BRCA1 and 2, genes whose proteins are supposed to
work as tumor suppressors and also repair DNA damage, were the first known risk factor genes for familial breast cancer as well as ovarian and other cancers.
«These results showed us that epithelial TRPV1 normally
works as a tumor suppressor in the intestines,» said de Jong.
In a series of in vitro experiments, the researchers demonstrated that C / EBPα indeed
works as a tumor suppressant by restraining the expression of another molecule known to play a role in triggering and maintaining tumor growth.
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.
His
work indicates that this cell surface marker could serve
as a target for a novel brain cancer vaccine or T - cell therapies engineered to recognize and kill
tumors carrying that neoantigen.
As researchers learn more about genetic profile of various cancers, other
work is charging ahead to deliver personalized vaccines targeted to a patient's own
tumor cells
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.
«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.
A glioblastoma
tumor requires large amounts of energy
as it grows, and the dietary intervention
works by drastically limiting the
tumor's supply of glucose, Reynolds said.
Chemotherapy aimed at killing single cells may not
work as efficiently against bands of spreading
tumor cells, she said.
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.
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.
This cytokine they thought was a treatment for cancer was actually
working as an endogenous
tumor promoter.
The
work also reinforces the importance of finding
tumor cell clusters in the blood
as a mechanism of detecting cancer metastasis earlier.
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.
Early - stage data suggests the investigative LAMP - Vax technology
works by fusing
tumor antigens to a cellular protein known
as LAMP (Lysosomal - Associated Membrane Protein).
«But the immune system can get overwhelmed when there is too much
tumor, and not
work as effectively
as possible,» he says.
Sanford Research scientists are published in Nature Cell Biology for their
work developing a model to explore therapies for a pediatric brain
tumor known
as choroid plexus carcinoma.
Looking forward, Gimi's
work will focus on using these microencapsulated cells to stimulate the immune system to act against
tumors,
as well
as activating drug synthesis.
This causes genomic instability in developing immune cells and, in the absence of a
working tumor suppressor protein such
as p53, an aggressive form of lymphoma develops in mice.
The scientist explains that the nanoparticle
works as a bridge of antitumor activation between
tumor cells and T lymphocytes.
This
work shows that the
tumor microenvironment itself can compromise the efficacy of targeted therapies and should be taken into account
as new treatment approaches are developed.»
In their previous
work, the scientists suspected that C / EBPα may act
as a
tumor suppressant in normal cells, but the mechanism by which its absence promoted lung cancer
tumors remained unclear.
IP5
worked as well
as cisplatin in reducing the volumes of the
tumors, the team reports today in Cancer Research.
As Fiebig found in his early
work,
tumor samples do not always successfully graft onto the mice.
Although there is new data coming from Dr. Michel Sadelain's lab and others where they have made a molecule that may
work as a CAR T cell that would then bind to NY - ESO - 1 peptides displayed on the surface of a
tumor cell.
«Our
work supports the idea of exploring the use of Onyx - 015 in
tumors that we presumed would be immune to the drug because they were thought to frequently have p53 genes, such
as such
as melanoma and glioblastoma [a form of brain cancer].
Drugs used in chemotherapy, such
as ifosfamide and doxorubicin hydrochloride,
work in different ways to stop the growth of
tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading.
To develop new drugs and determine what treatments are most appropriate for different
tumor stages, scientists need to
work out what changes occur at a molecular and genetic level
as a
tumor progresses.
Since starting her new role
as an investigator in the In Vivo Pharmacology group at Novartis Oncology, Bhang has been
working on using the ClonTracer library to monitor clonal dynamics following drug treatment in cell line and primary
tumor xenograft models.
As an active researcher, much of her
work is focused on regulation of angiogenesis in pediatric solid
tumors, including Wilms»
tumor, neuroblastoma, and hepatoblastoma.
DCEG investigators are also
working to identify novel molecular and genomic signatures in
tumors that are linked to germline genetic variants and environmental exposures, such
as cigarette smoking and ionizing radiation.
Their
work encompasses several strategies, including: developing FL - HCC animal models to characterize
tumor - immune interactions, exploring if a mutated protein associated with FL - HCC could be targeted by immunotherapy, identifying immune checkpoints that could potentially serve
as targets for immunotherapy
as well
as biomarkers for analyzing patients, and evaluating the effectiveness of immunotherapy strategies against FL - HCC patient samples in the lab.
The lab also found that apoptotic
tumor cells serve
as potent instigators of the T cell immune response and has
worked on developing cancer vaccines to mimic PND
tumor immunity.
It's called molecular - targeted therapy and it
works as advertised: The drugs do disable the molecules that drive growth — but, again,
tumors figure out a new way to grow.
As part of our Melanoma Moon Shot, our team of clinicians and scientists
work together to study blood and
tumors that are collected from patients on these trials.
During his 11 years of extensive
work experience in the fields of cell and cancer biology (including
work on the famous
tumor suppressor gene BRCA1), and biochemistry he has successfully published in peer - reviewed journals such
as Molecular and Cell Biology and Cancer Research.
Dual Approach Better for Liver Cancer A combined treatment for liver cancer that uses one oral drug and another delivered directly to
tumors in a method known
as chemoembolization appears to
work better against liver cancer.
Data generated by the
working group, which includes molecular profiling of over 10,000
tumors across 33
tumor types
as well
as a series of results on immune -
tumor interaction and response mechanisms, will provide rich characterizations of the relationship between
tumors and the immune microenvironment and its impact on patient outcomes.
In combination with this approach, inhibitors of DNA methylation and / or histone deacetylases are expected to relieve repression of DAPK
tumor suppressors, whose epigenetic silencing has emerged
as a recurring theme from our
work and throughout the literature.
A unique focus of my
work is on the impact of heterogeneity within
tumors and
tumor cell populations, including subpopulations commonly referred to
as «cancer stem cells», on the immune response.
Recently, Swanton gave a talk at his older daughter's school on his recent
work that uncovered HLA loss
as a way
tumors avoid being recognized by the immune system.
Working with James Hicks, a biologist at USC, the team was able to detect
tumor DNA in tiny fragments that had likely been loosed
as tumor cells died and broke up.
I had a hunch based on this
work that microRNA expression would be different in breast cancer stem cells than in more differentiated
tumor cells or normal tissue and that it would change
as the stem cells differentiated to form a
tumor.
Researchers led by St. Jude Children's Research Hospital scientists have
worked out how a crucial cancer - related protein, a «histone writer» called Ezh2, plays a role in suppressing
as well
as driving the most aggressive form of the brain
tumor medulloblastoma.
Building on each other's
work, the five award recipients demonstrated how this normal self - defense mechanism can be hijacked by
tumors as a way to evade immune surveillance and dodge an attack.
Prior to
working at City of Hope, she
worked as a research associate in Dr. Peter Lee's lab at Stanford University since 2006 and facilitated in investigating mechanisms causing immune dysfunction in melanoma and breast cancer patients» peripheral blood, lymph node and
tumor specimens utilizing techniques including microarray analysis, RT - PCR, Phospho - flow cytometry, histoloogy, and functional FACS studies.
While the drug blocks the effect of estrogen in breast tissue or
tumors, it can help estrogen do beneficial
work in other parts of the body, such
as the heart and bones.
According to Lewis Cantley, director of the Cancer Center at Beth Israel Deaconess Medical Center at Harvard Medical School,
as much
as 80 percent of all cancers are «driven by either mutations or environmental factors that
work to enhance or mimic the effect of insulin on the incipient
tumor cells,» Gary Taubes reports, vii adding:
Some of these treatments such
as Gerson Therapy
work to strengthen and balance the immune system and take some time to be effective while other treatments, such
as High Dose Vitamin C intravenous therapy, target cancer cells safely and
work right away to decrease
tumor load, allowing time for the nutritional program to
work.