Vortex's system uses a microfluidic chip to generate tiny vortices that trap larger, more deformable
cancer cells from a blood plasma sample.
The device has been used to separate different blood components, to separate
cancer cells from blood and to manipulate nanorod motors inside living cells, to name only a few research areas.
So my field is science and technology, so my work is circulating tumor cells where I isolate
cancer cells from blood of patients and isolate their DNA and RNA and try to sequence them and try to device treatments for cancer treatment and therapy.
The experimental test uses a plastic chip whose microscopic inner surfaces are covered in antibodies to grab
cancer cells from the blood.
Memorial Sloan Kettering Cancer Center's Dr. Howard Scher notes in the NCI piece that plucking
the cancer cells from blood is just the start.
The chip would allow the filtering of
cancer cells from a blood sample, which would be an easier way to harvest cancer cells, rather than the current method of taking them from tumor sites in the body.
Not exact matches
Consider: Last year alone, the FDA approved two treatments,
from Novartis and Gilead, that literally reengineer patients» immune T -
cells to target and destroy
blood cancers.
This new kind of approach to fighting
blood cancers is truly personalized; immune T -
cells are extracted
from patients, genetically tinkered to home in on an destroy cancerous
cells, multiplied in a lab, and then jolted back into the patient's body within about two weeks.
It offers cardio protection, it helps lower bad cholesterol, it may help prevent the progression of multiple sclerosis, it has the ability to regenerate brain
cells after a stroke, it has the ability to cross the
blood - brain barrier to potentially ward off Alzheimer's disease, apparently it's good at wiping amyloid plaque
from the brain (which studies haves linked to Alzheimer's), it may help to prevent certain types of
cancer, and studies have shown that it inhibits
cancer cell growth and metastases (meaning it keeps
cancer from spreading).
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.
In their latest study, they tested compounds against
cells from nine different types of human
cancer, including common types affecting
blood, colon, breast, prostate, ovaries, kidneys, and lungs.
The results of the empirical study show a clear distinction between the damage to the white
blood cells from patients with
cancer, with pre-cancerous conditions and
from healthy patients.
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.
Adding two
blood - borne proteins associated with
cancer cell migration increases the predictive ability of the current biomarker for pancreatic cancer to detect early stage disease, a research team from The University of Texas MD Anderson Cancer Center reports in the Journal of the National Cancer Inst
cancer cell migration increases the predictive ability of the current biomarker for pancreatic
cancer to detect early stage disease, a research team from The University of Texas MD Anderson Cancer Center reports in the Journal of the National Cancer Inst
cancer to detect early stage disease, a research team
from The University of Texas MD Anderson
Cancer Center reports in the Journal of the National Cancer Inst
Cancer Center reports in the Journal of the National
Cancer Inst
Cancer Institute.
In experiments on normal and MLL
cells from mice and humans, the researchers demonstrated that beta - catenin is activated in
cancer stem
cells that prompt leukaemic
blood cells to multiply.
Researchers at Dana - Farber / Boston Children's
Cancer and
Blood Disorders Center report promising outcomes
from a clinical trial with patients with a rare form of bone marrow failure who received a hematopoietic stem
cell transplant (HSCT) after pre-treatment with immunosuppressive drugs only.
From a simple
blood draw, the test reads the DNA of the patient's immune repertoire to find the immune
cell barcodes associated with the
cancer.
A DEVICE that filters
cancer cells from human
blood using sound could help to identify tumour
cells that have spread.
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.
The
cancer cells spread
from one place in the body to another, through the
blood vessel.
Metastatic
cancer cells have the ability to break free
from tissue, circulate in the
blood stream, and form tumors all over the body, in a way acting like
blood cells.
The stem
cells, derived
from human umbilical cord -
blood and coaxed into an embryonic - like state, were grown without the conventional use of viruses, which can mutate genes and initiate
cancers, according to the scientists.
Scientists
from the German
Cancer Research Center (DKFZ) have developed a way to equip mouse
blood stem
cells with a fluorescent marker that can be switched on
from the outside.
«We began with stem
cells taken
from cord -
blood, which have fewer acquired mutations and little, if any, epigenetic memory, which
cells accumulate as time goes on,» says Zambidis, associate professor of oncology and pediatrics at the Johns Hopkins Institute for
Cell Engineering and the Kimmel
Cancer Center.
In this study, researchers took
cells from patients with
blood cancer MDS and turned them into stem
cells to study the deletions of human chromosome 7 often associated with this disease.
In a process called cellular reprogramming, researchers at Icahn School of Medicine at Mount Sinai have taken mature
blood cells from patients with myelodysplastic syndrome (MDS) and reprogrammed them back into iPSCs to study the genetic origins of this rare
blood cancer.
Lymphoma is a type of
blood cancer that affects the white
blood cells — called lymphocytes — that help protect the body
from infection.
In their investigation, Greaves and colleagues discovered incipient
cancer cells in routine
blood samples taken
from the child at birth, strongly suggesting that the transmission happened in utero.
Now a team of researchers in China has developed a new microfluidic chip that can quickly and efficiently segregate and capture live circulating tumor
cells (CTCs)
from a patient's
blood, with potential applications for
cancer screenings and treatment assessments.
As a result, these
blood vessels will be structured more tightly, which can prevent
cancer cells from spreading to other organs.
«FDG PET shows tumor DNA levels in
blood are linked to NSCLC aggressiveness: Insights derived
from FDG PET could improve treatment selection for patients with advanced non-small
cell lung
cancer.»
To make the vaccine,
cancer cells are harvested
from a tumor after surgery and stripped of their proteins; then those proteins are cultured with dendritic
cells, a subclass of white
blood cells, drawn
from the patient's
blood.
He did, however, publish a paper last year documenting a study in which he infused three
cancer patients with white
blood cells from young donors who had been injected with G - CSF.
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.
Living in overcrowded conditions appears to protect children and young adults against developing a particular type of Hodgkin lymphoma (HL), a
cancer that originates
from the lymphocytes (white
blood cells).
To understand how these multi-colored lesions originated they examined
blood from these mice and found that tumor
cells in circulation frequently occurred as clusters comprised of different colored
cancer cells.
Some of the first evidence for
cancer stem
cells came
from studies of leukemia in the 1990s, which showed that only a small subset of the cancerous
blood cells could propagate the disease in mice.
Analyzing white
blood cells from 934 patients and 1,698 healthy controls, they found BRCA1 methylation among 6.4 % of patients diagnosed with ovarian
cancer, contrasting 4.2 % among controls.
Next, T
cells — the immune system's foot soldiers — are harvested
from the patient's
blood and infected with the virus, which rewrites their genetic code to recognize and destroy
cancer cells.
In recent studies of
cancer patients who received a bone marrow transplant, genes
from the marrow's white
blood cells were found in the patient's tumor
cells.
The SC3 tool was then used to analyse single -
cell RNA - sequence data
from two patients diagnosed with myeloproliferative neoplasm (MPN)
blood cancers.
HSCT is effectively used today as a form of «replacement» therapy for patients with hard - to - treat
blood cancers, providing healthy
cells from either the patient (autologous transplantation) or
from a donor (allogeneic transplantation) to better equip patients to fight the disease on their own.
Cheng, an assistant professor of medicine in hematology / oncology at Feinberg, provided the
cell lines and NanoFlare targets the researchers used to model
blood samples taken
from breast
cancer patients.
Abatacept, when added to the standard drug regimen used to prevent GvHD, reduced the occurrence of acute, grade III - IV GvHD
from 32 to 3 percent in pediatric and adult patients who underwent mismatched unrelated donor stem
cell transplants to treat advanced
cancer and other
blood disorders.
Adds Liu: «With metastatic
cancers accounting for around 90 % of deaths
from solid tumors, the hope is that one day a device that can enable the analysis of single tumor
cells circulating in the
blood could make a big difference in early diagnosis, detection and monitoring of numerous types of
cancer, without invasive biopsies.»
The researchers identified the LSC17 score by sampling the leukemia stem
cell properties of
blood or bone marrow samples
from 78 AML patients
from the
cancer centre combined with molecular profiling technology that measures gene expression.
Recently, scientists have engineered
cells from a patient's own immune system to fight
blood cancers.