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Clonal evolution in cancer

Jesse J. Salk
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The article was published on 2010-01-01 and is currently open access. It has received 817 citations till now. The article focuses on the topics: Somatic evolution in cancer & Cancer.

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Citations
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Identification of large-scale genomic variation in cancer genomes using in silico reference models

TL;DR: A method that uses available breakpoint information to generate models of structural variations and uses these models as references to align previously unmapped and discordant reads from a genome is developed.
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Is lineage decision-making restricted during tumoral reprograming of haematopoietic stem cells?

TL;DR: Evidence is examined to support the notion that whilst cells that initiate leukemia have multi-lineage potential, leukemia stem cells are reprogrammed by further oncogenic insults to restrict their lineage decision-making and the idea that leukemia, like normal haematopoiesis, is a hierarchically organized tissue is examined.
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Complex Chromosomal Rearrangements in B-Cell Lymphoma: Evidence of Chromoanagenesis? A Case Report

TL;DR: A case of possible chromoanagenesis in a patient with diffuse large B-cell lymphoma is reported, illustrating that lymphomagenesis can be complex and may arise from a catastrophic event resulting in multiple complex chromosome rearrangements.
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Targeting transcriptional regulators for treatment of anaplastic thyroid cancer.

TL;DR: An emerging notion is that many different oncogenic signaling pathways activated by multiple upstream driver mutations might ultimately converge on the transcriptional responses, which would provide an opportunity to target transcriptional regulators for treatment of ATC.
References
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Metastatic colonization by circulating tumour cells

TL;DR: An improved understanding of the mechanistic determinants of such colonization is needed to better prevent and treat metastatic cancer.
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Clonal evolution in breast cancer revealed by single nucleus genome sequencing

TL;DR: The data show that aneuploid rearrangements occurred early in tumour evolution and remained highly stable as the tumour masses clonally expanded, which has important implications for the diagnosis, therapeutic treatment and evolution of chemoresistance in breast cancer.