«Considering that frequent amplification of MET accounts
for resistance to therapies now in development and to poor prognosis, not only in ovarian cancer but in other cancers too, our findings pinpoint an important new signaling hub, involving the role of FER in MET activation.
Whilst further study is needed, we are building evidence to show that genetic diversity in a bacterial infection or in a tumour being treated could lay the foundation
for resistance to the therapy and affect how quickly resistance develops.»
Not exact matches
I won't reveal yet who my favorites are, but I will say that these young scientist - founders came up with very creative solutions
for preventing infections in some common surgeries, tackling
resistance in targeted antibody drugs, improving gene vectors
for cell
therapies, helping the vision - impaired «see» faces and better read their environments, imaging hard -
to - see spots in the lungs and other organs, improving genetic risk analysis, and expediting the logistical operations of hospitals.
Currently, many patients who acquire
resistance to EGFR - targeted
therapy undergo a tumor biopsy and are designated as either positive or negative
for specific secondary mutations.
Now a University of Colorado Cancer Center study published online ahead of print in the journal Oncogene offers compelling evidence explaining this failure and offering a possible strategy
for the use of retinoic acid or other retinoids against some breast cancers: Because early clinical trials are often offered
to patients who have already tried other more established
therapies, breast cancer cells may have been pushed past an important tipping point that offers retinoic acid
resistance.
Tissue engineering provides a more practical means
for researchers
to study cell behavior, such as cancer cell
resistance to therapy, and test new drugs or combinations of drugs
to treat many diseases.
The analysis suggests that alternative
therapies for certain mild infections — which may be easier
to develop — could indirectly slow development of antibiotic
resistance in more dangerous bugs.
Many leukemias acquire a
resistance to the TKIs used
for the
therapy over time, and the patient suffers a relapse.
If these peptides are developed
for therapeutic use, the researchers anticipate that they could be used either in stand - alone
therapy or together with traditional antibiotics, which would make it more difficult
for bacteria
to evolve drug
resistance.
To compensate for this shortcoming, combination therapy attempts to hit a virus at so many places simultaneously that it can not develop resistance to them al
To compensate
for this shortcoming, combination
therapy attempts
to hit a virus at so many places simultaneously that it can not develop resistance to them al
to hit a virus at so many places simultaneously that it can not develop
resistance to them al
to them all.
«We believe this discovery is a promising avenue
for developing a new
therapy to reduce chemo -
resistance in women with this deadly disease,» said Dr. Dar - Bin Shieh, collaborative partner from National Cheng Kung University of Taiwan.
Insulin
resistance allows hibernating bears
to break down their fat stores, and finding out how they do it could lead
to therapies for type 2 diabetes
«By helping us understand that lower levels of RNF125 confer
resistance to BRAF inhibitors, we have a new strategy
to stratify patients
for currently approved
therapy versus participation
for human clinical trials
to investigate whether targeting JAK1 will be more effective in patients whose tumors exhibit reduced RNF125,» said Keith T. Flaherty, M.D., associate professor, Harvard Medical School, and director of Developmental Therapeutics, Cancer Center, Massachusetts General Hospital, and co-author of the study.
In future, Bandyopadhyay says, better understanding how chemotherapy agents impact specific biological pathways should allow drug trials
to focus on patients who are more likely
to respond
to the drugs being tested and enable clinicians
to identify targeted or combination
therapies for patients with a genetic predisposition
to resistance.
In their report that has received advance online publication in Nature Nanotechnology, a research team based at the Wellman Center
for Photomedicine at Massachusetts General Hospital (MGH) describes how a nanomedicine that combines photodynamic
therapy — the use of light
to trigger a chemical reaction — with a molecular
therapy drug targeted against common treatment
resistance pathways reduced a thousand-fold the dosage of the molecular
therapy drug required
to suppress tumor progression and metastatic outgrowth in an animal model.
The other study — Combination
therapy with potent PI3K and MAPK inhibitors overcomes adaptive kinome
resistance to single agents in preclinical models of glioblastoma — published March 30, shows how drugs targeting PI3K and MAPK could represent promising candidates
for glioblastoma
therapy.
However, these patients will eventually develop
resistance to EGFR TKI
therapy and a further EGFR mutation called T790M accounts
for 60 % of this acquired
resistance.
These findings identify specific BRCA1 mutations that are more likely
to develop
therapy resistance, which may lead
to more accurate predictions and personalized treatments
for breast and ovarian cancers.
The researchers say their method offers a new explanation
for how
to prevent cancer cells from becoming treatment - resistant and how combinations
therapies can be developed
to overcome drug
resistance.
«Understanding how the drugs work gives us the opportunity
to investigate new treatments,
for example by using combination
therapies, or altering the dosage and timing of treatment
to prevent drug
resistance from emerging,» Dr Glaser said.
«Using a novel model we developed
to facilitate discoveries about the growth and spread of lymph node metastases, we show that angiogenesis does not occur in lymph node metastases, providing a mechanism
for resistance to angiogenic
therapy in these situations.»
Shokat and his colleagues wanted
to get ahead of this problem, and began thinking about third - generation mTOR inhibitors without waiting
for patients
to develop
resistance to the latest
therapies.
«Figuring out why
resistance to targeted
therapies develops has been the focus of our research
for a long time,» says Paul Mischel, the paper's co-corresponding author, at the Ludwig Institute
for Cancer Research at the University of California, San Diego.
Increasing
resistance to existing antiviral
therapies and the short time - frame in which these agents are effective highlight the critical need
for new treatments, such as Eritoran.
«It would be very difficult
for the virus
to develop
resistance against a
therapy that targets a cellular protein,» says Palese.
Given that AR - V7 has been associated with
resistance to hormone
therapy but not chemotherapy, the authors speculated that AR - V7 - positive patients should probably be offered chemotherapy rather than hormone
therapy as initial treatment
for mCRPC.
«HER3 is thought
to be an important mediator of
resistance to the HER2 inhibitors class of anti-cancer
therapies, which are used
to treat HER2 - positive breast cancer representing approximately 20 percent of all breast cancers,» said principal author Eric P. Wehrenberg - Klee, MD, from Massachusetts General Hospital in Boston, Mass. «Imaging of HER3 expression may allow
for better understanding of how prevalent HER3 over-expression is among HER2 positive breast cancer patients, which in turn may allow
for appropriate patient selection
for the addition of HER3 inhibitors currently in clinical development.»
«Given the alarming trend of
resistance to our current antimalarial
therapies, this is really an exciting finding,» says Dr. Mota, the senior author of the study, «and we are already working
to develop Torin molecules suitable
for clinical trials of antimalarial activity in humans.»
This work provides direct evidence in mice that cyclin D2 is needed
for a successful response
to a broad spectrum of insulin
resistance, and points toward potential
therapies that can be harnessed
for preventing and curing type 2 diabetes.
We seek
to «Track and Treat» the cancer cells present in patients» tissues by using lineage tracing, as well as sequencing technologies,
to determine the molecular mechanisms responsible
for the dissemination of cancer cells
to various organs, and
resistance to current
therapies.
The bioinformatics team uses sophisticated algorithms
to elucidate markers of response and
resistance to therapy, as well as determine how patients can be stratified appropriately
for the most relevant
therapies under study.»
These models are used
for both basic and translational research, including studies
to investigate the role of tumor initiating cells in tumor relapse, tumor metastasis and
therapy resistance.
We hope CBS - based combination
therapy will open up a new horizon
for the treatment of infection caused by superbugs, serving as a new and more economical
therapy to solve the problem of antimicrobial
resistance (AMR).»
World Health Organization Global Plan
for Artemisinin
Resistance Containment is a call
to action that outlines measures
to protect the value of artemisinin - based combination
therapies for Plasmodium falciparum malaria.
Areas covered by Cancer Cell include, but are not limited
to, molecular and cellular mechanisms of cancer, mechanisms
for the sensitivity and the
resistance to cancer
therapies, and development of better cancer
therapies.
These results show that acquisition of a JAK inhibitor - resistant mutation such as the Y931C in cells dependent on activated JAK2 V617F
for growth is a potential mechanism of secondary
resistance to JAK inhibitor
therapy in MPN patients.
My studies of cancer genomes have led
to characterization of multiple pediatric and adult tumor types,
to development of methods that identify and characterize changes in genomic heterogeneity,
to defining acquired
resistance mechanisms
to targeted
therapies and
to designing novel, personalized vaccines
for individual patients.
The broader impact of this finding
for this disease is that it provides a relatively noninvasive readout of
resistance to PARP inhibitors, and likely
to platinum - based agents, and will allow
for personalization of
therapy based on this readout.
Numerous international publications testify
to the research group's commitment
to identifying metabolic and molecular pathways as potential targets
for innovative
therapies that combine nutraceutical intervention and physical exercise,
for the prevention and treatment of insulin
resistance, of diabetes and associated complications.
These results show that acquisition of a JAK inhibitor resistant mutation such as the F958C in cells dependent on activated JAK1
for growth is a potential mechanism of secondary
resistance to JAK inhibitor
therapy.
My research efforts are focused on identifying novel combination
therapies for breast cancer and the mechanisms that lead
to drug
resistance.
In 2016, Dmitry I. Gabrilovich, M.D., Ph.D., program leader of Wistar's Translational Tumor Immunology program, and his research team identified a marker
for myeloid - derived suppressor cells (MDSCs), a population of immune cells implicated in tumor
resistance to various types of cancer treatment, including targeted
therapies, chemotherapy and immunotherapy.
This work, and that of colleagues Brian Druker and Novartis, led
to the development of the kinase inhibitor imatinib (Gleevec) as primary
therapy for chronic myelogenous leukemia (CML), and the discovery that imatinib
resistance is caused by BCR - ABL kinase domain mutations.
My go -
to herbalist, author and American Herbalist Guild member David Winston of Broadway, New Jersey, says in his book, Herbal
Therapy and Supplements: A Scientific and Traditional Approach, that animal and test - tube studies are convincing enough
to recommend eating maitake regularly as part of a treatment plan
for high cholesterol, high blood pressure, insulin
resistance, and even hepatitis B. (Placebo - controlled studies in people have yet
to be conducted.)
He's not a huge fan of water but has tolerated our request and done really well in the
resistance pool
for therapy - it's helping relieve some of the extra stress he puts on the front half of his body and is a fantastic workout
for him as he does need
to lose a few pounds.
In addition
to needless expense
for owners, and antibiotics potentially having their own adverse side effects, unnecessary administration of antibiotics may lead
to the development of antibiotic
resistance which may further complicate
therapy in the true «Lyme - ill» patient.
In addition
to needless expense
for owners, and antibiotics potentially having their own adverse side effects, unnecessary administration of antibiotics may lead
to the development of antibiotic
resistance which may further complicate
therapy in the true «Anaplasma - ill» patient.
Incorrect
therapy of urinary tract disease, overuse and misuse of antimicrobials can have negative effects on patient health (e.g. failure
to resolve infections), the allocation of resources (e.g. need
for repeated or prolonged treatment), and public health (e.g. antimicrobial
resistance) and may raise regulatory concerns (e.g. antimicrobial use)[13].
In addition
to needless expense
for owners, and antibiotics potentially having their own adverse side effects, unnecessary administration of antibiotics may lead
to the development of antibiotic
resistance which may further complicate
therapy in the true «Ehrlichia - ill» patient.
Antimicrobial
therapy may need
to be continued
for up
to 2 mo, which may promote emergence of antimicrobial
resistance.