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First Whole Cancer Genome Sequenced
dooling writes "A paper detailing the sequencing of the first human cancer genome will be published in the 6 November 2008 issue of Nature. This is not only the first cancer genome published, it is the first female genome as well. You can read the paper's abstract, DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome, or the story in Science News. This issue of Nature also has articles on the sequencing of the first African and Asian genomes. The sequencing in all three articles was done using the Illumina Genome Analyzer, one of the massively parallel, next-generation genome sequencing platforms."
Just wait until nanopore sequencing really takes off. Now that shit is awesome.
We figured out a long time ago that it's easier to elect seven judges than to elect 132 legislators.
The Science News article says that they sequenced both a cancer cell and a non-cancer cell from this woman. So we can specifically say "these are the bases that are different" and from there (with luck) to "this is the mutation that happened".
That should prove quite illuminating.
1) "genetic instability does not seem to be a general feature of AML genomes."
Are they on crack? Perhaps I don't fully understand the context of this statement; genetic instability and evolution are seen in most cases of AML.
2) "Alternatively, all may have occurred simultaneously in the same leukaemia-initiating cell, but only a subset of the mutations (or an as-yet undetected mutation) is truly important for pathogenesis (that is, disease 'drivers' versus passengers). Although we suggest that the latter hypothesis is very unlikely on the basis of our current understanding of tumour progression"
Simultaneously occurring? Again, this flies in the face of common knowledge. The theory is the hematopoietic stem cell is extremely long lived and only divides once a year and so has plenty of time to accumulate genetic mutations. This explains both the average relapse time of one year and also the genetic homogeneity of the leukemic clone. Thus many of their new found eight mutations may be accidental and not disease causing.
Does anyone have any new light to shed on this? I am not a doctor and would benefit from some guidance on this issue.