Evidence map›Paper›PMID 37329481›Full record

ArticleMolecular biology reports2023

Polysaccharide extracted from the Sargassum fusiforme induces cell cycle arrest and apoptosis of B16F10 melanoma cells through the PI3K/AKT pathway.

Feng Xu, Haomiao Ding, Zhifang Liu, Xinyu Jiang, Yizhao Ma, Diancheng Wang, Suling Xu

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

Feng Xu *Department of Dermatology, The First Affiliated Hospital of Ningbo University, 247 Renmin Road, Ningbo, 315000, China.ORCID http://orcid.org/0000-0003-0471-4716
Haomiao Ding *College of Biological and Environmental Sciences, Zhejiang Wanli University, 8 Qianhu South Road, Ningbo, 315100, China.
Zhifang LiuDepartment of Dermatology, The First Affiliated Hospital of Ningbo University, 247 Renmin Road, Ningbo, 315000, China.
Xinyu JiangDepartment of Dermatology, The First Affiliated Hospital of Ningbo University, 247 Renmin Road, Ningbo, 315000, China.
Yizhao MaDepartment of Dermatology, The First Affiliated Hospital of Ningbo University, 247 Renmin Road, Ningbo, 315000, China.
Diancheng WangDepartment of Dermatology, The First Affiliated Hospital of Ningbo University, 247 Renmin Road, Ningbo, 315000, China.
Suling XuDepartment of Dermatology, The First Affiliated Hospital of Ningbo University, 247 Renmin Road, Ningbo, 315000, China. xusuling@nbu.edu.cn.ORCID http://orcid.org/0000-0002-2472-0403
Ningbo University · CNZhejiang Wanli University · CN

Funding

The Medical and Health Research Project of Zhejiang Province 2022KY1145The Ningbo Public Welfare Projects 2022S065The Project of Ningbo Leading Medical & Health Discipline 2022-F23The Research Startup Project of Advanced Talents of The First Affiliated Hospital of Ningbo University 2022KYQDJ-XF
6 · The paper itself

Abstract

backgroundSARGASSUM FUSIFORME: (S. fusiforme) is a brown alga that has been utilized as a medicine for a long time. Polysaccharides extracted from S. fusiforme demonstrate antitumor activities.

methodsThe impact of S. fusiforme polysaccharides (SFPS 191,212) on the proliferation, apoptosis, and cell cycle kinetics of B16F10 murine melanoma cells were thoroughly investigated in this work. The anticancer activities of the SFPS 191,212 compounds were assayed in the B16F10 cells at both transcriptional and translational levels.

resultsThe compound exhibited concentration-dependent effects. Moreover, SPFS 191,212 increased the numbers of apoptotic cells and arrested the cell cycle in the S phase of the quantitative real-time PCR. From western blotting, it was verified that the SFPS 191,212 treatment improved the expression of Bax, Caspase-9, and Caspase-3 genes and proteins, while it reduced phosphatidylinositol 3 kinase and Bcl-2 genes and proteins, suggesting the involvement of mitochondria.

conclusionOverall, SFPS 191,212 can be further explored as a potential functional food or adjuvant agent for the prevention or treatment of melanoma.

Indexed as

MelanomaSargassumAnimalsApoptosisCell Cycle CheckpointsEdible SeaweedsMicePhosphatidylinositol 3-KinasesPolysaccharidesProto-Oncogene Proteins c-aktPhosphatidylinositol 3-KinasesPolysaccharidesProto-Oncogene Proteins c-aktApoptosisB16F10 cellsCell arrestPolysaccharidesSargassum fusiforme

Identifiers

PMID37329481
OpenAlexW4381054701

What OpenQuestion holds

Textmetadata
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.