Evidence map›Paper›PMID 34940569›Full record

ArticleMetabolites2021

AMPK-Mediated Metabolic Switching Is High Effective for Phytochemical Levo-Tetrahydropalmatine (l-THP) to Reduce Hepatocellular Carcinoma Tumor Growth.

Xunzhe Yin, Wenbo Li, Jiaxin Zhang, Wenjing Zhao, Huaxing Cai, Chi Zhang, Zuojia Liu, Yan Guo, Jin Wang

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. High-Throughput Sequencing Reveals ThatJournal of personalized medicine · 2023
    Article
  7. Review
  8. Article
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

9 authors at 3 institutions in 2 countries.

Xunzhe YinSchool of Pharmacy, Changchun University of Chinese Medicine, Changchun 130117, China.
Wenbo LiState Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China.
Jiaxin ZhangState Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China.
Wenjing ZhaoState Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China.
Huaxing CaiSchool of Pharmacy, Changchun University of Chinese Medicine, Changchun 130117, China.
Chi ZhangSchool of Pharmacy, Changchun University of Chinese Medicine, Changchun 130117, China.
Zuojia LiuState Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China.ORCID 0000-0002-1770-3998
Yan GuoSchool of Pharmacy, Changchun University of Chinese Medicine, Changchun 130117, China.
Jin WangDepartment of Chemistry and Physics, Stony Brook University, Stony Brook, NY 11794-3400, USA.
Chinese Academy of Sciences · CNChangchun University of Chinese Medicine · CNStony Brook University · US

Funding

Ministry of Science and Technology of China 2013YQ170585Ministry of Science and Technology of China 2016YFA0203200National Natural Science Foundation of China 21721003National Natural Science Foundation of China 81573448Science and Technology Development Plan of Jilin Province 20200301009RQScientific Instrument Developing Project of the Chinese Academy of Sciences YJKYYQ20180038
6 · The paper itself

Abstract

Targeting cancer cell metabolism has been an attractive approach for cancer treatment. However, the role of metabolic alternation in cancer is still unknown whether it functions as a tumor promoter or suppressor. Applying the cancer gene-metabolism integrative network model, we predict adenosine monophosphate-activated protein kinase (AMPK) to function as a central hub of metabolic landscape switching in specific liver cancer subtypes. For the first time, we demonstrate that the phytochemical levo-tetrahydropalmatine (l-THP), a

Indexed as

AMPKautophagycancer metabolismhepatocellular carcinomalevo-tetrahydropalmatine

Identifiers

PMID34940569
PMCPMC8703446
OpenAlexW3216757381

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.