GSK-3和BCL-XL抑制降低了apc突变型结直肠癌细胞的竞争优势。

IF 5.9 2区 医学 Q1 ONCOLOGY
Le Zhang, Lidia Atencia Taboada, Selami Baglamis, Maartje de Kroon, Carolien Elshout, Prashanthi Ramesh, Roxan F C P A Helderman, Arezo Torang, Kate Cameron, Milou S van Driel, Valérie M Wouters, Sanne M van Neerven, Jan Paul Medema
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引用次数: 0

摘要

BCL-XL是一种重要的抗凋亡蛋白,在结直肠癌(CRC)的进展过程中支持肠细胞的存活。虽然用BH3模拟物靶向BCL-XL是有效的,但其显著的毒性突出了替代方法的必要性。重要的是,肠道转化的早期阶段以正常干细胞和转化干细胞之间的竞争为特征,其中突变细胞由于分泌WNT抑制剂而获得超竞争优势。通过多种人类和小鼠CRC模型,我们发现GSK-3抑制对BH3模拟物诱导的杀伤具有强烈的敏感性。正如预期的那样,GSK-3抑制显著上调了WNT通路,但也导致BH3模拟物诱导的细胞凋亡显著增强,这是通过线粒体BAX聚集、Caspase-3激活和碘化啶排除来测量的。此外,由于WNT通路的再激活,GSK-3抑制在与apc突变体竞争时为野生型肠道类器官提供了优势。更引人注目的是,GSK-3和BCL-XL联合抑制深刻影响了apc突变型肠道细胞对野生型的超竞争。实际上,联合疗法增强了野生型细胞的竞争适应度,并导致apc突变类器官的杀伤,这表明一种新的联合疗法可以进一步用于腺瘤和CRC的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GSK-3 and BCL-XL inhibition mitigates the competitive advantage of APC-mutant colorectal cancer cells.

BCL-XL is a crucial anti-apoptotic protein that supports survival of intestinal cells during the progression and in established colorectal cancer (CRC). While targeting BCL-XL with BH3 mimetics is effective, its significant toxicity highlights the need for alternative approaches. Importantly, the early steps in intestinal transformation are marked by a competition between normal and transformed stem cells in which the mutant cells gain a supercompetitive advantage due to the secretion of WNT inhibitors. Using multiple human and murine CRC models, we revealed that GSK-3 inhibition strongly sensitized to BH3 mimetic-induced killing. As expected, GSK-3 inhibition significantly upregulated the WNT pathway, but also led to marked enhancement of BH3 mimetic-induced apoptosis, as measured by mitochondrial BAX aggregation, Caspase-3 activation and Propidium Iodide exclusion. Furthermore, GSK-3 inhibition provided an advantage to wild-type intestinal organoids in competition with APC-mutant counterparts due to reactivation of the WNT pathway. More strikingly, combining GSK-3 and BCL-XL inhibition profoundly affected the supercompetition APC-mutant intestinal cells exert over the wild-types. In effect, the combination therapy enhanced the competitive fitness of wild-type cells and resulted in the killing of APC-mutant organoids, pointing to a novel combination therapy that can be further exploited in the treatment of adenomas and CRC.

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来源期刊
Oncogenesis
Oncogenesis ONCOLOGY-
CiteScore
11.90
自引率
0.00%
发文量
70
审稿时长
26 weeks
期刊介绍: Oncogenesis is a peer-reviewed open access online journal that publishes full-length papers, reviews, and short communications exploring the molecular basis of cancer and related phenomena. It seeks to promote diverse and integrated areas of molecular biology, cell biology, oncology, and genetics.
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