A team of researchers from the College of Design and Engineering, the N.1 Institute for Health and the Cancer Science Institute of Singapore at the National University of Singapore has recently engineered in vitro tumor models to better understand the crosstalk between liver cancer cells and their microenvironment. Using lab-grown mini liver tumors co-cultured with endothelial cells—these are cells that form the lining of blood vessels—to conduct their study, the research team investigated the role of endothelial cells in liver cancer progression.
“The conventional understanding is that endothelial cells are structural cells that form blood vessels. Our latest findings suggest that these cells also give ‘instructions’ to liver cancer cells to increase the production of a protein called CXCL1, which is associated with poor survival outcome in liver cancer patients,” explained Assistant Professor Eliza Fong, who led the research study.
CXCL1 is a type of chemokine, which are signaling proteins secreted by cells to regulate the infiltration of different immune cells into tumors. Hence, these molecules affect tumor immunity and may influence therapeutic outcomes in patients.
“Our results pave the way for new therapeutic targets to control tumor development, and further our team’s understanding of the mechanisms behind the progression of liver cancer,” Dr. Toh Tan Boon added, who is also a key member of the research team.
The team’s results were published in the journal Biomaterials on 16 April 2022.
Breakthrough in understanding liver cancer progression
Hepatocellular carcinoma (HCC) is the sixth most commonly occurring cancer and remains the second leading cause of cancer worldwide. While several therapeutics have been approved in the recent years to treat advanced HCC, the impact of anti-angiogenic treatment on the overall survival of HCC patients remains elusive.
Previous studies have shown that tumor growth is facilitated by a biological process called angiogenesis (the development of blood vessels) which provides the tumor with oxygen and nutrients to grow. Unfortunately, the benefits of angiogenesis inhibitors are only temporary, following which the tumor resumes growth.
To find new therapeutic targets to better control tumor development, the NUS team decided to study the role of endothelial cells in cancer development using engineered in vitro tumor models.
Unlike previously reported models that rely on the use of immortalized cancer cell lines, the NUS team incorporated patient-derived xenograft organoids and endothelial cells in their new model, which led the team to their significant discovery.
“We found that the ‘communication’ between liver cancer cells and endothelial cells contribute to the generation of macrophages. These immune cells are pro-inflammatory and pro-angiogenesis, potentially creating a very conducive microenvironment for tumor expansion,” explained Associate Professor Edward Chow, also a key member on the research team.
Advancing cancer research using complex tumor models
This latest study, which is a continuation from their previous work in 2018, highlight the significance of setting up such complex co-cultures to better understand the liver cancer milieu.
Importantly, these co-culture models may be useful for drug development studies looking to target liver cancer and can also serve as valuable platforms to better understand how inflammation is promoted in liver cancer, and how it contributes to cancer progression.
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