WASHINGTON (May 17, 2017)-- A new investigation of more than 48,000 stored
tumor samples finds evidence of a key deficiency in a repair mechanism designed to keep DNA from being mutated and causing cancer.
A new investigation of more than 48,000 stored
tumor samples finds evidence of a key deficiency in a repair mechanism designed to keep DNA from being mutated and causing cancer.
Not exact matches
She and her colleagues sequenced genomic DNA in the
tumor samples but did not
find any new driver gene mutations in the metastatic
samples compared to the primary
tumor samples, said McDonald, who completed clinical training under Iacobuzio - Donahue at Johns Hopkins.
However, many studies have
found the inconsistency of EGFR mutation status in plasma DNA
samples as compared to
tumor tissue DNA
samples.
The team also compared the animals» responses to the therapy's effects in laboratory cell
samples and
found that in vitro studies did not predict how well the viral therapy and immune response would fight
tumor cells in vivo.
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.
They analyzed bacterial DNA
found in breast tissue
samples from 58 women who were undergoing lumpectomies or mastectomies for either benign or cancerous
tumors, as well as from 23 healthy women who had undergone breast reductions or enhancements.
They
found that the levels of two specific tRNAs were significantly higher in metastatic cells and metastatic
tumors than in primary
tumors that did not metastasize or healthy
samples.
«And we
found all three types of «gain - of - function» mutations in the estrogen receptor gene ESR1 in the
tumor samples.»
The researchers were able to replicate this
finding by comparing the healthy thyroid tissues in GTEx to 500
samples taken from thyroid
tumors, compiled by The Cancer Genome Atlas, and giving support to the extensive impact of FOXE1 on cellular state.
An additional set of 18 prostate cancer tissue
samples was analyzed by qPCR and five lncRNAs were
found to be significantly higher in prostate
tumor tissues compared with matched normal tissues.
«Our
findings show that high - intensity circulating
tumor DNA sequencing is possible and may provide invaluable information for clinical decision - making, potentially without any need for
tumor tissue
samples,» said lead study author Pedram Razavi, MD, PhD, a medical oncologist and instructor in medicine at Memorial Sloan Kettering Cancer Center (MSK) in New York, NY.
After sequencing the
tumor samples, the authors
found that the JAK2 gene was more frequently amplified in chemotherapy - treated TNBC than in
tumors before treatment.
Researchers have
found a group of circulating
tumor cells in prostate cancer patient blood
samples which are linked to the spread of the disease, according to new research presented at the National Cancer Research Institute (NCRI) Cancer Conference in Liverpool.
Overall, including all genomic variations present in most if not all
tumor cells (clonal) as well as those present only in subsets of the cancer cells (subclonal) from
tumor tissue, the researchers detected a total of 864 genetic changes in tissue
samples across the three
tumor types, and 627 (73 %) of those were also
found in the blood.
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.
Notably, the researchers
found that, using their methods, highly reactive TILs could be obtained from some 90 % of the ovarian cancer patients whose
tumor samples they examined.
«Based on our
findings, the next phase will be to measure exosomes and exomeres in plasma
samples to help predict organs that may be targeted for metastasis during
tumor progression,» said Dr. Lyden.
As Fiebig
found in his early work,
tumor samples do not always successfully graft onto the mice.
Perhaps the most intriguing — and contentious —
finding of the paper (as highlighted by GT's In Sequence magazine and Keith Robison on Omics Omics) was that few of the somatic mutations in the metastasis were detected in the primary
tumor sample from 9 years earlier.
Another collaboration was unfolding among the cancer geneticists, sequencing experts, clinical researchers, and surgical oncologists at Johns Hopkins, MD Anderson, and Baylor College of Medicine to study 32 pairs of head and neck
tumor and normal tissue
samples by whole - exome sequencing and validate the
findings in an additional 88
samples.
Further, for each plasmid in the kit, the transcript most commonly
found across all TCGA
tumor samples is represented, making the results of any such study as clinically relevant as possible.
There is considerable interest in
finding CNAs that affect the same chromosomal region in multiple
tumor samples.
Because of small
sample size, the changes in
tumor - initiating cell number were not significant (P > 0.05), but these data are supportive of the in vitro
findings and suggest that hypoxia may have a positive effect on the
tumor - initiating cell population in ER - α — positive breast cancers and a negative effect in ER - α — negative
tumors.
Outside retinoblastoma experts say they're excited about the
finding because they've never been able to grab
samples of the
tumors they treat without removing the eye.
For example, proteins related to angiogenesis, the process through which new blood vessels form to ensure supply of oxygen and nutrients to a tissue such as a
tumor, are
found to be clearly associated to clinical outcome in HPV - positive
samples.
When the researchers compared average cytokine levels in CFS patients versus the healthy control
samples, they
found that only 2 of the 51 substances they tested for were significantly different: One, called
tumor growth factor beta, was higher in CFS patients, while the other, called resistin, was lower.
Closely monitoring several markers of cell damage (including creatine kinase, lactate dehydrogenase, prostaglandin - E and
tumor necrosis factor - alpha) in their
sample of 18 male athletes (who used 20 grams of creatine monohydrate per day for five days, mixed with 60 grams of maltodextrine), the researchers
found levels of these markers were reduced after the race, compared to 16 control subjects who took only the maltodextrine.
What they
found: Denosumab delayed and prevented
tumor growth in the tissue
samples and the mice.
The study
found that it's now feasible in dogs to collect a
tumor sample and perform molecular profiling in less than a week's time, a clinically practical window.
They also
found that just over half the
tumors samples analyzed carry genetic mutations that could be targeted by therapies that are already on the market.