It may even be possible to modify
the cancer blood vessel cells to secrete factors that would inhibit cancer cell growth.
Not exact matches
Breast
cancer tumors can fuse with
blood vessel cells, allowing clumps of
cancer cells to break away from the main tumor and ride the bloodstream to other locations in the body, suggests preliminary research.
For over one hundred years, scientists have debated the question of the origins of the lymphatic system — a parallel system to the
blood vessels that serves as a conduit for everything from immune
cells to fat molecules to
cancer cells.
Cancer cells can break away from a primary tumor, penetrate into lymphatic and
blood vessels, circulate through the bloodstream, and grow in a distant focus (metastasize) in normal tissues elsewhere in the body.
The researchers confirmed this hypothesis by showing that if they blocked YAP1 they could inhibit stem
cells from undergoing self - renewal, forming
blood vessel - like structures, and reduce lung
cancer cell growth in mice.
Opioids also may make
blood vessels leaky, making tissues more receptive to
cancer cells looking for places to build a tumor, Moss says.
An experimental drug in early development for aggressive brain tumors can cross the
blood - brain tumor barrier, kill tumor
cells and block the growth of tumor
blood vessels, according to a study led by researchers at the Ohio State University Comprehensive
Cancer Center — Arthur G. James
Cancer Hospital and Richard J. Solove Research Institute (OSUCCC — James).
To seed in the brain, a
cancer cell must dislodge from its tumor of origin, enter the bloodstream, and cross densely packed
blood vessels called the
blood - brain barrier.
Dr. Massagué is particularly interested in the ability of tumor
cells to hug
blood vessels, as he suspects this behavior may be essential for the survival of metastatic
cancer cells not only in the brain but also in other parts of the body where metastatic tumor growth can occur.
Fat
cells cultured from the body mass index of a morbidly obese patient cause multiple myeloma
cells to anchor to a much greater extent than normal
cells and produce a significantly larger number of
blood vessels to sustain the
cancer cells.
When the scientists inserted human colorectal
cancer cells into zebrafish embryos and allowed them to grow for 4 days, the resulting tumors showed three hallmarks of human solid tumors: rapid
cell division, formation of
blood vessels to supply nutrients, and the ability to spread to other locations in the body.
The
cancer cells spread from one place in the body to another, through the
blood vessel.
In this study, we found that chloroquine not only has an effect on the growth of the
cancer cells, but also makes the tumor environment less aggressive by normalizing the abnormal
blood vessels in the tumor,» says Patrizia Agostinis.
As a result, these
blood vessels will be structured more tightly, which can prevent
cancer cells from spreading to other organs.
In other words, the same «old» medicine simultaneously targets the
cancer cells themselves and the
blood vessels with great efficiency.
When BRCA1 is mutated, ANG1 switches on, new
blood vessels are formed, and
cancer cells get the nutrients critical to their survival.
This
blood vessel normalization results in an increased barrier function on the one hand — thereby blocking
cancer cell dissemination and metastasis - and in enhanced tumor perfusion on the other hand, which increases the response of the tumor to chemotherapy.
For the subset of more recent patients, the researchers assessed tumor
cell behavior — in particular,
cancer cells» ability to cross the endothelium (inner layer) of
blood vessels.
They found that besides traveling in the bloodstream, melanoma
cells could also move along the abluminal, or outside, surface of
blood vessels by way of angiotropism, a biological interaction between the
cancer cells and the
blood vessel cells.
With angiotropism and EVMM, the
cancer cells may replace a type of
cell called a pericyte, which normally resides on the outsides of
blood vessels.
Based on the pioneering work of Dr. Claire Lugassy and Dr. Raymond Barnhill at UCLA's Jonsson Comprehensive
Cancer Center, a new study provides additional support for a process by which melanoma cells, a deadly form of skin cancer, can spread throughout the body by creeping like tiny spiders along the outside of blood vessels without ever entering the blood stream, and that this process is exacerbated by exposure to ultraviolet (UV)
Cancer Center, a new study provides additional support for a process by which melanoma
cells, a deadly form of skin
cancer, can spread throughout the body by creeping like tiny spiders along the outside of blood vessels without ever entering the blood stream, and that this process is exacerbated by exposure to ultraviolet (UV)
cancer, can spread throughout the body by creeping like tiny spiders along the outside of
blood vessels without ever entering the
blood stream, and that this process is exacerbated by exposure to ultraviolet (UV) light.
A study combining tumor
cells from patients with breast
cancer with a laboratory model of
blood vessel lining provides the most compelling evidence so far that a specific trio of
cells is required for the spread of breast
cancer.
«UV light accelerates
cancer cells that creep along outside of
blood vessels.»
In earlier studies involving animal models and human
cancer cell lines, researchers found that breast
cancer spreads when three specific
cells are in direct contact: an endothelial
cell (a type of
cell that lines the
blood vessels), a perivascular macrophage (a type of immune
cell found near
blood vessels), and a tumor
cell that produces high levels of Mena, a protein that enhances a
cancer cell's ability to spread.
Aifantis, the chair of the Department of Pathology at NYU Langone and a member of its Perlmutter
Cancer Center, and an early career scientist at the Howard Hughes Medical Institute, says experiments in his laboratory had shown that leukemia - initiating
cells concentrate in the bone marrow near CXCL12 - producing
blood vessels.
Researchers with the U.S. Department of Energy (DOE)'s Lawrence Berkeley National Laboratory (Berkeley Lab) have identified the microenvironment surrounding microvasculature — the small
blood vessels that transport
blood within tissues — as a niche where dormant
cancer cells reside.
To determine whether endothelial
cells — the
cells that line the interior surface of
blood vessels — directly influence breast
cancer cell growth, they then created unique organotypic models of lung and bone marrow microvascular niches, in which endothelial
cells formed
blood vessel - like structures in culture as they would in the original organ.
This neural highway might be especially important in pancreatic
cancer, they say, because it grows fewer
blood vessels that can carry
cancer cells to the rest of the body.
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 toxicity of chokeberry extract on normal
blood vessel lining
cells was tested and found to have no effects up to the highest levels used (50 ug / ml), suggesting that the
cell death effect is happening in a way other than through preventing new
blood vessel formation (anti-angiogenesis), a process that is important in
cancer cell growth.
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.
They also used a model which simulated the
cancer cells flowing through the
blood vessels, and got the same result.
«Loophole for
cancer cells found: Cancer cells kill blood vessel cells so that they can slip through the vascular wall, form metastases.&
cancer cells found:
Cancer cells kill blood vessel cells so that they can slip through the vascular wall, form metastases.&
Cancer cells kill
blood vessel cells so that they can slip through the vascular wall, form metastases.»
These
cells have different factors on their surfaces which determines how «sticky» the
cells are and whether they are responsible for mediating the
cancer cells binding to the
blood vessel walls.
One drug attacks
cancer cells; the other inhibits
cancer cell formation and the growth of
blood vessels at tumor sites.
Cancer cells and tumors at first rely on nearby
blood vessels to get what they need to survive, but, as tumors grow, they need to form new
vessels.
Dr Kat Arney,
Cancer Research UK's science communications manager, said: «This exciting research may have cracked how healthy cells in the blood vessels are protecting against cancer treat
Cancer Research UK's science communications manager, said: «This exciting research may have cracked how healthy
cells in the
blood vessels are protecting against
cancer treat
cancer treatments.
By engineering red
blood cells to have «sticky» proteins on their surface, a team of researchers has given the
cells the ability to carry anything from drugs to treat immune disorders or
cancer to radioactive molecules used in imaging of
blood vessels.
Lymphovascular invasion (LVI) means that malignant
cancer cells «invade» the
blood vessels and lymphatic system, from whence they can be transported onwards.
Dr. Nagy is renowned for his work in stem
cells,
blood vessel biology, and creating genetic tools in
cancer cells, among other areas.
The team's experiments in
cell cultures, conducted with funding from an American Brain Tumor Association Discovery Grant, showed that coibamide A cuts off the
cancer cells» ability to communicate with
blood vessels and other
cells, eventually starving the
cell and triggering its death.
Due to the lack of oxygen in the
cancer cells, VEGF - A (Vascular Endothelial Growth Factor) is formed and this promotes the formation of new
blood vessels to supply the tumor.
In another, a
cancer cell trails sticky appendages as it rolls through a
blood vessel and attempts to gain purchase on the
vessel wall.
According to a new study, these «
cancer stem
cells» reside in
blood vessels.
The dendrimer, an extremely tiny nanoparticle, takes advantage of certain physical characteristics that
blood vessels leading to
cancer cells have, but healthy ones do not.
«Scientists discover how breast
cancer cells spread from
blood vessels.»
This study sheds light on how
cancer cells leave the
blood vessels to travel to a new part of the body, using a technique that allows researchers to map how
cancer cells interact and exchange information with
cells that make up the
blood vessels.
Researchers at Emory University School of Medicine were testing whether GM - CSF (granulocyte - macrophage colony stimulating factor), already used to restore white
blood cell numbers during
cancer treatment, could help heal
blood vessels damaged by atherosclerosis.
Dr Claus Jorgensen, who led the research at The Institute of
Cancer Research, London, and at Cancer Research UK's Manchester Institute at the University of Manchester, said: «The next step is to figure out how to keep this receptor switched on, so that the tumour cells can't leave the blood vessels — stopping breast cancer spreading and making the disease easier to treat successfully.&
Cancer Research, London, and at
Cancer Research UK's Manchester Institute at the University of Manchester, said: «The next step is to figure out how to keep this receptor switched on, so that the tumour cells can't leave the blood vessels — stopping breast cancer spreading and making the disease easier to treat successfully.&
Cancer Research UK's Manchester Institute at the University of Manchester, said: «The next step is to figure out how to keep this receptor switched on, so that the tumour
cells can't leave the
blood vessels — stopping breast
cancer spreading and making the disease easier to treat successfully.&
cancer spreading and making the disease easier to treat successfully.»
When
cancer cells interact with the walls of the
blood vessels, EPHA2 is activated and the tumour
cells remain inside the
blood vessels.