Gene study uncovers origins of many common cancers

LONDON Wed Aug 14, 2013 1:09pm EDT

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LONDON (Reuters) - Researchers in Britain have set out the first comprehensive map of mutational processes behind the development of tumors - work that should in future lead to better ways to treat and prevent a wide range of cancers.

In a study published in the journal Nature on Wednesday, researchers who analyzed more than 7,000 genomes, or genetic codes, of common forms of cancer uncovered 21 so-called "signatures" of processes that mutate DNA.

"(This) is an important step to discovering the processes that drive cancer formation," said Serena Nik-Zainal of the Wellcome Trust Sanger Institute who worked on the research.

"Through detailed analysis, we can start to use the overwhelming amounts of information buried deep in the DNA of cancers to our advantage in terms of understanding how and why cancers arise."

All cancers are caused by mutations in DNA occurring in cells of the body during someone's lifetime.

Scientists are clear about some things, such as that chemicals in tobacco smoke cause mutations in lung cells that lead to lung cancers, or that ultraviolet light triggers mutations in skin cells that lead to skin cancers.

But they have yet to figure out the biological processes that cause mutations behind most common cancers.

"We're beginning to know quite a lot about what the consequences of those mutations are. But actually we have a really rudimentary understanding of what is causing the mutations in the first place," said Mike Stratton, the Sanger Institute's director and the lead researcher on this study.

"And after all, the things that are causing those mutations are the causes of cancer."

The team analyzed the genetic codes of 7,042 cases of cancer in people from around the world, covering 30 different types of the disease, to see if they could find patterns, or signatures, of mutational processes.

They discovered that all the cancers contained two or more signatures - a finding that shows the variety of processes that work together when a cancer develops.

They also found that different cancers have different numbers of mutational processes. While two mutational processes underlie the development of ovarian cancer, there are six behind the development of liver cancer, the researchers said

And some signatures are found in multiple cancer types, while others are only found in one type. Out of the 30 cancers, 25 had signatures from mutational processes linked to ageing.

In a suggestion of what might be behind many common cancers, the team also discovered that a family of enzymes called APOBECs, known to mutate DNA, was linked to more than half of the cancer types studied.

APOBECs can be activated when the body is responding to a viral infection. The researchers said it may be that the resulting "signatures" are collateral damage on the human genome caused by the enzymes acting to protect cells from viruses.

Stratton described the results as like uncovering the "archaeological traces" of the many mutational processes that lead to most cancers.

"This compendium of mutational signatures and the consequent insights into the mutational processes underlying them has profound implications for the understanding of cancer."

(Editing by Mark Heinrich)

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Comments (3)
LynnJ wrote:
If there is a major link between aging and cancer (25 of 30 kinds of cancer in this study) it would seem that, if one lives long enough, cancer is almost certain. Whether this is due to repeated exposure to viruses, reduced ability of the immune system to respond, or other deficits remains to be seen; but perhaps one of the best ways to reduce cancer would be to focus on aging processes in general.

Aug 15, 2013 1:40pm EDT  --  Report as abuse
branchltd wrote:
This is not as novel a study as the article seems to indicate.

Aug 15, 2013 2:41pm EDT  --  Report as abuse
sylvan wrote:
Excellent. The power of a study with 7000 participants is staggering. The results showing that all cancers have at least two drivers, explains why many of the specific compound oncologic agents are or become ineffective, even when the gene defect is detected. This is truly a major step and hopefully these geniuses for the public good can also derive metabolites of the processes’ and develop easy to use blood or urine tests to use as screens, saving billions in non-evidence-based screenings now widely used, like mammograms and PSAs. This is why we need to invest in basic scientific research. Thank you to the trust that funded this analysis.

Aug 18, 2013 8:38am EDT  --  Report as abuse
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