Evidence map›Paper›PMID 36303309›Full record

ArticleYonsei medical journal2022

Antitumor Effect of Low-Dose of Rapamycin in a Transgenic Mouse Model of Liver Cancer.

Hyung Soon Lee, Joon Ye Kim, Simon Weonsang Ro, Myoung Soo Kim, Haeryoung Kim, Dong Jin Joo

Open access · goldAbstract read
In one paragraph

Article in Yonsei medical journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Role of cellular senescence in hepatic diseases (Review).International journal of molecular medicine · 2025
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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

6 authors at 4 institutions in 1 country.

Hyung Soon LeeDepartment of Surgery, National Health Insurance Service Ilsan Hospital, Goyang, Korea.ORCID https://orcid.org/0000-0001-9825-8648
Joon Ye KimThe Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-1180-2899
Simon Weonsang RoDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin, Korea.ORCID https://orcid.org/0000-0003-2187-3698
Myoung Soo KimThe Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-8975-8381
Haeryoung KimDepartment of Pathology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea. haeryoung.kim@snu.ac.kr.ORCID https://orcid.org/0000-0002-4205-9081
Dong Jin JooThe Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-8405-1531
Yonsei University · KRKyung Hee University · KRNational Health Insurance Service Ilsan Hospital · KRSeoul National University Hospital · KR

Funding

GC Biopharma Corp. Korea
6 · The paper itself

Abstract

purposeWe investigate whether low-dose rapamycin is effective in preventing hepatocellular carcinoma (HCC) growth and treating HCC after tumor development in transgenic mice. MATERIALS AND

methodsWe established transgenic mice with HCC induced by activated HrasG12V and p53 suppression. Transgenic mice were randomly assigned to five experimental groups: negative control, positive control, tacrolimus only, rapamycin only, and tacrolimus plus rapamycin. The mice were further divided into two groups according to time to commencement of immunosuppressant treatment: de novo treatment and post-tumor development.

resultsIn the de novo treatment group, marked suppression of tumor growth was observed in the rapamycin only group. In the post-tumor development group, the rapamycin only group displayed no significant suppression of tumor growth, compared to the positive control group. In T lymphocyte subset analysis, the numbers of CD4

conclusionLow-dose rapamycin might be effective to prevent HCC growth, but may be ineffective as a treatment option after HCC development.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAnimalsCell Line, TumorMiceMice, TransgenicSirolimusTacrolimusSirolimusTacrolimuscarcinomahepatocellularLivermicesirolimustransgenic

Identifiers

PMID36303309
PMCPMC9629903
OpenAlexW4308054443

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.