Not exact matches
Immunotherapy differs
from more traditional cancer treatments, such as surgery (cutting malignant cells out of the body), chemotherapy and radiation (poisoning the deadly mutants), and even the newer, more precise molecular drugs that attempt to jam the
protein signals that tell
tumor cells to keep dividing and conquering.
Chicago, GenomeWeb — A new study by researchers
from Memorial Sloan Kettering Cancer Center has demonstrated the predictive power of an AR - V7
protein expression test using Epic Sciences» non-EPCAM-based circulating
tumor cell detection platform, which could help guide treatment decisions for men with metastatic castration - resistant prostate cancer.
We examined COX - 2
protein abundance in
tumors extracted
from mouse skin.
Both TRPV1 / WT and KO mice treated with capsaicin and TPA together exhibited higher COX - 2
protein levels than groups treated with TPA alone (Fig. 2A), and
tumors from TRPV1 / KO mice expressed the highest level of COX - 2 as a result of treatment with capsaicin and TPA together (Fig. 2A).
Researchers at NYU School of Medicine found that the value of the drug infliximab, marketed as Remicade, in both applications proceeds
from its ability to block the contribution of the
protein tumor - necrosis factor alpha, or TNF alpha, to problem - causing inflammation.
«We're interrogating the
tumor microenvironment,» she says, «by looking at suppressive cues as well as cells and secreted
proteins that protect
tumors from the immune response.»
«We found that fat cells
from obese or morbidly obese patients secreted a high amount of inflammatory
proteins, which contributed to
tumor progression,» DeCicco - Skinner said.
That gene's
protein usually holds immune cells back
from attacking
tumors.
Along with finding that the
tumor suppressor
protein SIRT6 is inactive in around 30 percent of cases of pancreatic ductal adenocarcinoma (PDAC), the team identified the precise pathway by which SIRT6 suppresses PDAC development, a mechanism different
from the way it suppresses colorectal cancer.
Researchers
from the «Angiogenesis signaling pathways» research group of the Institute of Biomedical Investigation of Bellvitge (IDIBELL), led by Dr. Mariona Graupera, have unveiled the potential therapeutic benefit of a selective inhibitior of the PI3 - kinase (PI3K)
protein in pancreatic neuroendocrine
tumors (PanNETs).
PTEN prevents
tumor cells
from growing uncontrollably, and mutations in the gene encoding this
protein are commonly found in many different types of cancer.
The team integrated three, complementary gene sequencing approaches to look for mutations in
tumor cells
from SS patients: whole - genome sequencing in six subjects, sequencing of all
protein - coding regions (exomes) in 66 subjects, and comparing variation in the number of copies of all genes across the genome in 80 subjects.
RNA sequencing of both single and clustered CTCs
from breast cancer patients identified several genes expressed at elevated levels in CTC clusters, one of which — a
protein called plakoglobin — also was overexpressed in the primary
tumors of patients with reduced survival.
Damage occurs when metastatic
tumor cells recruit pre-osteoclast cells to the bone and then induce their differentiation into mature bone - degrading cells, which results in the release of
proteins from the bone matrix that promote
tumor cell growth.
To make the vaccine, cancer cells are harvested
from a
tumor after surgery and stripped of their
proteins; then those
proteins are cultured with dendritic cells, a subclass of white blood cells, drawn
from the patient's blood.
One
protein that keeps healthy cells
from behaving this way is a
tumor suppressor named p53.
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 team of medical and engineering researchers at The Ohio State University previously determined that modifying a single gene to reduce this
protein's level in breast cancer cells lowered the cells» ability to migrate away
from the
tumor site.
For the CRISPR trial, a UPenn - led team wants to remove T cells
from patients and use a harmless virus to give the cells a receptor for NY - ESO - 1, a
protein that is often present on certain
tumors but not on most healthy cells.
When the
protein is present, these cells that start out round and stuck together in a pattern resembling cobblestones become irregularly shaped and tend to detach
from the
tumor site in an uncoordinated way — hallmarks of metastasis.
The researchers next will turn to analyzing the presence of myoferlin in samples
from numerous human
tumor types available in an Ohio State tissue bank, which will allow them to compare
protein levels in
tumors to clinical outcomes for the patients who provided the samples.
But the cells also changed shape and other properties in the absence of the
protein in ways that reduced the likelihood that they would travel away
from the
tumor — a sign that myoferlin not only changes genes in cancer cells, but also alters the cells» mechanical properties.
Using a fluorescent
protein to detect Rgs16 expression, the investigators found that this gene is induced by pancreatic
tumor formation starting
from its earliest manifestation as ductal neoplasm all the way to advanced solid
tumor in a spatially and temporally coincidental manner.
CAR T cells are T cells that are removed
from a patient, genetically engineered to grow a
protein «sensor» that targets them to
tumor cells, and then re-injected into the patient.
Further research could test these cancer stem cell gene expression at the RNA and
protein level in circulating
tumor cells and biopsies
from patients on trial.
«
From brain
tumors to memory: A very multifunctional
protein.»
Scientists
from the Crick Institute, London and the Hebrew University, Jerusalem, discover a
protein that plays a key role in turning cancer
tumor cells into cancer stem cells that are able to renew outbreaks of the disease
However, many
tumor proteins do not provoke T cells to attack, so T cells must be removed
from the patient and programmed to attack a specific
tumor molecule.
Results showed that
tumor cells containing the
protein carried anywhere
from 10 to 17 times fewer breast stem cells, and
tumors grown
from the injected cells were about three times smaller than those in mice who had received
tumor cells with depleted levels of HOXA5.
Research
from other scientists at Johns Hopkins, he says, had suggested that some
tumors, particularly those that affect the nervous system, have mutations in the ATRX gene, which produces
proteins that appear to maintain the length of telomeres, repetitive segments of DNA on the ends of chromosomes that typically shorten each time a cell divides.
Many of the peptides being tested have been isolated
from proteins that are secreted by
tumors.
Over the past two years, investigators
from the Perelman School of Medicine at the University of Pennsylvania have reported results
from a human trial in GBM using chimeric antigen receptor (CAR) T cell therapy, through which patients» own T cells were engineered to track down and kill cancer cells that express a
tumor - specific
protein known as EGFRvIII.
A better approach, Monje said, would be to develop drugs that specifically block the
tumor - stimulating activities of neuroligin - 3, such as a drug that stops the
protein from being secreted into the area around the cancer cells.
Findings by scientists
from the Max F. Perutz Laboratories (MFPL) of the University of Vienna and the Medical University of Vienna reveal a surprising role for histone deacetylase 1 (HDAC1)-- a member of a family of chromatin modifying
proteins — in the development of skin
tumors.
To confirm that the missing mutations were important for generating an immune response, the researchers cultured a subset of the neoantigen
protein fragments containing the
tumor mutations with immune cells taken
from three patients» blood samples.
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.
A widespread cancer - causing
protein called MYC promotes the growth of
tumor cells in part by ensuring that RNA transcripts are properly spliced, according to latest work
from A * STAR researchers.
«Eliminating endothelial CD146 by conditional knockout in two different mouse models of colitis significantly reduced the severity of inflammation and decreased
tumor incidence and
tumor progression in a mouse model of CAC,» reports lead investigator Xiyun Yan, PhD,
from the Key Laboratory of
Protein and Peptide Pharmaceuticals, Institute of Biophysics, Chinese Academy of Sciences, Beijing.
Studying mice with breast
tumors transplanted
from patients, researchers at Washington University School of Medicine in St. Louis, The Broad Institute of MIT and Harvard, and Baylor College of Medicine have analyzed the
proteins present in these
tumors.
Another reason to prioritize the systematic study of
proteins in
tumors — cancer proteomics — is that the vast majority of cancer therapies developed
from genetic studies actually target
proteins.
She also collected visceral fat tissue
from women undergoing hysterectomies and found that when the fat secretions had more of the FGF2
protein, more of the cells formed cancerous
tumors when transferred into mice.
When researchers at Johns Hopkins University in Baltimore, Maryland, examined
tumor tissue
from the original man with colon cancer who responded to a PD - 1 inhibitor, they found a clue: His
tumor had mutations in «mismatch repair» genes, so - called because their encoded
proteins fix errors in DNA bases when cells replicate their DNA.
VIC - 008 is a fusion
protein combining an immune - activating
protein from the tuberculosis bacteria with a small antibody fragment targeting mesothelin, a
protein expressed in several types of
tumor — including mesothelioma, pancreatic and ovarian cancer.
Berkeley researchers isolated circulating
tumor cells
from the blood of breast cancer patients, then used microscale physics to design a precision test for
protein biomarkers, which are indicators of cancer.
Once settled in the microwell, the circulating
tumor cells were burst open and the
proteins released
from inside each cell were separated according to differences in size or mass.
Pembrolizumab blocks the action of the
tumor - surface
protein PD - 1, which many cancers use to hide themselves
from immune system T cells.
Zhang, who earned an M.D.
from the Peking University Health Science Center in China and a Ph.D.
from the National University of Singapore, was recruited in 2007 to the Texas team that expected to see an increase of brain metastasis when PTEN, a known
tumor - inhibiting
protein, was artificially deleted in a
tumor cell.
-- In silico basic and systems biology: We develop innovative approaches to reverse engineer biological networks
from omics data, model
tumor progression at the genomic, transcriptomic and epigenetic level, automatically annotate new
proteins and functional elements through integration of complex and heterogeneous data, including data obtained
from high - throughput sequencing or time - lapse video - microscopy.
Vincent Brichard, Thomas Wölfel, and Thierry Boon identify the first CTL - defined
tumor antigen derived
from a melanoma differentiation
protein, tyrosinase.
Perform
protein extraction
from tumor tissue or cell pellets, upon request (with additional charge), for use in the reverse phase
protein array studies (see pricing below).