Evidence map›Paper›PMID 39125863›Full record

ArticleInternational journal of molecular sciences2024

Kuwanon C Inhibits Tumor Cell Proliferation and Induces Apoptosis by Targeting Mitochondria and Endoplasmic Reticulum.

Gangxiang Yuan, Peng Qian, Lin Chen, Ningjia He

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. 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

4 authors.

Gangxiang YuanState Key Laboratory of Resource Insects, Southwest University, Chongqing 400715, China.ORCID 0000-0002-5455-0791
Peng QianState Key Laboratory of Resource Insects, Southwest University, Chongqing 400715, China.
Lin ChenState Key Laboratory of Resource Insects, Southwest University, Chongqing 400715, China.ORCID 0000-0002-1463-3242
Ningjia HeState Key Laboratory of Resource Insects, Southwest University, Chongqing 400715, China.ORCID 0000-0002-7322-7113

Funding

Chongqing Research Program of Basic Research and Frontier Technology cstc2021yszx-jcyj0004Innovation Research 2035 Pilot Plan of Southwest University SWU-XDZD22008National Key R&D Program of China 2022YFD1201602
6 · The paper itself

Abstract

Kuwanon C is a unique flavonoid found in the mulberry family, characterized by two isopentenyl groups. While previous research has focused on various properties of kuwanon C, such as antioxidant, hypoglycemic, antimicrobial, food preservation, skin whitening, and nematode lifespan extension, little attention has been given to its potential role in oncological diseases. In this study, we investigate the antitumor effect of kuwanon C in cervical cancer cells and elucidate its specific mechanism of action. We assessed the antitumor effects of kuwanon C using various experimental techniques, including cell proliferation assay, wound healing assays, EdU 488 proliferation assay, mitochondrial membrane potential assay, ROS level assay, cell cycle, apoptosis analysis, and studies on kuwanon C target sites and molecular docking. The results revealed that kuwanon C significantly impacted the cell cycle progression of HeLa cells, disrupted their mitochondrial membrane potential, and induced a substantial increase in intracellular ROS levels. Moreover, kuwanon C exhibited notable anti-proliferative and pro-apoptotic effects on HeLa cells, surpassing the performance of commonly used antitumor drugs such as paclitaxel and cisplatin. Notably, kuwanon C demonstrated superior efficacy while also being more easily accessible compared to paclitaxel. Our study demonstrates that kuwanon C exerts potent antitumor effects by its interaction with the mitochondrial and endoplasmic reticulum membranes, induces a significant production of ROS, disrupts their normal structure, inhibits cell cycle progression, and stimulates apoptotic signaling pathways, ultimately resulting in the death of HeLa tumor cells. As an isopentenyl compound derived from

Indexed as

ApoptosisCell ProliferationEndoplasmic ReticulumMembrane Potential, MitochondrialMitochondriaReactive Oxygen SpeciesAntineoplastic AgentsCell CycleFemaleHeLa CellsHumansMolecular Docking SimulationUterine Cervical NeoplasmsAntineoplastic AgentsReactive Oxygen SpeciesapoptosiscancerflavonoidHeLakuwanon Cmitochondria

Identifiers

PMID39125863
PMCPMC11312418

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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.