Not exact matches
A high degree of
aneuploidy is a feature of high - grade
tumors and is associated with poor prognosis.
Many
tumors are characterized by «
aneuploidy,» meaning they display an abnormal number of chromosomes and chromosomal segments.
«Unfortunately our paper suggests that
tumors don't even need to be heterogeneous genetically, the very fact that they have
aneuploidy could lead to very variable outcomes, and that represents a significant challenge for cancer therapy,» Amon says.
Elledge argues that simply losing or gaining one copy of a gene through
aneuploidy can influence
tumor growth as well.
Aneuploidy (an abnormal number of chromosomes) is the most common genetic alteration in human
tumors and a major cause for birth defects (Figure 4).
Errors in chromosome segregation are a major cause for birth defects and embryonic lethality in humans, and the most common genetic alteration in human
tumors is aberrant chromosome numbers, called
aneuploidy.
Errors in chromosome segregation can cause birth defects and embryonic lethality in humans and cause
aneuploidy, the most common genetic alteration in
tumors.
The efficient compaction of DNA during cellular division ensures equal distribution of DNA into daughter cells and prevents
aneuploidy, which has been implicated as a major driver of
tumor development.
This case includes the majority of
tumor samples and perhaps genomes with mosaic
aneuploidy.
Moreover, many human
tumors have highly abnormal numbers of chromosomes (that is, they are aneuploid), with initial chromosomal loss participating in the early steps of the transformation cascade in inherited cancers caused by heterozygous mutation in
tumor suppressor genes and the more widespread
aneuploidy characteristic of advance
tumors thought to drive acquisition of malignant growth properties.??
Using a series of genetically - matched euploid and aneuploid cell lines, we have demonstrated that
aneuploidy can paradoxically function as a barrier to
tumor growth.
By identifying phenotypes that are shared among
tumors with different
aneuploidies, we hope to discover pathways that can be manipulated to selectively eliminate aneuploid cells or to block
aneuploidy's non-cell autonomous effects.
Nearly all
tumors exhibit a condition known as
aneuploidy — their cells contain the wrong number of chromosomes.
About 90 % of solid
tumors display whole - chromosome
aneuploidy, while many
tumors with diploid karyotypes nonetheless harbor segmental or arm - length
aneuploidies that also result in significant gene copy number alterations.
Swanton's new lab set out to identify specific genes that, when inhibited, result in the death of
tumor cells that displayed
aneuploidy, meaning they had more or less than the normal set of 46 chromosomes.