«Importantly, while the overall number of new investigational cardiovascular drugs has declined, we also found a relative growth in
the number of drugs targeting novel biological pathways,» Kesselheim said.
The increasing
number of drugs targeting specific proteins implicated in tumourigenesis and the commercial promotion of relatively affordable genome - wide analyses has led to an increasing expectation among patients with cancer that they can now receive effective personalised treatment based on the often complex genomic signature of their tumour.
Friedman notes that, even with the increasing
number of drugs targeting specific molecular abnormalities that drive tumor growth, most patients are only treated with one such drug at a time.
Researchers in Sweden have just identified
a number of drug targets that can be used in the development of new efficient treatment strategies with minimum side effects.
Not exact matches
She says a
number of experimental
drugs now in clinical trials are designed to
target serotonin in other ways in the brain, and may have better success than the SSRIs.
From accelerating the identification and validation
of novel therapeutic
targets, to creating better animal models
of human diseases in a shorter time frame, to reducing the
number of failed products, Crispr looks set to shave millions off R&D costs and boost
drug discovery, she says.
«The
number of protein functions that are currently
targeted by
drugs is incredibly small compared to the total
number of protein interactions that could be
targeted for therapeutic benefit,» says Geoffrey Wahl, a professor in Salk's Gene Expression Laboratory.
It is triggered by the immune system, and new insights into immune processes have thrown up a
number of exciting
drug targets.
Structure - based
drug design, in which the physical structure
of a
targeted protein is used to help identify compounds that will interact with it, has already been used to generate therapeutic agents for a
number of infectious and metabolic diseases.
Unsurprisingly, then, MET is the
target of a
number of drug development efforts, which have in common the aim
of blocking MET's activation.
A
number of drugs that
target the p53 pathway, like Nutlin - 3, are currently in clinical development.
In an effort to expand the
number of cancer gene mutations that can be specifically
targeted with personalized therapies, researchers at University
of California San Diego School
of Medicine and Moores Cancer Center looked for combinations
of mutated genes and
drugs that together kill cancer cells.
Further, a significant percentage
of these complex mutations are found in well - known cancer genes that could be
targeted by existing
drugs, potentially expanding the
number of cancer patients who may benefit.
Mardinoglu says the team's network modeling approach, which relied on data from the Sweden - based Human Protein Atlas project and The Genotype - Tissue Expression (GTEx) project consortia, can be used in the identification
of drug targets and eventually in the development
of efficient strategies for treating a
number of chronic liver diseases.
However, the reality is that nanocarriers may not always reach their intended
target in sufficient
numbers because
of a constraint on their ability to transit through the blood vessel wall at the tumor site, leading the encapsulated
drugs to be diverted or lost before they can deliver their payload.
Thus, the glutamate pathway has become the
target of a
number of new
drug therapies.
A small
number of these mutations have been found previously in other cancers, and
drugs have been developed to
target these mutations,» said lead author Raphael Bueno, MD, chief
of the Division
of Thoracic Surgery at BWH and co-director
of the BWH Lung Center.
Although a small
number of repurposed and new
drugs have recently become available to treat
drug - resistant TB (including bedaquiline, delamanid, and linezolid), the authors warn that without accurate diagnostic tests to deliver individually
targeted treatments, clear prescription guidelines on appropriate use and improved control efforts to prevent transmission, optimal dosing and administration, and well - functioning health care systems, the effectiveness
of the
drugs could be rapidly lost.
To narrow down the
number of chemical compounds that could be potential
drug candidates, scientists utilize computer models that can predict how a particular chemical compound might interact with a biological
target of interest — for example, a key protein that might be involved with a disease process.
He thinks a
number of cancer cell subsets are never really affected by most
targeted anticancer
drugs currently used.
Ahead
of us now is the major task
of exploring the potential
of new
drug targets, so that hopefully we can prevent the
number of people with untreatable infections from escalating further,» says Professor Anders Miki Bojesen, who coordinates the UC - Care research activities at the Department
of Veterinary Clinical and Animal Sciences.
Research led by scientists at the University
of Birmingham shows more precisely how G protein - coupled receptors, which are the key
target of a large
number of drugs, work.
«We are working to increase our understanding
of Alzheimer's disease all the time, and there are already a
number of drugs in clinical testing that are
targeted against amyloid.
It can be used in the identification
of drug targets and eventually in the development
of efficient strategies for treating a
number of chronic liver diseases.
Lung cancer treatment is an evolving field
of science, currently there are several pathways under investigation as a possible treatment target.1 - 3
Targeted treatment is currently considered to be more efficient compared to the non-specific cytotoxic
drugs, however; the small
number of patients identified with mutations, limit the application
of these
drugs.
Vescor, advised by its scientific founders White and Kimmelman, whose research has shown inhibition
of autophagy can dramatically impact tumor growth in pre-clinical models, will develop small molecule inhibitors
of a
number of protein
targets at critical nodes
of the autophagy cascade, perform investigational new
drug (IND) enabling studies, and move these into clinical development.
In the search for compounds that might alter a protein's behavior or function — such as that
of alpha - synuclein —
drug companies often rely on so - called
target - based screens that test the effect large
numbers of compounds have on the protein in question in rapid, automated fashion.
Horizontal transfer
of genes
of bacterial origin has contributed to some
of the metabolic differences in these parasites, and a
number of novel potential
drug targets have been identified.
The study includes a detailed picture
of the proteins that are linked to cancer, the
number of proteins present in the bloodstream, and the
targets for all approved
drugs on the market.
Fortunately, there are a
number of targeted drugs in phase III clinical trials.
They expect that many genes will overlap and affect the same cellular process, which will help them narrow down the
number of potential
drug targets.
We are applying it to evaluate large
number of potential
drug targets in a faster and more systematic way than before and to select the best ones to work on.
Knowledge
of these mutations could potentially identify a greater
number of patients with treatable mutations because many potent cancer
drugs that
target these mutations already exist.
In fact, a predominant
number of current
drugs target the GPCR signaling.
To understand the selection mechanism behind mutations, network - based studies were used to estimate the importance
of a mutated protein compared to non-mutated ones in signalling and protein — protein interaction networks.10, 11,12,13 Proteins mutated in cancer were found having a high
number of interacting partners (i.e., a high degree
of connectivity), which indicates high local importance.10 Mutated proteins are also often found in the centre
of the network, in key global positions, as quantified by the
number of shortest paths passing through them if all proteins are connected with each other (i.e., they have high betweenness centrality; hereafter called betweenness).11, 12 Mutated proteins also have high clustering coefficients, which means their neighbours are also neighbours
of each other.10, 13 Moreover, neighbourhood analysis
of mutated proteins have been previously successfully used to predict novel cancer - related genes.14, 15 However, to the best
of our knowledge, no study has concentrated particularly on the topological importance
of first neighbours
of mutated proteins in cancer, and their usefulness as
drug targets themselves.
This led to the development
of a
number of drugs that
targeted and blocked specific receptors in this pathway.
Police will soon be launching their national campaign which will
target drink drivers, as the
number of drink and
drug driving offences increases hugely around the Christmas time.
Goals: Formalise and rationalise the collection
of data in the region; reduce by half the
number of Aboriginal and Torres Strait Islander children on long - term care and protection orders by 2008; Achieve a
target of 90 %
of Aboriginal and Torres Strait Islander children enrolled in pre-primary and kindergarten programs by 2008; reduction in truancy rates; achieve 20 % increase in participation rates in sport and recreation; reduce
number of alcohol related and
drug related incidents in community.