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.
They note that targeting inflammation
to treat infections offers an advantage over antibiotic
therapy, as the former hinders gene transfer and the evolution
of pathogens, while the latter promotes bacterial evolution and, ultimately, antibiotic
resistance.
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.
The study «provided the surprising result that one new
therapy currently being explored
to lower insulin
resistance promotes, rather than decreases, the formation
of bone in mice,» says Darwin Prockop, a stem cell researcher at Texas A&M College
of Medicine in Temple, who was not involved in the work.
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.
They have also discovered that a protein named Wnt5A promotes metastatic progression,
resistance to therapy and poorer prognosis, and one
of the ways in which it is regulated is by the anti-aging protein Klotho.
The researchers predict that the Thailand border area, which has used the artemisinin - based
therapy since the mid-1990s, will see these levels
of resistance within the next two
to six years.
My cancer systems biology team at the University
of California, Merced, is tackling diagnosis and treatment
of therapy - resistant cancers by elucidating the network
of changes within cells as a way
to identify new drug targets and circumvent cancer
resistance.
However,
resistance to therapy might go beyond cancer mutations that usually alter the function
of genes.
While the combination
of targeted
therapies improves patient outcomes, any remaining cancer cells can lead
to drug
resistance.
«This is a step forward in understanding pancreatic cancer's
resistance to standard
therapies,» said principal investigator Gregory Beatty, MD, PhD, an assistant professor
of Hematology / Oncology at Penn and a member
of Penn's Abramson Cancer Center.
«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.
Sometimes they respond
to renewed treatment, but then develop a
resistance against all methods
of therapy.
This discovery is an important step in the personalisation
of the treatment
of colorectal cancer, as the presence
of this mutation is associated with an increased
resistance compared
to standard
therapies.
«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.
«One criticism
of the PARP drugs is they are not active in patients who have developed
resistance to other
therapies, but we found veliparib appears
to be effective in some platinum - resistant patients with recurrent or persistent disease,» said Robert L. Coleman, MD, lead author
of the study and professor and vice chair
of clinical research at the University
of Texas MD Anderson Cancer Center, Houston.
Just as chemotherapy often requires several drugs
to combat
resistance in cancerous cells, successful antimicrobial
therapy against some pathogens requires a combination
of drugs.
The threat
of antibiotic
resistance is nothing
to scoff at: The World Health Organization predicts (pdf) that some diseases, including malaria, tuberculosis, and pneumonia, could have «no effective
therapies within the next 10 years.»
Until RDTs became widespread, almost all fevers were treated as if they were malaria, leading
to the overuse
of the new generation
of «wonder drugs,» artemisinin - based combination
therapies (ACTs), which were in danger
of being lost
to drug
resistance.
Cancer stem cells are strongly associated with the growth and recurrence
of all cancers and are especially difficult
to eradicate with normal treatment, which also leads
to tumours developing
resistance to other types
of therapy.
«There has been a groundswell
of interest in the idea
of reversing
resistance to androgen deprivation
therapy.
They enabled health workers in remote villages in Africa and Asia
to accurately and almost instantly diagnose malaria, making them less likely
to overuse the new generation
of «wonder drugs,» artemisinin - based combination
therapies (ACTs), which were in danger
of being lost
to drug
resistance.
This high mortality is primarily caused by
resistance to therapy and the diagnosis
of ovarian cancer after it has already metastasized, which occurs in approximately 80 percent
of patients.
The emphasis now is
to store samples from almost every major study with correlative science in mind, and this is essential if we are
to understand disease biology, mechanism
of response and
resistance to therapy in the era
of targeted
therapy and precision medicine.»
«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.
Loss
of the tumor suppressor p53 often contributes
to therapy resistance in tumors.
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 over-prescribing
of anti-malarials puts evolutionary pressure on the malaria parasite that risks hastening its
resistance to artemisinin - based combination
therapy — the frontline drugs used
to treat malaria in Africa,» Stoler said.
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.
«
Resistance to hormonal
therapy is a major clinical problem in the treatment
of most breast cancers.
As a clinician - scientist with a translational research focus, Dr. Deininger is heading an extramurally funded research laboratory that is dedicated
to the study
of signaling pathways, drug
resistance, and new molecular
therapies in leukemia.
This finding is
of particular concern, Murakami says, because if the bacterium is not eradicated after the recommended
therapy, it could indicate potential
resistance to drugs
of choice.
Field reports suggest that not all K13 mutations are capable
of causing
resistance, and the genetic system developed by Dr. Fidock
to study K13, based on DNA repair approaches that are being used in human gene
therapy studies, will be critical in identifying real hot spots
of resistance.
Though malaria deaths have dropped by 30 percent worldwide since the introduction
of artemisinin - based combination
therapies (ACTs) in the late 1990s, these gains are now threatened by the emergence
of resistance to the core artemisinin component
of ACTs in Southeast Asia.
Gene
therapy could impart this kind
of resistance to others.
The tumors often develop
resistance to existing
therapies, and in general only 50 %
of people with the cancer live longer than 15 months.
«Globally,
resistance to some strains
of pneumonia is increasing, so it is imperative
to increase development in the R&D pipeline
of new antibacterial
therapies, especially infections that are acquired in - hospitals, where the pathogens are highly resistant.»
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.
And while new
therapies have been effective in releasing the immune system's restraints
to unleash the body's own cancer - fighting powers, they only work in about half
of melanoma patients and often lose their potency as the cancer develops
resistance.
The study also adds
to our understanding
of disease development and
therapy resistance,» Theodorescu says.
«This may be compensatory and a mechanism
of resistance to anti-psoriasis
therapy, and it suggests that the solenopsin compounds could be used in combination with existing approaches,» Arbiser says.
«Current
therapies take advantage
of this by using targeted drugs such as Trastuzumab or Lapatinib
to specifically inhibit ERBB2, but eventually they become ineffective as the cancer develops
resistance to those drugs.»
«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.
Researchers developed the strategy as a way
to develop inhibitors
of «undruggable» proteins and overcome drug
resistance, a common shortcoming
of targeted
therapies.
This visual abstract depicts how Wei et al. utilize single - cell phosphoproteomic analysis
of patient derived glioblastoma models
to identify shifts in signaling coordination following short - term treatment with kinase inhibitors, which facilitates the design
of combination
therapy approaches with reduced
resistance and improved efficacy.
«We have previously demonstrated the role
of MDSCs as important mediators
of resistance to immune
therapy approaches.