Evidence map›Paper›PMID 39516823›Full record

ArticleBMC complementary medicine and therapies2024

Effect and mechanisms of shikonin on breast cancer cells in vitro and in vivo.

Chuyi Yu, Haoyu Xing, Xiaguo Fu, Yingying Zhang, Xiufang Yan, Jianjia Feng, Zhouqin He, Li Ru, Chunlong Huang, Jianming Liang

Abstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
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

10 authors.

Chuyi YuThe First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Haoyu XingArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Xiaguo FuArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Yingying ZhangArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Xiufang YanArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Jianjia FengArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Zhouqin HeArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Li RuArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Chunlong HuangGuangdong Provincial People's Hospital Zhuhai Hospital, Zhuhai Golden Bay Center Hospital, Zhuhai, 519090, China. tommyhuang1988@foxmail.com.
Jianming LiangThe First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510405, China. liangjianming@gzucm.edu.cn.

Funding

Natural Science Foundation of Guangdong Province 2022A1515011312Special Projects in Key Areas of Colleges and Universities in Guangdong Province 2022ZDZX2015
6 · The paper itself

Abstract

backgroundBreast cancer seriously affects physical and mental health of women. Despite advances in the clinical use of different treatments, breast cancer remains a major cause of mortality. Therefore, it is imperative to identify promising treatment options. In the present study, we investigated the effects of shikonin on 4T1 breast cancer cells and its potential mechanisms of action.

methodsBALB/c-derived mouse breast cancer 4T1 is very close to human breast cancer in growth characteristics and systemic response, so 4T1 cells were selected for further experiments. Cell viability, apoptosis, intracellular reactive oxygen species (ROS), mitochondrial activity, and cellular calreticulin (CRT) exposure were assessed to evaluate the antitumor effects and mechanisms of shikonin in vitro. Orthotopic tumor growth inhibition and splenic immune cell regulation by shikonin were evaluated in 4T1 breast cancer orthotopic mice in vivo.

resultsIn vitro, shikonin could inhibit cell proliferation, cause apoptosis, disrupt mitochondrial activity, and induce ROS production and CRT exposure. In vivo, shikonin inhibited tumor growth, increased the proportion of CD8

conclusionsShikonin inhibits the growth of 4T1 breast cancer cells by disrupting mitochondrial activity, promoting oxidative stress, and regulating immune function.

Indexed as

ApoptosisBreast NeoplasmsMice, Inbred BALB CNaphthoquinonesReactive Oxygen SpeciesAnimalsCell Line, TumorCell ProliferationCell SurvivalFemaleHumansMiceMitochondriaNaphthoquinonesReactive Oxygen SpeciesshikoninBreast cancerImmunomodulationIntracellular reactive oxygen speciesMitochondrial activityShikonin

Identifiers

PMID39516823
PMCPMC11549804

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.