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Tissue Regeneration in the Chronically Inflamed Tumor Environment: Implications for Cell Fusion Driven Tumor Progression and Therapy Resistant Tumor Hybrid Cells

机译:慢性炎症肿瘤环境中的组织再生:对细胞融合驱动的肿瘤进展和抗肿瘤治疗的杂交细胞的影响。

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摘要

The biological phenomenon of cell fusion in a cancer context is still a matter of controversial debates. Even though a plethora of in vitro and in vivo data have been published in the past decades the ultimate proof that tumor hybrid cells could originate in (human) cancers and could contribute to the progression of the disease is still missing, suggesting that the cell fusion hypothesis is rather fiction than fact. However, is the lack of this ultimate proof a valid argument against this hypothesis, particularly if one has to consider that appropriate markers do not (yet) exist, thus making it virtually impossible to identify a human tumor cell clearly as a tumor hybrid cell. In the present review, we will summarize the evidence supporting the cell fusion in cancer concept. Moreover, we will refine the cell fusion hypothesis by providing evidence that cell fusion is a potent inducer of aneuploidy, genomic instability and, most likely, even chromothripsis, suggesting that cell fusion, like mutations and aneuploidy, might be an inducer of a mutator phenotype. Finally, we will show that “accidental” tissue repair processes during cancer therapy could lead to the origin of therapy resistant cancer hybrid stem cells.
机译:在癌症背景下细胞融合的生物学现象仍是一个有争议的辩论问题。尽管在过去的几十年中已经发表了大量的体外和体内数据,但仍缺乏有关肿瘤杂交细胞可能起源于(人类)癌症并可能促进疾病进展的最终证据,这表明细胞融合假设是虚构而非事实。然而,缺乏这种最终证据是对这一假设的有效论据,特别是如果必须考虑(尚)不存在合适的标记物的情况下,因此实际上不可能将人肿瘤细胞清楚地鉴定为肿瘤杂交细胞。在本综述中,我们将总结支持癌症概念中细胞融合的证据。此外,我们将通过提供证据证明细胞融合是非整倍性,基因组不稳定和最有可能发生的染色体突变的有效诱因,来完善细胞融合假说,表明细胞融合(如突变和非整倍性)可能是突变体表型的诱导剂。 。最后,我们将证明癌症治疗过程中的“偶然”组织修复过程可能导致具有治疗抗性的癌症杂交干细胞的起源。

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