Azacytidine and Decitabine induce gene - specific and non-random DNA demethylation
in human cancer cell lines
To validate their computer modeling predictions, researchers performed experiments
in human cancer cell lines, mouse liver samples and primary human hepatocytes.
Not exact matches
Introducing
human prostate
cancer cell lines into mice, Wu and his colleagues saw a particular enzyme called MAOA activate a cascade of signals that made it easier for tumor
cells to invade and grow
in bone.
«This model was trained on genetic data from
human tumors
in The
Cancer Genome Atlas and was able to predict response to certain inhibitors that affect cancers with overactive Ras signaling in an encyclopedia of cancer cell lines,» Greene
Cancer Genome Atlas and was able to predict response to certain inhibitors that affect
cancers with overactive Ras signaling
in an encyclopedia of
cancer cell lines,» Greene
cancer cell lines,» Greene said.
Professor Ali Tavassoli, who led the study with colleague Dr. Ishna Mistry, explains: «
In an effort to better understand the role of HIF - 1 in cancer, and to demonstrate the potential for inhibiting this protein in cancer therapy, we engineered a human cell line with an additional genetic circuit that produces the HIF - 1 inhibiting molecule when placed in a hypoxic environmen
In an effort to better understand the role of HIF - 1
in cancer, and to demonstrate the potential for inhibiting this protein in cancer therapy, we engineered a human cell line with an additional genetic circuit that produces the HIF - 1 inhibiting molecule when placed in a hypoxic environmen
in cancer, and to demonstrate the potential for inhibiting this protein
in cancer therapy, we engineered a human cell line with an additional genetic circuit that produces the HIF - 1 inhibiting molecule when placed in a hypoxic environmen
in cancer therapy, we engineered a
human cell line with an additional genetic circuit that produces the HIF - 1 inhibiting molecule when placed
in a hypoxic environmen
in a hypoxic environment.
The researchers observed the effect of the synthetically produced molecule, JK - 31, on the growth and proliferation of a model
human breast
cancer cell line and found that it effectively blocked the protein cyclin - dependent kinase 1 (CDK1), which plays a key part
in the process of the division of
cancer cells, and therefore inhibited the proliferation of the
cells.
They found out that TiY is capable of distinguishing TICs from non-TICs
in various
human lung
cancer cell lines and patient - derived lung tumors.
Beyond lung
cancer, TiY is able to target TICs
in 28 types of
human cell lines derived from the central nervous system, melanoma, breast, renal, ovarian, colon, and prostate
cancer.
«Our study results suggest a new drug cocktail that is effective
in both
human lung
cancer cell lines and fly models,» says Cagan.
Through these effects, the PERY peptide reduced the proliferation of several (but not all)
cancer cell lines in culture and inhibited the growth of a
human breast
cancer xenograft
in mice.
In earlier studies involving animal models and human cancer cell lines, researchers found that breast cancer spreads when three specific cells are in direct contact: an endothelial cell (a type of cell that lines the blood vessels), a perivascular macrophage (a type of immune cell found near blood vessels), and a tumor cell that produces high levels of Mena, a protein that enhances a cancer cell's ability to sprea
In earlier studies involving animal models and
human cancer cell lines, researchers found that breast
cancer spreads when three specific
cells are
in direct contact: an endothelial cell (a type of cell that lines the blood vessels), a perivascular macrophage (a type of immune cell found near blood vessels), and a tumor cell that produces high levels of Mena, a protein that enhances a cancer cell's ability to sprea
in direct contact: an endothelial
cell (a type of
cell that
lines the blood vessels), a perivascular macrophage (a type of immune
cell found near blood vessels), and a tumor
cell that produces high levels of Mena, a protein that enhances a
cancer cell's ability to spread.
The researchers showed that cabazitaxel worked better than docetaxel
in human prostate
cancer cells lines that were resistant hormone treatment, both
in terms of slowing
cancer -
cell growth and
in its ability to kill
cancer cells.
In addition to the afatinib - resistant NSCLC
cells, the researchers tested the neratinib and valproic acid combination on
cell lines derived from
human pancreatic and ovarian
cancers containing K - Ras mutations and N - Ras mutations, respectively.
A team of researchers
in Germany and Denmark led by Steven Johnsen, Professor at the University Medical Center Göttingen, Germany, used
human prostate
cancer cell lines and depleted them of the DNA - binding protein CHD1.
He is researching the functions and properties of
human sulfotransferase (EST) enzymes
in human breast
cancer cell lines.
Slashing the amount of HSF1
in several
lines of
human cancer cells diminished growth and survival.
«We've seen this
in six different types of
human cancer cell lines in the lab,» Choudhury said.
In studies of laboratory - grown
human tumor
cell lines, the drug disrupted tumor
cell division and prevented growth of advanced
cancer 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 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.
It demonstrates that alterations
in these
cells lines do indeed match changes
in samples of
human bladder
cancer.
In a paper published online May 17, 2016 in the journal Nature Communications, de Jong and co-first author Koji Taniguchi, MD, PhD, and colleagues, report that treating both ERK1 / 2 and the compensatory pathway, ERK5, concurrently with a combination of drug inhibitors halted colorectal cancer growth more effectively in both mouse models and human colorectal cancer cell line
In a paper published online May 17, 2016
in the journal Nature Communications, de Jong and co-first author Koji Taniguchi, MD, PhD, and colleagues, report that treating both ERK1 / 2 and the compensatory pathway, ERK5, concurrently with a combination of drug inhibitors halted colorectal cancer growth more effectively in both mouse models and human colorectal cancer cell line
in the journal Nature Communications, de Jong and co-first author Koji Taniguchi, MD, PhD, and colleagues, report that treating both ERK1 / 2 and the compensatory pathway, ERK5, concurrently with a combination of drug inhibitors halted colorectal
cancer growth more effectively
in both mouse models and human colorectal cancer cell line
in both mouse models and
human colorectal
cancer cell lines.
The goal of the first experiment was to see whether lncRNAs are differentially expressed
in prostate
cancer by measuring total RNA from prostate
cancer cell lines and normal epithelial prostatic
cells using NCode
human ncRNA array and SurePrint G3
human lncRNA microarrays.
Dr. Bauman and her colleagues treated
human head and neck
cancer cells in the laboratory with varying doses of sulforaphane and a control, and compared them to normal, healthy
cells that
line the throat and mouth.
Recent studies with
human breast
cancer cell lines have also shown that Shp2 mediates survival signals
in cancer cells.
For the time course study,
cells were treated with 20 μM of EGCG for 12, 24, 48, 72, or 144 h.
Human colon
cancer cell line HT - 29 and prostate
cancer cell line PC3 were obtained from American Type Culture Collection (Manassas, VA), and were grown
in McCoy's 5A and RPMI 1640 containing 10 % fetal bovine serum, respectively.
To determine whether the reactivation of methylation - silenced genes by EGCG is a general phenomenon that also occurs
in other
cell lines, we studied the effects of EGCG treatment on the methylation status and mRNA levels of p16INK4a or RARβ
in three other
human cancer cell lines (Fig. 3C) ⇓.
The example shown reveals that these estrogen agonists show the strongest connectivity to each other
in MCF7, a
human breast
cancer cell line that expresses the estrogen receptor.
Interestingly, two recent reports that have catalogued recurrent focal deletions
in large cohorts of
human tumors and
cancer cell lines.
Sphere - forming
cell subpopulations with
cancer stem
cell properties
in human hepatoma
cell lines.
Decreased functional expression of Grp78 and Grp94 inhibits proliferation and attenuates apoptosis
in a
human gastric
cancer cell line in vitro.
Significantly increased expression of OCT4 and ABCG2
in spheroid body - forming
cells of the
human gastric
cancer MKN - 45
cell line.
The researchers then injected AAV2 into
human breast
cancer cell line - derived tumors
in mice without functioning immune systems.
They fused mouse B
cells — antibody - producing
cells of the immune system — with
human myeloma (also known as B
cell cancer)
cell lines in a new technique called hybridoma technology.
Using cutting - edge techniques enabled by next - generation sequencing, the authors generated complete methylome maps at single nucleotide resolution
in a low - passage breast
cancer cell line and normal breast tissue (primary
human mammary epithelial
cells).
Ab7291 staining alpha tubulin
in human breast
cancer cell line by ICC / IF (Immunocytochemistry / Immunofluorescence).
Pim - 3, a Proto - Oncogene with Serine / Threonine Kinase Activity, Is Aberrantly Expressed
in Human Pancreatic
Cancer and Phosphorylates Bad to Block Bad - Mediated Apoptosis
in Human Pancreatic
Cancer Cell Lines
«Basically, this study shows that the genetic makeup of individual
human embryonic stem
cell lines is unique
in the numbers of copies of certain genes that may control traits and things like disease susceptibility,» said Teitell, who also is an associate professor of pathology and laboratory medicine and a researcher at UCLA's Jonsson Comprehensive
Cancer Center.
I wanted to inactivate the gene BRAF (a kinase implicated
in several
human cancers)
in A549
cells (a
human lung
cancer cell line), armed only with viruses obtained through Addgene's viral service and the methods sections of scientific articles (gasp).
The goal was to deepen the knowledge about the pharmacological and cytotoxic effects of the drug Temodex
in vitro
in different
human brain
cancer cell lines.
(a kinase implicated
in several
human cancers)
in A549
cells (a
human lung
cancer cell line), armed only with viruses obtained through Addgene's viral service and the methods sections of scientific articles (gasp).
The
human breast
cancer cell line SKBR3 was purchased from the Duke University Cell Culture Facility and was maintained in McCoy's 5A medium (Life Technologies) supplemented with 10 % FBS (Life Technologies) and antibiot
cell line SKBR3 was purchased from the Duke University
Cell Culture Facility and was maintained in McCoy's 5A medium (Life Technologies) supplemented with 10 % FBS (Life Technologies) and antibiot
Cell Culture Facility and was maintained
in McCoy's 5A medium (Life Technologies) supplemented with 10 % FBS (Life Technologies) and antibiotics.
In a series of lab experiments with cell lines, human xenograft tumors in mice and primary human prostate cancer samples, the researchers demonstrated that miR - 34a inhibits prostate cancer stem cells by suppressing CD4
In a series of lab experiments with
cell lines,
human xenograft tumors
in mice and primary human prostate cancer samples, the researchers demonstrated that miR - 34a inhibits prostate cancer stem cells by suppressing CD4
in mice and primary
human prostate
cancer samples, the researchers demonstrated that miR - 34a inhibits prostate
cancer stem
cells by suppressing CD44.
In studies using
human cancer cell lines, a new, never - described compound known as BMH - 21 destroyed this critical communication pathway.
Inhibition of growth, production of insulin - like growth factor - II (IGFII), and expression of IGF - II mRNA of
human cancer cell lines by antagonistic analogs of growth hormone - releasing hormone
in vitro.
canSAR contains information on the entire
human proteome — the protein equivalent of the
human genome - as well as linking to information on more than 1,000
cancer cells lines, used by researchers to study the effect of new drugs
in the lab.
Cultures of the
human triple negative breast
cancer cell line, HCC1806, were maintained
in RPMI 1640 medium supplemented with 10 % FBS.
On the basis of studies on the XMRV - producing
human prostate
cancer cell lines CWR22Rν1 and CWR - R1 and their progenitor tumour xenograft CRW22, they concluded that XMRV infections were caused by contamination during
in vivo passaging
in nude mice.
Growth hormone (GH) receptors
in prostate
cancer: gene expression
in human tissues and
cell lines and characterization, GH signaling and androgen receptor regulation
in LNCaP
cells.
Important features of XMRV biology include (1) tropism for a variety of
cell lines, including prostate
cancer DU145 and LNCaP
cells [27], [43], [48], and
human neural
cell types [57], (2) adaptations that promote growth
in prostate epithelium and
human - derived prostate
cancer cell lines including an androgen response element
in the promoter region [58] and downregulation of APOBEC3G [59], and (3) cellular effects with potential oncogenic properties including increased tumor aggressiveness mediated by downregulation of p27 [60] and differential regulation of several microRNAs [61].