Evidence map›Paper›PMID 27559001›Full record

ArticleGut and liver2017

Generation of Multilayered 3D Structures of HepG2 Cells Using a Bio-printing Technique.

Hyeryeon Jeon, Kyojin Kang, Su A Park, Wan Doo Kim, Seung Sam Paik, Sang-Hun Lee, Jaemin Jeong, Dongho Choi

Open access · diamondAbstract read
In one paragraph

Article in Gut and liver, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 109 citations in OpenAlex.

  1. Article
  2. Cell therapy for liver disorders: past, present and future.Nature reviews. Gastroenterology & hepatology · 2025
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  13. iScience · 2022
    Review
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  15. Article
  16. Review
  17. Article
  18. Emerging liver organoid platforms and technologies.Cell regeneration (London, England) · 2021
    Review
  19. Alginate and alginate composites for biomedical applications.Asian journal of pharmaceutical sciences · 2021
    Review
  20. 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

8 authors at 2 institutions in 1 country.

Hyeryeon JeonDepartment of Surgery, Hanyang University College of Medicine, Seoul, Korea.
Kyojin KangDepartment of Surgery, Hanyang University College of Medicine, Seoul, Korea.
Su A ParkDepartment of Nature-Inspired Nano Convergence Systems, Korea Institute of Machinery and Materials, Daejeon, Korea.
Wan Doo KimDepartment of Nature-Inspired Nano Convergence Systems, Korea Institute of Machinery and Materials, Daejeon, Korea.
Seung Sam PaikDepartment of Pathology, Hanyang University College of Medicine, Seoul, Korea.
Sang-Hun LeeDepartment of Biomedical Science, Graduate School of Biomedical Science Engineering, Hanyang University, Seoul, Korea.
Jaemin JeongDepartment of Surgery, Hanyang University College of Medicine, Seoul, Korea.
Dongho ChoiDepartment of Surgery, Hanyang University College of Medicine, Seoul, Korea.
Hanyang University · KRKorea Institute of Machinery and Materials · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsChronic liver disease is a major widespread cause of death, and whole liver transplantation is the only definitive treatment for patients with end-stage liver diseases. However, many problems, including donor shortage, surgical complications and cost, hinder their usage. Recently, tissue-engineering technology provided a potential breakthrough for solving these problems. Three-dimensional (3D) printing technology has been used to mimic tissues and organs suitable for transplantation, but applications for the liver have been rare.

methodsA 3D bioprinting system was used to construct 3D printed hepatic structures using alginate. HepG2 cells were cultured on these 3D structures for 3 weeks and examined by fluorescence microscopy, histology and immunohistochemistry. The expression of liverspecific markers was quantified on days 1, 7, 14, and 21.

resultsThe cells grew well on the alginate scaffold, and liver-specific gene expression increased. The cells grew more extensively in 3D culture than two-dimensional culture and exhibited better structural aspects of the liver, indicating that the 3D bioprinting method recapitulates the liver architecture.

conclusionsThe 3D bioprinting of hepatic structures appears feasible. This technology may become a major tool and provide a bridge between basic science and the clinical challenges for regenerative medicine of the liver.

Indexed as

Printing, Three-DimensionalAlginatesCell ProliferationGlucuronic AcidHep G2 CellsHexuronic AcidsHumansImmunohistochemistryLiverMicroscopy, FluorescenceReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionRNA, MessengerTissue EngineeringTissue ScaffoldsAlginatesGlucuronic AcidHexuronic AcidsRNA, MessengerHep G2 cellPrinting, three-dimensional

Identifiers

PMID27559001
PMCPMC5221869
OpenAlexW2514830645

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.