Evidence map›Paper›PMID 40422575›Full record

ReviewDiseases (Basel, Switzerland)2025

Anticancer Mechanisms of Ginsenoside Compound K: A Review.

Yu-Po Lee, Hui-Ting Chan, Tzu-Hsuan Li, Lichieh Julie Chu, Sheau-Long Lee, Yu-Quan Chang, Robert Yl Wang

Abstract readReview
In one paragraph

Review in Diseases (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Yu-Po LeeBiotechnology Industry Master and Ph.D. Program, Chang Gung University, Taoyuan 333323, Taiwan.ORCID 0009-0009-1927-892X
Hui-Ting ChanBiotechnology Industry Master and Ph.D. Program, Chang Gung University, Taoyuan 333323, Taiwan.
Tzu-Hsuan LiWellhead Biological Technology Corp., Taoyuan 325019, Taiwan.
Lichieh Julie ChuGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan 333323, Taiwan.ORCID 0000-0002-8488-9614
Sheau-Long LeeWellhead Biological Technology Corp., Taoyuan 325019, Taiwan.
Yu-Quan ChangWellhead Biological Technology Corp., Taoyuan 325019, Taiwan.
Robert Yl WangBiotechnology Industry Master and Ph.D. Program, Chang Gung University, Taoyuan 333323, Taiwan.ORCID 0000-0002-1322-3890

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer, also known as malignant tumors, is formed due to abnormal mutations and the proliferation of human cells. Cancer cells not only demonstrate accelerated proliferation but also show robust invasive and metastatic potential, disseminating from a primary affected region of the body to multiple areas and potentially culminating in organ dysfunction or failure, thereby jeopardizing the individual's life. The rapid growth of the biopharmaceutical market has given rise to numerous novel medicines, thereby precipitating a paradigm shift in contemporary drug development methodologies. This modification is focused on identifying methodologies that can effectively target cancerous cells while minimizing damage to normal cells. There is an increasing societal movement that supports the utilization of natural ingredients derived from plants. In recent years, traditional herbal medicine has experienced a surge in popularity within the global cancer market. In comparison with the use of more toxic chemotherapy methods, there has been an increasing focus on advanced therapies that exhibit reduced side effects. Ginsenoside compound K (CK) is derived from the natural components in ginseng through biotransformation. The utilization of CK in cancer research is a practice engaged in by numerous scientists. The underlying rationale is that CK exhibits a multitude of effects within the realm of cancer research, including but not limited to the mitigation of inflammation, the suppression of cancerous cell proliferation, and the safeguarding of cardiovascular, hepatic, and renal functions. This review methodically identifies and organizes CK-related journals according to the following key points of cancer treatment: the effects on cancer cells themselves, angiogenesis inhibition, modulation of immune response to identify cancer cells, and inflammation regulation. The intricate interplay between ginsenoside CK and cells is elucidated through a graphical representation. The present review focuses on the results of CK in in vitro tests. It is our hope that the present article will aid future studies on the results of CK in vivo tests, clarify the correlation between cellular mechanisms in vivo and in vitro tests, and assist in the development of drugs.

Indexed as

angiogenesiscancerchronic inflammationginsenoside compound Kstromal cell-derived factor 1

Identifiers

PMID40422575
PMCPMC12110123

What Socratic 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 Socratic graph.