Curcumin — Improves * detoxification of oestrogen by supporting safe, tissue - protective oestrogen metabolite, reduces * oxidative damage, inhibition
of the growth of breast cancer cells [2] Lycopene - Powerful antioxidant, inhibition of cancer cell proliferation [3], reduction * of DNA damage from estrogen [4],
Not exact matches
In 2010, researchers from the University
of Michigan Comprehensive
Cancer Center published a study in the journal Clinical Cancer Research showing that sulforaphane had the ability to kill breast cancer stem cells in mice and in lab cultures, and it also prevented the growth of new tumor
Cancer Center published a study in the journal Clinical
Cancer Research showing that sulforaphane had the ability to kill breast cancer stem cells in mice and in lab cultures, and it also prevented the growth of new tumor
Cancer Research showing that sulforaphane had the ability to kill
breast cancer stem cells in mice and in lab cultures, and it also prevented the growth of new tumor
cancer stem
cells in mice and in lab cultures, and it also prevented the
growth of new tumor
cells.
Cancer: Flaxseed may protect against breast cancer, prostate cancer, and colon cancer by inhibiting tumor growth and blocking enzymes that are involved in the spread of tumor
Cancer: Flaxseed may protect against
breast cancer, prostate cancer, and colon cancer by inhibiting tumor growth and blocking enzymes that are involved in the spread of tumor
cancer, prostate
cancer, and colon cancer by inhibiting tumor growth and blocking enzymes that are involved in the spread of tumor
cancer, and colon
cancer by inhibiting tumor growth and blocking enzymes that are involved in the spread of tumor
cancer by inhibiting tumor
growth and blocking enzymes that are involved in the spread
of tumor
cells.
Breast cancer is the uncontrollable
growth of malignant
cells in the
breasts.
For example, in experiments, they have been found to stimulate the
growth of breast cancer cells and feminize male fish.
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.
Isoflavones have been shown to slow the
growth of breast cancer cells in laboratory studies, and epidemiological analyses in East Asian women with
breast cancer found links between higher isoflavone intake and reduced mortality.
Moreover, epalrestat, a drug that inhibits AKR1B1 and is approved in Japan to treat peripheral neuropathies associated with diabetes, was similarly able to block the
growth and metastasis
of human basal - like
breast cancer cells.
Women with the KRAS - variant are also more susceptible to triple - negative
breast cancer, tumors whose
growth is not fueled by the hormones estrogen and progesterone, or by the presence
of a particular genetic mutation known as HER2, which promotes
cancer cell growth.
The substance vigorously inhibited the
growth of cultured tumor
cells from colon, lung, and
breast cancers, the team reports in the 20 January issue
of Angewandte Chemie.
Overexpression
of ZMYND11 in an osteosarcoma
cell line and a triple - negative
breast cancer cell line inhibited tumor
growth.
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.
Until now, little was known in preclinical models about the mechanisms that allow
breast cancer cells to leave the latent state and even less is known in patients,» explains Roger Gomis, head of the Growth Control and Cancer Metastasi
cancer cells to leave the latent state and even less is known in patients,» explains Roger Gomis, head
of the
Growth Control and
Cancer Metastasi
Cancer Metastasis Lab.
In animal and
cell culture studies, the drug inhibited
growth both in estrogen - dependent
breast cancer cells and in
cells that had developed resistance to the anti-estrogen tamoxifen and / or to the aromatase inhibitors, two
of the most widely used types
of drugs to prevent and treat estrogen - dependent
breast cancer.
«Both the natural and the synthetic substances inhibit the
growth and spread
of cancer stem
cells in
breast cancer cell lines.
A drug approved in Europe to treat osteoporosis has now been shown to stop the
growth of breast cancer cells, even in cancers that have become resistant to current targeted therapies, according to a Duke Cancer Institute
cancer cells, even in
cancers that have become resistant to current targeted therapies, according to a Duke
Cancer Institute
Cancer Institute study.
If the stem
cells lose Numb, however, p53 levels plunge and the
cells proliferate uncontrollably, leading to the emergence
of cancer stem
cells that drive the
growth of breast tumors.
«Osteoporosis drug stops
growth of breast cancer cells, even in resistant tumors, study suggests.»
However, when the tips
of these blood
cells begin to sprout, the thrombospondin - 1 proteins give way to TGF - beta 1 and periostin proteins in the neovasculature, turning it into a metastatic niche that not only permits but accelerates the
growth of breast cancer cells.
To determine whether endothelial
cells — the
cells that line the interior surface
of blood vessels — directly influence
breast cancer cell growth, they then created unique organotypic models
of lung and bone marrow microvascular niches, in which endothelial
cells formed blood vessel - like structures in culture as they would in the original organ.
«We have shown that blocking the activity
of FAK not only reduces the
growth of breast cancer stem
cells, but also improves sensitivity to radiotherapy.
Other studies have found that nutrients in dark, leafy greens may inhibit the
growth of tumor
cells in
breast, skin, lung and stomach
cancers and that green tea may thwart
cancer development in colon, liver,
breast and prostate
cells.
About 20 percent
of breast cancer patients have overexpressed
growth receptors, known as Her2 + receptors, on the
cancer cells, which cause uncontrolled tumor
growth.
«In lab tests, the antimicrobial ingredient triclosan spurs
growth of breast cancer cells.»
Their study, published in the ACS journal Chemical Research in Toxicology, found that triclosan, as well as another commercial substance called octylphenol, promoted the
growth of human
breast cancer cells in lab dishes and
breast cancer tumors in mice.
It can promote
cancer cell survival and
growth of ER +
breast cancer cells.
Capsaicin, an active ingredient
of pungent substances such as chilli or pepper, inhibits the
growth of breast cancer cells.
Now, results
of a new study by Johns Hopkins Kimmel
Cancer Center scientists suggests a powerful role for the protein in normal
breast cells, acting as a tumor suppressor that halts abnormal
cell growth.
«Never before has PTK6 inhibition been shown to inhibit
growth and induce
cell death
of ER +
breast cancer cells, including those resistant to standard treatments for this subtype such as tamoxifen,» said Hanna Irie, MD, PhD, Assistant Professor of Medicine (Hematology and Medical Oncology) and Oncological Sciences at The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, and senior author of the
cancer cells, including those resistant to standard treatments for this subtype such as tamoxifen,» said Hanna Irie, MD, PhD, Assistant Professor
of Medicine (Hematology and Medical Oncology) and Oncological Sciences at The Tisch
Cancer Institute, Icahn School of Medicine at Mount Sinai, and senior author of the
Cancer Institute, Icahn School
of Medicine at Mount Sinai, and senior author
of the study.
«Spicy molecule inhibits
growth of breast cancer cells.»
In a development that could lead to a new generation
of drugs to precisely treat a range
of diseases, scientists from the Florida campus
of The Scripps Research Institute (TSRI) have for the first time designed a drug candidate that decreases the
growth of tumor
cells in animal models in one
of the hardest to treat
cancers — triple negative
breast cancer.
Recent mouse studies have found that a stiffer extracellular matrix triggers the production
of proteins that promote the
growth of precancerous
breast cancer cells.
The data suggests that high levels
of Myc and low levels
of TXNIP promote triple negative
breast cancer cell growth and survival.
The
growth rate
of the
cells exploded, and they quickly became disorganized masses characteristic
of early stage, aggressive
breast cancer, the team reports in the 7 February issue
of the Journal
of Experimental Medicine.
When a chemical that inhibits entosis was applied to a line
of breast cancer cells, colony formation — an indicator
of tumor
growth in vitro — increased 10-fold.
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.
Additionally, overexpression
of POSTN in human mammary epithelial and
breast cancer cells resulted in enhanced tumor
growth and metastasis (Wang et al., 2013), which is similar to a colon
cancer cell model where overexpression
of POSTN resulted in an increase in the number and size
of liver metastases (Bao et al., 2004).
Biologically, hypermethylation often silences genes that keep runaway
cell growth in check, and its appearance in the DNA code
of breast cancer - related genes shed into the blood may indicate that a patient's
cancer growth is increasing and the disease has worsened.
In this way they were able to reactivate the senescence program and stop the
growth of the
breast cancer cells.
Now Javier Menendez at the Northwestern University Feinberg School
of Medicine in Chicago and his team have shown that oleic acid, the major fatty acid component
of olive oil, blocks the production
of a protein that boosts the
growth of breast cancer cells.
Tamoxifen prevents oestrogen from stimulating
growth of breast cancer cells but some tumours can eventually develop resistance to the treatment, making the drug ineffective.
Mutations in the gene increase rat susceptibility to mammary
cancer and FRY reduced the
growth of highly aggressive human
breast cancer cells.
These therapies are relatively young, but researchers have had success with treatments that introduce antibodies to the body that inhibit the
growth of breast cancer cells.
The current study shows that NUDT5 is operates in the nucleus
of hormone - driven
breast cancer cells, to produce energy for the expression
of genes important for
cancer growth.
Now, in Stem
Cells Translation Medicine, the group
of Shu Wang at the National University
of Singapore describe the derivation
of EPCs from human iPSCs, their therapeutic modification, and their ability to inhibit tumor
growth in a mouse
breast cancer model [4].
AAV2 mediated
cell killing
of multiple
breast cancer cell lines representing both low and high grades
of cancer and targeted the
cancer cells independent
of hormone or
growth factor classification.
Many
breast cancers use hormones, such as oestrogen, to drive their
growth and current treatment options aim to block the hormonal activity in order to halt the
growth of the
breast cancer cells.
They demonstrated that this new molecule can stop the
growth of breast cancer cells in laboratory experiments.
Injections
of iPSC - EPCs did not however have significant effect on tumor
growth or on overall survival, but transducing
cells with a baculovirus expressing CD40L, a member
of the TNF gene family which can induce apoptosis [6, 7], and injection into the
breast cancer lung metastasis, increased levels
of pro-apoptotic cytokines in lung tissues, indicating the induction
of apoptosis by CD40L carried by the EPCs (See figure).
Subpopulations
of breast cancer cells sometimes cooperate to aid tumor
growth, according to Penn State College
of Medicine researchers, who believe that understanding the relationship between
cancer subpopulations could lead to new targets for
cancer treatment.