Evidence map›Paper›PMID 32426183›Full record

ArticlePeerJ2020

Hellebrigenin anti-pancreatic cancer effects based on apoptosis and autophage.

Xiaolu Wei, Jing He, Bo Gao, Lingyu Han, Yingqiu Mao, Haiyu Zhao, Nan Si, Hongjie Wang, Jian Yang, Baolin Bian

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Comparative Evaluation of the Potential Antitumor ofPlants (Basel, Switzerland) · 2022
    Article
  7. Article
  8. 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

10 authors at 4 institutions in 1 country.

Xiaolu WeiInstitute of Chinese Materia Medica, China Academy of Chinese Medicine Sciences, Beijing, China.
Jing HeSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, The Key Unit of Exploring Effective Substances of Classical and Famous Prescription of SATCM, Beijing, China.
Bo GaoChina Resources Sanjiu Medical and Pharmaceutical Co. Ltd., Shenzhen, China.
Lingyu HanInstitute of Chinese Materia Medica, China Academy of Chinese Medicine Sciences, Beijing, China.
Yingqiu MaoBeijing University of Chinese Medicine, Beijing, China.
Haiyu ZhaoInstitute of Chinese Materia Medica, China Academy of Chinese Medicine Sciences, Beijing, China.
Nan SiInstitute of Chinese Materia Medica, China Academy of Chinese Medicine Sciences, Beijing, China.
Hongjie WangInstitute of Chinese Materia Medica, China Academy of Chinese Medicine Sciences, Beijing, China.
Jian YangInstitute of Chinese Materia Medica, China Academy of Chinese Medicine Sciences, Beijing, China.
Baolin BianInstitute of Chinese Materia Medica, China Academy of Chinese Medicine Sciences, Beijing, China.
China Academy of Chinese Medical Sciences · CNInstitute of Chinese Materia MedicaBeijing University of Chinese Medicine · CNChina Resources (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hellebrigenin is a natural product found in the toad skin secretions and plants of Urginea, including Hellebores and Kalanchoe genera. It has been shown to be active against Leishmania chagasi promastigotes and Trypanosoma cruzi trypomastigotes and also reported to play an anti-tumor effect on several cancer cell lines in vitro, including pancreatic cancer. This study is aimed to investigate the effects of Hellebrigenin on pancreatic carcinoma cells, SW1990 and BxPC-3 in vitro and its molecular mechanism involved in antitumor activities. Our results showed that Hellebrigenin effectively inhibited the proliferation of SW1990 and BxPC-3 cells in dose- and time-dependent manner. Flow cytometry results showed that Hellebrigenin induced the G0/G1 arrest in both of SW1990 and BxPC-3 cells and promoted cell early apoptosis and autophagy according to morphological observation. Immunofluorescence staining results further confirmed that cell apoptosis and autophagy also increased upon the Hellebrigenin treatment. Moreover, higher dose of Hellebrigenin further increased the cell apoptosis rate while decrease the mitochondrial membrane potential 24 h after treatment. The autophagy rate increased 48 h after treatment with significant difference (

Indexed as

AntitumorHellebrigeninPancreatic cancer

Identifiers

PMID32426183
PMCPMC7213012
OpenAlexW3022274220

What OpenQuestion 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 OpenQuestion graph.