«If you show
it works in tumor studies, I have no trouble with it being the guideline for tumor studies,» he says.
«Researchers are using newer technologies to look directly into tumors,» she says, «to make sure immunotherapies induce a response that
works in the tumor.»
Drugs like pembrolizumab boost the response in tumors where immune cells are present but don't
work in tumors where there is no immune response to boost.
He says that the mechanism is unlikely to
work in all tumor types or metastases, but that it is definitely worth exploring its potential ability to turn some fatal cancers into chronic diseases.
Not exact matches
The Kamens claim the main thing that distinguishes their foundation from other brain
tumor foundations is their focus on pediatric brain cancer specifically, as well as their close ties with pharmaceutical and biotech companies
working in the fields of immunotherapy and target gene therapy.
Kneaders found a partner
in Huntsman Cancer Institute, an organization that is
working with the University of Utah to conduct research into how DNA from elephants, which are resistant to
tumors, could be used to cure childhood cancer.
Previous
work in Weinberg's lab had shown that after a
tumor forms
in one part of the body, some of the cancer cells undergo EMT, Mani explains.
For some years now, a new class of drugs called antibody - drug conjugates (ADCs) have been used, which
work in two ways: they consist of an antibody that binds selectively to the
tumor cell receptor and interrupts the signal to propagate; they also act as a transport vehicle for a chemical substance that enters the cancer cells with the antibody and triggers their death.
In a recent study, working with a team of researchers, Danino demonstrated that bacteria in pancreatic tumors degrade a chemotherapy drug — Gemcitabine — most commonly used to treat patients who have pancreatic cance
In a recent study,
working with a team of researchers, Danino demonstrated that bacteria
in pancreatic tumors degrade a chemotherapy drug — Gemcitabine — most commonly used to treat patients who have pancreatic cance
in pancreatic
tumors degrade a chemotherapy drug — Gemcitabine — most commonly used to treat patients who have pancreatic cancer.
The
work, reported online today
in Science, could one day lead to a tool for routinely screening people and catching
tumors before they cause symptoms, when chances are best for a cure.
«Our
work strongly supports that cancer stem cells are the main source of growth
in these
tumors and, as such, should be considered promising targets for treatment,» says Mario Suvà, MD, PhD, of the MGH Department of Pathology, co-senior author of the Nature paper.
For some cancer patients, viruses engineered to zero
in on
tumor cells
work like a wonder drug.
The virus, redesigned using sophisticated protein engineering techniques,
works: With its shield and its adapter, these viral gene shuttles efficiently infected
tumor cells
in laboratory animals.
In demonstrating that FOXO4 works to prevent the spread of cancerous tumors by binding to and inhibiting the protein RUNX2, the team identified a circuit that controls metastatic progression in prostate cance
In demonstrating that FOXO4
works to prevent the spread of cancerous
tumors by binding to and inhibiting the protein RUNX2, the team identified a circuit that controls metastatic progression
in prostate cance
in prostate cancer.
«Different types of cancer cells with different strengths and weaknesses are both present
in the
tumor at the same time and can
work together to spread faster and more efficiently.
Working with colleagues at St. Vincent's Hospital
in Sydney, Martin identified two individuals who had the characteristics of hereditary nonpolyposis colorectal cancer, which is usually caused by a mutation that inactivates one of a person's two copies of the
tumor suppressor gene MLH1, but who showed no signs of mutation.
Maria Zajac - Kaye, Ph.D., an associate professor
in the College of Medicine's department of anatomy and cell biology, and Rony François, an M.D. / Ph.D. student who
works with her, found a new drug combination that inhibits one form of pancreatic cancer
tumor and kills its cells.
The company is also
working on a similar test
in solid
tumors for early diagnosis of relapse, and is developing tests that will help diagnose some lymphomas that are notoriously tricky to detect.
Cells suspended
in a stiff matrix were more likely to
work their way through the matrix to other side of a serum gradient, analogous to how metastasizing cancer cells break free from their
tumors.
A case of cancer was diagnosed
in his family, and Delahaye decided to spend his postdoc
working on
tumor immunogenetics
in the laboratory of Laurence Zitvogel at the Institut Gustave Roussy
in Paris.
«Despite the low infection levels of mouse cells with oHSV, we were able to cause a delay
in tumor growth
in one of the cancer models and even cure many of the mice
in a second model,» said first author Jennifer Leddon, who conducted much of the laboratory
work during a research experience
in the Center for Childhood Cancer and Blood Diseases.
«The effective immune response didn't happen
in every
tumor model we tested, so we still need to figure out exactly what triggered the
tumor shrinkage and how to predict which
tumors will shrink
in response to virotherapy,» said Leddon, who is also
working toward her medical and doctoral degrees at the University of Cincinnati.
But as noted
in a recent Science news story, targeted therapies don't
work as well on solid
tumors, which usually develop resistance and start growing again.
Previous
work on cartilage
tumors has been done using models based on genetic mutations that occurred only rarely
in enchondromas; however, IDH mutations are present
in a high percentage of enchondromas.
Dr. Preul directs the Neurosurgery Research Laboratory of the Barrow Neurosurgical Institute, which has carried out the pioneer
work in applying and developing confocal laser endomicroscopy for brain
tumors.
The
work demonstrates that BRAF - mutated melanoma requires autophagy for
tumor development and blocking autophagy could have therapeutic value, particularly
in combination with BRAF inhibition.
«Hodgkin lymphoma is unusual among cancers
in that it consists of a small number of
tumor cells
in a sea of inflammatory cells and immune system cells, including T cells that don't
work very effectively.»
His
work on RMP - 7 came to naught
in 1998: «We demonstrated
in the Phase 1 and 2 trials that when RMP - 7 was delivered directly into the carotid artery that fed the
tumor, we could open the blood - brain barrier and get clinical responses to the chemo.
The class of medications that he conceived, known as immune checkpoint inhibitors,
works counterintuitively: By turning off one of the immune system's built -
in safeguards, the inhibitors allow T cells — the system's foot soldiers — to attack
tumors more effectively.
«Now we're investigating how the protein
works in order to be able to develop a drug that could prevent
tumor metastasis.»
Frank Ruscetti, who had discovered HTLV - 1 while
working in Robert Gallo's Laboratory of
Tumor Cell Biology at the NCI
in 1980, was Mikovits's primary collaborator.
In a previous study, his team
worked with other collaborators to identify the potential role of extra copies of the
tumor suppressor gene (p53) that increase the elephant's ability to eliminate pre-cancerous cells with DNA damage.
In a study published in the Journal of NeuroOncology, TGen researchers report that PPF works to limit the spread of glioblastoma multiforme, or GBM — the most common primary tumor of the brain and central nervous system — by targeting a protein called TRO
In a study published
in the Journal of NeuroOncology, TGen researchers report that PPF works to limit the spread of glioblastoma multiforme, or GBM — the most common primary tumor of the brain and central nervous system — by targeting a protein called TRO
in the Journal of NeuroOncology, TGen researchers report that PPF
works to limit the spread of glioblastoma multiforme, or GBM — the most common primary
tumor of the brain and central nervous system — by targeting a protein called TROY.
«By understanding how stress accelerates invasion
in aggressive breast
tumor cells, this
work will inform future studies into whether beta - blockers could be a useful adjuvant therapy
in the treatment of some aggressive breast cancers.»
The
work also reinforces the importance of finding
tumor cell clusters
in the blood as a mechanism of detecting cancer metastasis earlier.
«We had a hypothesis about how these treatments would
work together, and when we did biopsies of patients»
tumors we found that they were cooperating
in just the way we thought they would,» says lead author Antoni Ribas, director of the Immunology Program at the UCLA Jonsson Comprehensive Cancer Center.
Previous
work also suggested synergistic impact of isoprenoids on
tumor growth, a finding remaining to be confirmed
in prostate cancer.
The Oncotarget study demonstrated that Brenner's antibody
worked in animal models of
tumors that made cadherin - 11.
Combining their strategy with an existing immunotherapy treatment that
works by releasing the «brakes» on immune cells, they found they could shrink melanoma
tumors, and prolong survival
in preclinical models for melanoma.
«We have shown that our molecule
works on cancer cells
in the lab, but the next step is to see if it
works on real
tumors in animals.
«Our
work paves the way to discovering many more of these unusual RNAs and how they contribute to cancer, which could reveal new mechanisms and druggable pathways involved
in tumor progression.»
Published
in Nature Photonics, this
work might lay a foundation for
in vivo experiments that use light
in biomedical imaging, optogenetics,
tumor treatment, and for recharging implanted medical devices.
The finding warrants research into adding drugs that could prevent the cancer from hijacking patients» repressive gene regulatory machinery, which might allow the original therapy to
work long enough to eradicate the
tumor, the researchers report
in their National Institutes of Health - funded study, published
in the current issue of Science Translational Medicine.
Working in mouse models of primary, non-metastatic
tumors, the researchers increased the production of the tRNAs, and found that these cells became much more invasive and metastatic.
How aspirin
works is a longstanding puzzle, but Harris and others theorize that it may help inhibit cancer by blocking cyclooxygenase - 2, or COX - 2, an enzyme commonly found
in malignant
tumors.
«Radioimmunotherapy not only
worked against these cancers but,
in addition, the radioactivity was confined entirely to the
tumor masses, leaving healthy tissues undamaged,» said senior study co-author Ekaterina Dadachova, an associate professor of nuclear medicine and of microbiology and immunology at Einstein.
«The use of a mouse
tumor - derived matrix would limit any future applications of these organoid technologies
in humans, and this
work opens the door to research directed specifically for clinical applications,» noted Asma Nusrat, study co-author and the Aldred Scott Warthin Professor and Director of Experimental Pathology
in the University of Michigan's School of Medicine.
They
work particularly well if the cancer cells they attack already have defects
in the corresponding DNA repair pathways, as it frequently occurs
in breast cancer and other
tumors.
Drugs like fluorouracil, oxaliplatin and irinotecan
work by mimicking and damaging DNA molecules, or inhibiting enzymes involved
in cell and DNA replication, slowing the uncontrolled growth of
tumor cells.
In the future, their
work could help scientists to better understand the formation of
tumors.