Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
1996-10-11
pubmed:abstractText
Progression of gliomas to more malignant phenotypes involves numerous molecular genetic alterations. The genes affected by these alterations, the steps in malignant progression for which they are responsible, their normal function in controlling diverse cellular functions such as differentiation, signal transduction, cell cycle progression and angiogenesis and how they may act in concert with other tumour suppressor genes or oncogenes are some of the questions finally coming into focus and being studied. As other genes are discovered, their association with tumour progression can be assessed, coupled with current histopathology and used to determine more accurately patient prognosis and strategies for intervention. With the generation of specific reagents, such as monoclonal antibodies directed to glioma derived antigens or emerging gene therapy techniques designed to deliver toxic, antisense or reconstituting genes specifically to tumour tissue, new approaches will be devised that may finally be used to treat these tumours effectively.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0261-2429
pubmed:author
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
233-75
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:8718522-Animals, pubmed-meshheading:8718522-Astrocytoma, pubmed-meshheading:8718522-Brain Neoplasms, pubmed-meshheading:8718522-Chromosome Mapping, pubmed-meshheading:8718522-Chromosomes, Human, pubmed-meshheading:8718522-Disease Susceptibility, pubmed-meshheading:8718522-Gene Therapy, pubmed-meshheading:8718522-Genes, Retinoblastoma, pubmed-meshheading:8718522-Genes, p53, pubmed-meshheading:8718522-Glioblastoma, pubmed-meshheading:8718522-Glioma, pubmed-meshheading:8718522-Humans, pubmed-meshheading:8718522-Immunotherapy, pubmed-meshheading:8718522-Mice, pubmed-meshheading:8718522-Mice, Knockout, pubmed-meshheading:8718522-Mice, Transgenic, pubmed-meshheading:8718522-Receptor, Epidermal Growth Factor, pubmed-meshheading:8718522-Receptor, Platelet-Derived Growth Factor alpha, pubmed-meshheading:8718522-Receptors, Platelet-Derived Growth Factor
pubmed:year
1995
pubmed:articleTitle
Genetics and malignant progression of human brain tumours.
pubmed:affiliation
Ludwig Institute for Cancer Research, University of California San Diego, La Jolla 92093-0660, USA.
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't