ReviewAsian Pacific journal of cancer prevention : APJCP2025
Omics in Cutaneous Melanoma.
Review in Asian Pacific journal of cancer prevention : APJCP, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Metformin Enhances 2-Aminoethyl Dihydrogen Phosphate-Induced Mitochondrial Dysfunction and Apoptosis in Melanoma Cells.International journal of molecular sciences · 2026Article
- Targeting Peptidergic Systems for Melanoma Treatment.Cancers · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The advancement of multidimensional omics technologies holds immense promise for the future of medical treatment, particularly in addressing a wide range of human illnesses. Melanoma, which ranks among the most aggressive malignant pathologies affecting the skin, is a complex and heterogeneous oncological condition. There exist mutations that are tightly intertwined with the biological behavior of tumors, significantly influencing the course and outcome of the disease. Specifically, a subset of these mutations has been identified as mutually exclusive, involving specific signaling molecules and signaling cascades. Simultaneously, it has now been well established that inactivation of one component can activate alternative signaling pathways, ultimately leading to a more pronounced intensification of carcinogenesis. Consequently, this study not only reveals the impact of transcription factors and growth factors on carcinogenesis, but also emphasizes the importance of non-coding RNA (microRNAs), which constitute a unique set of biomarkers that determine the biological and molecular characteristics of tumors. It is important to note that genomic, transcriptomic, and proteomic profiling of tumors do not provide a complete assessment of their invasive and metastatic potential. The article provides contemporary insights into multimodal approaches for identifying molecular subtypes of melanoma.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.