Creatine,
the organic acid that is popularly taken as a supplement by athletes and
bodybuilders, serves as a molecular battery for immune cells by storing and
distributing energy to power their fight against cancer, according to new UCLA
research.
The study,
conducted in mice and published in the Journal of Experimental Medicine, is the
first to show that creatine uptake is critical to the anti-tumor activities of
CD8 T cells, also known as killer T cells, the foot soldiers of the immune
system. The researchers also found that creatine supplementation can improve
the efficacy of existing immunotherapies.
"Because
oral creatine supplements have been broadly utilized by bodybuilders and
athletes for the past three decades, existing data suggest they are likely safe
when taken at appropriate doses," said Lili Yang, a member of the Eli and
Edythe Broad Center of Regenerative Medicine and Stem Cell Research at UCLA and
the study's senior author. "This could provide a clear and expedient path
forward for the use of creatine supplementation to enhance existing cancer
immunotherapies."
The findings
of the paper stem from the Yang lab's research into the metabolic needs of
tumor-infiltrating lymphocytes, immune cells that travel into tumors to fight
cancer. Examining these cells, the team observed that killer T cells taken from
inside of tumors possessed a large number of creatine transporter molecules,
which sit on cells' surfaces and control creatine uptake into cells.
"As
biologists, we are always asking 'why?'" said Yang, who is also an
assistant professor of microbiology, immunology and molecular genetics and a
member of the UCLA Jonsson Comprehensive Cancer Center. "We could see that
these tumor-battling T cells had increased their capacity to take in creatine,
likely for a good reason, so we designed experiments to determine what happens
when they can't get it."
The lab
genetically engineered mouse models so that their killer T cells were deficient
in a gene called CrT, or Slc6a8, which is responsible for producing creatine
transporter molecules. They found that mice whose killer T cells could not take
in creatine were less capable of fighting tumors.
The team
then tried validating their hypothesis from the opposite angle, giving
non-engineered mice a daily dose of creatine comparable to the safe dose
recommended to athletes and bodybuilders. This creatine boost—which was given
to some mice via injection and others as an oral supplement—made both groups
better equipped to suppress both skin and colon cancer tumor growth.
"Taken
together, these findings suggest that killer T cells really need creatine to
fight cancer," Yang said. "Without it, they simply can't do their
jobs effectively."
Creatine is
naturally occurring in humans and other vertebrates; it is primarily produced
in the liver and kidneys. Most humans take in additional creatine through their
diets, with meat and fish as major sources. In addition to these natural
sources, creatine supplements are widely popular among athletes and
bodybuilders looking to gain muscle mass and improve performance.
The
popularity of creatine supplements stems from the knowledge that cells with
high-energy demands, like those found in muscle and brain tissue, use creatine
to store excess energy for when they most need it.
These new
findings add killer T cells to the list of creatine-dependent cells, all of
which utilize two distinct sources of power, much like hybrid cars. The first
power source is a metabolic process that is similar to a fuel engine,
converting nutrients like glucose, amino acids and lipids into ATP, the energy
currency of cells. The secondary power source is creatine, which—like a hybrid
car's battery—absorbs excess energy (in this case, ATP) and stores it to be
released when fuel is in short supply to keep the cells working until more fuel
can be burned.
"This
creatine-powered hybrid engine system enables killer T cells to make the most
of their available energy supply in an environment where they have to compete
with fast-growing tumor cells for nutrients," Yang said.
Next, the
team tried combining creatine supplementation with PD-1/PD-L1 blockade therapy,
a form of cancer immunotherapy that prevents T cell exhaustion and has been
approved to treat a broad range of cancers including melanoma, lymphoma, colon,
lung, liver, kidney and cervical. They found that creatine supplementation and
anti-PD-1 blockade therapy worked synergistically, tipping the metabolic scales
in T cells' favor and enabling them to avoid exhaustion and fight cancer
effectively for an extended period.
Four out of
five mice that received this combination therapy were found to have completely
eradicated their colon cancer tumors and remained tumor-free for over three
months. Furthermore, when they were given a second round of tumor cells, all
these "cancer survivor" mice were protected from tumor recurrence and
remained tumor-free for an additional six months.
As a next
step, the team is repeating these experiments using special mouse models that
harbor human tumor grafts and human immune cells. If they are able to replicate
these effects in human cells, the team will work to determine the proper dose,
timing and method to give people creatine supplements to enhance existing
immunotherapies. Because the strategy has proven effective in mouse models of
both melanoma and colon cancer, the team expects the findings could apply to a
range of cancers.
The
experimental combination therapy described above was used in preclinical tests
only and has not been tested in humans or approved by the Food and Drug
Administration as safe and effective for use in humans. This newly identified
therapeutic strategy is covered by a patent application filed by the UCLA
Technology Development Group on behalf of the Regents of the University of
California, with Yang and Stefano Di Biase as co-inventors.
The
researchers recommend that people consult a doctor before incorporating a new
supplement such as creatine into their routine as supplements can carry risks
of drug interactions and other harmful side effects. There is concern that
long-term use of creatine at high doses could damage the liver, kidneys or heart.
Provided by University of California, Los Angeles