Jeffrey Settleman of the Massachusetts General Hospital Cancer Center in Charlestown and his colleagues treated
tumour cells with cancer drugs.
The researchers concluded that patients with circulating
tumour cells with more N - terminals than C - terminals had the androgen receptor variants.
Not exact matches
When placed at the site of a cancerous
tumour in a rodent and «activated» by a scope
with a light source, the compounds eradicated up to 100 % of cancer
cells.
«Recent data have shown that a variant of the androgen receptor called AR - V7, found in
tumour cells circulating in the blood of patients
with metastatic CRPC, predicted resistance to treatment
with enzalutamide and abiraterone,» she will say.
After 16 days, mice injected
with the
tumour - specific Th17
cells had barely detectable
tumours, compared
with mice injected
with tumour cells alone.
Molecular characterization of the
cells that undergo
cell fate transition upon oncogenic Pik3ca expression demonstrated a profound oncogene - induced reprogramming of these newly formed
cells and identified gene expression signatures, characteristic of the different
cell fate switches, which was predictive of the cancer
cell of origin,
tumour type and clinical outcomes in women
with breast cancers.
Approximately one year after successful treatment
with cytotoxic chemotherapy and radiotherapy, patients
with advanced Small
Cell Lung Cancer (SCLC), which primarily affects heavy smokers, generally relapse
with recurrence of
tumours that are resistant to further chemotherapy.
These results were facilitated by the permanent cultivation of circulating
tumour cells of patients
with advanced SCLC in Vienna.
Cancer stem - like
cells are thought to be the root cause of chemotherapy resistance, leading to treatment failure in patients
with advanced disease and the triggers of
tumour recurrence and metastasis (regrowth).
The Lund University research team has looked at how cancer
cells communicate
with surrounding
cells and how this encourages the development of malignant
tumours.
«
With this breakthrough it is possible to generate cell models with the same alterations as observed in tumour cells from patients, which will allow us to study their role in tumour development,» says CNIO researcher Sandra Rodríguez - Pera
With this breakthrough it is possible to generate
cell models
with the same alterations as observed in tumour cells from patients, which will allow us to study their role in tumour development,» says CNIO researcher Sandra Rodríguez - Pera
with the same alterations as observed in
tumour cells from patients, which will allow us to study their role in
tumour development,» says CNIO researcher Sandra Rodríguez - Perales.
«Patients
with stage 1 non-seminomatous germ
cell tumours have to make a difficult choice of whether to be watched or to receive chemotherapy to reduce the risk of relapse.
When chlorotoxin is tagged
with a fluorescent dye, it will illuminate a
tumour — a trick that makes the surgeon's job easier by helping to pinpoint cancerous growth and ensure that all the cancerous
cells are removed and healthy tissue spared.
«The study of this type of
tumours has been problematic up to now due to the lack of
cell models and the appropriate animal models,» says CNIC researcher Juan Carlos Ramírez, who adds that the difficulty of generating these chromosomal translocations had limited the availability of
cells with this mark of the disease.
Around 15 per cent of women
with breast cancer have this form of the disease, in which
tumour cells lack the three receptors that most drugs target.
According to Eckmann, «The special thing about these processes is that they involve known molecules
with very long evolutionary histories, previously receiving attention as suppressors of
tumour formation within the context of normal
cell division.
Anne Goriely of the University of Oxford and her colleagues took
tumour cells from men
with benign testicular
tumours and looked for specific mutations in the FGFR3 and HRAS genes.
«We could get some shrinkage of the
tumours with other types of treatment we tried before, but we never got a complete
cell kill,» he says.
Cell lines from human
tumours did exist, but were considered unsafe: what if cancerous
cells were transferred along
with the vaccine?
Now, the researchers have discovered an alternative in a mouse model: in the case of breast
tumours with a specific defect in DNA repair, the animals can be cured using already established, cheap chemotherapy drugs, if enough DNA damage can be inflicted on the resting
tumour cells.
The five year disease - free and overall survival rates for patients
with high - risk malignant germ
cell tumours remains less than 50 %, and so accurate diagnosis and monitoring is crucial to improving outcomes for patients.
The researchers found five different sub-types of HL among the patients studied: 247 cases of the nodular sclerosis (NS) type, in which the
tumour nodules are large; 105 of mixed cellularity, where a mixture of different types of inflammatory
cells are involved; 58 lymphocyte rich, the sub-type
with the best outcome; 68 «others»; and 143 «not otherwise specified» (NOS).
Tumours spread
with the help of enzymes called matrix metalloproteinases (MMPs), which destroy the connective tissue between
cells and organs, allowing
tumour cells to break out of the original site and enter new ones.
Using an approach developed at Maisonneuve - Rosemont, consisting of an autograft to reduce
tumour mass followed by a family allograft three to four months later to clean the bone marrow of myeloma
cells with immune
cells from a family donor (immunotherapy), the study resulted in a total cure rate of 41 %, a record level using this strategy.
Cancer stem
cells are strongly associated
with the growth and recurrence of all cancers and are especially difficult to eradicate
with normal treatment, which also leads to
tumours developing resistance to other types of therapy.
KEYNOTE - 024 investigated the efficacy of pembrolizumab compared to standard of care
with platinum - based chemotherapy in untreated patients
with advanced NSCLC and high PD - L1 expression (defined as expression in at least 50 % of
tumour cells).
Patients
with TILs do much better because they already have cancer - fighting
cells in their
tumours.
Dr Sophie Roerink, joint first author from the Wellcome Sanger Institute, said: «We found mutational processes in these cancer
cells that are just not seen in normal
cells, leading to a huge increase in mutation rate for
tumours compared
with normal
cells.
The research team
with international collaborators analysed more than 100 patient samples from ovarian and other cancer types to discover a distinct population of
cells found in some
tumours.
The team worked on tissue from three patients
with colorectal cancer, taking normal bowel stem
cells and
cells from four different areas of the
tumours.
The discovery could pave the way for new treatments that are able to block
cell signals switched on in
tumours with low levels of PTEN.
This unfortunate and rare side effect of the biopsy provided Nicola Valeri at the Institute of Cancer Research in London and his colleagues
with a kind of stopwatch — an exact point in time when a few
cells left as the needle was withdrawn began their two year evolution into a
tumour.
The researchers, working
with cell cultures, first observed how individual
tumour cells kill specific
cells in the vascular wall, called endothelial
cells.
Professor Geoff Pilkington, study co-author and Head of the Brain
Tumour Research Centre, said: «Although this work is still at an early stage, we have demonstrated key elements that are associated with tumour cell binding to blood vessels and this may provide a target for future drug development to prevent the development of secondary tumours in the
Tumour Research Centre, said: «Although this work is still at an early stage, we have demonstrated key elements that are associated
with tumour cell binding to blood vessels and this may provide a target for future drug development to prevent the development of secondary tumours in the
tumour cell binding to blood vessels and this may provide a target for future drug development to prevent the development of secondary
tumours in the brain.
In collaboration
with Dr Gabriele Bonatz from the Augusta clinics in Bochum (Brustzentrum), Hatt's team confirmed the existence of TRPV1 in
tumour cells in nine different samples from patients suffering from breast cancer.
It could have implications for HIV patients, both
with and without cancer, as it can work on HIV reservoirs and
tumour cells independently.
Therefore, «this finding may represent a future therapeutic strategic to combine
with other strategies, such as immunotherapy, chemotherapy or inhibitors against specific signalling routes of the
tumour cells.»
A team working at the Institute of Cancer Research and the Royal Marsden Hospital in London, in collaboration
with scientists at the National Cancer Institute in Bethesda, Maryland, has found that tamoxifen also works by encouraging the
cells surrounding a
tumour to produce a «growth factor».
When
tumours are treated
with drugs, some resistant cancer
cells can survive and continue to grow, leading to disease relapse.
«The high efficiency of the materials along
with cheap, scalable synthesis makes them very attractive as next generation emitters for fluorescent lamps, LEDs and for biological imaging, for example for highlighting
tumours or
cell division.»
In the mice, the neuron - like
cells did not grow as quickly as the original cancer
cells, and analyses of the
tumour tissue from patients show that those
with a high level of the estrogen receptor have a better survival rate that those
with a low.
When they loaded sperm
cells with doxorubicin, a common chemo agent, and released them in a dish containing mini cervical cancer
tumours, the sperm swam towards the
tumours, killing 87 per cent of their
cells within three days.
This has always been a worry
with tissues produced from embryonic stem
cells, as these have the capability to form
tumours if any are left in their original state in the transplanted tissue.
When cancer
cells interact
with the walls of the blood vessels, EPHA2 is activated and the
tumour cells remain inside the blood vessels.
When they injected the soil bacterium Clostridium [ck] novyi into the bloodstream of mice
with tumours, it spread throughout the necrotic region, consuming living
tumour cells as well as dead tissue.
Directly derived from patient
tumours without any genetic manipulation, these new products provide the assurance of primary
cells with long - term reproducibility and scalability
Discovery of synonymous cancer driver mutations in human
tumours associated
with changes in the splicing of oncogenes (Lehner group,
Cell 2014).
She has worked in prestigious Institutions like the NIH - NCI, Bethesda, Md and the MIT, Cambridge, MA and developed an internationally recognised research profile in
tumour cell migration and invasion
with over 65 publications and 2 patents to her name.
These drugs can be targeted to interfere
with signalling within the
tumour microenvironment or activate other processes which will kill the cancer
cells.
Combining a cancer therapy
with a second drug therapy that helps suppress
tumour blood vessels found in cancer
cells can help to significantly reduce the spread of breast cancer
tumours while also causing cancer
cell death.