TY - JOUR
T1 - Tumour evolution in hepatocellular carcinoma
AU - Craig, Amanda J.
AU - von Felden, Johann
AU - Garcia-Lezana, Teresa
AU - Sarcognato, Samantha
AU - Villanueva, Augusto
N1 - Funding Information:
The work of A.V. is supported by the U.S. Department of Defense (CA150272P3). The work of J.v.F. is supported by Deutsche Forschungsgemeinschaft (FE1746/1-1). The work of T.G.-L is supported by Asociación Española para el Estudio del Hígado (AEEH).
Publisher Copyright:
© 2019, Springer Nature Limited.
PY - 2020/3/1
Y1 - 2020/3/1
N2 - Hepatocellular carcinoma (HCC), the most common form of primary liver cancer, typically develops on the background of chronic liver disease and is an aggressive disease with dismal prognosis. Studies using next-generation sequencing of multiple regions of the same tumour nodule suggest different patterns of HCC evolution and confirm the high molecular heterogeneity in a subset of patients. Different hypotheses have been proposed to explain tumour evolution, including clonal selection or neutral and punctuated acquisition of genetic alterations. In parallel, data indicate a fundamental contribution of nonmalignant cells of the tumour microenvironment to cancer clonal evolution. Delineating these dynamics is crucial to improve the treatment of patients with HCC, and particularly to help understand how HCC evolution drives resistance to systemic therapies. A number of new minimally invasive techniques, such as liquid biopsies, could help track cancer evolution in HCC. These tools might improve our understanding of how systemic therapies affect tumour clonal composition and could facilitate implementation of real-time molecular monitoring of patients with HCC.
AB - Hepatocellular carcinoma (HCC), the most common form of primary liver cancer, typically develops on the background of chronic liver disease and is an aggressive disease with dismal prognosis. Studies using next-generation sequencing of multiple regions of the same tumour nodule suggest different patterns of HCC evolution and confirm the high molecular heterogeneity in a subset of patients. Different hypotheses have been proposed to explain tumour evolution, including clonal selection or neutral and punctuated acquisition of genetic alterations. In parallel, data indicate a fundamental contribution of nonmalignant cells of the tumour microenvironment to cancer clonal evolution. Delineating these dynamics is crucial to improve the treatment of patients with HCC, and particularly to help understand how HCC evolution drives resistance to systemic therapies. A number of new minimally invasive techniques, such as liquid biopsies, could help track cancer evolution in HCC. These tools might improve our understanding of how systemic therapies affect tumour clonal composition and could facilitate implementation of real-time molecular monitoring of patients with HCC.
UR - http://www.scopus.com/inward/record.url?scp=85075996358&partnerID=8YFLogxK
U2 - 10.1038/s41575-019-0229-4
DO - 10.1038/s41575-019-0229-4
M3 - Review article
C2 - 31792430
AN - SCOPUS:85075996358
SN - 1759-5045
VL - 17
SP - 139
EP - 152
JO - Nature Reviews Gastroenterology and Hepatology
JF - Nature Reviews Gastroenterology and Hepatology
IS - 3
ER -