Another lab ran into a similar problem when it tried to replicate work by Stanford stem cell biologist Irving Weissman and his colleagues, who reported in 2012 in the Proceedings of the National Academy of Sciences that an antibody to
a tumor cell surface receptor called CD47 can slow tumor growth in mice.
Not exact matches
His work indicates that this
cell surface marker could serve as a target for a novel brain cancer vaccine or T -
cell therapies engineered to recognize and kill
tumors carrying that neoantigen.
At the end of September, the European Commission approved a marketing application for Lutathera, a radioactive molecule that targets specific receptors found on the
surface of neuroendocrine
tumor cells.
Many
tumors release
cells with distinctive antigens on their
surfaces, and affinity - based techniques can pull these
cells out of the blood sample relatively easily.
The immune system depends on molecules called T
cell receptors on the
surface of T
cells to recognize and respond to foreign antigens from virus - infected
cells,
tumors and other threats.
Several studies have used
cell -
surface markers — proteins found on the outer membranes of
tumor cells — to identify glioblastoma stem
cells; but the specific markers used have been controversial and can not reflect molecular processes going on within
tumor cells.
To begin the research, the scientists screened human DIPG
tumor cultures for
surface molecules that could act as targets for CAR - T
cells.
SapC - DOPS binds with exposed patches of the phospholipid phosphatidylserine (PtdSer) on the
surface of
tumor cells;
Most cancer vaccines developed to date have been designed to recognize and attack a specific known molecule — such as a
cell -
surface receptor — that is likely to be found on cancerous
cells in any patient with that type of
tumor.
Instead of displaying the full complement of incriminating proteins on the
tumor cell's
surface, the dog cancer displays just a few, obfuscating the invasion underway.
The
tumor cells»
surfaces presented no antigens and thus, no identity card at all.
Liang Xu, Ph.D. member of the KU Cancer Center's Drug Discovery, Delivery and Experimental Therapeutics program and associate professor of molecular biosciences at KU, has discovered that targeting a
cell -
surface receptor called «CD44s» can block pancreatic
tumor formation and recurrence after radiotherapy.
In collaboration with the group of Valerian Kagan, Ph.D., D.Sc., at the University of Pittsburgh, Gabrilovich and colleagues analyzed in great detail the events that take place in the DCs from
tumor - bearing mice models and found that impaired cross-presentation, which occurred in the presence of
tumor - derived factors, was associated with defective trafficking of the antigen - MHC complex to the
cell surface.
Images of the
tumor cells are immediately created on an LCD screen observed as the surgeon scans the instrument across the
tumor or brain
surface.
The protein sits on the
surface of T
cells and helps dampen the activity of the
cells after an immune response, but
tumors have found ways to hide from T
cell attack by flipping on the PD - 1 switch themselves.
The tool sprays a microscopic stream of charged solvent onto the tissue
surface to gather information about its molecular makeup and produces a color - coded image revealing the nature and concentration of
tumor cells.
Researchers from BUSM and the University of Cyprus compared the markers on the
surface of the cancer
cells to gene expression profile of breast
tumors deposited by researchers in international public databases and found that a molecule named IL13RA2 (IL13R alpha2) was abundant in metastatic or late - stage BLBC.
«Beta blockers may lead to new novel triple negative breast cancer treatments: New research suggests that adrenaline can act on
tumor cells via a
cell surface receptor called the beta2 - adrenoceptor and that changes in signaling within the
cell make it highly invasive.»
The new study revealed that pancreatic cancer
cells not only send signals that make macrophages produce abnormal amounts of dectin - 1
surface receptors, but also that make
tumor cells themselves express high levels of galectin - 9.
The ability to track
tumor cells in the bloodstream based on genetic content located within the
cell itself, as opposed to using proteins located on the
cell's
surface (current technology)
In this study, we examined the effectiveness of a vaccination targeting
tumors that produced IL - 15 and its
cell surface receptor called IL - 15R - alpha -LRB--RRB- and examined their ability to up - regulate (or increase) immune responses to
tumor antigens,» Morris says.
Using microfluidic design principles, Liu's group engineered vortices in their device to increase the chance that
tumor cells will collide with the
surface of the flow channel.
PDGFRα is a
cell surface tyrosine kinase receptor involved in organ development and
tumor progression, it is present in multiple
cell types such as mesenchymal
cells, neurons, astrocytes, megakaryocytes and oligodendrocyte progenitor.
Since cancer
cells bear very specific antigens on the
surface, the corresponding antibodies bind to these molecules and thus inhibit
tumor growth.
While fibers aligned perpendicular to the
surface of the
tumor provide a path for the
tumor cells to follow and encourage spreading.
IL - 6 is a cytokine, a signal molecule that is produced and secreted both by immune
cells and by
tumor cells and binds specifically to a receptor (IL - 6R) that is found on the
surfaces of many
cell types.
But the full potential of CARs for treating solid
tumors has not been reached because they have targeted molecules found on the
surface of both normal
cells and cancer
cells, resulting in serious side effects.
Working in mouse models of breast cancer and breast
tumor samples from patients, Longmore and his colleagues showed that a protein that sits on the
surface of
tumor cells, called DDR2, binds to collagen and activates a multistep pathway that encourages
tumor cells to spread.
F3 can detect the expression of a protein called nucleolin, which is a marker on the
surface of
tumor cells.
Once activated, the circuit expresses proteins designed to direct the immune system to target the
tumor cells, including
surface T
cell engagers, which direct T
cells to kill the
cells.
Pembrolizumab blocks the action of the
tumor -
surface protein PD - 1, which many cancers use to hide themselves from immune system T
cells.
In breast cancer, CSCs or
tumor - initiating
cells were first identified by using a combination of
cell surface markers, CD24 − / CD44 + / ESA (EpCAM) + (2).
Hu14.18 K332A is a laboratory - produced antibody designed to activate the immune response against
tumor cells by recognizing and binding to an antigen found on the
surface of most neuroblastoma
tumor cells.
Although there is new data coming from Dr. Michel Sadelain's lab and others where they have made a molecule that may work as a CAR T
cell that would then bind to NY - ESO - 1 peptides displayed on the
surface of a
tumor cell.
The serologically unique
cell surface antigen of Zajdela ascitic hepatoma is also its
tumor - associated transplantation antigen.
Once the sensors have traveled into a
tumor's leaky blood vessels, they use special targeting molecules to bind to receptors on the
surface of blood vessel
cells.
Gold nanotubes engineered to a specified length, modified
surfaces, and to have other desirable characteristics showed expected abilities to enter
tumor cells in laboratory studies, and to distribute to tissues within live mice as intended.
Further research uncovered a broad spectrum of
cell surface stem
cell markers (e.g., CD133, CD44, and CD24) that allow the identification of CSCs in human solid
tumors, including brain, breast, prostate, pancreas, liver, ovary, skin, colon cancers, and melanoma (3 - 6)(Figure 1 based on 7).
Specifically, they analyzed the
tumors» epigenome, an array of molecules that covers the
surface of DNA and helps regulate gene activity, acting like a control switch to decide which genes are active or inactive in the
cell.
Recently, there has been progress in the treatment of patients with malignancy through targeting receptors on the
surface of CD8 + T
cells that inhibit their activity within the highly suppressive
tumor microenvironment.
Miller said that other proteins anchored to the
cell surface in a similar fashion are known to play roles in
cell proliferation, suggesting a possible mechanism for how HYAL2 might be involved in
tumor formation.
Igaki identified the ligand Sas and the receptor - type tyrosine phosphatase PTP10D as the
cell -
surface ligand - receptor system that drives
tumor - suppressive
cell competition.
Through a genetic screen in Drosophila, Igaki identified the ligand Sas and the receptor - type tyrosine phosphatase PTP10D as the
cell -
surface ligand - receptor system that drives
tumor - suppressive
cell competition.
By means of a non-obese diabetic / severe combined immunodeficiency disease (NOD / SCID) xenotransplant assay in combination with specific
cell surface markers (CD44 + CD24 - / low), CSCs were enriched from metastatic and primary breast
tumors and were shown to have the ability to reestablish
tumor heterogeneity after transplantation [1].
From there they showed that cancer
cells had lost structural polarity, resulting in random distribution of CAR receptors on their
surface, thereby allowing the virus to attach to and infect the
tumor cells.
We have invented new biomaterial
surfaces based on natural halloysite nanotubes, that capture rare circulating
tumor cells (CTCs) from blood while simultaneously repelling white blood
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.
Metastatic
tumors develop when cancer
cells spread from another area of cancer by breaking away from the primary
tumor and traveling through the body by way of the blood, lymphatic vessels or membranous
surfaces.
Most of these CSCs have been identified using
surface markers that identify their corresponding normal tissue stem and progenitor
cells, thus reinforcing the resemblance of
tumor development to normal organogenesis.
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.