TY - JOUR
T1 - Advances for studying clonal evolution in cancer
AU - Ding, Li
AU - Raphael, Benjamin J.
AU - Chen, Feng
AU - Wendl, Michael C.
N1 - Funding Information:
The authors are supported by grants from the NIH (U01HG006517, U54HG003079, R01HG005690, R01DK081592, and R01DK087960). We thank Joshua McMichael for help with figure preparation and Michael D. McLellan for providing cross-study comparison.
PY - 2013/11/1
Y1 - 2013/11/1
N2 - The "clonal evolution" model of cancer emerged and "evolved" amid ongoing advances in technology, especially in recent years during which next generation sequencing instruments have provided ever higher resolution pictures of the genetic changes in cancer cells and heterogeneity in tumors. It has become increasingly clear that clonal evolution is not a single sequential process, but instead frequently involves simultaneous evolution of multiple subclones that co-exist because they are of similar fitness or are spatially separated. Co-evolution of subclones also occurs when they complement each other's survival advantages. Recent studies have also shown that clonal evolution is highly heterogeneous: different individual tumors of the same type may undergo very different paths of clonal evolution. New methodological advancements, including deep digital sequencing of a mixed tumor population, single cell sequencing, and the development of more sophisticated computational tools, will continue to shape and reshape the models of clonal evolution. In turn, these will provide both an improved framework for the understanding of cancer progression and a guide for treatment strategies aimed at the elimination of all, rather than just some, of the cancer cells within a patient.
AB - The "clonal evolution" model of cancer emerged and "evolved" amid ongoing advances in technology, especially in recent years during which next generation sequencing instruments have provided ever higher resolution pictures of the genetic changes in cancer cells and heterogeneity in tumors. It has become increasingly clear that clonal evolution is not a single sequential process, but instead frequently involves simultaneous evolution of multiple subclones that co-exist because they are of similar fitness or are spatially separated. Co-evolution of subclones also occurs when they complement each other's survival advantages. Recent studies have also shown that clonal evolution is highly heterogeneous: different individual tumors of the same type may undergo very different paths of clonal evolution. New methodological advancements, including deep digital sequencing of a mixed tumor population, single cell sequencing, and the development of more sophisticated computational tools, will continue to shape and reshape the models of clonal evolution. In turn, these will provide both an improved framework for the understanding of cancer progression and a guide for treatment strategies aimed at the elimination of all, rather than just some, of the cancer cells within a patient.
KW - Cancer
KW - Clonal evolution
KW - Tumor heterogeneity
UR - http://www.scopus.com/inward/record.url?scp=84887610979&partnerID=8YFLogxK
U2 - 10.1016/j.canlet.2012.12.028
DO - 10.1016/j.canlet.2012.12.028
M3 - Review article
C2 - 23353056
AN - SCOPUS:84887610979
SN - 0304-3835
VL - 340
SP - 212
EP - 219
JO - Cancer Letters
JF - Cancer Letters
IS - 2
ER -