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简明综述:可传播动物肿瘤作为癌症干细胞过程的模型。

Concise review: transmissible animal tumors as models of the cancer stem-cell process.

机构信息

de l'immeuble 3, Centre d'Affaires Poincaré, 3 Rue Poincaré, Nice, France.

出版信息

Stem Cells. 2011 Dec;29(12):1909-14. doi: 10.1002/stem.751.

Abstract

Tasmanian devil facial tumor disease (DFTD) and canine transmissible venereal tumor (CTVT) are highly unusual cancers capable of being transmitted between animals as an allograft. The concept that these tumors represent a cancer stem-cell process has never been formally evaluated. For each, evidence of self-renewal is found in the natural history of these tumors in the wild, tumor initiation in recipient animals, and serial transplantation studies. Additional data for stem-cell-specific genes and markers in DFTD also exist. Although both tumor types manifest as undifferentiated cancers, immunocytohistochemistry supports a histiocytic phenotype for CTVT and a neural crest origin, possibly a Schwann-cell phenotype, for DFTD. In these data, differential expression of lineage markers is seen which may suggest some capacity for differentiation toward a heterogeneous variety of cell types. It is proposed that DFTD and CTVT may represent and may serve as models of the cancer stem-cell process, but formal investigation is required to clarify this. Appreciation of any such role may act as a stimulus to ongoing research in the pathology of DFTD and CTVT, including further characterization of their origin and phenotype and possible therapeutic approaches. Additionally, they may provide valuable models for future studies of their analogous human cancers, including any putative CSC component.

摘要

塔斯马尼亚恶魔面部肿瘤病(DFTD)和犬传染性性病肿瘤(CTVT)是两种非常特殊的癌症,能够作为同种异体移植物在动物之间传播。这些肿瘤代表癌症干细胞过程的概念从未得到过正式评估。对于每一种肿瘤,在这些肿瘤的自然史、受者动物中的肿瘤起始以及连续移植研究中都发现了自我更新的证据。DFTD 中还存在与干细胞特异性基因和标记物相关的其他数据。尽管这两种肿瘤类型都表现为未分化的癌症,但免疫细胞化学支持 CTVT 的组织细胞表型和 DFTD 的神经嵴起源,可能是施万细胞表型。在这些数据中,可以看到谱系标记物的差异表达,这可能表明它们具有向多种异质细胞类型分化的一些能力。因此,DFTD 和 CTVT 可能代表并可作为癌症干细胞过程的模型,但需要进行正式研究以澄清这一点。对这种作用的认识可能会刺激对 DFTD 和 CTVT 病理学的持续研究,包括对其起源和表型的进一步表征以及可能的治疗方法。此外,它们可能为未来研究类似的人类癌症提供有价值的模型,包括任何推测的 CSC 成分。

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