Zhang's group is moving beyond bulk sequencing
of tumor samples and is now conducting genomics on single cells.
She has sequenced hundreds
of tumor samples from across the island in an effort to understand how it evolves and how that affects the devils» survival rates.
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 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.
The ambitious plan was to create a new shared resource
of tumor samples with attached patient information.
The model, called COXEN (CO-eXpression gENe analysis), sorts through the massive genetic data of thousands
of tumor samples to discover differences between tumors that responded and tumors that did not.
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.
Cells were extracted from the biopsy
of her tumor sample for use in research without her knowledge or consent.
«Furthermore, analysis
of tumor samples from large cohorts of colorectal cancer patients revealed that activation of the loop is associated with metastasis,» Hermeking reports.
Thirty companies and academic groups will receive the same set
of tumor samples from individual patients and will try to predict the best neoantigens.
In collaboration with Dr. Omer Iqbal, from the Department of Pathology, they are analyzing the genetics and biology
of tumor samples to find how they differ from samples of tumors not linked to radiation.
Labmatrix aligns each patient's details with genetic and biological analysis
of their tumor samples, as well as the results of drug screening in laboratory flasks and biological models.
This case includes the majority
of tumor samples and perhaps genomes with mosaic aneuploidy.
To help the patient, and also make some advances in tech development, Jones and his colleagues did whole - genome and RNA - Seq
of the tumor samples and matched normals.
In the group's initial scan
of the tumor samples, researchers identified gene mutations that would increase RTK / RAS / RAF pathway activity in 62 percent of the samples.
Not exact matches
Interest in liquid biopsy has escalated in recent years due to the minimally invasive
sampling method, potential to overcome the challenges
of tumor heterogeneity, and the potential for longitudinal monitoring
of tumor burden through serial
sampling.
To determine how the cells switch from one type to another, they took three human uterine carcinosarcoma
samples and sequenced the genomes
of cells in two parts
of each
tumor: the carcinoma and sarcoma components.
For example, TCGA, with genomic data on 33
tumor types taken from
samples from 11,000 patients, is finishing 2018 by publishing a series
of papers and holding a symposium.
Many
tumors release cells with distinctive antigens on their surfaces, and affinity - based techniques can pull these cells out
of the blood
sample relatively easily.
The focus
of those hopes is the liquid biopsy: a test that could detect and analyze a solid
tumor from biomarkers in the bloodstream or other easily
sampled body fluids, such as saliva.
While the latter has a reputation for being hard to isolate, she explains that even degraded RNA generally contains enough intact sequence to analyze — provided investigators can detect the scarce
tumor signals against the immense background
of other RNA molecules in a
sample.
«The minimum
sample volume required is only 1 µL for analysis
of 92 proteins, which has been proven to be a great advantage for applications with limited
sample volumes, such as pediatric applications, fine - needle biopsies, and
tumor microbiopsies,» he says.
Even after initial purification
of the
sample, liquid biopsies typically contain much more nucleic acid from healthy cells than from
tumors.
While more sensitive assays have enabled doctors to take smaller
samples of some types
of solid
tumors, oncologists have long dreamed
of avoiding traditional biopsies altogether.
«Circulating
tumor cells have the advantage that they are... intact living cells,» says Michael Kazinski, senior director and head
of global product management for
sample technologies at Qiagen in Hilden, Germany.
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.
Analyzing a database
of nearly 800 multiple myeloma patient
samples, they discovered that 162 patients with low ADAR1 levels in their
tumor cells survived significantly longer over a three - year period compared to 159 patients with high ADAR1 levels.
Ependymomas also occur in adults, but in the study, none
of the adult
tumor samples had reduced H3K27me3.
The study's 31
samples of dog
tumors was compared to 40 normal canine tissues
samples as a way
of estimating the variance in gene expression.
Researchers used tissue and blood
samples to show that the gammopathy (a precursor to myeloma) in both mice and patients with Gaucher disease is triggered by specific lipids, and that the antibodies made by
tumor cells in nearly a third
of myeloma patients are directed against such lipids.
Biopsied
samples of glioblastoma
tumors contain high level
of STK17A.
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.
In blood
samples from 1005 patients with eight types
of tumors that had evidently not yet metastasized, the test detected between 33 % and 98 %
of cases, depending on the
tumor type (see graph, above).
The results
of a study
of more than 100 human
tumor samples show that the
tumors expressing a high level
of CCR3 present more frequent local dissemination.
A tissue slice, a
tumor biopsy, or a
sample of a bacterial culture yields a sequence representing the average
of all
of the cells within it, even though researchers know there can be tremendous variation between those cells.
After surgical removal, the metabolic processes in a
tumor change in a very short period
of time, so that valuable information about the
tumor tissue is lost during a conventional
sampling procedure.
However, many studies have found the inconsistency
of EGFR mutation status in plasma DNA
samples as compared to
tumor tissue DNA
samples.
31: The percentage
of genetic mutations shared by all the
tumor samples taken from a patient with kidney cancer.
Plasma
samples of patients with NSCLC is a less invasive method and has been used as surrogate
tumor tissues for detecting genetic alterations.
Plasma
samples also can not address the issue
of expression heterogeneity (primary
tumor vs. metastatic site (s)-RRB-.
«This gives us novel and exciting new therapeutic options to pursue based on results from drug screenings
of primary
tumor samples from patients.»
Researchers said the importance
of collecting tissue
samples from recurrent
tumors will grow as more targeted therapies become available.
To that end, in collaboration with the University
of Zurich and MD Anderson Cancer Center, the researchers tested melanoma
tumor samples from human patients undergoing treatment with the same targeted therapies.
The investigators looked at 4,278
tumor samples from a tissue repository
of patients with GI tract cancers.
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.
A global analysis
of metabolites and small molecules in urine
samples from patients with adrenal cancer has identified four biochemicals that, when measured together, can distinguish malignant from benign adrenal
tumors, according to study results presented at the 2015 Annual Clinical Congress
of the American College
of Surgeons.
Analysis
of blood and tissue
samples from one patient revealed that plakoglobin was expressed in CTC clusters but not single CTCs and also was expressed in some portions
of both the primary
tumor and metastases.
The researchers analyzed the
samples using immunohistochemistry and RNA sequencing to study the changes in the
tumor immune microenvironment
of patients who received and did not receive chemotherapy, and changes before and after chemotherapy.
The latter, presented by Eric Lander
of the Broad Institute in Cambridge, Massachusetts, would systematically sequence
tumor samples for mutations involved in cancer to speed up the search for new drugs and diagnostics.
Using
tumor samples from the Women's Healthy Eating and Living clinical trial, researchers identified stem - like
tumor cells as being characterized by low levels
of the molecule p53 upregulated modulator
of apoptosis (PUMA).