Evidence map›Paper›PMID 31391058›Full record

ArticleBMC complementary and alternative medicine2019

Jingfukang induces anti-cancer activity through oxidative stress-mediated DNA damage in circulating human lung cancer cells.

Zujun Que, Zhiyi Zhou, Bin Luo, Changsheng Dong, Yi Jiang, Hegen Li, Jianhui Tian

Open access · goldAbstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 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

7 authors at 2 institutions in 1 country.

Zujun QueOncology Institute of Traditional Chinese Medicine, Shanghai Research Institute of Traditional Chinese Medicine, No. 725, South Wanping Road, Shanghai, 200032, China.
Zhiyi ZhouDepartment of Oncology, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, No. 725, South Wanping Road, Shanghai, 200032, China.
Bin LuoDepartment of Oncology, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, No. 725, South Wanping Road, Shanghai, 200032, China.
Changsheng DongOncology Institute of Traditional Chinese Medicine, Shanghai Research Institute of Traditional Chinese Medicine, No. 725, South Wanping Road, Shanghai, 200032, China.
Yi JiangDepartment of Oncology, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, No. 725, South Wanping Road, Shanghai, 200032, China.
Hegen LiDepartment of Oncology, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, No. 725, South Wanping Road, Shanghai, 200032, China. shlaogen@163.com.
Jianhui TianOncology Institute of Traditional Chinese Medicine, Shanghai Research Institute of Traditional Chinese Medicine, No. 725, South Wanping Road, Shanghai, 200032, China. hawk7150@hotmail.com.
Longhua Hospital Shanghai University of Traditional Chinese Medicine · CNShanghai University of Traditional Chinese Medicine · CN

Funding

Clinical Science and technology innovation project of Shanghai Shenkang Hospital Development Center SHDC12016114Excellent Academic Leaders of Health and Family Planning System in Shanghai 2017BR044Longhua Medical Scholar LYTD-39National Natural Science Foundation of China 81373621National Natural Science Foundation of China 81774166Sponsored by Shanghai Sailing Program 17YF1419700
6 · The paper itself

Abstract

backgroundMetastasis is the main cause of lung cancer death. As a seed of metastasis, circulating tumor cells are an important target for metastasis intervention. The traditional Chinese medicine, Jinfukang, has been clinically available for the treatment of non-small cell lung cancer (NSCLC). In this study, we investigated the action and underlying mechanisms of Jinfukang against circulating lung tumor cells.

methodsThe cell counting kit-8 (CCK-8), colony formation and cell cycle assays were used to study the cell proliferation ability. Flow cytometry was used to detect the apoptosis and the expression level of ROS and Caspase-3. Comet and TUNEL assays were used to detect DNA damage. DNA damage related pathway protein was detected by western blot.

resultsJinfukang significantly inhibits the proliferation of CTC-TJH-01 cells by inducing G1 phase arrest and inhibits their colony formation in a dose-dependent manner. Moreover, Jinfukang induces apoptosis in CTC-TJH-01 cells through the ROS-mediated ATM/ATR-p53 pathway and DNA damage.

conclusionsOur findings suggest that Jinfukang may be a potential drug for lung cancer metastasis.

Indexed as

Antineoplastic Agents, PhytogenicApoptosisAtaxia Telangiectasia Mutated ProteinsCarcinoma, Non-Small-Cell LungCell Cycle CheckpointsCell Line, TumorCell ProliferationDNA DamageDrugs, Chinese HerbalHumansNeoplastic Cells, CirculatingOxidative StressReactive Oxygen SpeciesTumor Suppressor Protein p53Antineoplastic Agents, PhytogenicAtaxia Telangiectasia Mutated ProteinsDrugs, Chinese HerbaljinfukangReactive Oxygen SpeciesTumor Suppressor Protein p53ApoptosisCirculating tumor cellJinfukangNon-small cell lung cancerOxidative stress

Identifiers

PMID31391058
PMCPMC6686466
OpenAlexW2965868999

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.