Not exact matches
Researchers led
by Patricia Donahoe and Xiaolong Wei of Massachusetts General Hospital and Harvard Medical School found that the common chemotherapy agent doxorubicin actually encourages the growth of
ovarian cancer stem
cells.
Chemotherapy drugs designed to kill tumors may actually encourage
ovarian cancer by stimulating the growth of
cells that give rise to the malignancy, a new study finds.
The research shows that ONA reduces the progression of malignant
ovarian cancer tumors
by interfering with the pro-tumor function of myeloid
cells.
«In pancreatic,
ovarian and liver
cancers, we hope that
by adding anti-cancer stem
cell drugs to standard of care, we can control proliferating
cells within the tumor that could otherwise help the tumor regenerate in the face of existing chemotherapies.»
«For this reason, we decided to combine vitamin C with a PARP inhibitor, a drug type known to cause
cancer cell death
by blocking the repair of DNA damage, and already approved for treating certain patients with
ovarian cancer.»
The researchers treated 63
cancer cell lines (26 breast, 14 colorectal and 23
ovarian) with low - dose 5 - azacitidine (AZA), an FDA - approved drug for myelodysplastic syndrome, that reverses epigenetic changes
by stripping off the methyl group that silences the gene.
The researchers then exposed
cells from each of these lines to a panel of 31 different drug treatments — including 23 chemotherapy compounds approved
by the FDA for breast and
ovarian cancers, six targeted
cancer drugs, and two common drug combinations.
«We think that
by isolating the CA125 - negative tumor
cells we have uncovered this reservoir of carboplatin - resistant high - grade serous
ovarian cancer cells.»
While previous research had shown some effectiveness of this molecule in a mouse model of
ovarian cancer, that benefit was limited
by the immunosuppressive environment within tumors, particularly the presence of regulatory T
cells (Tregs).
Led
by Ludwig Lausanne investigator Alexandre Harari and George Coukos, director of the Ludwig Institute for
Cancer Research, Lausanne, the study shows that
ovarian tumors harbor highly reactive killer T
cells — which kill infected and cancerous
cells — and demonstrates how they can be identified and selectively grown for use in personalized,
cell - based immunotherapies.
The class of compounds that includes GDC - 0449 could also help contain other
cancers, such as
ovarian and colorectal
cancers, that are not triggered in the same way as medulloblastoma or basal
cell carcinoma but that are still partly driven
by aberrant Hedgehog signaling.
Currently, she is investigating how inhibiting aldehyde dehydrogenase can kill
ovarian cancer stem
cells by inducing necroptosis.
Growth inhibition induced
by antiprogestins RU - 38486, ORG - 31710, and CDB - 2914 in
ovarian cancer cells involves inhibition of cyclin dependent kinase 2.
$ 1.8 M Supports
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Cancer Ribbon?
Coukos, who is currently leading an
ovarian cancer clinical trial sponsored
by CRI's Clinical Accelerator, sought to understand why PD - 1 / PD - L1 immunotherapies are often ineffective for these patients, even though
ovarian tumors are often infiltrated
by «killer» T
cells that recognize tumor - specific neoantigens and express high levels of PD - 1.
Surveillance of the tumor mutanome
by T
cells during progression from primary to recurrent
ovarian cancer.
Review of «Induced Pluripotent Stem
Cell - Derived Natural Killer
Cells for Treatment of
Ovarian Cancer» from Stem
Cells by Stuart P. Atkinson
Matsuzaki J, Gnjatic S, Mhawech - Fauceglia P, Beck A, Miller A, Tsuji T, Eppolito C, Qian F, Lele S, Shrikant P, Old LJ, Odunsi K. (2010) NY - ESO - 1 specific tumor infiltrating CD8 + T
cells in human
ovarian cancer: negative regulation
by LAG - 3 and PD - 1.
The approach developed
by the MGH team starts with the engineered protein, which in this case fuses an antibody fragment targeting a protein called mesothelin — expressed on the surface of such tumors as mesothelioma,
ovarian cancer and pancreatic
cancer — to a protein from the tuberculosis bacteria that stimulates the activity of dendritic and other immune
cells.
The research team confirmed those results
by testing the four compounds at a low dose in mice injected with
ovarian cancer cells.
In 80 percent of women,
by the time
ovarian cancer is diagnosed, it has spread to the pad of fat
cells, called the omentum.
Sulforaphane induces
cell cycle arrest
by protecting RB - E2F - 1 complex in epithelial
ovarian cancer cells.
According to experts,
by modulating the secretion of angiogenic factors in
ovarian cancer cells, ginger is can be one of the most potent natural ingredients against this disease.
According to the American
Cancer Society, ginger can combat ovarian cancer by blocking the cancer cells from growing, preventing it from spreading and causing more harm to the
Cancer Society, ginger can combat
ovarian cancer by blocking the cancer cells from growing, preventing it from spreading and causing more harm to the
cancer by blocking the
cancer cells from growing, preventing it from spreading and causing more harm to the
cancer cells from growing, preventing it from spreading and causing more harm to the body.