Evidence map›Paper›PMID 31689494›Full record

ReviewSeminars in cancer biology2020

Translational pathology, genomics and the development of systemic therapies for acral melanoma.

Yian Ann Chen, Jamie K Teer, Zeynep Eroglu, Jheng-Yu Wu, John M Koomen, Florian A Karreth, Jane L Messina, Keiran S M Smalley

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cancer biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 11% 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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. SPP1Cell death & disease · 2026
    Article
  6. Article
  7. The Roles of PTEN in Melanoma Suppression.Pigment cell & melanoma research · 2025
    Review
  8. Article
  9. Adoptive Cell Transfer of Tumor-Infiltrating Lymphocytes for Metastatic Acral Lentiginous Melanoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. A nomogram incorporating Ki67 to predict survival of acral melanoma.Journal of cancer research and clinical oncology · 2023
    Article
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Yian Ann ChenDepartment of Biostatistics and Bioinformatics, Moffitt Cancer Center, Tampa, FL, United States. Electronic address: ann.chen@moffitt.org.
Jamie K TeerDepartment of Biostatistics and Bioinformatics, Moffitt Cancer Center, Tampa, FL, United States.
Zeynep ErogluDepartment of Cutaneous Oncology, Moffitt Cancer Center, Tampa, FL, United States.
Jheng-Yu WuDepartment of Tumor Biology, Moffitt Cancer Center, Tampa, FL, United States.
John M KoomenDepartment of Molecular Oncology, Moffitt Cancer Center, Tampa, FL, United States.
Florian A KarrethDepartment of Molecular Oncology, Moffitt Cancer Center, Tampa, FL, United States.
Jane L MessinaDepartment of Cutaneous Oncology, Moffitt Cancer Center, Tampa, FL, United States.
Keiran S M SmalleyDepartment of Cutaneous Oncology, Moffitt Cancer Center, Tampa, FL, United States; Department of Tumor Biology, Moffitt Cancer Center, Tampa, FL, United States. Electronic address: keiran.smalley@moffitt.org.
Moffitt Cancer Center · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

Acral melanomas arise on the non-hair bearing skin of the palms, soles and in the nail beds. These rare tumors comprise 2-3 % of all melanomas, are not linked to UV-exposure, and represent the most frequent subtype of melanomas in patients of Asian, African and Hispanic origin. Although recent work has revealed candidate molecular events that underlie acral melanoma development, this knowledge is not yet been translated into efficacious local, regional, or systemic therapies. In the current review, we describe the clinical characteristics of acral melanoma and outline the genetic basis of acral melanoma development. Further discussion is given to the current status of systemic therapy for acral melanoma with a focus on ongoing developments in both immunotherapy and targeted therapy for the treatment of advanced disease.

Indexed as

Genetic Predisposition to DiseaseGenomicsBiomarkers, TumorDisease ManagementHumansMelanomaMutationPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSignal TransductionSkin NeoplasmsTranslational Research, BiomedicalBiomarkers, TumorPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanAcral melanomaSystemic therapiesTranslational genomics

Identifiers

PMID31689494
PMCPMC7771370
OpenAlexW2983195778

What OpenQuestion holds

Textmetadata
LicenceTDM
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.