Evidence map›Paper›PMID 35528507›Full record

ArticleOxidative medicine and cellular longevity2022

N-((1-(4-Fluorophenyl)-1H-1,2,3-triazol-4-yl)methyl)-2-methylene-3-oxo-olean-12-en-28-amide Induces Apoptosis in Human Breast Cancer Cells by Stimulating Oxidative Stress and Inhibiting the Notch-Akt Signaling Pathway.

Xiaorui Li, Shisheng Wang, Ning Deng, Xiangyu Guo, Meiyi Fu, Yiwen Ma, Tao Sun

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Notch signaling, hypoxia, and cancer.Frontiers in oncology · 2023
    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

7 authors at 1 institution in 1 country.

Xiaorui LiCancer Hospital of Dalian University of Technology Liaoning Cancer Hospital & Institute, Shenyang, China.
Shisheng WangCollege of Pharmaceutical Science and Technology, Dalian University of Technology, Dalian, China.
Ning DengCancer Hospital of Dalian University of Technology Liaoning Cancer Hospital & Institute, Shenyang, China.
Xiangyu GuoCancer Hospital of Dalian University of Technology Liaoning Cancer Hospital & Institute, Shenyang, China.
Meiyi FuCancer Hospital of Dalian University of Technology Liaoning Cancer Hospital & Institute, Shenyang, China.
Yiwen MaCancer Hospital of Dalian University of Technology Liaoning Cancer Hospital & Institute, Shenyang, China.
Tao SunCancer Hospital of Dalian University of Technology Liaoning Cancer Hospital & Institute, Shenyang, China.ORCID https://orcid.org/0000-0001-5931-386X
Dalian University of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is of the leading causes of cancer-related deaths and the most frequently diagnosed cancer among females worldwide. Despite advancements in breast cancer therapy, the disease eventually progresses in most patients because of de novo or secondary resistance. Thus, discovering novel drugs with high effectiveness and low toxicity for systemic therapy is essential. In this study, we investigated whether a new oleanolic derivative N-((1-(4-fluorophenyl)-1H-1,2,3-triazol-4-yl)methyl)-2-methylene-3-oxo-olean-12-en-28-amide (ZQL-4c) exhibits potential anticancer effects against breast cancer. We determined that ZQL-4c strongly inhibited cell proliferation and invasion and induced G2/M phase arrest and apoptosis in breast cancer cells. We then found that ZQL-4c induced the production of reactive oxygen species (ROS). We then found that ZQL-4c significantly inhibited Notch-AKT signaling pathways that are related to oxidative stress. Taken together, this study is the first to show that ZQL-4c can significantly suppress the growth and invasion of breast cancer by blocking Notch-Akt signaling pathways, which are mainly regulated by ROS-mediated oxidative stress. Thus, ZQL-4c might be considered a novel and potential anticancer drug for breast cancer treatment.

Indexed as

AmidesBreast NeoplasmsProto-Oncogene Proteins c-aktReceptors, NotchSignal TransductionApoptosisCell Line, TumorCell ProliferationHumansOxidative StressReactive Oxygen SpeciesAmidesProto-Oncogene Proteins c-aktReactive Oxygen SpeciesReceptors, Notch

Identifiers

PMID35528507
PMCPMC9068303
OpenAlexW4224988976

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.