Evidence map›Paper›PMID 31485597›Full record

ArticleOncology reports2019

Silymarin induces inhibition of growth and apoptosis through modulation of the MAPK signaling pathway in AGS human gastric cancer cells.

Sung-Hyun Kim, Gang-Sik Choo, Eun-Seon Yoo, Joong-Seok Woo, So-Hee Han, Jae-Han Lee, Ji-Youn Jung

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Oncology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05631041 (The Possible Anticancer Effect of Silymarin in Patients With Metastatic Colorectal Cancer Receiving Chemotherapy.), which is not on this map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.5field-weighted citation impact, top 5% 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.

NCT05631041 phase3unknown statusnot on this mapstarted 2022, after this paper: background citation

The Possible Anticancer Effect of Silymarin in Patients With Metastatic Colorectal Cancer Receiving Chemotherapy.

TypeinterventionalSponsorTanta UniversityRan2022 to 2024Enrolled64ConditionsMetastatic Colorectal CancerArmsSilymarin
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. International journal of molecular sciences · 2026
    Review
  3. Targetable pathways for drug repurposing in gastric cancer.World journal of gastroenterology · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. A review of therapeutic potentials of milk thistle (Iranian journal of basic medical sciences · 2022
    Review
  19. Review
  20. 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 at 1 institution in 1 country.

Sung-Hyun KimDepartment of Companion and Laboratory Animal Science, Kongju National University, Yesan 340‑702, Republic of Korea.
Gang-Sik ChooDepartment of Companion and Laboratory Animal Science, Kongju National University, Yesan 340‑702, Republic of Korea.
Eun-Seon YooDepartment of Companion and Laboratory Animal Science, Kongju National University, Yesan 340‑702, Republic of Korea.
Joong-Seok WooDepartment of Companion and Laboratory Animal Science, Kongju National University, Yesan 340‑702, Republic of Korea.
So-Hee HanDepartment of Companion and Laboratory Animal Science, Kongju National University, Yesan 340‑702, Republic of Korea.
Jae-Han LeeDepartment of Companion and Laboratory Animal Science, Kongju National University, Yesan 340‑702, Republic of Korea.
Ji-Youn JungDepartment of Companion and Laboratory Animal Science, Kongju National University, Yesan 340‑702, Republic of Korea.
Kongju National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apoptosis is regarded as a therapeutic target because it is typically disturbed in human cancer. Silymarin from milk thistle (Silybum marianum) has been reported to exhibit anticancer properties via regulation of apoptosis as well as anti‑inflammatory, antioxidant and hepatoprotective effects. In the present study, the effects of silymarin on the inhibition of proliferation and apoptosis were examined in human gastric cancer cells. The viability of AGS human gastric cancer cells was assessed by MTT assay. The migration of AGS cells was investigated by wound healing assay. Silymarin was revealed to significantly decrease viability and migration of AGS cells in a concentration‑dependent manner. In addition, the number of apoptotic bodies and the rate of apoptosis were increased in a dose‑dependent manner as determined by DAPI staining and Annexin V/propidium iodide double staining. The changes in the expression of silymarin‑induced apoptosis proteins were investigated in human gastric cancer cells by western blotting analysis. Silymarin increased the expression of Bax, phosphorylated (p)‑JNK and p‑p38, and cleaved poly‑ADP ribose polymerase, and decreased the levels of Bcl‑2 and p‑ERK1/2 in a concentration‑dependent manner. The in vivo tumor growth inhibitory effect of silymarin was investigated. Silymarin (100 mg/kg) significantly decreased the AGS tumor volume and increased apoptosis, as assessed by the TUNEL assay, confirming its tumor‑inhibitory effect. Immunohistochemical staining revealed elevated expression of p‑JNK and p‑p38 as well as reduced expression of p‑ERK1/2 associated with silymarin‑treatment. Silymarin was revealed to reduce tumor growth through inhibition of p‑ERK and activation of p‑p38 and p‑JNK in human gastric cancer cells. These results indicated that silymarin has potential for development as a cancer therapeutic due to its growth inhibitory effects and induction of apoptosis in human gastric cancer cells.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicCell Line, TumorCell ProliferationCell SurvivalGene Expression Regulation, NeoplasticHumansMaleMAP Kinase Signaling SystemMiceSilymarinStomach NeoplasmsTreatment OutcomeXenograft Model Antitumor AssaysAntineoplastic Agents, PhytogenicSilymarin

Identifiers

PMID31485597
PMCPMC6775811
OpenAlexW2970406218

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.