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两种间隙连接细胞间通讯缺陷型“癌症干细胞”的癌症预防与治疗

Cancer Prevention and Therapy of Two Types of Gap Junctional Intercellular Communication⁻Deficient "Cancer Stem Cell".

作者信息

Trosko James E

机构信息

Department Pediatrics & Human Development, College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.

出版信息

Cancers (Basel). 2019 Jan 14;11(1):87. doi: 10.3390/cancers11010087.

Abstract

Early observations showed a lack of growth control and terminal differentiation with a lack of gap junctional intercellular communication (GJIC). Subsequent observations showed that epigenetic tumor promoters and activated oncogenes, which block gap junction function, provide insights into the multi-stage, multi-mechanism carcinogenic process. With the isolation of embryonic induced pluri-potent stem cells and organ-specific adult stem cells, gap junctions were linked to early development. While tumors and tumor cell lines are a heterogeneous mixture of "cancer stem cells" and "cancer non-stem cells", the cancer stem cells seem to be of two types, namely, they express (a) no connexin genes or (b) connexin genes, but do not have functional GJIC. These observations suggest that these "cancer stem cells" originate from normal adult stem cells or from the de-differentiation or re-programming of somatic differentiated cells. This "" provides a hypothesis that "cancer stem cells" either originate from (a) organ-specific adult stem cells before the expression of the connexin genes or (b) organ-specific adult stem cells that just express gap junction genes but that the connexin proteins are rendered dysfunctional by activated oncogenes. Therefore, cancer prevention and therapeutic strategies must account for these two different types of "cancer stem cell".

摘要

早期观察结果显示,缺乏生长控制和终末分化,同时缺乏间隙连接细胞间通讯(GJIC)。随后的观察表明,阻断间隙连接功能的表观遗传肿瘤启动子和激活的癌基因,为多阶段、多机制致癌过程提供了见解。随着胚胎诱导多能干细胞和器官特异性成体干细胞的分离,间隙连接与早期发育联系了起来。虽然肿瘤和肿瘤细胞系是“癌症干细胞”和“癌症非干细胞”的异质混合物,但癌症干细胞似乎有两种类型,即它们要么(a)不表达连接蛋白基因,要么(b)表达连接蛋白基因,但没有功能性的GJIC。这些观察结果表明,这些“癌症干细胞”起源于正常成体干细胞,或体细胞分化细胞的去分化或重编程。这就提出了一个假说,即“癌症干细胞”要么起源于(a)连接蛋白基因表达之前的器官特异性成体干细胞,要么起源于刚刚表达间隙连接基因但连接蛋白被激活的癌基因使其功能失调的器官特异性成体干细胞。因此,癌症预防和治疗策略必须考虑这两种不同类型的“癌症干细胞”。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/6356618/9e4990cb0688/cancers-11-00087-g001.jpg

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