the future.”
Microbes play a critical role in affecting cancer susceptibility and tumor progression, particularly in colorectal cancers. However, emerging evidence suggests that they are also integral components of the tumor tissue itself in a broad range of cancer types, such as pancreatic cancer, lung cancer, and breast cancer. Microbial features are linked to cancer risk, prognosis, and treatment responses, yet the biological functions of tumor-resident microbes in tumor progression remain unclear.
Whether these microbes are passengers or drivers of tumor progression has been an intriguing question. “Tumor cells hijacked by microbes could be more common than previously thought, which underscores the broad clinical value of understanding the exact role of the tumor-resident microbial community in cancer progression,” Cai says.
To address this gap, Cai and his collaborators used a mouse model of breast cancer with significant amounts of bacteria inside cells, similar to human breast cancer. They found that the microbes can travel through the circulatory system with the cancer cells and play critical roles in tumor metastasis. Specifically, these passenger bacteria are able to modulate the cellular actin network and promoted cell survival against mechanical stress in circulation.
“We were surprised initially at the fact that such a low abundance of bacteria could exert such a crucial role in cancer metastasis. What is even more astonishing is that only one shot of bacteria injection into the breast tumor can cause a tumor that originally rarely metastasizes to start to metastasize,” Cai says. “Intracellular microbiota could be a potential target for preventing metastasis in broad cancer types at an early stage, which is much better than having to treat it later on.”
Although the study revealed a clear role of intratumor bacteria in promoting cancer cell metastatic colonization, the authors did not exclude the possibility that the gut microbiome and immune system may act together with intratumor bacteria to determine cancer progression. In the future, further in-depth analysis of how bacteria invade tumor cells, how intracellular bacteria are integrated into the host cell system, and how bacteria-containing tumor cells interact with the immune system will provide insights on how to properly implement antibiotics for cancer therapeutics in the clinic.
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