Evidence map›Paper›PMID 38059303›Full record

ArticleIntegrative cancer therapies

Anti-Colorectal Cancer Effects of Fucoidan Complex-Based Functional Beverage Through Retarding Proliferation, Cell Cycle and Epithelial-Mesenchymal Transition Signaling Pathways.

Chun-Hao Chan, Yue-Hua Deng, Bou-Yue Peng, Pao-Chang Chiang, Li-An Wu, Yen-Yung Lee, Wen Tsao, Hsiang-Hsun Mao, Chia-Yu Wu, Win-Ping Deng

Open access · goldAbstract read
In one paragraph

Article in Integrative cancer therapies. 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
2.1field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Fucoidan in cancer therapy: from biomedical application to medicinal chemistry approach.Journal of materials science. Materials in medicine · 2025
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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

10 authors at 4 institutions in 1 country.

Chun-Hao ChanSchool of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 110301, Taiwan.
Yue-Hua DengSchool of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 110301, Taiwan.
Bou-Yue PengSchool of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 110301, Taiwan.
Pao-Chang ChiangSchool of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 110301, Taiwan.
Li-An WuStem Cell Research Center, College of Oral Medicine, Taipei Medical University, Taipei 110301, Taiwan.
Yen-Yung LeeStem Cell Research Center, College of Oral Medicine, Taipei Medical University, Taipei 110301, Taiwan.
Wen TsaoSchool of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 110301, Taiwan.
Hsiang-Hsun MaoStem Cell Research Center, College of Oral Medicine, Taipei Medical University, Taipei 110301, Taiwan.
Chia-Yu WuSchool of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 110301, Taiwan.
Win-Ping DengSchool of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 110301, Taiwan.ORCID 0000-0002-7826-7595
Taipei Medical University · TWTaipei Medical University Hospital · TWFu Jen Catholic University · TWWan Fang Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background

objectiveColorectal cancer (CRC) remains a significant cause of mortality, particularly in metastatic cases. Therefore, the urgent need for novel alternative medicines that comprehensively inhibit CRC persists. In this investigation, we assess the impact of VMW-FC on CRC cell proliferation, cell cycle dynamics, metastasis,

methodsCell growth was assessed using MTT and colony formation assays, while metastatic potential was evaluated through wound healing and transwell migration assays. The underlying signaling mechanisms were elucidated through qPCR and western blot analysis.

resultsOur findings demonstrate that VMW-FC significantly impedes CRC proliferation and migration in a dose- and time-dependent manner. Furthermore, it induces sub-G1 cell cycle arrest and an increase in apoptotic cell populations, as confirmed through flow-cytometric analysis. Notably, VMW-FC also suppresses xenograft tumor growth in NOD/SCID mice without causing renal or hepatic toxicity.

conclusionThe integrative herbal concoction VMW-FC presents a promising approach for inhibiting CRC by slowing proliferation and migration, inducing cell cycle arrest and apoptosis, and suppressing markers associated with proliferation (Ki-67, PCNA, and CDKs) and epithelial-mesenchymal transition (EMT) (Vimentin, N-cadherin, and β-catenin).

Indexed as

Colorectal NeoplasmsAnimalsCell Line, TumorCell MovementCell ProliferationEpithelial-Mesenchymal TransitionHumansMiceMice, Inbred NODMice, SCIDPolysaccharidesSignal TransductionfucoidanPolysaccharidesapoptosiscell cyclecolorectal cancerepithelial–mesenchymal transition (EMT)fucoidanintegrative herbal medicine

Identifiers

PMID38059303
PMCPMC10704951
OpenAlexW4389443073

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.