Author
Listed:
- Weiwei Zhai
(Genome Institute of Singapore, Agency for Science, Technology and Research)
- Tony Kiat-Hon Lim
(Singapore General Hospital)
- Tong Zhang
(Genome Institute of Singapore, Agency for Science, Technology and Research)
- Su-Ting Phang
(National Cancer Centre)
- Zenia Tiang
(Genome Institute of Singapore, Agency for Science, Technology and Research)
- Peiyong Guan
(Genome Institute of Singapore, Agency for Science, Technology and Research)
- Ming-Hwee Ng
(Genome Institute of Singapore, Agency for Science, Technology and Research
School of Biological Sciences, Nanyang Technological University)
- Jia Qi Lim
(Genome Institute of Singapore, Agency for Science, Technology and Research
School of Biological Sciences, Nanyang Technological University)
- Fei Yao
(Genome Institute of Singapore, Agency for Science, Technology and Research)
- Zheng Li
(Genome Institute of Singapore, Agency for Science, Technology and Research)
- Poh Yong Ng
(Genome Institute of Singapore, Agency for Science, Technology and Research)
- Jie Yan
(Genome Institute of Singapore, Agency for Science, Technology and Research)
- Brian K. Goh
(Singapore General Hospital)
- Alexander Yaw-Fui Chung
(Singapore General Hospital)
- Su-Pin Choo
(National Cancer Centre)
- Chiea Chuen Khor
(Genome Institute of Singapore, Agency for Science, Technology and Research)
- Wendy Wei-Jia Soon
(Genome Institute of Singapore, Agency for Science, Technology and Research)
- Ken Wing-Kin Sung
(Genome Institute of Singapore, Agency for Science, Technology and Research
School of Computing, National University of Singapore, 13 Computing Drive)
- Roger Sik-Yin Foo
(Genome Institute of Singapore, Agency for Science, Technology and Research
Cardiovascular Research Institute, National University of Singapore, National University Healthcare System)
- Pierce Kah-Hoe Chow
(National Cancer Centre
Singapore General Hospital
Office of Clinical Sciences, Duke-NUS Graduate Medical School)
Abstract
Hepatocellular carcinoma (HCC) has one of the poorest survival rates among cancers. Using multi-regional sampling of nine resected HCC with different aetiologies, here we construct phylogenetic relationships of these sectors, showing diverse levels of genetic sharing, spanning early to late diversification. Unlike the variegated pattern found in colorectal cancers, a large proportion of HCC display a clear isolation-by-distance pattern where spatially closer sectors are genetically more similar. Two resected intra-hepatic metastases showed genetic divergence occurring before and after primary tumour diversification, respectively. Metastatic tumours had much higher variability than their primary tumours, suggesting that intra-hepatic metastasis is accompanied by rapid diversification at the distant location. The presence of co-existing mutations offers the possibility of drug repositioning for HCC treatment. Taken together, these insights into intra-tumour heterogeneity allow for a comprehensive understanding of the evolutionary trajectories of HCC and suggest novel avenues for personalized therapy.
Suggested Citation
Weiwei Zhai & Tony Kiat-Hon Lim & Tong Zhang & Su-Ting Phang & Zenia Tiang & Peiyong Guan & Ming-Hwee Ng & Jia Qi Lim & Fei Yao & Zheng Li & Poh Yong Ng & Jie Yan & Brian K. Goh & Alexander Yaw-Fui Ch, 2017.
"The spatial organization of intra-tumour heterogeneity and evolutionary trajectories of metastases in hepatocellular carcinoma,"
Nature Communications, Nature, vol. 8(1), pages 1-9, April.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms14565
DOI: 10.1038/ncomms14565
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