دورية أكاديمية

Heterogeneity and molecular landscape of melanoma: implications for targeted therapy.

التفاصيل البيبلوغرافية
العنوان: Heterogeneity and molecular landscape of melanoma: implications for targeted therapy.
المؤلفون: Beigi YZ; Laboratory of System Biology and Bioinformatics (LBB), Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran., Lanjanian H; Software Engineering Department, Engineering Faculty, Istanbul Topkapi University, Istanbul, Turkey., Fayazi R; Laboratory of System Biology and Bioinformatics (LBB), Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran., Salimi M; Department of Medical Genetics, Institute of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran., Hoseyni BHM; Laboratory of System Biology and Bioinformatics (LBB), Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran., Noroozizadeh MH; Negah Eye Hospital, Tehran, Iran., Masoudi-Nejad A; Laboratory of System Biology and Bioinformatics (LBB), Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran. amasoudin@ut.ac.ir.
المصدر: Molecular biomedicine [Mol Biomed] 2024 May 10; Vol. 5 (1), pp. 17. Date of Electronic Publication: 2024 May 10.
نوع المنشور: Journal Article; Review; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Springer Singapore Country of Publication: Singapore NLM ID: 9918283581406676 Publication Model: Electronic Cited Medium: Internet ISSN: 2662-8651 (Electronic) Linking ISSN: 26628651 NLM ISO Abbreviation: Mol Biomed Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Singapore : Springer Singapore, [2020]-
مواضيع طبية MeSH: Melanoma*/genetics , Melanoma*/pathology , Melanoma*/therapy , Melanoma*/drug therapy , Molecular Targeted Therapy*/methods , Genetic Heterogeneity* , Uveal Neoplasms*/genetics , Uveal Neoplasms*/therapy , Uveal Neoplasms*/pathology, Humans ; Neoplastic Cells, Circulating/metabolism ; Neoplastic Cells, Circulating/pathology ; Biomarkers, Tumor/genetics ; Mutation ; Circulating Tumor DNA/genetics ; Circulating Tumor DNA/blood ; Liquid Biopsy/methods
مستخلص: Uveal cancer (UM) offers a complex molecular landscape characterized by substantial heterogeneity, both on the genetic and epigenetic levels. This heterogeneity plays a critical position in shaping the behavior and response to therapy for this uncommon ocular malignancy. Targeted treatments with gene-specific therapeutic molecules may prove useful in overcoming radiation resistance, however, the diverse molecular makeups of UM call for a patient-specific approach in therapy procedures. We need to understand the intricate molecular landscape of UM to develop targeted treatments customized to each patient's specific genetic mutations. One of the promising approaches is using liquid biopsies, such as circulating tumor cells (CTCs) and circulating tumor DNA (ctDNA), for detecting and monitoring the disease at the early stages. These non-invasive methods can help us identify the most effective treatment strategies for each patient. Single-cellular is a brand-new analysis platform that gives treasured insights into diagnosis, prognosis, and remedy. The incorporation of this data with known clinical and genomics information will give a better understanding of the complicated molecular mechanisms that UM diseases exploit. In this review, we focused on the heterogeneity and molecular panorama of UM, and to achieve this goal, the authors conducted an exhaustive literature evaluation spanning 1998 to 2023, using keywords like "uveal melanoma, "heterogeneity". "Targeted therapies"," "CTCs," and "single-cellular analysis".
(© 2024. The Author(s).)
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فهرسة مساهمة: Keywords: Circulating tumor cells (CTCs); Heterogeneity; Liquid biopsy; Single-cell analysis; Targeted therapy; Uveal melanoma (UM)
المشرفين على المادة: 0 (Biomarkers, Tumor)
0 (Circulating Tumor DNA)
تواريخ الأحداث: Date Created: 20240509 Date Completed: 20240509 Latest Revision: 20240802
رمز التحديث: 20240802
مُعرف محوري في PubMed: PMC11082128
DOI: 10.1186/s43556-024-00182-2
PMID: 38724687
قاعدة البيانات: MEDLINE
الوصف
تدمد:2662-8651
DOI:10.1186/s43556-024-00182-2