Evidence map›Paper›PMID 35198910›Full record

ArticleiScience2022

Single-cell multiomics reveals heterogeneous cell states linked to metastatic potential in liver cancer cell lines.

Shanshan Wang, Jiarui Xie, Xuanxuan Zou, Taotao Pan, Qichao Yu, Zhenkun Zhuang, Yu Zhong, Xin Zhao, Zifei Wang, Rui Li and 8 more

Abstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Single-cell Technologies Provide Novel Insights into Liver Physiology and Pathology.Journal of clinical and translational hepatology · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
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

18 authors.

Shanshan WangCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Jiarui XieSchool of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China.
Xuanxuan ZouCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Taotao PanBGI-Shenzhen, Shenzhen 518083, China.
Qichao YuCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Zhenkun ZhuangSchool of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China.
Yu ZhongBGI-Shenzhen, Shenzhen 518083, China.
Xin ZhaoCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Zifei WangCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Rui LiBGI-Shenzhen, Shenzhen 518083, China.
Ying LeiBGI-Shenzhen, Shenzhen 518083, China.
Jianhua YinBGI-Shenzhen, Shenzhen 518083, China.
Yue YuanCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Xiaoyu WeiCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Longqi LiuBGI-Shenzhen, Shenzhen 518083, China.
Shiping LiuBGI-Shenzhen, Shenzhen 518083, China.
Huanming YangCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Liang WuCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common liver cancer with a high rate of metastasis. However, the molecular mechanisms that drive metastasis remain unclear. We combined single-cell transcriptomic, proteomic, and chromatin accessibility data to investigate how heterogeneous phenotypes contribute to metastatic potential in five HCC cell lines. We confirmed that the prevalence of a mesenchymal state and levels of cell proliferation are linked to the metastatic potential. We also identified a rare hypoxic subtype that has a higher capacity for glycolysis and exhibits dormant, invasive, and malignant characteristics. This subtype has increased metastatic potential. We further identified a robust 14-gene panel representing this hypoxia signature and this hypoxia signature could serve as a prognostic index. Our data provide a valuable data resource, facilitate a deeper understanding of metastatic mechanisms, and may help diagnosis of metastatic potential in individual patients, thus supporting personalized medicine.

Indexed as

Cell biologyOmicsTranscriptomics

Identifiers

PMID35198910
PMCPMC8850337

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.