Suppr超能文献

无机多聚磷酸盐通过瞬时受体电位阳离子通道亚家族M成员8(TRPM8)受体信号通路促进结直肠癌生长。

Inorganic Polyphosphate Promotes Colorectal Cancer Growth via TRPM8 Receptor Signaling Pathway.

作者信息

Arrè Valentina, Balestra Francesco, Scialpi Rosanna, Dituri Francesco, Donghia Rossella, Coletta Sergio, Stabile Dolores, Bianco Antonia, Vincenti Leonardo, Fedele Salvatore, Shen Chen, Pettinato Giuseppe, Scavo Maria Principia, Giannelli Gianluigi, Negro Roberto

机构信息

Personalized Medicine Laboratory, National Institute of Gastroenterology "S. de Bellis", IRCCS Research Hospital, Via Turi 27, Castellana Grotte, 70013 Bari, Italy.

Data Science, National Institute of Gastroenterology "S. de Bellis", IRCCS Research Hospital, Via Turi 27, Castellana Grotte, 70013 Bari, Italy.

出版信息

Cancers (Basel). 2024 Sep 28;16(19):3326. doi: 10.3390/cancers16193326.

Abstract

BACKGROUND

Colorectal cancer (CRC) is characterized by a pro-inflammatory microenvironment and features high-energy-supply molecules that assure tumor growth. A still less studied macromolecule is inorganic polyphosphate (iPolyP), a high-energy linear polymer that is ubiquitous in all forms of life. Made up of hundreds of repeated orthophosphate units, iPolyP is essential for a wide variety of functions in mammalian cells, including the regulation of proliferative signaling pathways. Some evidence has suggested its involvement in carcinogenesis, although more studies need to be pursued. Moreover, iPolyP regulates several homeostatic processes in animals, spanning from energy metabolism to blood coagulation and tissue regeneration.

RESULTS

In this study, we tested the role of iPolyP on CRC proliferation, using in vitro and ex vivo approaches, in order to evaluate its effect on tumor growth. We found that iPolyP is significantly increased in tumor tissues, derived from affected individuals enrolled in this study, compared to the corresponding peritumoral counterparts. In addition, iPolyP signaling occurs through the TRPM8 receptor, a well-characterized Na and Ca ion channel often overexpressed in CRC and linked with poor prognosis, thus promoting CRC cell proliferation. The pharmacological inhibition of TRPM8 or RNA interference experiments performed in established CRC cell lines, such as Caco-2 and SW620, showed that the involvement of TRPM8 is essential, greater than that of the other two known iPolyP receptors, P2Y1 and RAGE. The presence of iPolyP drives cancer cells towards the mitotic phase of the cell cycle by enhancing the expression of , which encodes the Cyclin B protein. In vitro 2D and 3D data reflected the ex vivo results, obtained by the generation of CRC-derived organoids, which increased in size.

CONCLUSIONS

These results indicate that iPolyP may be considered a novel and unexpected early biomarker supporting colorectal cancer cell proliferation.

摘要

背景

结直肠癌(CRC)的特征是具有促炎微环境,并具有确保肿瘤生长的高能量供应分子。一种研究较少的大分子是无机多聚磷酸盐(iPolyP),它是一种高能线性聚合物,在所有生命形式中都普遍存在。iPolyP由数百个重复的正磷酸盐单元组成,对哺乳动物细胞的多种功能至关重要,包括增殖信号通路的调节。一些证据表明它参与了致癌过程,尽管还需要更多的研究。此外,iPolyP调节动物体内的几个稳态过程,从能量代谢到血液凝固和组织再生。

结果

在本研究中,我们使用体外和离体方法测试了iPolyP对CRC增殖的作用,以评估其对肿瘤生长的影响。我们发现,与相应的肿瘤旁组织相比本研究中纳入的受影响个体的肿瘤组织中iPolyP显著增加。此外,iPolyP信号通过TRPM8受体发生,TRPM8是一种特征明确的钠和钙离子通道,在CRC中常过度表达并与预后不良相关,从而促进CRC细胞增殖。在已建立的CRC细胞系(如Caco-2和SW620)中进行的TRPM8药理学抑制或RNA干扰实验表明,TRPM8的参与至关重要,比其他两个已知的iPolyP受体P2Y1和RAGE的作用更大。iPolyP的存在通过增强编码细胞周期蛋白B的的表达,促使癌细胞进入细胞周期的有丝分裂期。体外二维和三维数据反映了通过生成CRC来源的类器官获得的离体结果,这些类器官的大小增加。

结论

这些结果表明,iPolyP可能被认为是一种支持结直肠癌细胞增殖 的新型且意外的早期生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f54/11476407/47357b12d6a3/cancers-16-03326-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验