The researchers have devised a nanosensor that breaks apart in the presence of
ovarian tumor cells and sheds fragments of itself.
The resulting «map» of gene - drug interactions allowed the researchers to accurately predict the responses of multiple human cancer cell lines to different chemotherapy agents based on the cell lines» genetic profiles and also revealed new genetic factors that appear to determine the response of breast and
ovarian tumor cells to common classes of chemotherapy treatment.
«We found a striking difference between the metabolic profiles of poorly aggressive and highly aggressive
ovarian tumor cells, particularly with respect to their production and use of the amino acid glutamine,» said lead researcher Deepak Nagrath of Rice.
Claudin - 4 activity in
ovarian tumor cell apoptosis resistance and migration.
Not exact matches
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.
Shih, Wang and their colleagues tested fostamatinib's power to reduce
tumor size in mice implanted with human
ovarian cancer
cells that were resistant to paclitaxel.
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.»
The study published in Cancer
Cell shows that exosomes from
tumor cells of breast cancer (and other
tumor types such as
ovarian and endometrial) are different in size and composition than those of healthy
cells.
«While the presence of lymphocytes in
tumors is often associated with better clinical outcomes, this research adds clarity on the diversity of T
cells within the
tumor environment and their influence on
ovarian cancer outcomes,» says first author Kunle Odunsi, MD, PhD, FRCOG, FACOG, Deputy Director, M. Steven Piver Professor and Chair of Gynecologic Oncology, and Executive Director of the Center for Immunotherapy at Roswell Park.
One study showed that
ovarian tumors produce a signaling molecule that serves to attract regulatory T
cells, a subclass of adaptive immune
cells responsible for quieting other T
cells.
The lab of co-author Dr. Robert Bast Jr., an expert in
ovarian cancer and vice president for translational research at MD Anderson, inserted gel - bound carbon nanotubes into the ovaries of rodents to mimic the accumulations that are expected for nanotubes linked to special antibodies that recognize
tumor cells.
Researchers at Rice University's Laboratory for Systems Biology of Human Diseases analyzed the metabolic profiles of hundreds of
ovarian tumors and discovered a new test to determine whether
ovarian cancer
cells have the potential to metastasize.
Their results demonstrate that specific rhoptry and dense granule effector proteins that T. gondii secretes before and after host
cell invasion, respectively, control the development of an effective host antitumor response, and increase the survival of mice with
ovarian tumors.
A section of a
tumor organoid grown from
cells derived from a patient with high - grade serous
ovarian cancer (left) and a mini-
tumor treated with ReACp53, resulting in extensive cancer
cell death.
«We think that by isolating the CA125 - negative
tumor cells we have uncovered this reservoir of carboplatin - resistant high - grade serous
ovarian cancer
cells.»
«We expect that the proposed treatment will be especially effective in advanced stages of
ovarian cancers, where there are many cancer stem
cells in the
tumors that resist conventional drug treatment,» says Minko.
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).
They found that
tumor cells with the mutant genes were particularly sensitive to a drug, olaparib, recently approved for the treatment of hereditary
ovarian cancer.
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 3
ovarian cancer cases diagnosed before age 18 years were germ
cell tumors and included in the analysis (Table 1).
And a December 2014 study found that
ovarian tumors coax adult stem
cells into providing key metabolites they need to grow.
Next they treated the experimental
tumor cells with MIR506 to determine if it would behave in the same way it had with
ovarian and other cancers.
The earliest and one of the most striking came from observations that the presence of infiltrating T
cells (called «
tumor - infiltrating lymphocytes,» or TILs) in
ovarian tumors is positively and strongly associated with improved survival of patients with
ovarian cancer [1].
This separation may not be restricted to
ovarian cancer, or to the NCI60 panel of
tumor cells, they suggest, but could apply to a multitude of
tumor types.
He previously revealed the existence of spontaneous immune responses in
ovarian tumors as well as described how regulatory T
cells and
tumor blood vessels affect these responses.
The authors studied a standard panel of 60 established human
tumor cell lines representing nine different human cancers, as well as several specimens of human primary
ovarian cancer.
Their theory was first confirmed with
ovarian cancer
cell lines and then the Peter / Lengyel team tested HGMA2 protein levels in
tumor samples from 100 patients with
ovarian cancer.
The companies have launched a phase II trial of the antibody - drug conjugate, and are also testing it in other solid
tumors, including
ovarian and non — small -
cell lung cancers.
[2] Sato E, Olson SH, Ahn J, Bundy B, Nishikawa H, Qian F, Jungbluth AA, Frosina D, Gnjatic S, Ambrosone C, Kepner J, Odunsi T, Ritter G, Lele S, Chen YT, Ohtani H, Old LJ, Odunsi K. Intraepithelial CD8 +
tumor - infiltrating lymphocytes and a high CD8 + / regulatory T
cell ratio are associated with favorable prognosis in
ovarian cancer.
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NK
cells are a key part of the innate immune system with the ability to recognize and kill diverse types of
tumor cells, including
ovarian cancer.
The
tumor - suppressor gene ARHI (DIRAS3) suppresses
ovarian cancer
cell migration through inhibition of the Stat3 and FAK / Rho signaling pathways.
Growth inhibition of
ovarian tumor - initiating
cells by niclosamide.
Optical quantification of cellular mass, volume, and density of circulating
tumor cells identified in an
ovarian cancer patient.
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.
STC2 overexpression could promote
tumor cell proliferation, invasion, and metastasis in prostate cancer,
ovarian cancer, or neuroblastoma.
Dr. Matsuzaki has accumulated extensive expertise in T -
cell biology and mechanisms of immune suppression in periphery and
tumor microenvironments in patients with
ovarian cancer.
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.
«Visualizing how cancer
cells interact with a
tumor microenvironment that accurately reflects the complex biology of
ovarian cancer should help us understand the mechanisms underlying metastatic progression as well as identify new therapeutics that can inhibit this process,» said clinical gynecologic oncologist Ernst Lengyel, MD, PhD, senior author of the study and a professor of obstetrics and gynecology at the University of Chicago.
A novel approach to cancer immunotherapy — strategies designed to induce the immune system to attack cancer
cells — may provide a new and cost - effective weapon against some of the most deadly
tumors, including
ovarian cancer and mesothelioma.
In the experiments described in the paper, the MGH team confirmed that their mesothelin - targeting fusion protein binds to mesothelin on either
ovarian cancer or mesothelioma
cells, activates dendritic
cells, and enhances the
cells» processing and presentation of several different
tumor antigens, inducing a number of T -
cell - based immune responses.
Tags: checkpoint inhibitors, Clinical Research, immunotherapy, Lung Cancer, McGarry Houghton,
Ovarian Cancer, pembrolizumab, Philip D Greenberg, solid
tumors, T
cell, t
cell therapy, Transplant and Immunotherapy
Curcumin has been clinically shown to inhibit growth of various cancer
cells including: Bone Cancer, Breast Cancer, Brain
Tumors, Colon, Liver, Pancreatic, Stomach, Bladder, Kidney, Prostate, Leukemia,
Ovarian, Melanoma, and more!
The prolonged heat may also be the result of persistent high level of estrogen provoked by an
ovarian cyst or by a granulosa
cell tumor of the ovary.
Granulosa
cell and epithelial
tumors are the most common
ovarian tumors in bitches.
Tumors of ovarian stromal cells include granulosa cell tumors, thecomas and interstitial cell tumors (lute
Tumors of
ovarian stromal
cells include granulosa
cell tumors, thecomas and interstitial cell tumors (lute
tumors, thecomas and interstitial
cell tumors (lute
tumors (luteomas).
Some gerbils can have spontaneous seizures,
ovarian cysts,
tumors, and squamous
cell carcinomas.