Evidence map›Paper›PMID 36476645›Full record

ArticleNature communications2022

Multiregional single-cell dissection of tumor and immune cells reveals stable lock-and-key features in liver cancer.

Lichun Ma, Sophia Heinrich, Limin Wang, Friederike L Keggenhoff, Subreen Khatib, Marshonna Forgues, Michael Kelly, Stephen M Hewitt, Areeba Saif, Jonathan M Hernandez and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed
12.0field-weighted citation impact, top 1% 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

124 citing papers in PubMed, 150 citations in OpenAlex.

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64 more citing papers are in PubMed but not listed here.

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

17 authors at 5 institutions in 3 countries.

Lichun Ma *Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.ORCID 0000-0001-9809-775X
Sophia Heinrich *Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Limin WangLaboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Friederike L KeggenhoffDepartment of Medicine I, Lichtenberg Research Group, Johannes Gutenberg University, Mainz, Germany.
Subreen KhatibLaboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Marshonna ForguesLaboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Michael KellyFrederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, MD, 20701, USA.ORCID 0000-0003-0654-2778
Stephen M HewittLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.ORCID 0000-0001-8283-1788
Areeba SaifSurgical Oncology Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Jonathan M HernandezSurgical Oncology Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Donna MabryThoracic and GI Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Roman KloecknerDepartment of Medicine I, Lichtenberg Research Group, Johannes Gutenberg University, Mainz, Germany.ORCID 0000-0001-5492-4792
Tim F GretenThoracic and GI Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.ORCID 0000-0002-0806-2535
Jittiporn ChaisaingmongkolLaboratory of Chemical Carcinogenesis, Chulabhorn Research Institute, Bangkok, 10210, Thailand.ORCID 0000-0001-8019-5562
Mathuros RuchirawatLaboratory of Chemical Carcinogenesis, Chulabhorn Research Institute, Bangkok, 10210, Thailand.ORCID 0000-0001-6402-2442
Jens U MarquardtDepartment of Medicine I, Lichtenberg Research Group, Johannes Gutenberg University, Mainz, Germany.ORCID 0000-0002-8314-2682
Xin Wei WangLaboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA. xw3u@nih.gov.ORCID 0000-0001-9735-606X
National Cancer Institute · USJohannes Gutenberg University Mainz · DEChulabhorn Research Institute · THLeidos (United States) · USMedizinische Hochschule Hannover · DE

Funding

Liver Cancer ProgramZIABC011870 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WANG, XIN WEI · 2019 to 2025
$10.1M
Molecular signatures for liver cancer diagnosis and treatment stratificationZ01BC010313 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WANG, XIN WEI · 1999 to 2008
$1.8M
The role of cancer stem cells in liver cancer heterogeneity and subtypesZ01BC010876 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WANG, XIN · 2008 to 2008
$490k
The identification of human hepatocellular carcinoma metastasis genesZ01BC010877 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WANG, XIN · 2008 to 2008
$327k
Intramural NIH HHS Z01 BC010313Intramural NIH HHS Z01 BC010876Intramural NIH HHS Z01 BC010877Intramural NIH HHS ZIA BC011870
6 · The paper itself

Abstract

Intratumor heterogeneity may result from the evolution of tumor cells and their continuous interactions with the tumor microenvironment which collectively drives tumorigenesis. However, an appearance of cellular and molecular heterogeneity creates a challenge to define molecular features linked to tumor malignancy. Here we perform multiregional single-cell RNA sequencing (scRNA-seq) analysis of seven liver cancer patients (four hepatocellular carcinoma, HCC and three intrahepatic cholangiocarcinoma, iCCA). We identify cellular dynamics of malignant cells and their communication networks with tumor-associated immune cells, which are validated using additional scRNA-seq data of 25 HCC and 12 iCCA patients as a stable fingerprint embedded in a malignant ecosystem representing features of tumor aggressiveness. We further validate the top ligand-receptor interaction pairs (i.e., LGALS9-SLC1A5 and SPP1-PTGER4 between tumor cells and macrophages) associated with unique transcriptome in additional 542 HCC patients. Our study unveils stable molecular networks of malignant ecosystems, which may open a path for therapeutic exploration.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAmino Acid Transport System ASCEcosystemHumansMinor Histocompatibility AntigensTumor MicroenvironmentAmino Acid Transport System ASCMinor Histocompatibility AntigensSLC1A5 protein, human

Identifiers

PMID36476645
PMCPMC9729309
OpenAlexW4311579386

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.