Evidence map›Paper›PMID 39524792›Full record

ReviewHeliyon2024

Progress on the mechanism of action of emodin against breast cancer cells.

Ruoqing Chen, Hairong Zhang, Xue Zhao, Lin Zhu, XiaoYu Zhang, Yuning Ma, Lei Xia

Abstract readReview
In one paragraph

Review in Heliyon, 2024. 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
–field-weighted citation impact
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.

  1. Review
  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

7 authors.

Ruoqing ChenSchool of Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, 250355, PR China.
Hairong ZhangDepartment of Obstetrics and Gynecology, Shandong Provincial Third Hospital, Shandong University, Jinan, 250031, PR China.
Xue ZhaoSchool of Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, 250355, PR China.
Lin ZhuSchool of Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, 250355, PR China.
XiaoYu ZhangSchool of Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, 250355, PR China.
Yuning MaSchool of Acupuncture-Moxibustion and Tuina, Shandong University of Traditional Chinese Medicine, Jinan, 250355, PR China.
Lei XiaDepartment of Pathology, Shandong University of Traditional Chinese Medicine, Jinan, 250355, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

At present, the role of active ingredients of traditional Chinese medicine in tumor therapy has gradually attracted people's attention, and anthraquinones, which are structurally similar to adriamycin and epirubicin, are one of the hotspots of research. Emodin (1,3,8-trihydroxy-6-methylanthraquinone) is a natural anthraquinone compound isolated from rhubarb, Polygonum cuspidatum, and aloe vera. In recent years, emodin has received widespread attention for its remarkable anti-tumor effects, and its anti-breast cancer effects are manifested as induction of apoptosis, inhibition of tumor cell proliferation, inhibition of invasion and metastasis of tumor cells, and anti-tumor drug resistance. Moreover, emodin can act against multiple types of breast cancer cells by acting on different targets. In this paper, we reviewed the latest research progress on the anti-breast cancer effects of emodin and its anti-tumor mechanism, to provide reference and information for the treatment of breast cancer and the development of anti-tumor drugs.

Indexed as

Breast cancerEmodinHerbMolecular mechanismTumor

Identifiers

PMID39524792
PMCPMC11550755

What Socratic 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 Socratic graph.