Evidence map›Paper›PMID 38904694›Full record

ArticleArchives of dermatological research2024

Potential of cannabidiol as acne and acne scar treatment: novel insights into molecular pathways of pathophysiological factors.

Jun Hyo Lee, Ji Young Yoon, Dong Hyo Kim, Yoon Gyung Kwon, Geun-Hyeong Kim, Byoung Jun Park, Dae Hun Suh

Abstract read
In one paragraph

Article in Archives of dermatological research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
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.

Jun Hyo Lee *Department of Dermatology, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea.ORCID http://orcid.org/0000-0003-3567-8922
Ji Young Yoon *Acne, Rosacea, Seborrheic Dermatitis and Hidradenitis Suppurativa Research Laboratory, Seoul National University Hospital, Seoul, 03080, Republic of Korea.ORCID http://orcid.org/0009-0004-3882-1573
Dong Hyo KimDepartment of Dermatology, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea.ORCID http://orcid.org/0000-0002-0501-5418
Yoon Gyung KwonSkin and Natural Products Laboratory, Kolmar Korea Co., Ltd, Seoul, Republic of Korea.
Geun-Hyeong KimSkin and Natural Products Laboratory, Kolmar Korea Co., Ltd, Seoul, Republic of Korea.
Byoung Jun ParkSkin and Natural Products Laboratory, Kolmar Korea Co., Ltd, Seoul, Republic of Korea.
Dae Hun SuhDepartment of Dermatology, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea. daehun@snu.ac.kr.ORCID http://orcid.org/0000-0002-3371-7505

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cannabidiol (CBD), which is derived from hemp, is gaining recognition because of its anti-inflammatory and lipid-modulating properties that could be utilized to treat acne. We conducted experiments to quantitatively assess the effects of CBD on acne-related cellular pathways. SEB-1 sebocytes and HaCaT keratinocytes were exposed to various CBD concentrations. CBD exhibited a concentration-dependent impact on cell viability and notably reduced SEB-1 viability; furthermore, it induced apoptosis and a significant increase in the apoptotic area at higher concentrations. Additionally, CBD remarkably reduced pro-inflammatory cytokines, including CXCL8, IL-1α, and IL-1β. Additionally, it inhibited lipid synthesis by modulating the AMPK-SREBP-1 pathway and effectively reduced hyperkeratinization-related protein keratin 16. Simultaneously, CBD stimulated the synthesis of elastin, collagen 1, and collagen 3. These findings emphasize the potential of CBD for the management of acne because of its anti-inflammatory, apoptotic, and lipid-inhibitory effects. Notably, the modulation of the Akt/AMPK-SREBP-1 pathway revealed a novel and promising mechanism that could address the pathogenesis of acne.

Indexed as

Acne VulgarisApoptosisCannabidiolCell SurvivalKeratinocytesSignal TransductionAMP-Activated Protein KinasesAnti-Inflammatory AgentsCell LineCicatrixCollagen Type ICollagen Type IIIElastinHaCaT CellsHumansInterleukin-1alphaAMP-Activated Protein KinasesAnti-Inflammatory AgentsCannabidiolCollagen Type ICollagen Type IIICXCL8 protein, humanElastinIL1A protein, humanIL1B protein, humanInterleukin-1alphaInterleukin-1betaInterleukin-8Proto-Oncogene Proteins c-aktSterol Regulatory Element Binding Protein 1AcneCannabidiolInflammationKeratinocytesLipid modulationSebocytes

Identifiers

PMID38904694
PMCPMC11192675

What OpenQuestion holds

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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.