It is effective in
cancer cell samples and cell lines resistant to conventional therapies.
Not exact matches
Acquiring high - definition images of every
cancer cell found in a blood
sample, making characterization at single -
cell resolution possible.
Vortex's system uses a microfluidic chip to generate tiny vortices that trap larger, more deformable
cancer cells from a blood plasma
sample.
The diagnosis of
cancer and study of disease progression is often accomplished by examining a tumor
sample containing many billions or even trillions of
cells.
In
cancer research, our goal is to be able to start with a
sample of human tissue, extract many
cells of interest, and perform genetic analysis upon each of them separately.
An analysis of the HPV16 genome from 5,570 human
cell and tissue
samples revealed that the virus actually consists of thousands of unique genomes, such that infected women living in the same region often have different HPV16 sequences and variable risks to
cancer.
The test aims to detect and prevent the progression of HPV - induced cervical
cancer and other abnormalities in the female genital tract by
sampling cells from the outer opening of the cervix of the uterus and the endocervix.
To address this gap in knowledge, Mirabello and Schiffman teamed up with co-senior author Robert Burk of Albert Einstein College of Medicine to sequence the whole genomes of 5,570 HPV16 - infected
cell and tissue
samples from women around the world and to identify associations between HPV16 genetic variants and the risk of cervical precancer and
cancer.
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.
The team found that exposing
samples of human glioblastoma tumours grown in a dish to the Zika virus destroyed the
cancer stem
cells.
Studying such diseases is a good first step because they are
cancers of immune
cells themselves, and it's possible to analyze them with a mere blood
sample.
A technician then examines the
sample under a microscope for the oddly - shaped
cells that are a precursor to
cancer.
While testing the effect of many normal, non-cancerous, human
cells on the sensitivity of
cancer cells to chemotherapy, they found a specific
sample of normal human skin
cells that rendered pancreatic
cancer cells resistant to gemcitabine.
First, the research demonstrates that RB status can be tracked using
cell - free DNA
samples, an approach referred to as «liquid biopsy,» in prostate
cancer patient
samples.
The finding, reported by a Stand Up to
Cancer - Prostate Cancer Foundation Dream Team in the May 21 edition of the journal Cell, is based on an analysis of tumor samples from 150 men with metastatic prostate cancer that no longer responded to standard hormone - blocking th
Cancer - Prostate
Cancer Foundation Dream Team in the May 21 edition of the journal Cell, is based on an analysis of tumor samples from 150 men with metastatic prostate cancer that no longer responded to standard hormone - blocking th
Cancer Foundation Dream Team in the May 21 edition of the journal
Cell, is based on an analysis of tumor
samples from 150 men with metastatic prostate
cancer that no longer responded to standard hormone - blocking th
cancer that no longer responded to standard hormone - blocking therapy.
Spearheaded by first author Christopher McNair, PhD, a graduate student in the laboratory of Dr. Knudsen, the study undertook an extensive analysis of tumor
samples and
cell - free DNA
samples from patients with advanced, lethal - stage prostate
cancer.
Using tumor
samples from a patient, they do lab tests to determine which substances can first make the different types of
cancer cells uniform and then effectively kill them.
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.
From tissue and
cell samples from five glioblastoma patients, the scientists obtained 33 individual
cancer cells capable of reproduction, which grew into very different tumors in the lab.
Finding out involves passing a
sample of blood through a microfluidic device, in whose tiny channels
cancer cells can be captured and identified.
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.
Diagnosing
cancer today usually involves various imaging techniques, examining tissue
samples under a microscope, or testing
cells for proteins or genetic material.
This analysis, done on separate
samples from the same patient, revealed that many of the affected genes confer advantages to
cancer cells by, for example, enhancing
cell migration or resistance to chemotherapy.
Nana - Sinkam and his colleagues examined lung - tumor
samples from 81 patients with stage - 1 nonsmall -
cell lung
cancer and tumor -
cell lines.
A multicenter team of researchers reports that a full genomic analysis of tumor
samples from a small number of people who died of pancreatic
cancer suggests that chemical changes to DNA that do not affect the DNA sequence itself yet control how it operates confer survival advantages on subsets of pancreatic
cancer cells.
They treated a variety of healthy tissues and 23
samples of
cancer cells taken from leukemia patients with AG1295, a drug known to selectively block the kinase.
To validate their computer modeling predictions, researchers performed experiments in human
cancer cell lines, mouse liver
samples and primary human hepatocytes.
«Our study addressed an important safety issue — whether
cancer cells that might be present in testicular tissue
samples can survive the process to replicate the sperm - producing stem
cells,» said lead author Hooman Sadri - Ardekani, M.D., Ph.D., an instructor in urology and regenerative medicine at Wake Forest Baptist Medical Center.
Dr. Islam saw this phenomenon occur in
cell culture and in some
samples from patients with head and neck
cancers.
Researchers of KIT and the Center for Nanotechnology (CeNTech), Münster, have now developed a clinical method to reliably detect and isolate single
cancer cells in blood
samples in cooperation with the University Hospital of Hamburg - Eppendorf (UKE).
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.
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.
Then they collected the fluid that those Fam20C - deficient
cancer cells and non-manipulated
cancer cells were grown in and analyzed the proteins each
sample contained.
The images helped researchers to home in on PTEN levels in the
cancer cells while ignoring the other
cells in the
samples.
Toner pumped
samples of whole blood through the channels, which were coated with an antibody designed to trap any
cancer cell that carries a common surface protein, much as flypaper snags pesky insects.
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.
Samples of tumours from bowel
cancer patients given different doses of resveratrol showed that even lower doses can get into
cancer cells and potentially affect processes involved in tumour growth.
For example,
cancer cells floated above denser blood
cells, which could allow clinicians to spot rare circulating tumor
cells in a patient
sample.
In lab experiments, the research team used
cell lines derived from 40 patient tumour
samples to identify that CD151 contributes to the survival of
cells of high - grade serous ovarian
cancer origin.
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.
Through laser imaging at speeds up to 3,000 frames per second, a computer can capture images from all angles and reconstruct a model of all
cells in the given
sample, testing for all types of
cancer in a matter of minutes.
Because any
sample of
cancer cells is likely to contain thousands of mutations, advanced analytic tools are needed to distinguish harmless «passenger» mutations from the dangerous mutations driving the disease.
Once they had established the chemical and physical details about the nanocrystals, the team then tested the particles as «staining» agents on a tissue
sample containing liver
cancer cells held on a microscope slide.
For the new study, described in the October 23rd issue of Nature Communications, scientists at the Johns Hopkins Kimmel
Cancer Center and Dana Farber Cancer Institute in Boston collected tissue samples containing normal cells, ovarian cancers, metastases that had spread elsewhere, and small cancers found in the fallopian tubes, which included single cell layers of cancer called «p53 signatures» and serous tubal intraepithelial carcinoma, or STIC le
Cancer Center and Dana Farber
Cancer Institute in Boston collected tissue samples containing normal cells, ovarian cancers, metastases that had spread elsewhere, and small cancers found in the fallopian tubes, which included single cell layers of cancer called «p53 signatures» and serous tubal intraepithelial carcinoma, or STIC le
Cancer Institute in Boston collected tissue
samples containing normal
cells, ovarian
cancers, metastases that had spread elsewhere, and small
cancers found in the fallopian tubes, which included single
cell layers of
cancer called «p53 signatures» and serous tubal intraepithelial carcinoma, or STIC le
cancer called «p53 signatures» and serous tubal intraepithelial carcinoma, or STIC lesions.
Such targeting and ease of identification of
cancer cells could allow oncologists to spot even tiny numbers of diseased
cells in a biopsy
sample.
It demonstrates that alterations in these
cells lines do indeed match changes in
samples of human bladder
cancer.
The study of human astrocytes has faced issues related to access (
samples of living tissue must be obtained from brain
cancer or epilepsy surgeries or fetal tissue) and purification (breaking apart astrocytes away from other
cells often killed them and many experiments ended in failure).
Even more promising, Cui has
sampled a group of human volunteers and found that 10 to 15 percent have similar super
cancer - fighting white blood
cells.
Working in mouse models of breast
cancer and breast tumor
samples from patients, Longmore and his colleagues showed that a protein that sits on the surface of tumor
cells, called DDR2, binds to collagen and activates a multistep pathway that encourages tumor
cells to spread.
Samples with more of these
cells were more likely to come from patients whose
cancer had spread or was more aggressive.