Stress - surveillance contributes to anti-neoplastic immunity through the activation, on lymphocytes, of the NKG2D receptor that recognizes ligands (NKG2D - L)
expressed on cancer cells.
Not exact matches
«In addition, changes in how the genes are
expressed (turned
on or off) could be used in the future to predict how and when the
cancer cells will spread to other parts of the body and how fast they will grow.»
One way
cancer cells do this is by
expressing a protein ligand that binds to a receptor
on the T
cells to prevent the T
cell from recognizing and attacking the
cancer cell.
«The antibody binds to a specific protein, called CD44s, which is
expressed on the surface of pancreatic
cancer stem
cells.
They found that the number of copies of lncRNA genes
on a chromosome consistently change in 12 different
cancer types and lncRNA genes are widely
expressed in
cancer cells.
Ovarian
cancer researchers have identified a protein biomarker
expressed on the surface of tumour
cells in high - grade serous ovarian
cancer, the most common and lethal subtype of the disease.
Although myeloma is, like leukemias and lymphomas, a
cancer involving white blood
cells known as lymphocytes, myeloma
cells don't traditionally
express CD19
on their surface because they arise from the most mature type of lymphocytes — plasma
cells.
T
cells are collected from the patient's blood and genetically engineered to
express cell - surface proteins called CARs, which recognize specific molecules found
on the surface of
cancer cells.
In earlier research, Barbolina discovered that a fractalkine receptor — a protein found
on the
cell surface — is
expressed in the majority of ovarian
cancer cases.
The more it's
expressed only
on cancer cells, the more targeted the therapy becomes,» says Colin Weekes, MD, PhD, CU Cancer Center investigator and assistant professor in the Division of Oncology at the CU School of Med
cancer cells, the more targeted the therapy becomes,» says Colin Weekes, MD, PhD, CU
Cancer Center investigator and assistant professor in the Division of Oncology at the CU School of Med
Cancer Center investigator and assistant professor in the Division of Oncology at the CU School of Medicine.
To devise a potential new therapy, the investigators engineered a population of neural stem
cells to
express a potent version of a gene called TRAIL, which codes for a molecule that activates
cell - death - inducing receptors found only
on the surface of
cancer cells.
Blincyto (blinatumomab) is designed to treat
cancers expressing a molecule called CD19 — found
on the surface of B
cell ALL and also non-Hodgkin's lymphoma.
Injections of iPSC - EPCs did not however have significant effect
on tumor growth or
on overall survival, but transducing
cells with a baculovirus
expressing CD40L, a member of the TNF gene family which can induce apoptosis [6, 7], and injection into the breast
cancer lung metastasis, increased levels of pro-apoptotic cytokines in lung tissues, indicating the induction of apoptosis by CD40L carried by the EPCs (See figure).
Prostate
cancer cells that
express low levels of the protein give rise to
cancer stem
cells that are both hard to kill with existing drugs and highly capable of generating
cancer cells on a large scale.
It would indeed be of great interest to see whether ablation of stromal p16Ink4a -
expressing senescent
cells, in otherwise genetically intact INK - ATTAC animals without existing tumors, would lower the animals» risk for
cancer, and put any tumors they might develop
on a less malevolent trajectory, than untreated mice.
Neoantigens — called so because they are newly formed during
cancer development — may represent ideal immunotherapy targets as they are solely
expressed on tumor
cells.
We also found that the EphB4 receptor
expressed on the surface of breast
cancer cells can promote tumor xenograft growth by enhancing blood vessel formation through interactions with its preferred ligand, ephrin - B2, present in tumor endothelial
cells.
Several gene rearrangements have been engineered and their protein products have been
expressed in both normal
cells and
cancer cells to understand the effects of each rearrangement
on cell function and targeted drug effectiveness.
The approach developed by the MGH team starts with the engineered protein, which in this case fuses an antibody fragment targeting a protein called mesothelin —
expressed on the surface of such tumors as mesothelioma, ovarian
cancer and pancreatic
cancer — to a protein from the tuberculosis bacteria that stimulates the activity of dendritic and other immune
cells.
Aptamers targeted mucin - 1 (MUC1), a glycosylated surface protein overexpressed
on many
cancers, including MCF7 breast
cancer cells, and only minimally
expressed in MCF - 10A non-cancerous
cells.