浆液性液体
卵巢癌
生物
表型
浆液性癌
计算生物学
基因组
基因组学
癌症研究
卵巢癌
生物信息学
遗传学
基因
癌症
生物化学
作者
Alexandra Lahtinen,Kari Lavikka,Anni Virtanen,Yilin Li,Sanaz Jamalzadeh,Aikaterini Skorda,Anna Røssberg Lauridsen,Kaiyang Zhang,Giovanni Marchi,Veli‐Matti Isoviita,Valeria Ariotta,Oskari Lehtonen,Taru Muranen,Kaisa Huhtinen,Olli Carpén,Sakari Hietanen,Wojciech Senkowski,Tuula Kallunki,Antti Häkkinen,Johanna Hynninen,Jaana Oikkonen,Sampsa Hautaniemi
出处
期刊:Cancer Cell
[Elsevier]
日期:2023-05-18
卷期号:41 (6): 1103-1117.e12
被引量:45
标识
DOI:10.1016/j.ccell.2023.04.017
摘要
Ovarian high-grade serous carcinoma (HGSC) is typically diagnosed at an advanced stage, with multiple genetically heterogeneous clones existing in the tumors long before therapeutic intervention. Herein we integrate clonal composition and topology using whole-genome sequencing data from 510 samples of 148 patients with HGSC in the prospective, longitudinal, multiregion DECIDER study. Our results reveal three evolutionary states, which have distinct features in genomics, pathways, and morphological phenotypes, and significant association with treatment response. Nested pathway analysis suggests two evolutionary trajectories between the states. Experiments with five tumor organoids and three PI3K inhibitors support targeting tumors with enriched PI3K/AKT pathway with alpelisib. Heterogeneity analysis of samples from multiple anatomical sites shows that site-of-origin samples have 70% more unique clones than metastatic tumors or ascites. In conclusion, these analysis and visualization methods enable integrative tumor evolution analysis to identify patient subtypes using data from longitudinal, multiregion cohorts.
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