Evidence map›Paper›PMID 38426087›Full record

ReviewFrontiers in immunology2024

Immune escape and metastasis mechanisms in melanoma: breaking down the dichotomy.

Carl A Shirley, Gagan Chhabra, Deeba Amiri, Hao Chang, Nihal Ahmad

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Interleukin-1β Gene (Current oncology (Toronto, Ont.) · 2026
    Article
  5. Observational
  6. Article
  7. Review
  8. Circadian rhythms and lung cancer biology and immunotherapy: Emerging opportunities and challenges.Chinese medical journal pulmonary and critical care medicine · 2026
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

5 authors at 1 institution in 1 country.

Carl A Shirley *Department of Dermatology, University of Wisconsin, Madison, WI, United States.
Gagan Chhabra *Department of Dermatology, University of Wisconsin, Madison, WI, United States.
Deeba AmiriDepartment of Dermatology, University of Wisconsin, Madison, WI, United States.
Hao ChangDepartment of Dermatology, University of Wisconsin, Madison, WI, United States.
Nihal AhmadDepartment of Dermatology, University of Wisconsin, Madison, WI, United States.
University of Wisconsin–Madison · US

Funding

Functional and Therapeutic Significance of PLK4 in MelanomaR01CA261937 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Nihal Ahmad · 2022 to 2026
$2.9M
Combined inhibition of PLK1 and NOTCH for melanoma managementI01BX005917 · VA · WM S. MIDDLETON MEMORIAL VETERANS HOSP · PI AHMAD, NIHAL · 2023 to 2025
–
Role of sirtuin 6 in melanoma development and progressionI01CX002210 · VA · WM S. MIDDLETON MEMORIAL VETERANS HOSP · PI Nihal Ahmad · 2022 to 2026
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BLRD Research Career Scientist Award ApplicationIK6BX006041 · VA · WM S. MIDDLETON MEMORIAL VETERANS HOSP · PI AHMAD, NIHAL · 2022 to 2025
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BLRD VA I01 BX005917BLRD VA IK6 BX006041CSRD VA I01 CX002210CSRD VA I01 CX002308NCI NIH HHS R01 CA261937
6 · The paper itself

Abstract

Melanoma is one of the most lethal neoplasms of the skin. Despite the revolutionary introduction of immune checkpoint inhibitors, metastatic spread, and recurrence remain critical problems in resistant cases. Melanoma employs a multitude of mechanisms to subvert the immune system and successfully metastasize to distant organs. Concerningly, recent research also shows that tumor cells can disseminate early during melanoma progression and enter dormant states, eventually leading to metastases at a future time. Immune escape and metastasis have previously been viewed as separate phenomena; however, accumulating evidence is breaking down this dichotomy. Recent research into the progressive mechanisms of melanoma provides evidence that dedifferentiation similar to classical epithelial to mesenchymal transition (EMT), genes involved in neural crest stem cell maintenance, and hypoxia/acidosis, are important factors simultaneously involved in immune escape and metastasis. The likeness between EMT and early dissemination, and differences, also become apparent in these contexts. Detailed knowledge of the mechanisms behind "dual drivers" simultaneously promoting metastatically inclined and immunosuppressive environments can yield novel strategies effective in disabling multiple facets of melanoma progression. Furthermore, understanding progression through these drivers may provide insight towards novel treatments capable of preventing recurrence arising from dormant dissemination or improving immunotherapy outcomes.

Indexed as

MelanomaEpithelial-Mesenchymal TransitionHumansImmunotherapyacidosisdormancyearly disseminationEMThypoxiaimmune escapemetastasisneural crest stem cell genes

Identifiers

PMID38426087
PMCPMC10902921
OpenAlexW4391818823

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.