Evidence map›Paper›PMID 42027562›Full record

ArticleFrontiers in nutrition2026

Physicochemical characteristics and anti-colorectal cancer activity of

Xinran Wang, Jingjie Xu, Zhijun Liu, Kenan Huang, Fengjing Xu, Xinhua Song, Jianpeng Jiao, Shouhong Gao, Wansheng Chen

Abstract read
In one paragraph

Article in Frontiers in nutrition, 2026. 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
–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

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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.

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

9 authors.

Xinran Wang *Department of Pharmacy, Second Affiliated Hospital of Naval Medical University, Shanghai, China.
Jingjie Xu *Department of Pharmacy, Second Affiliated Hospital of Naval Medical University, Shanghai, China.
Zhijun Liu *Department of Pharmacy, Second Affiliated Hospital of Naval Medical University, Shanghai, China.
Kenan HuangDepartment of Thoracic Surgery, Shanghai Changzheng Hospital, Navy Military Medical University, Shanghai, China.
Fengjing XuDepartment of Pharmacy, Second Affiliated Hospital of Naval Medical University, Shanghai, China.
Xinhua SongDepartment of Pharmacy, Second Affiliated Hospital of Naval Medical University, Shanghai, China.
Jianpeng JiaoDepartment of Traditional Chinese Medicine, Shanghai Changzheng Hospital, Navy Medical University, Shanghai, China.
Shouhong GaoDepartment of Pharmacy, Second Affiliated Hospital of Naval Medical University, Shanghai, China.
Wansheng ChenDepartment of Pharmacy, Second Affiliated Hospital of Naval Medical University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Methods: In this study, a novel acidic polysaccharide (SMP-3) was extracted from Results: The purified SMP-3 exhibited a total polysaccharide content of 96.52% with a weight-average molecular weight of 61.3 kDa. Monosaccharide composition analysis revealed that SMP-3 was primarily composed of galacturonic acid, glucuronic acid, glucose, mannose, galactose, and rhamnose in a molar ratio of 52.6:24.1:7.5:6.8:6.0:3.0, preliminarily suggesting a possible pectin-like structural feature with uronic acids accounting for 76.7% of the total content. Structural characterization indicated the presence of both α- and β-glycosidic linkages, an amorphous structure, and an ordered conformation in aqueous solution. Biologically, SMP-3 exhibited dose- and time-dependent cytotoxicity against HCT116 cells while showing minimal toxicity to normal FHC cells. Notably, combination treatment with SMP-3 and REG demonstrated combined effects, significantly enhancing G0/G1 cell cycle arrest, apoptosis induction, and inhibition of cell migration and invasion compared to single-agent treatments. Mechanistically, the combination treatment upregulated p21, Bax, and caspase-3 expression while downregulating cyclin D1, CDK4, and Bcl-2, and profoundly suppressed the phosphorylation of STAT3, AKT, and ERK signaling pathways. Discussion: These findings suggest that SMP-3 possesses distinct structural characteristics and significant anti-tumor efficacy, making it a promising medical food candidate for colorectal cancer treatment.

Indexed as

apoptosiscolorectal cancercombined effectregorafenibSalvia miltiorrhiza polysaccharideSTAT3 signaling

Identifiers

PMID42027562
PMCPMC13099326

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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.