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肝癌发生中的细胞竞争

Cell competition in liver carcinogenesis.

作者信息

Marongiu Fabio, Laconi Ezio

机构信息

Department of Biomedical Sciences, Unit of Experimental Medicine, University of Cagliari, Cagliari 09124, Italy.

出版信息

World J Hepatol. 2020 Aug 27;12(8):475-484. doi: 10.4254/wjh.v12.i8.475.

DOI:10.4254/wjh.v12.i8.475
PMID:32952874
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7475782/
Abstract

Cell competition is now a well-established quality control strategy to optimize cell and tissue fitness in multicellular organisms. While pursuing this goal, it is also effective in selecting against altered/defective cells with putative (pre)-neoplastic potential, thereby edging the risk of cancer development. The flip side of the coin is that the molecular machinery driving cell competition can also be co-opted by neoplastic cell populations to expand unchecked, outside the boundaries of tissue homeostatic control. This review will focus on information that begins to emerge regarding the role of cell competition in liver physiology and pathology. Liver repopulation by normal transplanted hepatocytes is an interesting field of investigation in this regard. The biological coordinates of this process share many features suggesting that cell competition is a driving force for the clearance of endogenous damaged hepatocytes by normal donor-derived cells, as previously proposed. Intriguing analogies between liver repopulation and carcinogenesis will be briefly discussed and the potential dual role of cell competition, as a barrier or a spur to neoplastic development, will be considered. Cell competition is in essence a cooperative strategy organized at tissue level. One facet of such cooperative attitude is expressed in the elimination of altered cells which may represent a threat to the organismal community. On the other hand, the society of cells can be disrupted by the emergence of selfish clones, exploiting the molecular bar codes of cell competition, thereby paving their way to uncontrolled growth.

摘要

细胞竞争如今是一种成熟的质量控制策略,用于优化多细胞生物中的细胞和组织适应性。在追求这一目标的过程中,它还能有效地筛选出具有假定(前)肿瘤形成潜力的异常/缺陷细胞,从而降低癌症发生的风险。然而,问题的另一面是,驱动细胞竞争的分子机制也可能被肿瘤细胞群体利用,使其在组织稳态控制的范围之外不受限制地扩张。本综述将聚焦于有关细胞竞争在肝脏生理和病理过程中作用的新出现的信息。在这方面,正常移植肝细胞对肝脏的再填充是一个有趣的研究领域。这一过程的生物学特征有许多相似之处,表明细胞竞争是正常供体来源的细胞清除内源性受损肝细胞的驱动力,正如之前所提出的那样。我们将简要讨论肝脏再填充与肿瘤发生之间有趣的相似之处,并考虑细胞竞争作为肿瘤发展的屏障或促进因素的潜在双重作用。细胞竞争本质上是一种在组织层面组织起来的合作策略。这种合作态度的一个方面表现为清除那些可能对机体群落构成威胁的异常细胞。另一方面,细胞群落可能会被自私克隆的出现所破坏,这些克隆利用细胞竞争的分子标记,从而为其不受控制的生长铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72aa/7475782/52eafee26248/WJH-12-475-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72aa/7475782/a6c0711193f1/WJH-12-475-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72aa/7475782/52eafee26248/WJH-12-475-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72aa/7475782/a6c0711193f1/WJH-12-475-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72aa/7475782/52eafee26248/WJH-12-475-g002.jpg

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