Author/Authors :
Lim، نويسنده , , S.H. and Becker، نويسنده , , T.M. and Chua، نويسنده , , W. and Caixeiro، نويسنده , , N.J. and Ng، نويسنده , , W.L. and Kienzle، نويسنده , , N. and Tognela، نويسنده , , A. and Lumba، نويسنده , , S. and Rasko، نويسنده , , J.E.J. and de Souza، نويسنده , , P. and Spring، نويسنده , , K.J.، نويسنده ,
Abstract :
The detection of circulating tumour cells or circulating free tumour nucleic acids can potentially guide treatment and inform prognosis in colorectal cancer using minimally invasive “liquid biopsies”. Current literature supports the notion that high circulating tumour cell counts or presence of tumour nucleic acid correlate with inferior clinical outcomes for patients, but they are not yet part of routine clinical care. Future research evolves around the examination of the molecular phenotype of circulating tumour cells. The key unanswered areas include differentiating between circulating tumour cell presence and their proliferative capacity and dormancy, identifying tumour heterogeneity and understanding the epithelial–mesenchymal transition.
Keywords :
Circulating free DNA , Circulating free RNA , Personalised cancer therapy , Circulating tumour cells , Colorectal Cancer