A person’s lifetime risk for cancer may begin before they are even born, reports a paradigm-shifting study by Van Andel Institute scientists.
The findings, published in Nature Cancer, identified two distinct epigenetic states that arise during development and are linked to cancer risk. One of these states is associated with a lower lifetime risk while the other is associated with a higher lifetime risk.
If cancer does develop in the lower risk state, it is more likely to be a liquid tumor, such as leukemia or lymphoma. If cancer develops in the higher risk state, it is more likely to be a solid tumor, such as lung or prostate cancer.
Cancer risk increases as people age, thanks to an accumulation of DNA damage and other factors. Still, not every abnormal cell goes on to become cancer. In recent years, scientists have identified other influences, such as epigenetic errors, as additional contributors to cancer.
Epigenetics are processes that affect how and when the instructions in DNA are carried out. Problems with epigenetics can derail cellular quality control processes, enabling sick cells to survive and spread.
In their study, Pospisilik and collaborators found that mice with reduced levels of the gene Trim28 can have one of two patterns of epigenetic marks on cancer-related genes, despite being otherwise identical. These patterns are established during development. The strength of the patterns determines which of the two cancer risk states occur.
“Everyone has some level of risk but, when cancer does arise, we tend to think of it just as bad luck,” said Ilaria Panzeri, Ph.D., a research scientist in the Pospisilik Lab and the study’s first and co-corresponding author. “However, bad luck doesn’t fully explain why some people develop cancer and others don’t. Most importantly, bad luck cannot be targeted for treatment. Epigenetics, on the other hand, can be targeted. Our findings show that cancer’s roots may start during the sensitive period of development, offering a new perspective to study the disease and potential new options for diagnosis and treatment.”
The team found evidence of the two epigenetic states throughout tissues in the body, which suggests that developmental epigenetic risk may be common across cancers. In the future, they plan to explore the effects of these two states in individual cancer types.
(Newswise/YK)