Evidence map›Paper›PMID 35998012›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2022

Hepatocellular Carcinoma in Mongolia Delineates Unique Molecular Traits and a Mutational Signature Associated with Environmental Agents.

Laura Torrens, Marc Puigvehí, Miguel Torres-Martín, Huan Wang, Miho Maeda, Philipp K Haber, Thais Leonel, Mireia García-López, Roger Esteban-Fabró, Wei Qiang Leow and 20 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors at 10 institutions in 6 countries.

Laura Torrens *Liver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-3309-6200
Marc Puigvehí *Liver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
Miguel Torres-MartínLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0003-1589-8936
Huan WangSema4, Stamford, Connecticut.
Miho MaedaLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
Philipp K HaberLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0001-9685-9562
Thais LeonelLiver Unit, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), CIBEREHD, University of Barcelona, Barcelona, Spain.ORCID 0000-0003-2919-5676
Mireia García-LópezLiver Unit, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), CIBEREHD, University of Barcelona, Barcelona, Spain.ORCID 0000-0002-9643-7172
Roger Esteban-FabróLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-8173-3323
Wei Qiang LeowLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0001-6003-9837
Carla MontironiLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-1453-2193
Sara TorrecillaTranslational research in Hepatic Oncology, Liver Unit, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Hospital Clínic, University of Barcelona, Barcelona, Spain.
Ajay Ramakrishnan VaradarajanSema4, Stamford, Connecticut.
Patricia TaikSema4, Stamford, Connecticut.ORCID 0000-0003-0990-7832
Genís CampreciósLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-3155-1468
Chinbold EnkhboldHepato-Pancreatico-Biliary Surgery Department, National Cancer Center, Ulaanbaatar, Mongolia.
Erdenebileg TaivanbaatarNational Cancer Center, Ulaanbaatar, Mongolia.
Amankyeldi YerbolatNational Cancer Center, Ulaanbaatar, Mongolia.
Augusto VillanuevaLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
Sofía Pérez-Del-PulgarLiver Unit, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), CIBEREHD, University of Barcelona, Barcelona, Spain.ORCID 0000-0002-9890-300X
Swan ThungLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
Jigjidsuren ChinburenNational Cancer Center, Ulaanbaatar, Mongolia.
Eric LetouzéCentre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université de Paris, Université Paris 13, Functional Genomics of Solid Tumors Laboratory, Paris, France.ORCID 0000-0002-6369-2839
Jessica Zucman-RossiCentre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université de Paris, Université Paris 13, Functional Genomics of Solid Tumors Laboratory, Paris, France.ORCID 0000-0002-5687-0334
Andrew UzilovSema4, Stamford, Connecticut.ORCID 0000-0002-5411-9280
Jaclyn NeelyBristol Myers Squibb, Princeton, New Jersey.
Xavier FornsLiver Unit, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), CIBEREHD, University of Barcelona, Barcelona, Spain.ORCID 0000-0002-8188-1764
Sasan RoayaieDepartment of Surgery, White Plains Hospital, White Plains, New York.
Daniela SiaLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-9000-611X
Josep M LlovetLiver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0003-0547-2667
Tisch Hospital · USConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESStamford Hospital · USMongolian National University · MNInserm · FRBristol-Myers Squibb (Sweden) · SEInstitució Catalana de Recerca i Estudis Avançats · ESNational Center for Communicable Diseases · MNSingapore General Hospital · SGWhite Plains Hospital · US

Funding

THE TISCH CANCER INSTITUTE - CANCER CENTER SUPPORT GRANTP30CA196521 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Deanna L Benson · 2015 to 2026
$35.4M
Hepatic stellate cells in NASH fibrosis and HCCR01DK128289 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SCOTT L. FRIEDMAN · 2021 to 2026
$2.6M
Cancer Research UK 26813NCI NIH HHS P30 CA196521NIDDK NIH HHS R01 DK128289
6 · The paper itself

Abstract

purposeMongolia has the world's highest incidence of hepatocellular carcinoma (HCC), with ∼100 cases/100,000 inhabitants, although the reasons for this have not been thoroughly delineated. EXPERIMENTAL

designWe performed a molecular characterization of Mongolian (n = 192) compared with Western (n = 187) HCCs by RNA sequencing and whole-exome sequencing to unveil distinct genomic and transcriptomic features associated with environmental factors in this population.

resultsMongolian patients were younger, with higher female prevalence, and with predominantly HBV-HDV coinfection etiology. Mongolian HCCs presented significantly higher rates of protein-coding mutations (121 vs. 70 mutations per tumor in Western), and in specific driver HCC genes (i.e., APOB and TSC2). Four mutational signatures characterized Mongolian samples, one of which was novel (SBS Mongolia) and present in 25% of Mongolian HCC cases. This signature showed a distinct substitution profile with a high proportion of T>G substitutions and was significantly associated with a signature of exposure to the environmental agent dimethyl sulfate (71%), a 2A carcinogenic associated with coal combustion. Transcriptomic-based analysis delineated three molecular clusters, two not present in Western HCC; one with a highly inflamed profile and the other significantly associated with younger female patients.

conclusionsMongolian HCC has unique molecular traits with a high mutational burden and a novel mutational signature associated with genotoxic environmental factors present in this country.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsApolipoproteins BCoalFemaleHumansMongoliaMutationApolipoproteins BCoal

Identifiers

PMID35998012
PMCPMC7613712
OpenAlexW4292749631

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.