Molecular and histological correlations in liver cancer

被引:374
作者
Calderaro, Julien [1 ,2 ,3 ]
Ziol, Marianne [4 ,5 ,6 ]
Paradis, Valerie [7 ,8 ]
Zucman-Rossi, Jessica [4 ,9 ,10 ]
机构
[1] CHU Henri Mondor, AP HP, Dept Pathol, F-94000 Creteil, France
[2] Univ Paris Est Creteil, Fac Med, Creteil, France
[3] Inserm U955, Team 18, Creteil, France
[4] INSERM UMR 1162, Genom Fonct Tumeurs Solides, F-75010 Paris, France
[5] Univ Paris 13, Sorbonne Paris Cite, Bobigny, France
[6] Grp Hosp Paris Seine St Denis, Hop Jean Verdier, AP HP, Serv Anat & Cytol Pathol, Bondy, France
[7] Hop Univ Beaujon, Serv Anat & Cytol Pathol, AP HP, Clichy, France
[8] Univ Paris Diderot, CNRS, CRI, DHU,UNITY, Clichy, France
[9] Univ Paris 13, Univ Paris Descartes, Univ Paris Diderot, F-75010 Villetaneuse, France
[10] Hop Europeen Georges Pompidou, AP HP, Serv Oncol Med, Paris, France
关键词
Histology; Phenotype; Mutations; Hepatocellular carcinoma; HCC; Prognosis; Diagnosis; Treatment algorithms; TUMOR MUTATIONAL BURDEN; HEPATOCELLULAR-CARCINOMA; BETA-CATENIN; TRANSARTERIAL CHEMOEMBOLIZATION; IMMUNE MICROENVIRONMENT; BLADDER-CANCER; PD-1; BLOCKADE; KERATIN; 19; EXPRESSION; LANDSCAPE;
D O I
10.1016/j.jhep.2019.06.001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatocellular carcinoma (HCC) is a highly heterogeneous cancer, both at the molecular and histological level. High-throughput sequencing and gene expression profiling have identified distinct transcriptomic subclasses and numerous recurrent genetic alterations; several HCC subtypes characterised by histological features have also been identified. HCC phenotype appears to be closely related to particular gene mutations, tumour subgroups and/or oncogenic pathways. Non-proliferative tumours display a well-differentiated phenotype. Among this molecular subgroup, CTNNBI-mutated HCCs constitute a homogeneous subtype, exhibiting cholestasis and microtrabecular and pseudoglandular architectural patterns. Another non-proliferative subtype has a gene expression pattern similar to that of mature hepatocytes (G4) and displays a steatohepatitic phenotype. In contrast, proliferative HCCs are most often poorly differentiated, and notably include tumours with progenitor features. A novel morphological variant of proliferative HCC - designated "macrotrabecular-massive" - was recently shown to be associated with angiogenesis activation and poor prognosis. Altogether, these findings may help to translate our knowledge of HCC biology into clinical practice, resulting in improved precision medicine for patients with this highly aggressive malignancy. This manuscript reviews the most recent data in this exciting field, discussing future directions and challenges. (C) 2019 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:616 / 630
页数:15
相关论文
共 135 条
  • [1] Carcinosarcoma of the liver producing granulocyte-colony stimulating factor
    Aita, Kumi
    Seki, Kunihiko
    [J]. PATHOLOGY INTERNATIONAL, 2006, 56 (07) : 413 - 419
  • [2] Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma
    Ally, Adrian
    Balasundaram, Miruna
    Carlsen, Rebecca
    Chuah, Eric
    Clarke, Amanda
    Dhalla, Noreen
    Holt, Robert A.
    Jones, Steven J. M.
    Lee, Darlene
    Ma, Yussanne
    Marra, Marco A.
    Mayo, Michael
    Moore, Richard A.
    Mungall, Andrew J.
    Schein, Jacqueline E.
    Sipahimalani, Payal
    Tam, Angela
    Thiessen, Nina
    Cheung, Dorothy
    Wong, Tina
    Brooks, Denise
    Robertson, A. Gordon
    Bowlby, Reanne
    Mungall, Karen
    Sadeghi, Sara
    Xi, Liu
    Covington, Kyle
    Shinbrot, Eve
    Wheeler, David A.
    Gibbs, Richard A.
    Donehower, Lawrence A.
    Wang, Linghua
    Bowen, Jay
    Gastier-Foster, Julie M.
    Gerken, Mark
    Helsel, Carmen
    Leraas, Kristen M.
    Lichtenberg, Tara M.
    Ramirez, Nilsa C.
    Wise, Lisa
    Zmuda, Erik
    Gabriel, Stacey B.
    Meyerson, Matthew
    Cibulskis, Carrie
    Murray, Bradley A.
    Shih, Juliann
    Beroukhim, Rameen
    Cherniack, Andrew D.
    Schumacher, Steven E.
    Saksena, Gordon
    [J]. CELL, 2017, 169 (07) : 1327 - +
  • [4] [Anonymous], GUT
  • [5] [Anonymous], CANCERS
  • [6] [Anonymous], 2017, CLIN GENITOURIN CANC
  • [7] [Anonymous], MACSWEENS PATHOLOGY
  • [8] [Anonymous], LIVER INT
  • [9] [Anonymous], VIRCHOWS ARCH
  • [10] [Anonymous], 2014, Hepatology