After confirming in mouse models that cells from HER2 - positive breast cancers became resistant to anti-HER2 treatment when implanted into the brain but not into other tissues, the investigators found that HER3 is overexpressed in brain metastases of HER2 - positive breast cancers from
both mice and human patients.
This is the finding of a study in both
mice and human patients led by researchers at NYU Langone Medical Center and published online June 9 in the journal Cell.
Not exact matches
To better understand their findings, the team examined the animal model for APS1 (i.e.
mice with the same genetic defect as
human patients with the syndrome)
and found that male
mice spontaneously developed an inflammatory disease in their prostate glands — a so - called prostatitis —
and reacted to transglutaminase 4.
In the brain, his FFI
mice develop neuronal loss in the thalamus
and his CJD
mice experience spongiosis in the hippocampus
and the cerebellum, reflecting the damage seen in the brains of
human patients.
It works in cell studies
and in
mouse studies, but so far has proved frustratingly ineffective in
human patients.
Currently, Deng's laboratory is conducting additional preclinical studies using the
human - derived stem cells from Down syndrome
patients and mouse models to determine whether cellular
and behavioral abnormalities can be improved with minocycline therapy
and other candidate drugs.
In addition to looking at
mouse models of diabetes, the researchers also showed that exposure of
human pancreatic islet cells — both from healthy donors
and from
patients with Type 1 diabetes — to fasting - mimicking diet in a dish stimulated insulin production.
By promoting DNA demethylation, high - dose vitamin C treatment induced stem cells to mature,
and also suppressed the growth of leukemia cancer stem cells from
human patients implanted in
mice.
Many PD
patients typically show an increase in anxiety
and depression,
and in this respect the SNCA
mouse model did not replicate the
human condition.
Researchers have isolated exosomes from tumors
and from blood of
patients with breast cancer,
and from blood of
mice with
human tumors grown after breast implantation in
mice, called ortoxenogratfs.
This take on Michelangelo's famous Sistine Chapel image symbolizes the link between
human pain
patients and the
mouse model: The lab - designed SPR inhibitor (in green), shown within the active pocket of SPR itself (in gray with its atomic structure in colored lines), is the «bridge» between the two species.
The authors said that this result suggests that the reason bacterial numbers are so high in these
mice,
and, by extension,
human LAD
patients, is not because of a defect in the immune system's surveillance mechanism but because of the inflammation caused by the immune system's abnormal response to normal levels of bacteria in the gums.
By assessing the survival of the cells that engulf the particles
and measuring the levels of red or green light that they emitted, the researchers determined which formulation of particles performed best, then tested that formulation in
mice with
human brain cancer derived from their
patients.
They waited until
mice had had an EAE attack, akin to a flare - up of MS in
human patients,
and then administered Del - 1.
They created inflammation in the temporomandibular joints of the
mice,
and then measured bite force exerted by the
mice to assess jaw inflammation
and pain, similar to how TMJD pain is gauged in
human patients.
«These results are especially exciting because they show that we can take findings in the
mouse and possibly apply them at the
human patient population,» said Koenig.
Just as the technique restored kidney, muscle,
and insulin - producing function in the
mouse models, he sees a future for rejuvenating neuronal populations, maybe even one day in
human patients.
Hair thinning in a
human patient and mouse with inherited loss of function mutations in WNT10A is shown.
«Our studies took us back
and forth between
human patients and our
mouse model,» said Millar.
The researchers are now testing this approach in
mice,
and they envision that eventually the technology could be adapted to deliver the CRISPR components to treat infections or remove other unwanted bacteria in
human patients.
BMT was effective in
mice, but in
humans resulted in death before the new bone marrow grew
and expanded (called engraftment) in treated
patients.
The goal of the study was to explore whether fecal microbiota from
human IBS
patients with diarrhea has the ability to influence gut
and brain function in recipient
mice.
The new study — published October 18, 2016 in the journal Molecular Psychiatry — combined genetic analysis of more than 9,000
human psychiatric
patients with brain imaging, electrophysiology,
and pharmacological experiments in mutant
mice to suggest that mutations in the gene DIXDC1 may act as a general risk factor for psychiatric disease by interfering with the way the brain regulates connections between neurons.
In his current position at The Jackson Laboratory, he has overall responsibility for the ongoing operational development of the PDX resource, which generates, banks,
and distributes
patient - derived xenograft (PDX)
mouse models of
human cancers.
Though the findings were made in
mice, not
humans, the researchers say the crucial role of calcium may help explain another mystery: Why some hospital
patients and nursing home residents have a much higher risk of contracting C. diff infections
and the resulting diarrhea that carries its spores out of the body.
Tests in
mice and nonhuman primates had shown TGN1412 to be safe, but when it was injected into
humans — in a dose less than 1/500 of what was given to monkeys — it caused a massive release of infection - fighting T cells that overstimulated the
patients» immune systems, resulting in multiple organ failure.
The cells exhibited many functions associated with tumor progression; their presence within
mouse tumors substantially accelerated cancer growth,
and in
human lung tumors, a SiglecFhigh neutrophil signature was associated with poor
patient survival.
Extracts from the brains of FFI
patients transmitted disease to transgenic
mice expressing a chimeric
human -
mouse PrP gene about 200 days after inoculation
and induced formation of the 19 - kilodalton PrPSc fragment, whereas extracts from the brains of familial
and sporadic Creutzfeldt - Jakob disease
patients produced the 21 - kilodalton PrPSc fragment in these
mice.
Previous studies have shown the drug to be effective at spurring new bone growth in
mice and in
humans with osteoporosis,
and a U-M research team believes that it may spur new growth in brittle bone disease
patients as well.
Further testing found these
mice had lower - than - expected growth hormone
and insulin - like growth factor (IGF1) levels in the blood, potentially explaining the small stature
and delayed development seen in
human patients.
And while we successfully demonstrated that cardiolipin can improve the function of mitochondria in flies, mouse models and in human cells, we need to explore its effects in actual patients.&raq
And while we successfully demonstrated that cardiolipin can improve the function of mitochondria in flies,
mouse models
and in human cells, we need to explore its effects in actual patients.&raq
and in
human cells, we need to explore its effects in actual
patients.»
«More research is needed to evaluate the efficacy of this use of a cancer medication to alleviate risk of sudden cardiac death, but we are hopeful that what we observed in
mice will translate effectively to
humans, providing
patients and clinicians with a new paradigm for treating this common
and life - threatening illness,» Dudley said.
The researchers grafted breast or lung tumors in
mice, allowed the tumors to grow to small size
and removed these tumors surgically — essentially mimicking the situation in a
human tumor
patient in which the tumor is surgically removed as soon as possible after diagnosis.
The work highlights a previously unrecognized molecular pathway that contributes to the malfunction of insulin - producing pancreatic beta cells in T1D in
human patients and in
mice,
and shows that a chemical intervention can help beta cells function properly
and survive.
«If the
mouse models are indicative of
human disease, the combination therapy can increase the proportion of
patients who respond to therapy without additional adverse side effects
and can improve the quality of life for cancer
patients.»
Findings made in animal models do not always translate to
patients, but it appears that this important eye vessel functions very similarly in
mice and humans.
As a next step, Guha, Avadhani
and colleagues plan to extend this study to in vivo
mouse models
and will also investigate these mechanisms in tumor samples from
human breast cancer
patients.
The researchers studied tumour tissue from
patients, cultivated
human tumour cells
and tumours in
mouse models for neuroblastoma.
The
mice show many of the symptoms that
human patients do,
and so they were an especially good candidate to test iPS cells» abilities, says stem cell researcher Rudolf Jaenisch of the Whitehead Institute for Biomedical Research
and the Massachusetts Institute of Technology, both in Cambridge, who collaborated with Townes on the project.
North says his group has already generated a
human chimeric form of MAG - 1 that is equally effective as
mouse MAG - 1,
and they are now generating a humanized form for use in
patients.
For all panels, n = 53
mice per genotype, 28
patients with MCI - AD,
and 89
human controls.
Next steps include He's collaboration with Piedmont Atlanta Hospital to retrieve T cells, liver cancer cells
and healthy tissue normally removed from
patients during surgery, put the
mouse receptor genes on these T cells
and monitor in a dish both how those cells now fight the tumor
and react to healthy
human tissue.
In all analyses, n = 53
mice per genotype, 28
patients with MCI - AD,
and 89
human controls.
In their new paper in Journal of Immunology, Mandy Ford, Craig Coopersmith
and colleagues show that 2B4 levels are increased on certain types of T cells (CD4 + memory cells) in
human sepsis
patients and in a
mouse model of sepsis called CLP (cecal ligation + puncture).
Despite overexpression of mRNA from the XpdTTD allele relative to the wt allele (Figure 1E), TFIIH protein levels were reduced by 50 % in primary
mouse XpdTTD / TTD fibroblasts (Figure 4E
and 4F), thereby mimicking the situation in
human patients with TTD.
Of the 22
patients whose tumors successfully grafted, six died before data from the
mice were available, but in 13 of the remaining 16 cases, there was a positive correlation between
mouse and human results.2 In a second study, performed in collaboration with Manuel Hidalgo of the Spanish National Cancer Research Center, the team found that 6 of 13
patients with advanced solid tumors who were treated based on results from personalized PDX
mice had partial tumor remissions, even in cases where genetic sequencing of the tumor showed no actionable mutations.3
And, while the genetically - modified mice were made somewhat better by deactivating the HD gene in their hypothalamus, this approach isn't useable in human HD patients because their HD genes don't contain the sequences needed to turn them off with virus used by Petersen and colleagu
And, while the genetically - modified
mice were made somewhat better by deactivating the HD gene in their hypothalamus, this approach isn't useable in
human HD
patients because their HD genes don't contain the sequences needed to turn them off with virus used by Petersen
and colleagu
and colleagues.
They then examined the effect of a chemical that inhibits SRF
and found that glucose uptake rates increased in both
mice and human cells —
and that the effects were greater in cells from
patients who were insulin resistant or had type 2 diabetes.
Fleming researchers, using a Spondyloarthritis (SpA)
mouse model have found that Tnfr2 signaling is regulating polyarthritis
and a newly identified heart valve stenosis, which is a common comorbidity of SpA in
human patients.
A very large number of changes have been discovered in HD model
mice and then subsequently observed in
human HD
patients, suggesting the
mice are useful research tools, even if they don't really have Huntington's disease.