Mechanisms of HDAC inhibitor regulated gene
expression in cancer cells (Review).
When the researchers reduced the amount of IL13RA2
expression in the cancer cells, they found that the tumor growth was significantly slower in models.
Not exact matches
Curcumin
in turmeric has the ability to modulate genetic activity and
expression — both by destroying
cancer cells and by promoting healthy
cell function.
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.
«When we reduced this enzyme
expression in prostate
cancer cells, we found a lower prostate
cancer bone metastasis,» he said.
Without this regulation, lack of Sxl
expression in stem
cells can result
in the development of ovarian
cancer.
Molecular characterization of the
cells that undergo
cell fate transition upon oncogenic Pik3ca
expression demonstrated a profound oncogene - induced reprogramming of these newly formed
cells and identified gene
expression signatures, characteristic of the different
cell fate switches, which was predictive of the
cancer cell of origin, tumour type and clinical outcomes
in women with breast
cancers.
The idea to specifically study this group of patients was based on groundbreaking research Garon published
in the New England Journal of Medicine last year, which found that among patients who received pembrolizumab, those with PD - L1
expression on at least 50 percent of their
cancer cells showed the longest survival and disease control.
Protein
expression in these glioblastoma
cells more closely mimicked that
in real
cancer cells than
in 2D cultures of
cells, indicating that this method could be used to study
cancer (Nature Nanotechnology, DOI: 10.1038 / nnano.2010.23).
Bloch's colleagues at the National Institute of Environmental Health Sciences tested the oils
in gene
expression studies on lab - grown human breast
cancer cells and found that they could mimic estrogens, the primary female sex hormones, and inhibit androgens, the primary male sex hormones.
This study, published
in the journal Microarrays, shows that lack of SOST
in the bone microenvironment promotes the
expression of many genes associated with
cell migration and / or invasion, including long non-coding RNA MALAT1
in prostate
cancer, suggesting that SOST has an inhibitory effect on prostate
cancer invasion.
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.
Plakoglobin is a component of two important structures involved
in cell - to -
cell adhesion, and the investigators found that suppressing its
expression caused CTC clusters to fall apart, reducing their metastatic potential, and also disrupted
cell - to -
cell contact between breast
cancer cells but not normal breast tissue.
A molecule
in cells that shuts down the
expression of genes might be a promising target for new drugs designed to treat the most frequent and lethal form of brain
cancer, according to a new study by researchers at The Ohio State University Comprehensive Cancer Center — Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC — J
cancer, according to a new study by researchers at The Ohio State University Comprehensive
Cancer Center — Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC — J
Cancer Center — Arthur G. James
Cancer Hospital and Richard J. Solove Research Institute (OSUCCC — J
Cancer Hospital and Richard J. Solove Research Institute (OSUCCC — James).
Researchers from BUSM and the University of Cyprus compared the markers on the surface of the
cancer cells to gene
expression profile of breast tumors deposited by researchers
in international public databases and found that a molecule named IL13RA2 (IL13R alpha2) was abundant
in metastatic or late - stage BLBC.
To test this idea, they experimentally reduced the
expression of the DNM30S lncRNA, which resulted
in reduced ovarian
cancer cell migration and invasion.
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.
ONC201 may inhibit
cancer stem
cell self - renewals by altering their gene
expression, according to a study published August 2, 2017
in the open - access journal PLOS ONE by Varun Vijay Prabhu from Oncoceutics, Inc., USA and colleagues.
Further research could test these
cancer stem
cell gene
expression at the RNA and protein level
in circulating tumor
cells and biopsies from patients on trial.
Increasing
expression of a chemical cytokine called LIGHT
in mice with colon
cancer activated the immune system's natural
cancer - killing T -
cells and caused primary tumors and metastatic tumors
in the liver to shrink.
So far, Menendez and his colleagues have discovered the fatty acid cuts the
expression of the gene
in ovarian, stomach, and colon
cancer cell lines.
The team narrowed down the approximately 1000 microRNAs to a handful that induced strong fluorescence
in the system, and then reduced these to two that they confirmed could increase E-cadherin
expression in pancreatic
cancer cells.
Surprisingly, they found that although the patterns of gene
expression — as shown by the RNA sequencing — differed between the hepatocellular carcinomas and the liver
cancers with biliary phenotype and depended on the histological type, the overall pattern of mutations
in the
cells was actually similar between the tumors — of either type — that had emerged
in patients who had had infections with either hepatitis C or B, and were different
in patients without such infections.
In the current paper, knowing that MYC, a transcription factor that binds the genome through sites that are identical to the binding sites of BMAL1, the team hypothesized that aberrant MYC expression perturbs the clock by deregulating components of the circadian network in cancer cell
In the current paper, knowing that MYC, a transcription factor that binds the genome through sites that are identical to the binding sites of BMAL1, the team hypothesized that aberrant MYC
expression perturbs the clock by deregulating components of the circadian network
in cancer cell
in cancer cells.
What's more, the disrupted circadian oscillations
in the MYC - expressing
cancer cells could be partially rescued by inhibiting
expression of REV - ERBα.
In the new study, Burrows and colleagues focused on the protein HIC1, or «Hypermethylated in cancer 1, «so named because it was first identified in cancer cells; however, it also helps regulate gene expression in normal cell
In the new study, Burrows and colleagues focused on the protein HIC1, or «Hypermethylated
in cancer 1, «so named because it was first identified in cancer cells; however, it also helps regulate gene expression in normal cell
in cancer 1, «so named because it was first identified
in cancer cells; however, it also helps regulate gene expression in normal cell
in cancer cells; however, it also helps regulate gene
expression in normal cell
in normal
cells.
In preclinical experiments using human prostate cancer cell lines, Fu's team showed that increased PLK1 expression activated an oncogene known as c - RAF, which has previously been shown to play a role in regulating cell growth and divisio
In preclinical experiments using human prostate
cancer cell lines, Fu's team showed that increased PLK1
expression activated an oncogene known as c - RAF, which has previously been shown to play a role
in regulating cell growth and divisio
in regulating
cell growth and division.
In an effort to unravel that mystery, Rodriguez and his colleagues focused on the ways those
cancer cells regulate the
expression of genes or whether they make their constituent proteins.
Examination of gene
expression in patients with non-small
cell lung
cancer (NSCLC) showed the area adjacent to tumors is rich with
cancer markers.
In the lab, the scientific team used an approach that combined functional RNAi analysis with gene expression analysis in breast cancer - derived cell lines and in human breast cancers replicated in mic
In the lab, the scientific team used an approach that combined functional RNAi analysis with gene
expression analysis
in breast cancer - derived cell lines and in human breast cancers replicated in mic
in breast
cancer - derived
cell lines and
in human breast cancers replicated in mic
in human breast
cancers replicated
in mic
in mice.
For instance, a tumor influences the
expression of genes
in immune system
cells that are involved
in the body's response to
cancer.
«Our study reveals important differences and specificities
in the mechanism of action of high - and low - dose aspirin
in metastatic and nonmetastatic
cancer cells with different tumor origins and suggests that the ability of aspirin to prevent platelet - induced c - MYC [an oncoprotein]
expression might be selective for a nonmetastatic phenotype.»
What's really impressive about Babar's accomplishment is that he did the work for both papers — one on the role of a population of stem
cells in lung
cancer development (published
in Cell) the other on gene
expression in group A Streptococcus (published
in PNAS)-- as a participant
in summer undergraduate research programs.
In combination with a separate technique that measures the degree to which a gene is expressed, the researchers then identified genes that were either mutated or functionally altered through expression levels in these bladder cancer cell line
In combination with a separate technique that measures the degree to which a gene is expressed, the researchers then identified genes that were either mutated or functionally altered through
expression levels
in these bladder cancer cell line
in these bladder
cancer cell lines.
Loss of the PBRM1 gene function caused the
cancer cells to have increased
expression of other genes, including gene pathway known as IL6 / JAK - STAT 3, which are involved
in immune system stimulation.
This image shows an
expression of the stem
cell gene Musashi
in human pancreatic
cancer.
Cancer cells are shown in green, Musashi expression in red and blue includes cells within the cancer microenviro
Cancer cells are shown
in green, Musashi
expression in red and blue includes
cells within the
cancer microenviro
cancer microenvironment.
«We discovered that the BRD4 gene has more of a gene -
expression - guiding compound attached to it
in tumor
cells of a rare carcinoma (and several other
cancers) compared to non-cancerous
cells,» You said.
A study of gene
expression in leukemia
cells has identified an RNA binding protein that plays an important role
in driving the development of
cancer.
That would be a way to influence the
expression of many genes involved
in the proliferation of
cancer cells.»
The synergistic effect of the two drugs completely eliminated Stat3
expression in pancreatic
cancer cells.
Unlike most biomarkers for
cancer, DDX3 mRNA
expression only increased slightly
in the exposed breast
cells, but the corresponding proteins levels were significantly higher.
So the researchers developed synthetic promoters — DNA sequences designed to initiate gene
expression but only
in cancer cells.
By contrast,
in triple negative breast
cancer cells, the researchers discovered that Myc reduces the
expression of TXNIP.
«Given the link between 11C - sarcosine
cell uptake and PAT transport, the study provides first evidence that PAT
expression can be elevated
in prostate
cancer,» explains Morand Piert, MD, professor of radiology, Division of Nuclear Medicine at the University of Michigan, Ann Arbor, Michigan.
Based on analyses of over 600 drug and breast
cancer cell pairings, researchers showed that, for some
cells, drug exposure can cause significant changes
in gene
expression — indicating the successful action of a drug on its target — without affecting
cell growth or survival.
«Sight unseen: Gene
expression reveals «hidden» variability
in cancer cells» response to drugs.»
Altered promoters
in GC change the gene
expression profile of GC
cells and may confer its oncogenic properties, including
cell movement and
cancer signalling.
«Our experiments showed that restoring H19
expression hindered by too much p53 restored «protective differentiation» of osteoblasts to counter events of tumor growth early on
in bone
cancer,» said co-author, Ihor Lemischka, PhD, Director of The Black Family Stem
Cell Institute within the Icahn School of Medicine.
However, another report found that miR - 7
expression correlated with poorer prognosis of breast
cancer, and these apparently conflicting results suggest that miR - 7 may be differentially expressed
in a specific
cell population of breast
cancer (26).