«This is the first study to illustrate that a structural abnormality in the 3» untranslated region of the PD - L1 gene causes an abnormally high production of PD - L1 protein, consequently aiding
cancer immune escape,» says one of the lead authors, Keisuke Kataoka, at Kyoto University.
Not exact matches
But
cancer cells can
escape immune surveillance using a variety of techniques to disguise themselves.
This may explain how
cancer cells
escape detection by our body's
immune system.
In addition to formulating diagnostic strategies for
cancer immunotherapy agents, her team is focused on developing a deep understanding of tumor
immune biology as well as mechanisms associated with
immune response and
immune escape in
cancer patients, with the intent of generating rational strategies for the creation of combination therapies.
Therefore, having less MHC I molecules may allow
cancer cells to hide better and
escape detection by the
immune system.
Cancer cells can leverage such mechanisms to
escape the
immune system response.
Publishing in Nature, the study reports that genetic alterations affecting a part of the PD - L1 gene increases the production of the protein, allowing
cancer cells to
escape detection by the
immune system.
Then, they treated the dormant cells with a product of the
immune system, they found that dormant cells were susceptible to immunotherapy, and that quiescent, but not indolent
cancer cells, could not
escape from immunotherapy.
Publishing in Nature, a recent study reports that genetic alterations affecting a part of the PD - L1 gene increases the production of the protein, allowing
cancer cells to
escape detection by the
immune system.
Conversely, the
immune system contains triggers to blunt
immune responses, and antibodies that block these «off - switch» checkpoints might be able to further reduce the ability of these
cancers to
escape the
immune system.
A team of scientists from Singapore has discovered new ways in which
cancers can
escape the body's
immune system.
More recently, we have learned that it is critical to understand the biology of
cancer plasticity to identify the mechanisms that allow tumours to resist or
escape immune control.
Some of our next steps are to determine the biological process that causes
cancer cells to express non-mutated, shared antigens, and the means by which dormant metastases
escape immune elimination.
In fact, some researchers are even suggesting that lung
cancers use the PD - 1 pathway to
escape immune destruction in the first place.
What this suggests is that lung
cancers are able to take hold in the lungs by disarming T cells and
escaping the
immune system's control.
CRI postdoctoral fellow Dr. Haihui Lu at the Whitehead Institute for Biomedical Research in Cambridge, Massachusetts, is studying some of the unique characteristics that differentiate metastatic
cancer cells from primary tumor cells, and specifically aims to understand how these unique characteristics enable breast
cancer cells to
escape elimination by the
immune system.
This past October, led by postdoc Nicholas McGranahan and graduate student Rachel Rosenthal, Swanton's lab found one way that lung
cancers evolve to
escape detection by the
immune system.
Here, we review the current state of the art of somatic
cancer evolution and mechanisms of
immune control and
escape.
Cancer cells have developed a number of ways to survive, including ways to
escape detection and attack by our
immune system, but their ability to respond to viral infections is actually quite limited.
Based on this data, researchers concluded that learned helplessness in rats who couldn't
escape the shocks must have suppressed the
immune response known to fight off
cancer cells in tumors of this sort.