Evidence map›Paper›PMID 29993186›Full record

ArticleJournal of cellular and molecular medicine2018

Theabrownin triggers DNA damage to suppress human osteosarcoma U2OS cells by activating p53 signalling pathway.

Wangdong Jin, Li Zhou, Bo Yan, Li Yan, Fucun Liu, Peijian Tong, Wenhua Yu, Xiaoqiao Dong, Li Xie, Jin Zhang and 5 more

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

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  12. Green extraction, chemical composition, andCurrent research in food science · 2022
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  16. Predictive Study of the Active Ingredients and Potential Targets ofEvidence-based complementary and alternative medicine : eCAM · 2021
    Article
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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

15 authors.

Wangdong JinThe First Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China.
Li ZhouThe First Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China.
Bo YanThe First Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China.
Li YanThe First Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China.
Fucun LiuDepartment of Orthopaedics, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Peijian TongThe First Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China.
Wenhua YuHangzhou First People's Hospital, Hangzhou, China.
Xiaoqiao DongHangzhou First People's Hospital, Hangzhou, China.
Li XieAnalysis Center of Agrobiology and Environmental Science, Zhejiang University, Hangzhou, China.
Jin ZhangTheabio Co., Ltd, Hangzhou, China.
Yiqiao XuHunter Biotechnology, Inc, Hangzhou, China.
Chunqi LiHunter Biotechnology, Inc, Hangzhou, China.
Qiang YuanThe First Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China.
Letian ShanThe First Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China.ORCID 0000-0003-4926-0527
Thomas EfferthDepartment of Pharmaceutical Biology, Institute of Pharmacy and Biochemistry, Johannes Gutenberg University, Mainz, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma becomes the second leading cause of cancer death in the younger population. Current outcomes of chemotherapy on osteosarcoma were unsatisfactory to date, demanding development of effective therapies. Tea is a commonly used beverage beneficial to human health. As a major component of tea, theabrownin has been reported to possess anti-cancer activity. To evaluate its anti-osteosarcoma effect, we established a xenograft model of zebrafish and employed U2OS cells for in vivo and in vitro assays. The animal data showed that TB significantly inhibited the tumour growth with stronger effect than that of chemotherapy. The cellular data confirmed that TB-triggered DNA damage and induced apoptosis of U2OS cells by regulation of Mki67, PARP, caspase 3 and H2AX, and Western blot assay showed an activation of p53 signalling pathway. When P53 was knocked down by siRNA, the subsequent downstream signalling was blocked, indicating a p53-dependent mechanism of TB on U2OS cells (p53 wt). Using osteosarcoma cell lines with p53 mutations (HOS, SAOS-2 and MG63), we found that TB exerted stronger inhibitory effect on U2OS cells than that on p53-mut cell lines, but it also exerted obvious effect on SAOS-2 cells (p53 null), suggesting an activation of p53-independent pathway in the p53-null cells. Interestingly, theabrownin was found to have no toxicity on normal tissue in vivo and could even increase the viability of p53-wt normal cells. In sum, theabrownin could trigger DNA damage and induce apoptosis on U2OS cells via a p53-dependent mechanism, being a promising candidate for osteosarcoma therapy.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntineoplastic Agents, PhytogenicApoptosisBone NeoplasmsCaspase 3CatechinCell CycleCell Line, TumorCell SurvivalCisplatinDNA DamageHistonesHumansKi-67 AntigenLarvaAntineoplastic Agents, PhytogenicCASP3 protein, humanCaspase 3CatechinCisplatinH2AX protein, humanHistonesKi-67 AntigenMKI67 protein, humanPoly(ADP-ribose) PolymerasesRNA, Small InterferingtheabrowninTumor Suppressor Protein p53DNA damageosteosarcomaP53theabrowninzebrafish

Identifiers

PMID29993186
PMCPMC6111873

What OpenQuestion holds

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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.