In 89 % of patients, at least one genetic change
detected in the tumor was also detected in the blood.
In contrast, no PCR product was
detected in tumors from mice treated with trastuzumab alone.
«These tiny cells are very difficult to
detect in a tumor,» she says.
Not exact matches
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.
Paweletz and his colleagues are now developing a PCR - based test to
detect drug resistance mutations
in lung
tumors.
Nor are x-rays good at
detecting tumors in dense breast tissue, which also reads as white; many women younger than 50 have dense breasts.
A team of researchers has taken a major step toward one of the hottest goals
in cancer research: a blood test that can
detect tumors early.
He is now fashioning the lab's multidots — tiny crystalline beads encapsulated
in a special coating — into an actual product to
detect multiple biomarkers on
tumor cells.
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).
In contrast, our blood - based test is minimally invasive, inexpensive, and more sensitive, thus suitable for large population screening to
detect early - stage
tumors.»
The researchers demonstrated that blocking the PGD enzyme genetically or with a pharmacologic inhibitor reversed the epigenetic reprogramming and malignant gene expression changes
detected in distant metastases, and also strongly inhibited their
tumor - forming capacity, with no effect on normal cells or peritoneal pancreatic cancer controls.
The company is also working on a similar test
in solid
tumors for early diagnosis of relapse, and is developing tests that will help diagnose some lymphomas that are notoriously tricky to
detect.
The test
detects a combination of five
tumor proteins that appear to be a reliable signature of the disease, the researchers report
in the May 24...
«We did not
detect any clear change
in the long - term time trends
in the incidence of brain
tumors from 1998 to 2003
in any subgroup,» the researchers wrote
in the paper, which was published online Thursday
in the Journal of the National Cancer Institute (JNCI).
Instead, researchers told the European Breast Cancer Conference that their findings suggest that extending screening programs to older women results
in a large proportion of women being over-treated, and at risk from the harmful effects of such treatment, because these women were more likely to die from other causes than from any
tumors detected in the early stages of growth.
The new test uses a highly sensitive gene mutation detection method that is based on the partitioning of DNA into droplets to
detect specific circulating
tumor DNA mutations and RNA variants
in whole blood.
For example, just before von Eschenbach arrived, NCI had agreed to fund a now - $ 350 million screening trial to see if spiral computed tomography (CT) scans could
detect lung
tumors missed by x-ray imaging
in former smokers.
The reduction
in the number of potentially unnecessary biopsies appears to have occurred at the cost of
detecting fewer intermediate risk PCa
tumors.
They report that the test can
detect significant drops
in the metabolic activity levels of all three types of
tumors within 72 hours when exposed to an effective drug whereas
tumors that were resistant to a drug show no change.
New research led by Li Ding, Ph.D., of Washington University School of Medicine
in St. Louis, shows that current approaches to genome analysis systematically miss
detecting a certain type of complex mutation
in cancer patients»
tumors.
The approach was most successful
in making a difference
in samples from the two patients
in which the smaller - sized
tumor DNA was not readily apparent, which may represent patients with low
tumor burden and previously difficult to
detect circulating
tumor DNA.
The work also reinforces the importance of finding
tumor cell clusters
in the blood as a mechanism of
detecting cancer metastasis earlier.
«This development has the potential to enable earlier detection of solid
tumors through a simple blood draw by substantially improving our ability to
detect very low quantities of circulating DNA derived from
tumor cells,» says corresponding author Hunter Underhill, M.D., Ph.D., who initiated the research while
in the lab of senior author Jay Shendure, M.D., Ph.D., a professor
in genome sciences at the University of Washington.
Ben Stanger, MD, PhD, a professor
in the division of Gastroenterology, and first author Ravi Maddipati, MD, an instructor
in the division of Gastroenterology, say that these results may prove useful
in designing better targeted therapies to stop
tumor progression and provide an improved non-invasive method for
detecting early disease states
in this highly lethal cancer.
To see if PGD and the pentose phosphate pathway were tied to the epigenetic changes the researchers had
detected in distant metastases, they treated
tumor cells from different sites
in a single patient with the drug 6 - aminonicotinamide (6AN), which is known to inhibit PGD but is not used
in humans because of its severe side effects.
In the second study, researchers examined whether aspirin is associated with breast density, which is a widely accepted risk factor for both estrogen receptor minus (ER --RRB- and estrogen receptor positive (ER +) breast cancers, and can be a key factor in detecting tumors during routine mammogram
In the second study, researchers examined whether aspirin is associated with breast density, which is a widely accepted risk factor for both estrogen receptor minus (ER --RRB- and estrogen receptor positive (ER +) breast cancers, and can be a key factor
in detecting tumors during routine mammogram
in detecting tumors during routine mammograms.
Using a fluorescent protein to
detect Rgs16 expression, the investigators found that this gene is induced by pancreatic
tumor formation starting from its earliest manifestation as ductal neoplasm all the way to advanced solid
tumor in a spatially and temporally coincidental manner.
Northwestern University scientists now have demonstrated a simple but powerful tool that can
detect live cancer cells
in the bloodstream, potentially long before the cells could settle somewhere
in the body and form a dangerous
tumor.
The MRI imaging
detected metastatic
tumors, including micrometastases,
in lung, liver, lymph node, adrenal gland, bone, and brains of the mice.
Curious about the possibility of circular RNAs contributing to cancer, Pandolfi and his colleagues set out to see if they could
detect relevant changes
in tumors known to harbor distinct fusion proteins, which result when different chromosomes abnormally join together, melding two separate genes into a new centaur - like gene.
In the past few years, Vogelstein and Kinzler have shifted away from discovering new cancer genes to a less glamorous pursuit: using genetic tests to
detect common
tumors as early as possible, when they are easiest to cure.
Currently,
in another study, the researchers are focused on
detecting circulating
tumor cells
in the blood of patients with a diagnosis of breast cancer.
One of the candidates for this elastography, a variant of echography whereby the difference
in the rigidity of the
tumor and healthy tissue can be used to
detect cancer.
Deep convolutional networks are all the rage at Google, Facebook, Apple and other Silicon Valley companies seeking to automatically label images, translate speech to text,
detect pedestrians
in videos and find
tumors in breast scans.
Siva Vanapalli, an associate professor
in the Department of Chemical Engineering, at Texas Tech University, recently received two grants from the Cancer Prevention and Research Institute of Texas (CPRIT) to study the movement of
tumor cells throughout the body and new methods of
detecting cancer cells.
The technique is currently being tested
in a number of clinical applications, including imaging breast
tumors,
detecting skin cancer, and tracking blood oxygenation
in tissues.
Now, MIT engineers have developed a far more sensitive way to reveal ovarian
tumors:
In tests in mice, they were able to detect tumors composed of nodules smaller than 2 millimeters in diamete
In tests
in mice, they were able to detect tumors composed of nodules smaller than 2 millimeters in diamete
in mice, they were able to
detect tumors composed of nodules smaller than 2 millimeters
in diamete
in diameter.
In humans, colon cancer often spreads to the liver and forms small
tumors that are difficult to
detect, similar to ovarian
tumors.
This model showed that
in order to
detect tumors 5 millimeters
in diameter or smaller
in humans, the researchers would need to improve the system's sensitivity by at least one order of magnitude.
They
detected the presence of an enzyme that can induce
tumor metastasis, MMP - 2 (matrix metalloproteinase - 2)
in mice with cancer.
By combining these two refinements, the researchers were able to enhance the sensitivity of the sensor 15-fold, which they showed was enough to
detect ovarian cancer composed of small
tumors (2 millimeters
in diameter)
in mice.
They have
detected, for example, revved up signaling molecules involved
in inflammation, such as
tumor necrosis factor α (TNFα) and other cytokines; skewed populations of natural killer cells and other immune cells; imbalances
in the protein - destroying enzymes called proteases; and a shortening of the telomeres, the «end caps» on chromosomes, which indicates prematurely aged cells.
Although the existence of ChHV5 has been known for more than 20 years, the inability to grow the virus
in the laboratory hampered understanding of how it causes
tumors and the development of blood tests to
detect the virus.
In a study of 124 patients with advanced breast, lung, and prostate cancers, a new, high - intensity genomic sequencing approach
detected circulating
tumor DNA at a high rate.
MRI and computed tomography (CT) scans can be effective
in finding larger
tumors, but a patient's prognosis is poor by the time a
tumor is
detected.
This innovative approach — using high - intensity sequencing to
detect cancer from circulating
tumor DNA
in the bloodstream — heralds the development of future tests for early cancer detection.
Importantly, without any prior knowledge from the analysis of
tumor tissue, 76 % of «actionable» mutations (genetic changes that can be matched to an approved targeted therapy or one being tested
in clinical trials)
detected in tissue were also
detected in blood.
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.
So, for example, at the University of California
in San Francisco they are trying to engineer E. coli so that it can
detect cancer cells, it can invade
tumors, and then once it's inside they can release toxins; and so they are putting
in all sorts of genes from other bacteria to assemble this, you know, this sort of synthetic E. coli that could become basically a cancer torpedo.