Evidence map›Paper›PMID 26496199›Full record

ArticlePloS one2015

Qualitative and Quantitative Analysis of ROS-Mediated Oridonin-Induced Oesophageal Cancer KYSE-150 Cell Apoptosis by Atomic Force Microscopy.

Jiang Pi, Huaihong Cai, Hua Jin, Fen Yang, Jinhuan Jiang, Anguo Wu, Haiyan Zhu, Jianxin Liu, Xiaohui Su, Peihui Yang and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 36 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

11 authors at 2 institutions in 2 countries.

Jiang PiState Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau, China.
Huaihong CaiDepartment of Chemistry, Jinan University, GuangZhou, China.
Hua JinState Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau, China.
Fen YangState Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau, China.
Jinhuan JiangState Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau, China.
Anguo WuState Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau, China.
Haiyan ZhuDepartment of Chemistry, Jinan University, GuangZhou, China.
Jianxin LiuDepartment of Chemistry, Jinan University, GuangZhou, China; Department of Pharmacology, Hunan University of Medicine, HuaiHua, China.
Xiaohui SuState Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau, China.
Peihui YangState Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau, China.
Jiye CaiState Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau, China.
Macau University of Science and Technology · MOJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High levels of intracellular reactive oxygen species (ROS) in cells is recognized as one of the major causes of cancer cell apoptosis and has been developed into a promising therapeutic strategy for cancer therapy. However, whether apoptosis associated biophysical properties of cancer cells are related to intracellular ROS functions is still unclear. Here, for the first time, we determined the changes of biophysical properties associated with the ROS-mediated oesophageal cancer KYSE-150 cell apoptosis using high resolution atomic force microscopy (AFM). Oridonin was proved to induce ROS-mediated KYSE-150 cell apoptosis in a dose dependent manner, which could be reversed by N-acetylcysteine (NAC) pretreatment. Based on AFM imaging, the morphological damage and ultrastructural changes of KYSE-150 cells were found to be closely associated with ROS-mediated oridonin-induced KYSE-150 cell apoptosis. The changes of cell stiffness determined by AFM force measurement also demonstrated ROS-dependent changes in oridonin induced KYSE-150 cell apoptosis. Our findings not only provided new insights into the anticancer effects of oridonin, but also highlighted the use of AFM as a qualitative and quantitative nanotool to detect ROS-mediated cancer cell apoptosis based on cell biophysical properties, providing novel information of the roles of ROS in cancer cell apoptosis at nanoscale.

Indexed as

AcetylcysteineAntineoplastic Agents, PhytogenicApoptosisCell Line, TumorDiterpenes, KauraneDose-Response Relationship, DrugEpithelial CellsEsophagusFree Radical ScavengersHumansMembrane Potential, MitochondrialMicroscopy, Atomic ForceMitochondriaOxidative StressReactive Oxygen SpeciesAcetylcysteineAntineoplastic Agents, PhytogenicDiterpenes, KauraneFree Radical ScavengersoridoninReactive Oxygen Species

Identifiers

PMID26496199
PMCPMC4619704
OpenAlexW1850662201

What OpenQuestion holds

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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.