Evidence map›Paper›PMID 33391424›Full record

ArticleJournal of Cancer2021

Tephrosin induces apoptosis of human pancreatic cancer cells through the generation of reactive oxygen species.

Jie Du, Fan Jiang, Shen-Sheng Xu, Zi-Feng Huang, Li-Li Chen, Li Li

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Jie DuDepartment of Hepatobiliary Surgery, the Affiliated Puren Hospital of Wuhan University of Science and Technology, Wuhan, China.
Fan JiangDepartment of Hepatobiliary Surgery, the Affiliated Puren Hospital of Wuhan University of Science and Technology, Wuhan, China.
Shen-Sheng XuDepartment of Hepatobiliary Surgery, the Affiliated Puren Hospital of Wuhan University of Science and Technology, Wuhan, China.
Zi-Feng HuangDepartment of Hepatobiliary Surgery, the Affiliated Puren Hospital of Wuhan University of Science and Technology, Wuhan, China.
Li-Li ChenDepartment of Hepatobiliary Surgery, the Affiliated Puren Hospital of Wuhan University of Science and Technology, Wuhan, China.
Li LiDepartment of Centre for clinical teaching skills, the Affiliated Puren Hospital of Wuhan University of Science and Technology, Wuhan, China.
Wuhan University of Technology · CNWuhan University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tephrosin is a natural rotenoid isoflavonoid that has been shown to have potent anticancer activities. In this study, we reported the anticancer activity of tephrosin against pancreatic cancer cells. Tephrosin potently suppressed cell viability in various cancer cell lines and promoted apoptosis of PANC-1 and SW1990 pancreatic cancer cells evidenced by enhanced cleavage of caspase-3/-9 and PARP. Further studies showed that tephrosin increased the production of intracellular reactive oxygen species (ROS) and led to mitochondrial membrane potential depolarization, and subsequent cytochrome c release. DNA damage was also identified by increased tail DNA and phosphorylation of H2AX. Intracellular ROS production seems to be essential for the anticancer activity of tephrosin, alleviation of ROS production by ROS scavengers weakened the apoptotic effects of tephrosin. Importantly, in PANC-1 xenografted nude mice, potent antitumor activity and low toxicity of tephrosin were observed. In conclusion, these results indicated that tephrosin could be developed as a potential chemotherapeutic agent for the treatment of human pancreatic cancer.

Indexed as

apoptosispancreatic cancerreactive oxygen speciesTephrosin

Identifiers

PMID33391424
PMCPMC7738831
OpenAlexW3096413753

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.