This effect
on cell survival was not endothelial cell - specific, since IC50 values for kahweol treatment of several human tumoral cell lines were similar to those obtained for HUVEC (results not shown).
Zinc finger nuclease mediated knockout of ADP - dependent glucokinase in cancer cell lines: effects
on cell survival and mitochondrial oxidative metabolism.
GLP - 1 receptors are also found in the brain, and prior research has shown that activating them can boost the function of dopamine connections, act as an anti-inflammatory, improve energy production, and switch
on cell survival signals.
Not exact matches
Boldrini says that future research
on the aging brain will continue to explore how neural
cell proliferation, maturation, and
survival are regulated by hormones, transcription factors, and other inter-cellular pathways.
Cancers associated with Kaposi virus infection have an Achilles heel: their
cells» viability is directly dependent
on the
survival of the virus, which means that if the virus were to be eliminated cancer
cells would no longer proliferate, hence the cancer would be cured.
The receptor is often expressed
on epithelial
cells, the type of
cells that turn cancerous, and it promotes
cell survival.
The idea to specifically study this group of patients was based
on groundbreaking research Garon published in the New England Journal of Medicine last year, which found that among patients who received pembrolizumab, those with PD - L1 expression
on at least 50 percent of their cancer
cells showed the longest
survival and disease control.
The researchers then found that, while the drug continued to inhibit FGFR activity in the resistant
cells, its inhibition of FGFR signaling had no appreciable effect
on the
cells»
survival.
The creations had stored well at refrigerated temperatures and circulated in the body with
survival time
on par with that of original red
cells.
This mutation is
on a particular receptor, or docking site,
on the cancer
cells that is crucial to the
cell's growth and
survival.
The investigators utilized a targeting method called RNA interference (RNAi) which, when delivered via these natural nanoparticles or exosomes, zero in
on mutant KRAS in pancreas cancer
cells, impacting tumor burden and
survival in multiple pancreas cancer models.
PARP inhibitors target and block proteins which cancer
cells depend
on to repair DNA for their
survival.
Versions of ZMYND11 that could not bind to the trimethyl group
on H3.3 did not suppress cancer
cell growth or
survival.
When BRCA1 is mutated, ANG1 switches
on, new blood vessels are formed, and cancer
cells get the nutrients critical to their
survival.
A multicenter team of researchers reports that a full genomic analysis of tumor samples from a small number of people who died of pancreatic cancer suggests that chemical changes to DNA that do not affect the DNA sequence itself yet control how it operates confer
survival advantages
on subsets of pancreatic cancer
cells.
Combining their strategy with an existing immunotherapy treatment that works by releasing the «brakes»
on immune
cells, they found they could shrink melanoma tumors, and prolong
survival in preclinical models for melanoma.
Inglis attributes this success to the fact that the bacteriocin targets a receptor
on the bacteria's
cell surface that is essential to its
survival.
In particular, his laboratory focuses
on the regulation of key signaling networks that regulate cancer
cell growth and
survival.
In a four - year study conducted
on the mouse model in advanced breast cancer metastasis in the eye's anterior chamber, Petty and colleagues found that the new nanoparticle not only killed tumor
cells in the eye, but also extended the
survival of experimental mice bearing 4T1 tumors, a
cell line that is extremely difficult to kill.
Firstly, salt stress causes a delay in
cell division, leading to synchronization of
cell cycles; secondly,
survival probability depends
on the individual bacterial
cell's position in the
cell cycle at the time of the second exposure.
«The research showed that the aggressive form of basal breast cancer
cells may be dependent
on PLK4 for
survival and that depleting it induced
cell death,» says Dr. Mak.
But in individual
cells this effect is short - lived: after just 30 minutes, the
survival rate no longer depends
on the exposure history.
The Italian researcher faced prejudice and adversity as a woman and as a Jew, but went
on to elucidate a growth factor essential to the
survival of nerve
cells
«We're finding that leader and follower
cells have a symbiotic relationship and depend
on each for
survival and invasion,» he says.
The
cells»
survival relies
on a delicate balance between energy and reactive oxygen species (ROS) production.
Professor Ahmed and his team have identified how cancer
cells rely
on a process called NMD for their
survival.
«It appears that one or more of these proteins, either within the bacterial
cell envelope or
on its surface, are essential to its growth and
survival.
He managed to switch
on a
survival mode in bone
cells by inactivating the oxygen sensor PHD2 before implantation.
Matthew Paszek, assistant professor of chemical and biomolecular engineering at Cornell and Valerie Weaver, at the University of California, San Francisco, led the study
on glycoprotein - induced cancer
cell survival, published online in Nature.
A new study by a Cornell University researcher found this coating is especially thick and pronounced
on cancer
cells and is a crucial determinant of the
cell's
survival.
«This shows that the antibody not only can exert pressure
on the virus, but also can shorten the
survival of infected
cells,» says first author Ching - Lan Lu, a visiting student in Dr. Nussenzweig's lab.
Once the elongating fibers have established the appropriate synaptic contacts with the target
cells, the continued
survival of the innervating
cells in the ganglion appears to depend
on the availability of NGF.
The strategy of giving a higher proportion of plasma is based
on the belief that maintaining the balance of coagulation factors carried in plasma would reduce the overall amount of bleeding, requiring lower amounts of red blood
cells and improving
survival.
Based
on analyses of over 600 drug and breast cancer
cell pairings, researchers showed that, for some
cells, drug exposure can cause significant changes in gene expression — indicating the successful action of a drug
on its target — without affecting
cell growth or
survival.
Matthew Paszek, assistant professor of chemical and biomolecular engineering, led the study
on glycoprotein - induced cancer
cell survival, published online in Nature June 25.
Because cancer
cells acquire mutations in oncogenes — genes that can transform
cells into cancer
cells — to support their growth and
survival, a great deal of research has focused
on identifying oncogenes that could be targeted by cancer drugs.
Highly dependent
on their estrogen receptors for growth and
survival, these tumor
cells are sensitive to hormonal therapies, making drugs like tamoxifen and fulvestrant effective first - line therapies for many patients.
Thus, CXCR4 disruption had no impact
on cell viability, but conferred a significant
survival advantage in the presence of HIV strains that can use CXCR4 to infect
cells.
According to Whitehead Institute researchers, protein production or translation is tightly coupled to a highly conserved stress response — the heat shock response and its primary regulator, heat shock factor 1 (HSF1)-- that cancer
cells rely
on for
survival and proliferation.
That is why loss of autophagy in regulatory T
cells produces a two-fold effect
on both
survival and stability.»
Exon - Based Transcriptome Profiling Reveals Genes That Have Prognostic Impact
on the
Survival of Young High Risk Diffuse Large B -
Cell / Follicular Grade 3 Lymphoma Patients Treated with Dose - Dense Chemoimmuno - therapy and CNS Prophylaxis.
A national study
on conditional
survival, excess mortality and second cancer after high dose therapy with autologous stem
cell transplantation for non-Hodgkin lymphoma.
CAMBRIDGE, Mass. — Protein production or translation is tightly coupled to a highly conserved stress response that cancer
cells rely
on for
survival and proliferation, according to Whitehead Institute researchers.
Thus, treatment with X4 - ZFNs of both wild - type and ccr5Δ32 CD4 + T
cells confers stable cxcr4 disruption and a marked
survival advantage in the presence of R5X4 - HIV and X4 - HIV in vitro without any detectable effect
on cell growth or viability in the absence of HIV.
Thus, the
survival of XpdTTD / † XPCS (and XpdTTD / † XP)
cells likely represents a level of UV resistance that neither mutant allele can impart
on its own (Table 2).
The influence of the src - family kinases, Lck and Fyn,
on T
cell differentiation,
survival and activation.
Dr. Tu's research focuses
on the metabolic state of
cells and responses to conditions that induce or halt
cell division to promote
survival and homeostasis.
Thus, the improved UV
survival observed in compound heterozygote
cells (Figure 4A) and likely the rescue of TTD progeroid symptoms (Figure 3) were not due to normalisation of TFIIH levels, suggesting a qualitative rather than a quantitative effect
on these phenotypes in vivo.
Thirdly, the current, almost universal dependency of organoid culture
on the use of Matrigel as a replacement for the function of the extracellular basement matrix in providing structural support and
survival signals to the epithelial
cells hampers clinical application, considering its origin from a mouse sarcoma
cell line, its poorly defined composition and its mechanical rigidity after plating.
They found out that pre-organ transplant infusion of MSC in 1 or 2 doses [
on day - 7 and day - 1] induced a profound T
cell hyporesponsiveness and prolonged B6C3 cardiac allograft
survival.