Evidence map›Paper›PMID 35615883›Full record

ReviewIntegrative cancer therapies

Functional Mechanism of Ginsenoside Compound K on Tumor Growth and Metastasis.

Jinlong Liu, Yuchen Wang, Zhun Yu, Guangfu Lv, Xiaowei Huang, He Lin, Chao Ma, Zhe Lin, Peng Qu

Open access · goldAbstract readReview
In one paragraph

Review in Integrative cancer therapies. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Targeting Lysosomes for Enhanced Anti-Cancer Therapeutics and Immune Response.International journal of biological sciences · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Anti-leukemia effects of ginsenoside monomer: A narrative review of pharmacodynamics study.Current therapeutic research, clinical and experimental · 2024
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. 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

9 authors at 2 institutions in 2 countries.

Jinlong LiuChangchun University of Chinese Medicine, Changchun, Jilin, China.ORCID 0000-0002-9185-7688
Yuchen WangChangchun University of Chinese Medicine, Changchun, Jilin, China.
Zhun YuThird Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, Jilin, China.
Guangfu LvChangchun University of Chinese Medicine, Changchun, Jilin, China.
Xiaowei HuangChangchun University of Chinese Medicine, Changchun, Jilin, China.
He LinChangchun University of Chinese Medicine, Changchun, Jilin, China.
Chao MaChangchun University of Chinese Medicine, Changchun, Jilin, China.
Zhe LinChangchun University of Chinese Medicine, Changchun, Jilin, China.
Peng QuNational Institutes of Health, Frederick, MD, USA.ORCID 0000-0003-2304-1430
Changchun University of Chinese Medicine · CNNational Institutes of Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ginsenosides, as the most important constituents of ginseng, have been extensively investigated in cancer chemoprevention and therapeutics. Among the ginsenosides, Compound K (CK), a rare protopanaxadiol type of ginsenoside, has been most broadly used for cancer treatment due to its high anticancer bioactivity. However, the functional mechanism of CK in cancer is not well known. This review describes the structure, transformation and pharmacological activity of CK and discusses the functional mechanisms of CK and its metabolites, which regulate signaling pathways related to tumor growth and metastasis. CK inhibits tumor growth by inducing tumor apoptosis and tumor cell differentiation, regulates the tumor microenvironment by suppressing tumor angiogenesis-related proteins, and downregulates the roles of immunosuppressive cells, such as myeloid-derived suppressor cells (MDSCs). There is currently much research on the potential development of CK as a new strategy when administered alone or in combination with other compounds.

Indexed as

GinsenosidesNeoplasmsPanaxApoptosisHumansNeovascularization, PathologicTumor Microenvironmentginsenoside compound KGinsenosidesantimetastaticantitumorbiotransformationGinsenoside Compound Kpharmacological activity

Identifiers

PMID35615883
PMCPMC9152193
OpenAlexW4282919702

What Socratic 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 Socratic graph.