M032 kills tumor cells directly through oncolytic replication and then proceeds to infect tumor cells in proximity, continuing the process
of tumor destruction.
Not exact matches
The key to this approach is minimizing healthy tissue damage while maximizing cancerous
tumor destruction of the sort that improves recognition
of the
tumor by the immune system.
It can be used in computer simulations to optimize the
destruction of tumors in radiotherapy while sparing healthy tissue,» highlights Professor Matthias Kling
of the impact
of the work.
The selective pressure
of the competent immune system «edits» the
tumor by selecting for cells that can avoid immune
destruction.
Blood clots lead to both
destruction of the healthy and
tumor tissue and hypoxia, a shortage
of oxygen that drives more aggressiveness in the
tumor.
Longitudinal confocal microscopy imaging
of solid
tumor destruction following adoptive T cell transfer.
Interestingly, when parental d42m1 sarcoma cells were transplanted into wild - type mice, around 20 %
of recipients developed «escape»
tumors which evaded immune
destruction and progressed (escape clones).
They are important especially for the
destruction of cells infected by a virus or
of tumor cells.
Central to the concept
of immunoediting is the idea that T - cell recognition
of tumor - specific antigens drives the
destruction of early
tumors, and later the antigenic «sculpting»
of persistent
tumor cells.
In other words, T - cell
destruction of cells bearing mutant spectrin - B2 «sculpted» the
tumor cells into poorly immunogenic cells lacking the antigen, which progressed and grew out.
Through its various targets, MMP1 promotes not only
tumor invasion but also breast cancer colonization to bone by mechanisms that include the release
of membrane - bound EGF - like growth factors from
tumor cells, leading to activation
of EGF receptor signaling and suppression
of OPG expression in osteoblasts, which in turn promotes the differentiation and activation
of osteoclasts required for bone
destruction and enhanced
tumor growth in the bone microenvironment (32).
Tumors» mutations can encode the seeds
of their own
destruction, in the form
of immunogenic peptides recognized by T cells.
They found that
destruction of the cancer was mediated by killer T cells residing in the
tumor rather than newly infiltrating killer T cells.
A primary function
of CTLs is the selective recognition and
destruction of tumor cells.
Experiments in mice lacking CTLA - 4 and use
of CTLA - 4 antibodies demonstrated that absence
of CTLA - 4 or blocking its activity could lead to T cell activation and
tumor destruction.
Duntas (2015) articulates, «In susceptible individuals, iodine excess increases intra-thyroid infiltrating Th17 cells and inhibits T regulatory (Treg) cells development, while it triggers an abnormal expression
of tumor necrosis factor - related apoptosis - inducing ligand (TRAIL) in thyrocytes, thus inducing apoptosis and parenchymal
destruction» (31, p. 721).
GcMAF activity is essential to a healthy immune system and can also assist in the
destruction of tumors entirely.
When they do, the symptoms that we see are due to the physical
destruction of these organs as the
tumor grows and crowds out healthy cells.
I - 131 is only absorbed by tissue producing thyroid hormone; the radiation is then given off by the isotope, resulting in
destruction of the
tumor.
But a recent discovery in the world
of holistic medicine has shown very promising results in the reduction and
destruction of such
tumors...
In dogs, the most common cause
of secondary hypothyroidism is
destruction of pituitary thyrotrophs by an expanding, space - occupying
tumor.
There are a variety
of medications that can help brain
tumor patients using targeted
destruction of presence
of the
tumor, such as motor skills, speech, muscle strength and cognitive processes.