Evidence map›Paper›PMID 42183904›Full record

ArticleGlycoconjugate journal2026

3'-sialyllactose inhibits the migration and invasion of LPS-induced B16F10 mouse melanoma cells through inactivation of the NF-

Hee-Do Kim, Hyunju-Choi, Yu-Chan Chang, Cheorl-Ho Kim

Abstract read
In one paragraph

Article in Glycoconjugate journal, 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

4 authors.

Hee-Do KimDepartment of Biological Science, SungKyunkwan University, Janan-gu, Seoburo, Suwon, 16419, Republic of Korea.ORCID http://orcid.org/0009-0007-2111-3281
Hyunju-ChoiDepartment of Biological Science, SungKyunkwan University, Janan-gu, Seoburo, Suwon, 16419, Republic of Korea.
Yu-Chan ChangDepartment of Biomedicine Imaging and Radiological Sciences, National Yang Ming Chiao Tung University, Taipei, 112, Taiwan.ORCID http://orcid.org/0000-0003-0474-9935
Cheorl-Ho KimDepartment of Biological Science, SungKyunkwan University, Janan-gu, Seoburo, Suwon, 16419, Republic of Korea. chkimbio@skku.edu.ORCID http://orcid.org/0000-0002-6323-0714

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant melanoma has a high mortality rate and is aggressive. The development, metastasis, and angiogenesis of melanoma have all been connected to toll-like receptor 4 (TLR4). However, signal transduction mediated by TLR4 for accelerating melanoma progression is fully unclear. Because of this, the current research has been carried out to explore drug candidate possibility using 3'-Sialyllactose (3'-SL). We investigated the inhibitory effect of 3'-SL on migration and invasion, which are associated with treatment difficulty and mortality. The suppression of matrix metalloproteinases 9 (MMP-9) expression and activity by 3'-SL in B16F10 murine melanoma cells and concurrently downregulated the MAPK signaling pathway involved in this regulation. Therefore, our results demonstrate that 3'-SL may be a good candidate for the development of therapeutic agents to suppress malignancy associated with metastasis and invasion.

Indexed as

Cell MovementLactoseLipopolysaccharidesMelanoma, ExperimentalNF-kappa BSignal TransductionAnimalsCell Line, TumorMatrix Metalloproteinase 9MiceNeoplasm InvasivenessOligosaccharides3'-sialyllactoseLactoseLipopolysaccharidesMatrix Metalloproteinase 9NF-kappa BOligosaccharides3’-sialyllactose (3’-SL)Lipopolysaccharide (LPS)MMP-9NF-KB Signaling Pathway

Identifiers

PMID42183904
PMCPMC13201296

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Registered trials

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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.