Evidence map›Paper›PMID 40893218›Full record

ArticleACS omega2025

Potential Antiphotoaging Effect of Human Cathelicidin LL-37 Fragments and KR-12 Analogs on UVB-Induced HaCaT Cells and UVA-Induced HDF Cells.

Menggeng Li, Jing Wang, Peng Shu, Xueqing Chen, Yizhen Yan, Jiangming Zhong, Nan Zhao, Ling Liang, Zhao Liu

Abstract read
In one paragraph

Article in ACS omega, 2025. 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
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0citing papers in PubMed
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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.

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.

Menggeng LiHBN Research Institute and Biological Laboratory, Shenzhen Hujia Technology Co., Ltd., Shenzhen 518000, China.
Jing WangHBN Research Institute and Biological Laboratory, Shenzhen Hujia Technology Co., Ltd., Shenzhen 518000, China.
Peng ShuHBN Research Institute and Biological Laboratory, Shenzhen Hujia Technology Co., Ltd., Shenzhen 518000, China.ORCID https://orcid.org/0009-0004-6354-8716
Xueqing ChenHBN Research Institute and Biological Laboratory, Shenzhen Hujia Technology Co., Ltd., Shenzhen 518000, China.
Yizhen YanHBN Research Institute and Biological Laboratory, Shenzhen Hujia Technology Co., Ltd., Shenzhen 518000, China.
Jiangming ZhongHBN Research Institute and Biological Laboratory, Shenzhen Hujia Technology Co., Ltd., Shenzhen 518000, China.
Nan ZhaoHBN Research Institute and Biological Laboratory, Shenzhen Hujia Technology Co., Ltd., Shenzhen 518000, China.
Ling LiangHBN Research Institute and Biological Laboratory, Shenzhen Hujia Technology Co., Ltd., Shenzhen 518000, China.
Zhao LiuHBN Research Institute and Biological Laboratory, Shenzhen Hujia Technology Co., Ltd., Shenzhen 518000, China.ORCID https://orcid.org/0009-0000-5103-9923

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cathelicidin LL-37, an antimicrobial peptide (AMP) of the innate immune system, wards off bacterial infections. Recent research has identified plenty of biological functions of AMPs beyond their antimicrobial activity, including antioxidant, self-renewal, and procollagen properties, making them valuable for antiaging products. In this study, we assessed the antiphotoaging potential of cathelicidin LL-37 fragments and KR-12 analogs using human immortalized keratinocytes (HaCaT) and human dermal fibroblasts (HDF). Our results reveal that these peptides can modulate ultraviolet-radiation-induced photodamage, exhibiting anti-inflammatory and antioxidant properties. Notably, we proved the immune modulation effects of LL-23. Additionally, these peptides promote cell migration and collagen synthesis, inhibit glycation, and suppress melanin production. We propose that the antiphotoaging effects exhibited by LL-37 fragments and KR-12 analogs are related to the alleviation of inflammation, and we attempt to elucidate the possible underlying mechanisms. These findings support their efficacy as antiaging agents in dermatological applications.

Identifiers

PMID40893218
PMCPMC12392188

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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.