Evidence map›Paper›PMID 41258074›Full record

ReviewExperimental & molecular medicine2025

Emerging perspectives on the selective autophagy of melanosomes: melanophagy.

Na Yeon Park, Seong Hyun Kim, Doo Sin Jo, Dong-Hyung Cho

Abstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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

1 citing paper in PubMed.

  1. 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

4 authors.

Na Yeon ParkOrganelle Institute, Kyungpook National University, Daegu, Republic of Korea.ORCID http://orcid.org/0009-0004-3552-0062
Seong Hyun KimSchool of Life Sciences, BK21 FOUR KNU Creative BioResearch Group, Kyungpook National University, Daegu, Republic of Korea.
Doo Sin JoOrganelle Institute, Kyungpook National University, Daegu, Republic of Korea. doosinjo@gmail.com.
Dong-Hyung ChoOrganelle Institute, Kyungpook National University, Daegu, Republic of Korea. dhcho@knu.ac.kr.

Funding

Ministry of Health and Welfare (Ministry of Health, Welfare and Family Affairs) RS-2024-00342057Ministry of Trade, Industry and Energy (Ministry of Trade, Industry and Energy, Korea) P0025489National Research Foundation of Korea (NRF) RS-2024-00453488National Research Foundation of Korea (NRF) RS-2024-00463344
6 · The paper itself

Abstract

Melanosomes are highly specialized organelles responsible for melanin synthesis, storage and transport in melanocytes, playing a central role in pigmentation and skin homeostasis. Although melanosome biogenesis and trafficking have been well characterized, emerging evidence emphasizes the importance of melanosome degradation in regulating pigment levels. Among the degradation pathways, melanophagy-a selective form of autophagy targeting melanosomes-has recently emerged as an important mechanism for the turnover of damaged, immature, or excess melanosomes. Here we highlight current insights into melanophagy mechanisms, including molecular regulators and signaling pathways. We also discuss the potential of modulating melanophagy as a novel cosmetic or therapeutic approach for managing hyperpigmentation, offering an alternative to traditional strategies focused solely on inhibiting melanin synthesis. By emphasizing the role of organelle clearance, melanophagy provides a new paradigm in the regulation of skin pigmentation.

Indexed as

AutophagyMelanosomesAnimalsHumansMelaninsMelanocytesSignal TransductionSkin PigmentationMelanins

Identifiers

PMID41258074
PMCPMC12800028

What OpenQuestion holds

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LicenceCC BY
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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.