Evidence map›Paper›PMID 38196542›Full record

ArticleJournal of gastrointestinal oncology2023

Identification of acetylshikonin as a novel tubulin polymerization inhibitor with antitumor activity in human hepatocellular carcinoma cells.

Siming Hu, Yongchuan Li, Junqiu Zhou, Kun Xu, Yanqing Pang, Ralf Weiskirchen, Matthias Ocker, Fen Ouyang

Open access · diamondAbstract read
In one paragraph

Article in Journal of gastrointestinal oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
  3. 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 5 institutions in 2 countries.

Siming HuDepartment of Laboratory Medicine, Nanfang Hospital Taihe Branch, Guangzhou, China.
Yongchuan LiFirst Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, China.
Junqiu ZhouDepartment of Laboratory Medicine, Nanfang Hospital Baiyun Branch, Southern Medical University, Guangzhou, China.
Kun XuDepartment of Laboratory Medicine, Nanfang Hospital Baiyun Branch, Southern Medical University, Guangzhou, China.
Yanqing PangSecond Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, China.
Ralf WeiskirchenInstitute of Molecular Pathobiochemistry, Experimental Gene Therapy, and Clinical Chemistry (IFMPEGKC), RWTH University Hospital Aachen, Aachen, Germany.
Matthias OckerMedical Department, Division of Hematology, Oncology, and Cancer Immunology Campus Charité Mitte, Charité University Medicine Berlin, Berlin, Germany.
Fen OuyangDepartment of Laboratory Medicine, Nanfang Hospital Baiyun Branch, Southern Medical University, Guangzhou, China.
Guangzhou University of Chinese Medicine · CNNanfang Hospital · CNSouthern Medical University · CNCharité - Universitätsmedizin Berlin · DERWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Microtubules are attractive targets for anticancer drugs. However, the microtubule-targeting agents (MTAs) currently in clinical use exhibit inevitable drug resistance. Therefore, there is an urgent need to discover novel MTAs for the clinical treatment of cancer. Methods: Bioactive compounds extracted from Results: Acetylshikonin exhibited potent anti-proliferative activities against a panel of human cancer cell lines (IC Conclusions: In this study, acetylshikonin was identified as MTA against hepatocellular carcinoma and can serve as a promising lead compound for further development of anti-cancer drug, underscoring its potential clinical significance.

Indexed as

acetylshikoninanti-cancermicrotubule-targeting agent (MTA)Natural products (NPs)

Identifiers

PMID38196542
PMCPMC10772698
OpenAlexW4390350141

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.