Evidence map›Paper›PMID 31412862›Full record

ArticleBMC complementary and alternative medicine2019

Berberine inhibits NLRP3 Inflammasome pathway in human triple-negative breast cancer MDA-MB-231 cell.

Mingjiang Yao, Xiaodi Fan, Bo Yuan, Norio Takagi, Sai Liu, Xiao Han, Junguo Ren, Jianxun Liu

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 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
10.6field-weighted citation impact, top 1% 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

62 citing papers in PubMed, 1 synthesis or guideline pooled it, 116 citations in OpenAlex.

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  18. Current topics in medicinal chemistry · 2024
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2 more citing papers are in PubMed but not listed here.

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

8 authors at 5 institutions in 2 countries.

Mingjiang YaoXiyuan Hospital of China Academy of Chinese Medical Sciences, Institute of Basic Medical Sciences, No.1 Xiyuan Caochang, Haidian District, Beijing, 100091, China.
Xiaodi FanXiyuan Hospital of China Academy of Chinese Medical Sciences, Institute of Basic Medical Sciences, No.1 Xiyuan Caochang, Haidian District, Beijing, 100091, China.
Bo YuanLaboratory of Pharmacology, School of Pharmacy, Faculty of Pharmacy and Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado, Saitama, 350-0295, Japan.
Norio TakagiDepartment of Applied Biochemistry, School of Pharmacy, Tokyo University of Pharmacy & Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo, 192-0392, Japan.
Sai LiuXiyuan Hospital of China Academy of Chinese Medical Sciences, Institute of Basic Medical Sciences, No.1 Xiyuan Caochang, Haidian District, Beijing, 100091, China.
Xiao HanXiyuan Hospital of China Academy of Chinese Medical Sciences, Institute of Basic Medical Sciences, No.1 Xiyuan Caochang, Haidian District, Beijing, 100091, China.
Junguo RenXiyuan Hospital of China Academy of Chinese Medical Sciences, Institute of Basic Medical Sciences, No.1 Xiyuan Caochang, Haidian District, Beijing, 100091, China.
Jianxun LiuXiyuan Hospital of China Academy of Chinese Medical Sciences, Institute of Basic Medical Sciences, No.1 Xiyuan Caochang, Haidian District, Beijing, 100091, China. liujx0324@sina.com.
Institute of Basic Medical Sciences of the Chinese Academy of Medical SciencesChinese Academy of Medical Sciences & Peking Union Medical College · CNJosai University · JPTokyo University of Pharmacy and Life Sciences · JPXiyuan Hospital · CN

Funding

Major Research Plan 81873040Young Scientists Fund 81403141
6 · The paper itself

Abstract

backgroundBreast cancer is still the most common malignant tumor that threatens the female's life in the world, especially triple-negative breast cancer (TNBC), one of the most difficult subtypes. Lack of targeted therapies brings about urgent demand for novel treatments. In this study we aim to investigate the anti-tumor activity of Berberine (BBR), a Chinese plant-derived alkaloid, against the TNBC cell line MDA-MB-231 and elucidate its mechanism referring to anti-inflammation.

methodsCell inhibition rate was measured by Cell Proliferation Assay, the cytotoxic effects was detected by Lactate dehydrogenase (LDH) leakage assay, the colony formation and migration potential were evaluated by colony formation assay and wound healing assay, the release of inflammatory cytokines was detected by EMD multifactor detection, and alterations of proteins and genes related to the NLR family pyrin domain containing 3 (NLRP3) inflammasome pathway were analyzed using western blotting and real-time Polymerase Chain Reaction (PCR).

resultsBBR reduce the viability of MDA-MB-231 cells and increased the release of LDH from the cells in a dose-dependent manner, with and inhibition of colony formation potential and migration of the cells. BBR also caused a marked reduction in the secretion of proinflammatory cytokines, Interleukin-1α (IL-1α), Interleukin-1β (IL-1β), Interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α). Besides, a down-regulated behavior was observed with the expression of P2X purinoceptor 7 (P2X7), NLRP3, pro-caspase-1, apoptosis-associated speck-like protein containing a caspase-activation and recruitment domain (ASC), caspase-1 p20, Interleukin-18 (IL-18), IL-1β proteins and NLRP3, Caspase-1 and ASC mRNAs in the NLRP3 inflammasome cascade.

conclusionsOur results confirmed that BBR can effectively affect both tumor outgrowth and spontaneous metastasis in TNBC, and that we identified a new mechanism associated with inhibition the NLRP3 inflammasome pathway, suggesting its potential therapeutic relevance in clinical use.

Indexed as

ApoptosisBerberineCaspase 1Drugs, Chinese HerbalFemaleHumansInflammasomesInterleukin-18Interleukin-1betaInterleukin-6NLR Family, Pyrin Domain-Containing 3 ProteinTriple Negative Breast NeoplasmsTumor Necrosis Factor-alphaBerberineCaspase 1Drugs, Chinese HerbalIL18 protein, humanIL1B protein, humanInflammasomesInterleukin-18Interleukin-1betaInterleukin-6NLR Family, Pyrin Domain-Containing 3 ProteinTumor Necrosis Factor-alphaAnti-inflammationBerberineNLRP3 inflammasomeTriple-negative breast cancer

Identifiers

PMID31412862
PMCPMC6694465
OpenAlexW2968733355

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.