In the test tube, the nanogenerators killed leukaemia, lymphoma, breast, ovarian, neuroblastoma, and
prostate human cancer cells.
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.
In their latest study, they tested compounds against
cells from nine different types of
human cancer, including common types affecting blood, colon, breast,
prostate, ovaries, kidneys, and lungs.
FRESH insight into
prostate cancer has come in a study showing that the mitochondrial DNA of
human prostate cancer cells is riddled with mutations.
Serendipitously, the antimicrobial peptide shows promise for protecting
humans from
cancer; it can inhibit the growth of
prostate and bladder
cancer cells, as well as multi-drug resistant leukemic
cells.
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.
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.
«Plant oil suppresses viability of
human prostate cancer cells.»
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.
According to McCague, «the rarity of
human prostate cancer cell cultures makes studying tamandron's potential difficult in the test tube.»
This is a neat solution: blocking the uptake of a nutrient needed by
prostate cancer cells with nutrients that are commonly in the
human diet.
Next, the researchers tested the effects of RK - 33 and radiation in mice that had been injected with
human prostate cancer cells that highly express DDX3.
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 division.
Tadashi Matsuda of Hokkaido University and his colleagues in Japan investigated
human prostate cancer cells to determine if there is an unknown up - regulation mechanism in the EGFR pathway.
Their preliminary findings indicate that MUS81 - induced movement of DNA to the cytosol also occurs in
human cancer cells, including
prostate cancer, breast
cancer, colorectal
cancer, uterine
cancer, leukemia, and melanoma
cells.
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.
This compound killed
human breast,
prostate, lung, and liver
cancer cells, while sparing normal
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.
Reykjavik, ICELAND, 25 September 2011 — Scientists at deCODE Genetics and academic collaborators from Iceland, The Netherlands, Spain, Denmark, Germany, Sweden, the USA, the UK and Romania today report the discovery of a variant in the sequence of the
human genome associated with risk of developing basal
cell carcinoma of the skin (BCC), as well as
prostate cancer and glioma, the most serious form of brain
cancer.
Interactions between
human osteoblasts and
prostate cancer cells in a novel 3D in vitro model.
Further research uncovered a broad spectrum of
cell surface stem
cell markers (e.g., CD133, CD44, and CD24) that allow the identification of CSCs in
human solid tumors, including brain, breast,
prostate, pancreas, liver, ovary, skin, colon
cancers, and melanoma (3 - 6)(Figure 1 based on 7).
Although persistent loss of IGF - 1R expression ultimately induced
cell stasis and death, both of these processes are regulated by the tumor suppressor gene p53 that is commonly mutated in
human prostate cancers.
The Carboxyl Tail of Connexin32 Regulates Gap Junction Assembly in
Human Prostate and Pancreatic
Cancer Cells.
Mineralized
human primary osteoblast matrices as a model system to analyse interactions of
prostate cancer cells with the bone microenvironment.
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 CD44.
STAT5 promotes metastasis of
human prostate cancer cells (46) and has been implicated in the resistance of metastatic breast
cancer cells to targeted therapies (47).
«Theranostics» Simultaneously Kill and Image
Prostate Cancer Cells Experimenting with human prostate cancer cells and mice, cancer - imaging experts developed a method for finding and killing malignant cells while sparing healt
Prostate Cancer Cells Experimenting with human prostate cancer cells and mice, cancer - imaging experts developed a method for finding and killing malignant cells while sparing healthy
Cancer Cells Experimenting with human prostate cancer cells and mice, cancer - imaging experts developed a method for finding and killing malignant cells while sparing healthy
Cells Experimenting with
human prostate cancer cells and mice, cancer - imaging experts developed a method for finding and killing malignant cells while sparing healt
prostate cancer cells and mice, cancer - imaging experts developed a method for finding and killing malignant cells while sparing healthy
cancer cells and mice, cancer - imaging experts developed a method for finding and killing malignant cells while sparing healthy
cells and mice,
cancer - imaging experts developed a method for finding and killing malignant cells while sparing healthy
cancer - imaging experts developed a method for finding and killing malignant
cells while sparing healthy
cells while sparing healthy ones.
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].
In 2011, Paprotka, et al. reported that XMRV likely originated through recombination between 2 endogenous murine retroviruses, PreXMRV - 1 and PreXMRV - 2, during in vivo passaging of the
human prostate cancer xenograft CWR - R1, resulting in establishment of the XMRV - infected 22Rv1
cell line [38].
The test involves aggregating
human prostate cancer cells into microtissues in 96 - well plates and monitoring their growth over 90 days.
«Capsaicin inhibits the growth of
human prostate cancer cells in petri dishes and mice,» said lead researcher Dr. H. Phillip Koeffler, director of hematology and oncology at Cedars - Sinai Medical Center and a professor of medicine at the University of California, Los Angeles.
Serenoa repens (Permixon) inhibits the 5alpha - reductase activity of
human prostate cancer cell lines without interfering with PSA expression..
Ursolic acid, a naturally occurring triterpenoid, demonstrates anticancer activity on
human prostate cancer cells.
It rebalances acid / alkaline in the system and may help prevent other
cancers by inducing apoptosis in
human skin, thyroid, gastric, liver, colon, cervical and
prostate cancer cells.
Enhanced fat burning through green and white tea - brown fat
cells play key role 13.07.2017 Two cups of green tea daily results in more brown fat 25.04.2017 Animal study: half cup of green tea daily is life extending 15.04.2017 Speed up interval - training fat loss with supplement containing caffeine and green tea 19.01.2016 Green tea boosts fat burning after interval training 30.10.2015 Chin - Shin Oolong Tea contains growth hormone booster 02.10.2015 Green tea healthier and more effective on empty stomach 01.09.2015 EGCG speeds up muscle recovery after period of inactivity 19.05.2015 Green tea inhibits breakdown of fast muscle fibres during long - term inactivity 18.05.2015 Five cups of green tea daily rejuvenates skin 10.09.2014 Quercetin boosts inhibitory effect of green tea for
prostate cancer 27.01.2014 Slimming supplement containing ECGC, resveratrol and Grape Seed Extract shown to work in
human study 12.01.2014 Tea protects
prostate against testosterone 10.12.2013 Green tea speeds up muscle recovery after heavy training 11.11.2013 EGCG protects liver and kidneys, and extends life expectancy 04.08.2013 EGCG and caffeine supplement keeps the cold out 26.02.2013 N - oleyl - phosphatidyl - ethanolamine & EGCG combo makes weight - loss diet easier 03.02.2013 Green tea has a slightly anabolic effect on strength athletes 14.01.2013 Cup of green tea with a meal makes it easier to eat less 18.12.2012 Green tea keeps athletes fit as the years go by 24.10.2012 Mushrooms, green tea reduce chance of breast
cancer by factor of 10 13.10.2012 Combination of strength training and green tea gives elderly more muscle mass 12.10.2012 One cup of green tea burns five grams of fat 02.09.2012 Tiny amount of caffeine can burn fat — when combined with tea phenols 27.08.2012 Tea for temporary T boost 24.04.2012 Grow old healthily with green tea 11.03.2012 Tea drinkers have stronger bones 25.02.2012 Lose weight with Pu - Erh tea 17.08.2011 Tea supplement boosts T levels in animal study 30.10.2010 Almost no green tea in green tea sodas 13.10.2010 Drink green tea instead of water — and live longer 24.05.2010 Green tea stackers don't work without exercise 13.05.2010 Metastudy: slimming supplements with green tea do work 27.03.2010 Black tea reduces muscle soreness after training 20.03.2010 Cold brewed white tea contains most antioxidants 04.01.2010 Cup of tea inhibits uptake of mercury from fish 04.12.2009 Polyphenols in juice and tea clear bacteria from your teeth 22.10.2009 Drink three cups of tea a day and add five years to your life 11.09.2009 Bad breath from proteins?
Phytates have been shown to inhibit the growth of
human leukemia
cells, colon
cancer cells, both estrogen receptor - positive and negative breast
cancer cells, voicebox
cancer, cervical
cancer,
prostate cancer, liver tumors, pancreatic, melanoma, and muscle
cancers.