Computational Biology Helps Understand How Polyploid Giant Cancer Cells Drive Tumor Success.

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作者:Casotti Matheus Correia, Meira Débora Dummer, Zetum Aléxia Stefani Siqueira, Araújo Bruno Cancian de, Silva Danielle Ribeiro Campos da, Santos Eldamária de Vargas Wolfgramm Dos, Garcia Fernanda Mariano, Paula Flávia de, Santana Gabriel Mendonça, Louro Luana Santos, Alves Lyvia Neves Rebello, Braga Raquel Furlani Rocon, Trabach Raquel Silva Dos Reis, Bernardes Sara Santos, Louro Thomas Erik Santos, Chiela Eduardo Cremonese Filippi, Lenz Guido, Carvalho Elizeu Fagundes de, Louro Iúri Drumond
Precision and organization govern the cell cycle, ensuring normal proliferation. However, some cells may undergo abnormal cell divisions (neosis) or variations of mitotic cycles (endopolyploidy). Consequently, the formation of polyploid giant cancer cells (PGCCs), critical for tumor survival, resistance, and immortalization, can occur. Newly formed cells end up accessing numerous multicellular and unicellular programs that enable metastasis, drug resistance, tumor recurrence, and self-renewal or diverse clone formation. An integrative literature review was carried out, searching articles in several sites, including: PUBMED, NCBI-PMC, and Google Academic, published in English, indexed in referenced databases and without a publication time filter, but prioritizing articles from the last 3 years, to answer the following questions: (i) "What is the current knowledge about polyploidy in tumors?"; (ii) "What are the applications of computational studies for the understanding of cancer polyploidy?"; and (iii) "How do PGCCs contribute to tumorigenesis?"

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