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Cutaneous Malignant Melanoma

Cancer and Oncology · NLM MeSH · updated 2026-10-29 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 4 min read

A primary melanoma that originates from atypical skin melanocytes, especially from acquired and congenital melanocytic nevi, and dysplastic nevi.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (866 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

A primary melanoma that originates from atypical skin melanocytes, especially from acquired and congenital melanocytic nevi, and dysplastic nevi.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Where it fits in the MeSH classification

Broader topics
Melanoma; Skin Neoplasms
Narrower topics
Dysplastic Nevus Syndrome

Related concepts

  • Melanocytes
  • Melanocytic Nevi
  • Dysplastic Nevi

Research landscape

PubMed indexes 5,478 records tagged with the MeSH heading “Cutaneous Malignant Melanoma” (counts retrieved 2026-10-29). 2,653 of them (48.4%) were published from 2020 onward, and the busiest period so far is 2020 onward with 2,653 records.

Reviews account for 845 records (15.4%) and meta-analyses for 92. Randomized controlled trials number 62 (1.1%) as a share of all records on the topic. Randomized trials make up only a small share of this literature, so much of what is known comes from laboratory, observational or descriptive work.

PubMed records by publication periodthrough 1999: 612 records; 2000-2009: 278 records; 2010-2019: 1,935 records; 2020 onward: 2,653 records612through 19992782000-20091,9352010-20192,6532020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 1999612
2000-2009278
2010-20191,935
2020 onward2,653
Share of records by publication typeReviews: 15.4 percent; Meta-analyses: 1.7 percent; Randomized controlled trials: 1.1 percentReviews15.4% (845)Meta-analyses1.7% (92)Randomized controlled trials1.1% (62)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 5,478 PubMed records
TypeRecordsShare
Reviews84515.4%
Meta-analyses921.7%
Randomized controlled trials621.1%

Method: PubMed query "Cutaneous Malignant Melanoma"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-29.

Reading the evidence in cancer and oncology

Cancer research spans very different kinds of evidence. Laboratory studies in cell lines and animal models reveal mechanisms but often do not translate to patients. Early-phase trials mainly test safety and dosing, while phase 3 randomized trials and their meta-analyses are the usual basis for treatment conclusions. Outcomes also differ in meaning: tumour shrinkage, progression-free survival and overall survival are not interchangeable, and screening studies can be distorted by lead-time and overdiagnosis. When reading a result, check the cancer type and stage studied, the comparison treatment, and which outcome was measured.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Global trends in cutaneous malignant melanoma incidence and mortality
De Pinto G, Mignozzi S, La Vecchia C, Levi F, Negri E, Santucci C
2024Research article
Design not recorded in structured metadata
48cc by
PMID 38391175 · DOI · PMC11045545
FISH as an effective diagnostic tool for the management of challenging melanocytic lesions
Moore MW, Gasparini R
2011Research article
Design not recorded in structured metadata
36cc by
PMID 21834951 · DOI · PMC3162533
Nuclear ING2 expression is reduced in human cutaneous melanomas
Lu F, Dai DL, Martinka M, Ho V, Li G
2006Research article
Design not recorded in structured metadata
33cc by
PMID 16755297 · DOI · PMC2360493
The CUBED Versus ABCDE Recognition Tools in the Detection of Malignant Melanomas Arising in the Foot: An Analysis of Four Recent Case Studies in a Single NHS Community Trust
Sherratt A, Vaughan E, Huckerby N, Winn H, Swithenbank M
2026Research article
Design not recorded in structured metadata
0cc by
PMID 42056756 · DOI · PMC13128519

Global trends in cutaneous malignant melanoma incidence and mortality [1]

Research article De Pinto G, Mignozzi S, La Vecchia C, Levi F, Negri E, Santucci C · · 2024 · cited 48 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Mortality from cutaneous malignant melanoma (CMM) increased in the past, but trends have been favorable in more recent years in many high-income countries.
Closing excerpt
The increasing awareness of risk factors, mainly related to UV exposure, along with early diagnosis and progress in treatment for advanced disease played pivotal roles in reducing CMM mortality, particularly in Australia.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (238 words)

Mortality from cutaneous malignant melanoma (CMM) increased in the past, but trends have been favorable in more recent years in many high-income countries. However, incidence has been increasing in several countries. We provided an up-to-date overview of mortality trends from CMM. We analyzed death certification data from the WHO in selected countries worldwide from 1980 to the most recent available calendar years. We also reported incidence data derived from Cancer Incidence in Five Continents from 1990 to 2012. Separate analyses were performed for young adults aged 20-44 and middle-aged adults aged 45-64 years. Mortality from CMM in all age groups showed a favorable pattern in the majority of the countries considered. Mortality trends declined by 40 to 50% in Australia over the last decades, confirming the importance of prevention measures. Considering young adults aged 20-44, Australia, New Zealand and Northern Europe reported the highest death rates for both sexes (>0.90/100 000 in men and >0.60/100 000 in women) while Japan, the Philippines, and Latin America the lowest ones (<0.50/100 000 and <0.35/100 000 in men and women, respectively). Incidence trends were stable or upward in most countries, with higher rates among women. Our study highlights a global reduction of CMM mortality over the last three decades. The increasing awareness of risk factors, mainly related to UV exposure, along with early diagnosis and progress in treatment for advanced disease played pivotal roles in reducing CMM mortality, particularly in Australia.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 38391175 · DOI · PMC11045545

FISH as an effective diagnostic tool for the management of challenging melanocytic lesions [2]

Research article Moore MW, Gasparini R · · 2011 · cited 36 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
BackgroundThe accuracy of melanoma diagnosis continues to challenge the pathology community, even today with sophisticated histopathologic techniques.
Closing excerpt
ConclusionsBased on this study, inheritable genetic damage/instability identified by FISH testing is a hallmark of a progressive malignant process, and a valuable diagnostic tool for the identification of high risk lesions.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (191 words)

BackgroundThe accuracy of melanoma diagnosis continues to challenge the pathology community, even today with sophisticated histopathologic techniques. Melanocytic lesions exhibit significant morphological heterogeneity. While the majority of biopsies can be classified as benign (nevus) or malignant (melanoma) using well-established histopathologic criteria, there exists a cohort for which the prediction of clinical behaviour and invasive or metastatic potential is difficult if not impossible to ascertain on the basis of morphological features alone. Multiple studies have shown that there is significant disagreement between pathologists and even expert dermatopathologists in the diagnosis of this subgroup of difficult melanocytic lesions.MethodsA four probe FISH assay was utilized to analyse a cohort of 500 samples including 157 nevus, 176 dysplastic nevus and 167 melanoma specimens.ResultsReview of the lesions determined the assay identified genetic abnormalities in a total of 83.8% of melanomas, and 1.9% of nevus without atypia, while genetic abnormalities were identified in 6.3%, 6.7%, and 10.3% of nevus identified with mild, moderate and severe atypia, respectively.ConclusionsBased on this study, inheritable genetic damage/instability identified by FISH testing is a hallmark of a progressive malignant process, and a valuable diagnostic tool for the identification of high risk lesions.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 21834951 · DOI · PMC3162533

Nuclear ING2 expression is reduced in human cutaneous melanomas [3]

Research article Lu F, Dai DL, Martinka M, Ho V, Li G · · 2006 · cited 33 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Cutaneous malignant melanoma is a severe and sometimes life-threatening cancer.
Closing excerpt
Taken together, our results suggest that nuclear ING2 expression is significantly reduced in human melanomas and that reduced ING2 may be an important molecular event in the initiation of melanoma development.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (170 words)

Cutaneous malignant melanoma is a severe and sometimes life-threatening cancer. The molecular mechanism of melanomagenesis is incompletely understood. Deregulation of apoptosis is probably one of the key factors contributing to the progression of melanoma. The inhibitor of growth (ING) family proteins are candidate tumour suppressors which play important roles in apoptosis. Downregulated expression of ING proteins have been reported in several tumour types, including the loss of nuclear expression of p33ING1b in melanoma. As ING2 exhibits 58.9% homology with p33ING1b, we hypothesized that the aberrant expression of ING2 may be involved in melanomagenesis. Here, we used tissue microarray technology and immunohistochemistry to examine ING2 expression in human nevi and melanoma biopsies. Our data showed that nuclear ING2 expression was significantly reduced in radial growth phase (RGP), vertical growth phase (VGP), and metastatic melanomas compared with dysplastic nevi (P 0.05). Taken together, our results suggest that nuclear ING2 expression is significantly reduced in human melanomas and that reduced ING2 may be an important molecular event in the initiation of melanoma development.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 16755297 · DOI · PMC2360493

The CUBED Versus ABCDE Recognition Tools in the Detection of Malignant Melanomas Arising in the Foot: An Analysis of Four Recent Case Studies in a Single NHS Community Trust [4]

Research article Sherratt A, Vaughan E, Huckerby N, Winn H, Swithenbank M · · 2026

Abstract reading summary — source excerpts
Opening excerpt
BackgroundMelanoma of the foot and nail unit carries a worse prognosis than cutaneous melanoma elsewhere because lesions are frequently hidden, misdiagnosed, and therefore diagnosed at more advanced stages.
Closing excerpt
Wider education and adoption of CUBED alongside ABCDE may reduce misdiagnosis, shorten diagnostic delay, and improve clinical outcomes.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (267 words)

BackgroundMelanoma of the foot and nail unit carries a worse prognosis than cutaneous melanoma elsewhere because lesions are frequently hidden, misdiagnosed, and therefore diagnosed at more advanced stages. Traditional ABCDE criteria are often insufficient for foot and nail presentations; the CUBED recognition tool was developed to improve detection of atypical plantar and subungual lesions.AimTo evaluate four consecutive cases of foot melanoma seen in a single NHS community podiatry department, compare case characteristics against ABCDE and CUBED recognition tools, and describe service responses that aimed to improve early detection.MethodsA retrospective case series of four patients diagnosed with foot melanoma between 2019 and 2022 in one community podiatry service. Clinical features, referral timelines, diagnostic pathways, treatments, and outcomes were extracted and mapped against ABCDE and CUBED criteria. Shared-learning interventions developed by the department following these cases are described.ResultsAll four cases were toe-based melanomas (one lentigo maligna, one nail-bed malignant melanoma, two acral melanomas). Presentations commonly included irregular colour, bleeding or ulceration, delayed healing, diagnostic uncertainty, and lesion enlargement. CUBED criteria more consistently identified concerning features across the series than ABCDE criteria, prompting urgent dermatology referral in each case. Outcomes varied: one patient remains disease-free after excision, one developed distant metastasis and died, two underwent toe amputation and received systemic treatment. Departmental responses included case-based teaching and a poster campaign promoting CUBED and ABCDE recognition across local clinical networks.ConclusionPodiatrists are pivotal in early detection of foot melanoma. The CUBED tool demonstrated greater sensitivity for atypical foot and nail lesions in this series. Wider education and adoption of CUBED alongside ABCDE may reduce misdiagnosis, shorten diagnostic delay, and improve clinical outcomes.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 42056756 · DOI · PMC13128519

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi [5]
    Gandini S, Sera F, Cattaruzza MS, Pasquini P, Abeni D, Boyle P, et al. · Eur J Cancer · 2005 · cited 511 times (Europe PMC)
  • Research article A meta-analysis of nevus-associated melanoma: Prevalence and practical implications [6]
    Pampena R, Kyrgidis A, Lallas A, Moscarella E, Argenziano G, Longo C · J Am Acad Dermatol · 2017 · cited 141 times (Europe PMC)
  • Research article Pancreatic cancer and the FAMMM syndrome [7]
    Lynch HT, Fusaro RM, Lynch JF, Brand R · Fam Cancer · 2008 · cited 83 times (Europe PMC)
  • Research article What naevus is dysplastic, a syndrome and the commonest precursor of malignant melanoma? A riddle and an answer [8]
    Ackerman AB · Histopathology · 1988 · cited 80 times (Europe PMC)
  • Research article Precursors to skin cancer [9]
    Sober AJ, Burstein JM · Cancer · 1995 · cited 79 times (Europe PMC)
  • Research article Dysplastic nevi and melanoma [10]
    Goldstein AM, Tucker MA · Cancer Epidemiol Biomarkers Prev · 2013 · cited 65 times (Europe PMC)

References

  1. De Pinto G, Mignozzi S, La Vecchia C, Levi F, Negri E, Santucci C. Global trends in cutaneous malignant melanoma incidence and mortality. . 2024. PMID 38391175 · DOI · PMC11045545
  2. Moore MW, Gasparini R. FISH as an effective diagnostic tool for the management of challenging melanocytic lesions. . 2011. PMID 21834951 · DOI · PMC3162533
  3. Lu F, Dai DL, Martinka M, Ho V, Li G. Nuclear ING2 expression is reduced in human cutaneous melanomas. . 2006. PMID 16755297 · DOI · PMC2360493
  4. Sherratt A, Vaughan E, Huckerby N, Winn H, Swithenbank M. The CUBED Versus ABCDE Recognition Tools in the Detection of Malignant Melanomas Arising in the Foot: An Analysis of Four Recent Case Studies in a Single NHS Community Trust. . 2026. PMID 42056756 · DOI · PMC13128519
  5. Gandini S, Sera F, Cattaruzza MS, Pasquini P, Abeni D, Boyle P, et al.. Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi. Eur J Cancer. 2005. PMID 15617989 · DOI
  6. Pampena R, Kyrgidis A, Lallas A, Moscarella E, Argenziano G, Longo C. A meta-analysis of nevus-associated melanoma: Prevalence and practical implications. J Am Acad Dermatol. 2017. PMID 28864306 · DOI
  7. Lynch HT, Fusaro RM, Lynch JF, Brand R. Pancreatic cancer and the FAMMM syndrome. Fam Cancer. 2008. PMID 17992582 · DOI
  8. Ackerman AB. What naevus is dysplastic, a syndrome and the commonest precursor of malignant melanoma? A riddle and an answer. Histopathology. 1988. PMID 3056824 · DOI
  9. Sober AJ, Burstein JM. Precursors to skin cancer. Cancer. 1995. PMID 7804989 · DOI
  10. Goldstein AM, Tucker MA. Dysplastic nevi and melanoma. Cancer Epidemiol Biomarkers Prev. 2013. PMID 23549396 · DOI · PMC3616416

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-29.

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At a glance

5,478
PubMed records on this heading
48%
published since 2020
845
review articles
62
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-29; they show how much has been written, not how strong the evidence is.

Related topics See all →

  • MelanomaCancer and Oncology
  • GangliogliomaCancer and Oncology
  • Cutaneous Squamous Cell CarcinomaCancer and Oncology
  • GliomaCancer and Oncology
  • Basal Cell CarcinomaCancer and Oncology

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