We study the mechanisms by
which tumour cells are immortal and normal cells are mortal.
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.
Not exact matches
Although these spots themselves are harmless, if some of the spots are bigger than a 50 cent coin, then it could be due to Neurofibromatosis (NF),
which is a genetic disorder of the nervous system that causes abnormal
cell growth of nerve tissues or benign
tumours to form on the nerves anywhere in the body at any time.
We also detected circulating
tumour cells,
which were found in higher numbers in patients who had received more prior therapies.
There were no serious side effects — and no sign of
tumours,
which can be a potential risk in stem
cell therapies.
Because such
cells are derived from adult
cells, not pluripotent
cells —
which have the potential to form a kind of
tumour called a teratoma — they might be safer than iPS
cells.
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.
A «Trojan horse» treatment for an aggressive form of brain cancer,
which involves using tiny nanoparticles of gold to kill
tumour cells, has been successfully tested by scientists.
One reason for this is that the
tumour cells invade surrounding, healthy brain tissue,
which makes the surgical removal of the
tumour virtually impossible.
Tumours grow through a process of Darwinian evolution, where cancer
cells develop an advantageous mutation that allows them to survive and multiply, producing a population of
cells which can mutate further.
«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 - Perales.
Devil Facial
Tumour Disease (DFTD) is a rare contagious facial tumour, which emerged from a neural (Schwann) cell in a single Tasmanian devil more than 18 year
Tumour Disease (DFTD) is a rare contagious facial
tumour, which emerged from a neural (Schwann) cell in a single Tasmanian devil more than 18 year
tumour,
which emerged from a neural (Schwann)
cell in a single Tasmanian devil more than 18 years ago.
Within that sting lies a peptide called chlorotoxin,
which has an unusual property — it sticks strongly to
tumour cells while ignoring surrounding healthy tissue, by binding to a cancer - specific protein called matrix metalloproteinase - 2.
Infected individuals however, are constantly exposed to granulin - like proteins secreted by flukes,
which subsequently cause host
cells to proliferate uncontrollably, leading to
tumour growth.
This would then use the protein to recognise a foreign or
tumour cell, attach to it and release the toxin in a high local concentration,
which would cause the death of the
tumour cell.
In research funded by Sparks charity, Great Ormond Street Hospital Children's Charity and Cancer Research UK, researchers at the University of Cambridge have developed a test for blood and cerebrospinal fluid samples that looks for a specific panel of four pieces of short genetic code known as microRNAs,
which are found in greater quantities in malignant germ
cell tumours.
Until now, it was not clear
which form of
cell death is decisive for the development of malignant liver
tumours.
The result is increased
cell growth, also referred to as compensatory proliferation,
which can lead to
tumour development.
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.
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.
Saurabh Saha of BioMed Valley Discoveries in Kansas City, Missouri, and his colleagues wondered whether they could use the bacteria to selectively kill mammalian
cells within cancerous
tumours,
which often have a poor blood supply and therefore low oxygen levels.
«Brain metastases are a secondary brain
tumour,
which means they are caused by cancer
cells that escape from primary
tumours like lung, breast or melanoma, and travel to the brain,» said Mohini Singh, the study's primary author and a PhD candidate in biochemistry at the Michael G. DeGroote School of Medicine at McMaster.
To carry out the study, the team has analysed how different carbohydrates act on the surface of silver nanoparticles (Ag - NP) of around 50 nanometres,
which have been introduced into cultures of liver
cells and
tumour cells from the nervous system of mice.
Pembrolizumab works by binding to PD - 1 and blocking the interaction between PD - 1 and its ligands, PD - L1 and PD - L2, thereby activating T lymphocyte
cells which may affect both
tumour cells and healthy
cells.
But at the moment we have to use retroviruses to carry the foreign material into the
cells,
which could generate
tumours.
The experimental drug cediranib blocks the
cell surface receptor VEGF,
which stimulates the growth of new blood vessels to feed the growth of
tumours,» explains study researcher Dr Paul Symonds, of the Department Cancer Studies & Molecular Medicine at the University of Leicester, UK.
The CNIO researchers show that
cell defects caused by the inhibition of Cdh1 are independent of the presence of the p53 molecule,
which is mutated in different types of
tumours.
This bank of living
tumour cells allowed the team to study not only the genetics of the
cells, but also how genetic mutations in the mitochondria —
which drive energy production in the
cell — caused changes in the
cell's metabolism.
To do this, they switched from using dead
tumour cell samples to patient - derived
tumour cell lines, in
which fresh samples of a person's
tumour are grafted onto mice and grown to the required volumes.
This is very important for the
tumour cells which then spread into the surrounding nervous tissue.
Researchers from the University of Portsmouth's Brain
Tumour Research Centre of Excellence have identified molecules
which are responsible for metastatic lung cancer
cells binding to blood vessels in the brain.
Using genetic tools to establish in
which cells cancer - driving mutations originated and then propagated into other cancer
cells, they demonstrated that a distinct and rare subset of MDS
cells showed all the hallmarks of cancer stem
cells, and that no other malignant MDS
cells were able to propagate the
tumour.
While it is present on a number of different types of
cells in the body, it is expressed at higher levels on metastatic
tumour cells, including those
which have spread from the lung.
The TGF beta - 1 was produced by the stromal fibroblasts
which surrounded the
tumour cells.
Cancer stem
cells,
which fuel the growth of fatal
tumours, can be knocked out by a one - two combination of antibiotics and Vitamin C in a new experimental strategy, published by researchers at the University of Salford, UK.
Also characteristics of
tumour cells such as a protein
which is too abundant in the
cell envelope are called antigens.
Using a CRISPR - dCas9 epigenetic editing tool, the researchers methylated different genes in healthy breast
cells and found that those changes were sufficient to cause the
cells to undergo «hyperproliferation» — abnormally rapid
cell division
which is an early stage of
tumour initiation.
The study,
which is published in the journal Nature Communications, was conducted on human
tumour cells and on mice, and offers hope of a much improved therapy for a severe form of cancer.
The team plans to test the approach in a clinical trial in
which chemotherapy drug selection for each person will be guided by testing balls of their
tumour cells in the lab.
They sequenced the complete genomes of multiple regions in each
tumour and looked at
which mutations were present in all
cells and all regions of each
tumour, and
which were present in just some.
For cancer, he hopes to adopt a similar approach in
which the transplanted nodes will contain T
cells trained to hunt down the antigens produced by
tumour cells and kill them off.
There were no serious side effects — and no sign of
tumours,
which can be a risk in stem
cell - based therapies.
«This is because the stress led to poor function against the cancer by T -
cells,
which are very important in the immune system's control and surveillance of
tumours and are a major target in many immunotherapy treatments.»
The immune system also includes natural killer
cells (NK
cells),
which recognize and eliminate
tumour or virus - infected
cells.
For example, a gene called p53,
which normally acts as a brake on
cell division, turns out to be mutated or lost in about half of all
tumours.
That's the new picture emerging from recent studies,
which suggest that a small number of stem -
cell - like
cells within
tumours give rise to all the rest of the cancerous
cells.
The virus, code - named JX - 954, targets two genes involved in cancer
cell growth and blood supply,
which show increased activity in
tumours.
Scientists have identified for the first time the «
cell of origin» — in other words, the first
cell from
which the cancer grows — in basal
cell carcinoma, the most common form of skin cancer, and followed the chain of events that lead to the growth of these invasive
tumours.