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.
Not exact matches
HBI member V. Wee Yong, PhD and research associate Susobhan Sarkar, PhD, and their team including researchers from the Department of Clinical Neurosciences and the university's Southern Alberta Cancer Research Institute, looked at
human brain
tumor samples and discovered that specialized immune cells in brain
tumor patients are compromised.
While nivolumab improved survival rates in the overall study population, it appeared to be most successful in
patients whose
tumors were positive for the
human papillomavirus (HPV).
Human tumor cells (red) growing in a zebrafish embryo may help doctors choose how to treat cancer
patients.
Pancreatic
tumors taken from
human patients also carried the enzyme - producing bacteria.
The group examined over 100
human pancreatic
tumors to show that these particular bacteria with long CDD do live in the
patient's pancreatic
tumors.
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.
The common pathway found in mouse models was also found in
human tumors, suggesting that resistance could indeed be blocked in
patients with the same drug as in mice.
To that end, in collaboration with the University of Zurich and MD Anderson Cancer Center, the researchers tested melanoma
tumor samples from
human patients undergoing treatment with the same targeted therapies.
The first - in -
human PET / CT imaging of 75
patients with 18F - MPG was performed to show that this tracer can be used as a companion diagnostic to identify NSCLC
patients with EGFR activating mutant
tumors (primary
tumor or metastatic) with 84.3 % accuracy.
They found out that TiY is capable of distinguishing TICs from non-TICs in various
human lung cancer cell lines and
patient - derived lung
tumors.
Desgrosellier said the team will follow up with mouse models containing
tumor fragments from
patients to better reflect the diversity of cell types present in
human disease.
Horvath and Tell's research is the first reported study to compare breast cancer subtypes and gene expression patterns associated with STAT3 in the
tumors of
human patients.
«The next step is to test
tumors from more
human patients and see how the results compare to the response that the
patients have to chemotherapy,» said Walsh.
In order to test their hypothesis in a model that more closely mimicked
human disease, the researchers also tested the two drugs side - by - side on slices of
tumors removed from
patients during radical prostatectomy.
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.
To see if PGD and the pentose phosphate pathway were tied to the epigenetic changes the researchers had detected in distant metastases, they treated
tumor cells from different sites in a single
patient with the drug 6 - aminonicotinamide (6AN), which is known to inhibit PGD but is not used in
humans because of its severe side effects.
Now he and his team are putting cells from
human brain
tumors into the organoids, which have reached the level of development and complexity of a 20 - week - old
human fetus's, to see whether they reprise what happens in
patients.
Nagrath, director of Rice's Laboratory for Systems Biology of
Human Diseases, said the new metabolic analysis indicates that ovarian cancer may be susceptible to multidrug cocktails, particularly if the amounts of the drugs can be tailored to match the metabolic profile of a
patient's
tumor.
«By helping us understand that lower levels of RNF125 confer resistance to BRAF inhibitors, we have a new strategy to stratify
patients for currently approved therapy versus participation for
human clinical trials to investigate whether targeting JAK1 will be more effective in
patients whose
tumors exhibit reduced RNF125,» said Keith T. Flaherty, M.D., associate professor, Harvard Medical School, and director of Developmental Therapeutics, Cancer Center, Massachusetts General Hospital, and co-author of the study.
These are two pathways that are very commonly mutated in
human tumors, and we try to understand where those pathways are mutated, which type of
tumors, what are the mutations that co-occur with mutations in those pathways; and try to understand, if we try to inhibit those pathways, what can we expect in
patients.
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.
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.
Researchers from Uppsala University, Sweden, and the Broad Institute, USA, have identified both similarities and differences between a single
tumor type in multiple dogs breeds; a finding they believe parallels the situation in the cancer of
human patients.
But a new study of dogs with
tumors — as well as one
human cancer
patient — reveals that injecting certain bacteria directly into the growths can shrink or even eliminate them.
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.
Palanichamy, Chakravarti and their colleagues conducted this study using 13 primary GBM cell lines derived from
patient tumors, four commercially available GBM cell lines and normal
human astrocyte cells.
Past clinical trials of stem cell therapies for chronic stroke
patients used cells derived from
tumors in
humans and brain tissue from fetal pigs.
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 a 1988 paper summarizing his findings, Fiebig concluded that xenograft mice were wonderful models for broadly testing new drugs against
human tumors, but they «can not be used as a clinical routine method» for predicting
patient treatment.1 The idea of using xenograft mice as personal avatars for cancer
patients was discarded.
Using 80 of the successful
tumor xenografts — from the Greek «xenos» meaning «foreign» — he compared how the mouse's
tumor responded to a drug or drug combination with the treatment response of the corresponding
human patient.
A team of researchers led by Caltech scientists has shown that nanoparticles can function to target
tumors while avoiding adjacent healthy tissue in
human cancer
patients.
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
In the study, Davis and his colleagues examined gastric
tumors from nine
human patients both before and after infusion with a drug — camptothecin — that was chemically bound to nanoparticles about 30 nanometers in size.
An Open Label, Phase II Study of Neratinib in
Patients with Solid
Tumors with Somatic
Human Epidermal Growth Factor Receptor (EGFR, HER2, HER3) Mutations or EGFR Gene Amplification
These days, mice grafted with
human tumors, known as
patient - derived xenograft (PDX) mice, are common in cancer research laboratories.
NCI's efforts to develop new laboratory models of
human cancer includes vastly increasing the number of
human cancer cell lines (grown as two - dimensional and three - dimensional cultures) and
patient - derived
tumor xenografts.
Secondly, before considering the use of iPSC - derived organoids for transplantation / regenerative medicine in
human patients, the current protocols for expansion, reprogramming and differentiation of iPSCs in long - term cultures need further improvement to minimize the risk of oncogenic cellular mutations and teratoma, or
tumor formation, in the
patient.
Zebrafish larvae transplanted with
patients»
tumors respond as their
human donors do to chemotherapy.
Immunoblot analysis using mouse monoclonal antibody to
human IgM detected IgM to cytomegalovirus (CMV)- specific proteins (150, 42, 38, 32, and 28 kDa) in 74 (38 %) of 197 seropositive serum samples from 197 individuals in three subject groups: 43 surgical
patients, 31
patients with solid
tumors, and 123 healthy individuals.
These kind of mice are an extraordinary resource for modeling
human disease; for instance, research has found that mice that are genetically mutated to carry the BRCA1 gene (a
human breast cancer gene) behave more similarly to
human cancer
patients than those mice who have had a
tumor physically transplanted in.
His analysis of all publicly available cancer mutations and integration with all solved computational models of
human proteins has created a powerful roadmap for evaluating new mutations observed in
patient tumors.
Like doctors who have been using VR to assist in surgeries and pinpoint ailments — by generating 3D models of real
patient tumors from MRI scans, for example — science teachers are saying VR can help deepen understanding of subjects such as biology and anatomy, which require students to grasp the inner workings of cells and organs that are not visible to the
human eye.
The Gerson Institute in southern California has been using this premium calcium montmorillinite to treat
human cancer
patients with internal
tumors successfully.
With its internationally renowned school of veterinary medicine and its NCI - designated
human cancer center, UC Davis is uniquely positioned to evaluate novel treatments for companion dogs with spontaneous
tumors that may ultimately be effective in
human patients with cancer.