Evidence map›Paper›PMID 31658635›Full record

ArticleMolecules (Basel, Switzerland)2019

Alisol A Suppresses Proliferation, Migration, and Invasion in Human Breast Cancer MDA-MB-231 Cells.

Chenghua Lou, Xintong Xu, Yan Chen, Huajun Zhao

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Alisols A-C and their acetate derivatives: a review of natural occurrence, pharmacology, semisynthesis, pharmacokinetics, and metabolism.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
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  15. Chemical composition and pharmacological bio-efficacy ofSaudi journal of biological sciences · 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

4 authors.

Chenghua LouSchool of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou 310053, China. lou.chenghua@hotmail.com.
Xintong XuSchool of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou 310053, China. inclovers@163.com.
Yan ChenSchool of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou 310053, China. 13735558952@163.com.
Huajun ZhaoSchool of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou 310053, China. zhj@zcmu.edu.cn.

Funding

Natural Science Foundation of China no. 81774003Qianjiang Scholar Program funded by Zhejiang Province Huajun Zhaothe first level and third level (Zhiguo Zheng) in Zhejiang Province "151 talents project" Huajun Zhaothe Zhejiang Provincial Natural Science Foundation of China no. LY17H310007 and LZ15H310001Zhejiang Chinese Medical University Research Fund Project no. 2015ZR06
6 · The paper itself

Abstract

Natural products are a precious source of promising leads for the development of novel cancer therapeutics. Recently, triterpenoids in Alismatis rhizoma has been widely demonstrated for their anti-cancer activities in cancer cells. In this study, we examined the inhibitory effects of alisol A in human breast cancer cells. We demonstrated that alisol A exhibited significant anti-proliferative effects in MDA-MB-231 cells and this response was related to autophagy induction. Alisol A-induced autophagy was supported by the triggered autophagosome formation and increased LC3-II levels. Interestingly, autophagy inhibitor 3-MA significantly reversed the cytotoxic effects induced by alisol A. Meanwhile, alisol A-induced autophagy was significantly inhibited by 3-MA in MDA-MB-231 cells. Cell cycle analysis revealed that alisol A arrested the cell cycle at G0/G1 phase. The expression level of cell cycle regulatory proteins cyclin D1 was significantly down regulated. In addition, the suppression of NF-κB and PI3K/Akt/mTOR pathways in MDA-MB-231 cells was observed. Furthermore, alisol A significantly suppressed the migration and invasion of MDA-MB-231 cells by inhibiting the expression levels of MMP-2 and MMP-9. Taken together, our results demonstrated that alisol A could inhibit the proliferation and metastasis of MDA-MB-231 cells. It could be a promising agent for breast cancer therapy.

Indexed as

Autophagic Cell DeathBreast NeoplasmsCell Line, TumorCell MovementCholestenonesFemaleG1 Phase Cell Cycle CheckpointsHumansNeoplasm InvasivenessResting Phase, Cell CycleSignal Transductionalisol ACholestenonesalisol Aautophagybreast cancermetastasisproliferation

Identifiers

PMID31658635
PMCPMC6833085

What OpenQuestion holds

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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.