Evidence map›Paper›PMID 42652214›Full record

ReviewBiomedicines2026

Precision Medicine in Dermatology: MEK Inhibition and MAPK Pathway Modulation for Congenital Melanocytic Nevi.

Alyssa Forsyth, Ochuwa Precious Imokhai, Kayla Fure, Rafael do Valle, Reem Ayoub, Alejandra Sataray-Rodriguez, Gabriella Martinez, Amanda Brooks

Abstract readReview
In one paragraph

Review in Biomedicines, 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

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

8 authors.

Alyssa ForsythTexas College of Osteopathic Medicine, University of North Texas Health, Fort Worth, TX 76107, USA.
Ochuwa Precious ImokhaiMontana College of Osteopathic Medicine, Rocky Vista University, Billings, MT 59106, USA.ORCID 0009-0008-1015-7526
Kayla FureTexas College of Osteopathic Medicine, University of North Texas Health, Fort Worth, TX 76107, USA.
Rafael do ValleTexas College of Osteopathic Medicine, University of North Texas Health, Fort Worth, TX 76107, USA.
Reem AyoubTexas College of Osteopathic Medicine, University of North Texas Health, Fort Worth, TX 76107, USA.ORCID 0009-0009-5099-5652
Alejandra Sataray-RodriguezReno School of Medicine, University of Nevada, Reno, NV 89557, USA.
Gabriella MartinezMedical College of Wisconsin, Milwaukee, WI 53226, USA.
Amanda BrooksDepartment of Research and Scholarly Activity, Rocky Vista University, Ivins, UT 80112, USA.ORCID 0000-0001-9785-5969

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital melanocytic nevi (CMN) are pigmented skin lesions present at birth with a variable risk of developing into melanoma over time. The mitogen-activated protein kinase signaling (MAPK) pathway plays a critical role in the development and progression of CMN, making it a key target for therapeutic interventions. Precision medicine aims to optimize therapeutic efficacy while minimizing adverse effects by tailoring treatments to individuals' genetic and molecular profiles. This literature review examines the potential of precision medicine in managing CMN, with a specific focus on MEK inhibition within the MAPK pathway, summarizing current preclinical and clinical evidence, mechanisms of action, and therapeutic integration with surgical management strategies. Although early results are promising, the need for personalized treatment strategies, informed by genetic testing and biomarker profiling, is emphasized to improve the management of CMN and reduce the risk of malignant transformation. Further research is necessary to establish the long-term safety and effectiveness of MEK inhibition in CMN therapy, which could offer a more targeted and individualized approach to care.

Indexed as

congenital melanocytic neviMAPK pathwayMEK inhibitionpediatric dermatologyprecision medicinetargeted therapy

Identifiers

PMID42652214
PMCPMC13509157

What OpenQuestion holds

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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.