Evidence map›Paper›PMID 32973326›Full record

ArticleActa pharmacologica Sinica2021

Sodium propionate exerts anticancer effect in mice bearing breast cancer cell xenograft by regulating JAK2/STAT3/ROS/p38 MAPK signaling.

Hyun-Soo Park, Joo-Hui Han, Jeong Won Park, Do-Hyung Lee, Keun-Woo Jang, Miji Lee, Kyung-Sun Heo, Chang-Seon Myung

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 21% 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

47 citing papers in PubMed, 2 syntheses or guidelines pooled it, 76 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Propionate promotes CD8Journal for immunotherapy of cancer · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. The dialogue between breast cancer and microorganisms.Frontiers in cellular and infection microbiology · 2026
    Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  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

8 authors at 2 institutions in 1 country.

Hyun-Soo Park *Department of Pharmacology, Chungnam National University College of Pharmacy, Daejeon, 34134, Republic of Korea.
Joo-Hui Han *Department of Pharmacology, Chungnam National University College of Pharmacy, Daejeon, 34134, Republic of Korea.
Jeong Won ParkDepartment of Lifetech.Institute, iNtRON Biotechnology, Seongnam-si, 13202, Republic of Korea.
Do-Hyung LeeDepartment of Pharmacology, Chungnam National University College of Pharmacy, Daejeon, 34134, Republic of Korea.
Keun-Woo JangDepartment of Pharmacology, Chungnam National University College of Pharmacy, Daejeon, 34134, Republic of Korea.
Miji LeeDepartment of Pharmacology, Chungnam National University College of Pharmacy, Daejeon, 34134, Republic of Korea.
Kyung-Sun HeoDepartment of Pharmacology, Chungnam National University College of Pharmacy, Daejeon, 34134, Republic of Korea.
Chang-Seon MyungDepartment of Pharmacology, Chungnam National University College of Pharmacy, Daejeon, 34134, Republic of Korea. cm8r@cnu.ac.kr.
Chungnam National University · KRiNtRON (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Propionate is a short-chain fatty acid (SCFA) mainly produced from carbohydrates by gut microbiota. Sodium propionate (SP) has shown to suppress the invasion in G protein-coupled receptor 41 (GPR41) and GPR43-overexpressing breast cancer cells. In this study we investigated the effects of SP on the proliferation, apoptosis, autophagy, and antioxidant production of breast cancer cells. We showed that SP (5-20 mM) dose-dependently inhibited proliferation and induced apoptosis in breast cancer cell lines JIMT-1 (ER-negative and HER2-expressing) and MCF7 (ER-positive type), and this effect was not affected by PTX, thus not mediated by the GPR41 or GPR43 SCFA receptors. Meanwhile, we demonstrated that SP treatment increased autophagic and antioxidant activity in JIMT-1 and MCF7 breast cancer cells, which might be a compensatory mechanism to overcome SP-induced apoptosis, but were not sufficient to overcome SP-mediated suppression of proliferation and induction of apoptosis. We revealed that the anticancer effect of SP was mediated by inhibiting JAK2/STAT3 signaling which led to cell-cycle arrest at G

Indexed as

AnimalsAntineoplastic AgentsApoptosisAutophagyBreast NeoplasmsCell Line, TumorCell ProliferationFemaleG1 Phase Cell Cycle CheckpointsHumansMAP Kinase Signaling SystemMiceMice, NudePropionatesReactive Oxygen SpeciesXenograft Model Antitumor AssaysAntineoplastic AgentsPropionatesReactive Oxygen Speciessodium propionatebreast cancerJAK2p38 MAPKROSsodium propionateSTAT3

Identifiers

PMID32973326
PMCPMC8285538
OpenAlexW3088400341

What OpenQuestion holds

Textmetadata
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.