Evidence map›Paper›PMID 36613979›Full record

ArticleInternational journal of molecular sciences2022

Anti-Melanogenesis Effects of a Cyclic Peptide Derived from Flaxseed via Inhibition of CREB Pathway.

Ji Hye Yoon, Won Young Jang, Sang Hee Park, Han Gyung Kim, Youn Young Shim, Martin J T Reaney, Jae Youl Cho

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. 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
0.9field-weighted citation impact, top 29% 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, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
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 at 2 institutions in 2 countries.

Ji Hye YoonDepartment of Biocosmetics, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0000-0003-0470-7372
Won Young JangDepartment of Integrative Biotechnology, Biomedical Institute for Convergence at SKKU (BICS), Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0000-0001-8818-7698
Sang Hee ParkDepartment of Biocosmetics, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0000-0003-1175-4222
Han Gyung KimDepartment of Integrative Biotechnology, Biomedical Institute for Convergence at SKKU (BICS), Sungkyunkwan University, Suwon 16419, Republic of Korea.
Youn Young ShimDepartment of Integrative Biotechnology, Biomedical Institute for Convergence at SKKU (BICS), Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0000-0002-5039-8219
Martin J T ReaneyDepartment of Plant Sciences, University of Saskatchewan, Saskatoon, SK S7N 5A8, Canada.
Jae Youl ChoDepartment of Biocosmetics, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0000-0001-8141-9927
Sungkyunkwan University · KRUniversity of Saskatchewan · CA

Funding

National reseach foundation of Korea 2020H1D3A2A02110965
6 · The paper itself

Abstract

Linosorbs (Los) are cyclic peptides from flaxseed oil composed of the LO mixture (LOMIX). The activity of LO has been reported as being anti-cancer and anti-inflammatory. However, the study of skin protection has still not proceeded. In particular, there are poorly understood mechanisms of melanogenesis to LO. Therefore, we investigated the anti-melanogenesis effects of LOMIX and LO, and its activity was examined in mouse melanoma cell lines. The treatment of LOMIX (50 and 100 μg/mL) and LO (6.25-50 μM) suppressed melanin secretion and synthesis, which were 3-fold increased, in a dose-dependent manner, up to 95%. In particular, [1-9-NαC]-linusorb B3 (LO1) and [1-9-NαC]-linusorb B2 (LO2) treatment (12.5 and 25 μM) highly suppressed the synthesis of melanin in B16F10 cell lines up to 90%, without toxicity. LOMIX and LOs decreased the 2- or 3-fold increased mRNA levels, including the microphthalmia-associated transcription factor (MITF), Tyrosinase, tyrosinase-related protein 1 (TYRP1), and tyrosinase-related protein 2 (TYRP2) at the highest concentration (25 μM). Moreover, the treatment of 25 μM LO1 and LO2 inhibited the expression of MITF and phosphorylation of upper regulatory proteins such as CREB and PKA. Taken together, these results suggested that LOMIX and its individual LO could inhibit melanin synthesis via downregulating the CREB-dependent signaling pathways, and it could be used for novel therapeutic materials in hyperpigmentation.

Indexed as

FlaxMelanomaMelanoma, ExperimentalAnimalsCell Line, TumorCyclic AMP Response Element-Binding ProteinMelaninsMiceMicrophthalmia-Associated Transcription FactorMonophenol MonooxygenasePeptides, CyclicCyclic AMP Response Element-Binding ProteinMelaninsMicrophthalmia-Associated Transcription FactorMonophenol MonooxygenasePeptides, Cyclicanti-melanogenesisCREB pathwaycyclic peptideflaxseedlinusorbmelaninMITF

Identifiers

PMID36613979
PMCPMC9820828
OpenAlexW4313238218

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.