Conjugated linoleic acid (CLA) up - regulates the estrogen - regulated
cancer suppressor gene, protein tyrosine phosphatase gamma (PTPgama), in human breast cells.
Not exact matches
However, the impact of the two methylation - regulating enzymes was still seen at 10 to 15 months, when scientists found decreased expression of hundreds of
genes — many of which are key tumor
suppressor genes such as BMP3, SFRP2 and GATA4 — in the smoke - exposed cells and a five - or - more-fold increase in the signaling of the KRAS oncogene that is known to be mutated in smoking - related lung
cancers.
PTEN is known as a tumour
suppressor gene meaning that it typically slows the growth of cells and its loss can lead to
cancer.
«Over 40 % of prostate
cancers lose PTEN and some lose both PTEN and another tumour
suppressor gene, INPP4B, but we didn't previously have a clear picture of how this affects tumour growth,» says IMED Biotech Unit scientist Sabina Cosulich, at AstraZeneca.
Collateral lethality occurs when tumor
suppressor genes are deleted, a nearly universal occurrence in
cancer.
Working with colleagues at St. Vincent's Hospital in Sydney, Martin identified two individuals who had the characteristics of hereditary nonpolyposis colorectal
cancer, which is usually caused by a mutation that inactivates one of a person's two copies of the tumor
suppressor gene MLH1, but who showed no signs of mutation.
Inherited mutations of the tumour
suppressor gene CDKN2A are the strongest known risk factors for familial melanoma and mutations in this
gene also increase the risk of other
cancers.
Now, researchers studying mice have found one of the most powerful tumor
suppressor genes yet — animals lacking it have a startling 50 % chance of developing
cancer.
Now, in a provocative study that raises unsettling questions about the widespread use of vitamin supplements, Swedish researchers have showed that relatively low doses of antioxidants spur the growth of early lung tumors in
cancer - prone mice, perhaps by hindering a well - known tumor
suppressor gene.
The findings provide proof of principle that restoring the function of a single tumor
suppressor gene can cause tumor regression and suggest future avenues for developing effective
cancer treatments.
Spalax naturally have a variant in the p53
gene (a transcription factor and known tumor
suppressor), which is identical to a
cancer - related mutation in humans, Band said.
«Our data strongly suggest that KIF1Bβ, which is localized on chromosome 1p36, might be such a neuroblastoma tumor
suppressor gene,» says principal investigator Susanne Schlisio at the Department of Microbiology, Tumor and Cell Biology at Karolinska Institutet and Assistant Member at the Ludwig Institute for
Cancer Research in Stockholm, Sweden.
If tumors have this PPM1D mutation, they do not have another more common genetic mutation to the TP53
gene, a tumor
suppressor that, when defective, is linked to half of all
cancers.
In this research, the group looked at two variants of miR - 21, a microRNA «oncomiR» known to target tumor
suppressor genes and which is highly expressed in a number of
cancers as well as other proliferative diseases such as psoriasis.
Rather than target a tumor -
suppressor gene directly, Ideker and team took the approach of identifying genetic interactions between a tumor
suppressor gene and another
gene, such that simultaneous disruption of both
genes selectively kills
cancer cells.
«It wasn't known whether miR - 486 functioned as an oncogene or a tumor -
suppressor gene in lung
cancer,» says co-corresponding author Patrick Nana - Sinkam, MD, associate professor of medicine and a researcher with the OSUCCC — James Molecular Biology and Cancer Genetics Pr
cancer,» says co-corresponding author Patrick Nana - Sinkam, MD, associate professor of medicine and a researcher with the OSUCCC — James Molecular Biology and
Cancer Genetics Pr
Cancer Genetics Program.
Normal BRCA
genes encode proteins that are
cancer suppressors.
BRCA1 and 2,
genes whose proteins are supposed to work as tumor
suppressors and also repair DNA damage, were the first known risk factor
genes for familial breast
cancer as well as ovarian and other
cancers.
A study published in Molecular
Cancer Research reveals that a tumor
suppressor gene p16 is turned off by a histone mutation (H3.3 K27M), which is found in up to 70 percent of childhood brain tumors called diffuse intrinsic pontine glioma (DIPG).
The researchers further found that miR - 486 is itself regulated by the tumor -
suppressor gene p53, the most frequently altered
gene in human
cancers, and that activity of miR - 486 is partially dependent upon functional p53.
They tested these drugs one at a time for lethal interaction with 112 different tumor -
suppressor gene mutations in human
cancer cells growing in the lab.
Among them: some
genes believed to be tumor
suppressors turned on or became more active, whereas certain disease - promoting ones, including oncogenes (in the so - called RAS family that are implicated in both prostate and breast
cancer), were down - regulated or switched off.
All the fish had the human
cancer mutation BRAFV600E — found in most benign moles — and had also lost the tumor
suppressor gene p53.
The drug, lapatinib, activates the
suppressor called FOXO, in HER2 + breast
cancer cells, but then FOXO becomes a turncoat molecule, working with an epigenetic regulator that controls
gene expression.
«Identifying targets essential to cell survival in tumor
suppressor genes has long been an investigational goal with the aim of offering
cancer - specific vulnerabilities for targeted therapy,» said Ronald DePinho, M.D., professor of Cancer Biology, MD Anderson president, and senior author for the Nature
cancer - specific vulnerabilities for targeted therapy,» said Ronald DePinho, M.D., professor of
Cancer Biology, MD Anderson president, and senior author for the Nature
Cancer Biology, MD Anderson president, and senior author for the Nature paper.
By searching for
gene deletion patterns in
cancer through a concept the investigators call «synthetic essentiality,» the team identified a synthetic essential
gene known as chromatin helicase DNA - binding factor (CHD1) as a therapeutic target for prostate and breast
cancers lacking a tumor
suppressor gene called phosphatase and tensin homolog (PTEN).
«We reasoned that this retained synthetic essential
gene might be required for
cancer - promoting actions when the
cancers lose specific tumor
suppressor genes.»
They propose that normal tissue becomes primed for
cancer when oncogenes are activated and tumor
suppressor genes are silenced or lost, but that
cancer develops only when a cell in the tissue reverts to a more primitive, embryonic state and starts dividing.
A new method has been found for identifying therapeutic targets in
cancers lacking specific key tumor
suppressor genes.
The loss of the tumor
suppressor gene PTEN has been linked to tumor growth and chemotherapy resistance in the almost invariably lethal brain
cancer glioblastoma multiforme (GBM).
Tumor
suppressor genes are deleted in many
cancers leading to tumor formation and growth.
P53 is a tumor
suppressor gene, a protein that regulates cell growth, and it is the most frequently mutated
suppressor gene in
cancer.
A significant finding by the team was that either the mutant KRAS
gene or another
cancer gene is amplified, depending on which tumor
suppressor gene is affected and to what degree its function is impaired.
Another key finding was observing the inhibitor effect on tumor models with a
gene PTEN deficiency as a biomarker — of huge interest because PTEN, a tumor
suppressor, is known to be defective in as many as half of all advanced solid tumor
cancers.
This phenomenon could result in breakage in the human genome, and when a breakage impacts important
genes, such as tumor
suppressors, it could lead to
cancer development.
These complexes lead to mutations in the TP53 tumor
suppressor gene, which in turn initiate the process toward kidney
cancer.
2003 Chinese company Shenzhen SiBiono GeneTech gains approval for treating head and neck
cancer with Gendicine, a modified adenovirus carrying a tumour -
suppressor gene.
Or stem cells injected into a patient as therapy might be designed so that their tumor
suppressor genes are less likely to mutate and cause
cancer.
They observed that selected
genes including some oncogenes and tumor
suppressor genes are similarly altered in these two types of
cancers.
They discovered that the number of tumor
suppressor genes or oncogenes in a chromosome correlated with how often the whole chromosome or part of the chromosome was deleted or duplicated in
cancers.
Since 1971, the standard tumor
suppressor model has held that
cancer is caused by a «two - hit» cascade in which first one copy and then the second copy of a
gene becomes mutated.
They generated a list of suspected oncogenes and tumor
suppressor genes based on their mutation patterns — and found many more potential
cancer drivers than anticipated.
Poor repair of these «double - strand breaks» can activate
cancer - causing
genes or inactivate tumor -
suppressor genes.
In humans,
cancer develops when
genes that suppress
cancer, known as tumor
suppressors, are lost and when mutations or
genes that promote
cancer, known as oncogenes, are gained or activated.
When normal diploid cells lose one or both copies of tumor
suppressor genes,
cancers can form.
Polyploid cells, which carry additional copies of important tumor
suppressor genes, are better protected and more resistant to
cancer formation because they have these extra copies of the genome,» said Dr. Zhu, who is also an Assistant Professor of Pediatrics and Internal Medicine at UT Southwestern.
Analysis of genomic, epigenetic, and RNA sequencing data revealed that the combinations of mutations that lowered the levels of functioning BRCA1 and BRCA2 RNA —
genes that produce the breast
cancer tumor
suppressor proteins — were associated with significantly better survival outcomes.
But the idea fell out of fashion as researchers began to discover that mutations in specific oncogenes and tumor -
suppressor genes could set
cancer in motion.
The tumor
suppressor gene PTEN is known to play a major role in prostate
cancer; its partial loss occurs in up to 70 percent of primary prostate tumors.
«Inactive tumor
suppressor gene discovered in lung
cancer.»