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REVIEW article

Front. Cell Death
Sec. Non-Apoptotic Regulated Cell Death
Volume 3 - 2024 | doi: 10.3389/fceld.2024.1478258
This article is part of the Research Topic Cell Death in Drosophila View all 3 articles

Exploring advanced Drosophila cell death techniques and cancerrelated studies

Provisionally accepted
  • Genetic and epigenetic basis of Individuality and aging, Instituto de Neurociencias de Alicante (CSIC-UMH), San Joan d Alacant, Spain

The final, formatted version of the article will be published soon.

    Cell death is an essential physiological process for the survival of multicellular organisms. Our understanding of programmed cell death in development, immune function maintenance, and adult tissue repair has significantly advanced over the past decade. However, there are still gaps in our knowledge about the induction, regulation, and checkpoints of this process due to the diverse forms of cellular suicide and the rapid nature of the process. Molecular advancements such as specific cell death sensors, RNA-seq, single-cell RNA-seq, and metabolomics have allowed for identifying new factors and a better understanding of the molecular networks and pathways that regulate these processes. Programmed cell death also plays a role in cancer, both limiting and facilitating aspects of the malignant process, making its analysis and inhibition challenging. This review discusses the field's advancements using the model organism Drosophila melanogaster, the types of cell death in development and adult tissues, the techniques for studying it, and its role in cancer.

    Keywords: programmed cell death, Sensors, methods, -omics, development, Cancer, Drosophila

    Received: 09 Aug 2024; Accepted: 08 Nov 2024.

    Copyright: © 2024 Tendero-Lopez, Dominguez and Uribe. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Mary Luz Uribe, Genetic and epigenetic basis of Individuality and aging, Instituto de Neurociencias de Alicante (CSIC-UMH), San Joan d Alacant, Spain

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.