Evidence map›Paper›PMID 33764482›Full record

ReviewSeminars in liver disease2021

Organoids for the Study of Liver Cancer.

Haichuan Wang, Diego F Calvisi, Xin Chen

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in liver disease, 2021. 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
1.8field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Leveraging Patient-Derived Organoids for Personalized Liver Cancer Treatment.International journal of biological sciences · 2024
    Article
  11. Review
  12. Review
  13. Review
  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

3 authors at 3 institutions in 3 countries.

Haichuan WangDepartment of Liver Surgery, Liver Transplantation Division, West China Hospital, Sichuan University, Chengdu, China.
Diego F CalvisiInstitute of Pathology, University of Regensburg, Regensburg, Germany.
Xin ChenDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, California.
Sichuan University · CNUniversity of California, San Francisco · USUniversity of Regensburg · DE

Funding

UCSF Liver Core CenterP30DK026743 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Holger Willenbring · 1986 to 2026
$30.7M
Signaling cascades in cholangiocarcinoma developmentR01CA190606 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHEN, XIN · 2016 to 2020
$1.8M
Signaling pathways during hepatocarcinogenesisR01CA239251 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI CHEN, XIN · 2020 to 2024
$1.8M
2020HXBH006 West China Hospital, Sichuan University Post-Doctoral Research ProjectNCI NIH HHS R01 CA190606NCI NIH HHS R01 CA239251NIDDK NIH HHS P30 DK026743P30DK026743 National Institute of HealthR01CA190606 National Institute of HealthR01CA239251 National Institute of Health
6 · The paper itself

Abstract

Liver cancer is the second most lethal malignancy worldwide. Cell lines and murine models are the most common tools for modeling human liver carcinogenesis. Most recently, organoids with a three-dimensional structure derived from primary tissues or cells have been applied to liver cancer research. Organoids can be generated from induced pluripotent stem cells, embryonic or adult, healthy or diseased tissues. In particular, liver organoids have been widely employed in mechanistic studies aimed at delineating the molecular pathways responsible for hepatocarcinogenesis. The introduction of clustered regularly interspaced palindromic repeats (CRISPR)-associated protein 9 (Cas9) and microengineered miniorganoid technologies into liver organoids for cancer study has significantly accelerated these investigations. Translational advances have been made by utilizing liver tumor organoids for anticancer drug screening, biobanking, omics profiling, and biomarker discovery. This review summarizes the latest advances and the remaining challenges in the use of organoid models for the study of liver cancer.

Indexed as

Induced Pluripotent Stem CellsLiver NeoplasmsAnimalsBiological Specimen BanksCRISPR-Cas SystemsHumansMiceOrganoids

Identifiers

PMID33764482
PMCPMC8522208
OpenAlexW3128431578

What OpenQuestion holds

Textmetadata
LicenceTDM
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.