The acidic tumor microenvironment drives a stem-like phenotype in melanoma cells.

IF 4.2
Elena Andreucci, Silvia Peppicelli, Jessica Ruzzolini, Francesca Bianchini, Alessio Biagioni, Laura Papucci, Lucia Magnelli, Benedetta Mazzanti, Barbara Stecca, Lido Calorini
{"title":"The acidic tumor microenvironment drives a stem-like phenotype in melanoma cells.","authors":"Elena Andreucci,&nbsp;Silvia Peppicelli,&nbsp;Jessica Ruzzolini,&nbsp;Francesca Bianchini,&nbsp;Alessio Biagioni,&nbsp;Laura Papucci,&nbsp;Lucia Magnelli,&nbsp;Benedetta Mazzanti,&nbsp;Barbara Stecca,&nbsp;Lido Calorini","doi":"10.1007/s00109-020-01959-y","DOIUrl":null,"url":null,"abstract":"<p><p>Acidosis characterizes the microenvironment of most solid tumors and is considered a new hallmark of cancer. It is mainly caused by both \"aerobic\" and \"anaerobic\" glycolysis of differently adapted cancer cells, with the final product lactic acid being responsible of the extracellular acidification. Many evidences underline the role of extracellular acidosis in tumor progression. Among the different findings, we demonstrated that acidosis-exposed cancer cells are characterized by an epithelial-to-mesenchymal transition phenotype with high invasive ability, high resistance to apoptosis, anchorage-independent growth, and drug therapy. Acidic melanoma cells over-express SOX2, which is crucial for the maintenance of their oxidative metabolism, and carbonic anhydrase IX, that correlates with poor prognosis of cancer patients. Considering these evidences, we realized that the profile outlined for acid cancer cells inevitably remind us the stemness profile. Therefore, we wondered whether extracellular acidosis might induce in cancer cells the acquisition of stem-like properties and contribute to the expansion of the cancer stem cell sub-population. We found that a chronic adaptation to acidosis stimulates in cancer cells the expression of stem-related markers, also providing a high in vitro/in vivo clonogenic and trans-differentiating ability. Moreover, we observed that the acidosis-induced stem-like phenotype of melanoma cells was reversible and related to the EMT induction. These findings help to characterize a further aspect of stem cell niche, contributing to the sustainment and expansion of cancer stem cell subpopulation. Thus, the usage of agents controlling tumor extracellular acidosis might acquire great importance in the clinic for the treatment of aggressive solid tumor. KEY MESSAGES: • Extracellular acidosis up-regulates EMT and stem-related markers in melanoma cells • Acidic medium up-regulates in vitro self-renewal capacity of melanoma cells • Chronic acidosis adaptation induces trans-differentiation ability in melanoma cells • Melanoma cells adapted to acidosis show higher tumor-initiating potential than control cells • Extracellular acidosis promotes a stem-like phenotype in prostate and colorectal carcinoma cells.</p>","PeriodicalId":520678,"journal":{"name":"Journal of molecular medicine (Berlin, Germany)","volume":" ","pages":"1431-1446"},"PeriodicalIF":4.2000,"publicationDate":"2020-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s00109-020-01959-y","citationCount":"49","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of molecular medicine (Berlin, Germany)","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00109-020-01959-y","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/8/15 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 49

Abstract

Acidosis characterizes the microenvironment of most solid tumors and is considered a new hallmark of cancer. It is mainly caused by both "aerobic" and "anaerobic" glycolysis of differently adapted cancer cells, with the final product lactic acid being responsible of the extracellular acidification. Many evidences underline the role of extracellular acidosis in tumor progression. Among the different findings, we demonstrated that acidosis-exposed cancer cells are characterized by an epithelial-to-mesenchymal transition phenotype with high invasive ability, high resistance to apoptosis, anchorage-independent growth, and drug therapy. Acidic melanoma cells over-express SOX2, which is crucial for the maintenance of their oxidative metabolism, and carbonic anhydrase IX, that correlates with poor prognosis of cancer patients. Considering these evidences, we realized that the profile outlined for acid cancer cells inevitably remind us the stemness profile. Therefore, we wondered whether extracellular acidosis might induce in cancer cells the acquisition of stem-like properties and contribute to the expansion of the cancer stem cell sub-population. We found that a chronic adaptation to acidosis stimulates in cancer cells the expression of stem-related markers, also providing a high in vitro/in vivo clonogenic and trans-differentiating ability. Moreover, we observed that the acidosis-induced stem-like phenotype of melanoma cells was reversible and related to the EMT induction. These findings help to characterize a further aspect of stem cell niche, contributing to the sustainment and expansion of cancer stem cell subpopulation. Thus, the usage of agents controlling tumor extracellular acidosis might acquire great importance in the clinic for the treatment of aggressive solid tumor. KEY MESSAGES: • Extracellular acidosis up-regulates EMT and stem-related markers in melanoma cells • Acidic medium up-regulates in vitro self-renewal capacity of melanoma cells • Chronic acidosis adaptation induces trans-differentiation ability in melanoma cells • Melanoma cells adapted to acidosis show higher tumor-initiating potential than control cells • Extracellular acidosis promotes a stem-like phenotype in prostate and colorectal carcinoma cells.

Abstract Image

Abstract Image

Abstract Image

酸性肿瘤微环境驱动黑色素瘤细胞的茎样表型。
酸中毒是大多数实体肿瘤微环境的特征,被认为是癌症的新标志。它主要是由不同适应的癌细胞的“好氧”和“厌氧”糖酵解引起的,最终产物乳酸负责细胞外酸化。许多证据强调细胞外酸中毒在肿瘤进展中的作用。在不同的发现中,我们证明了酸中毒暴露的癌细胞具有高侵袭能力、高细胞凋亡抗性、不依赖锚定生长和药物治疗的上皮-间质转化表型。酸性黑色素瘤细胞过度表达SOX2和碳酸酐酶IX, SOX2对维持其氧化代谢至关重要,而碳酸酐酶IX与癌症患者预后不良相关。考虑到这些证据,我们意识到酸性癌细胞的轮廓不可避免地提醒我们干细胞的轮廓。因此,我们想知道细胞外酸中毒是否会诱导癌细胞获得干细胞样特性,并有助于癌症干细胞亚群的扩增。我们发现,对酸中毒的慢性适应刺激了癌细胞中干细胞相关标志物的表达,也提供了高的体外/体内克隆生成和反式分化能力。此外,我们观察到酸中毒诱导的黑色素瘤细胞干样表型是可逆的,并且与EMT诱导有关。这些发现有助于表征干细胞生态位的进一步方面,有助于维持和扩大癌症干细胞亚群。因此,使用控制肿瘤细胞外酸中毒的药物对侵袭性实体瘤的临床治疗具有重要意义。关键信息:•细胞外酸中毒上调黑色素瘤细胞中的EMT和干细胞相关标志物•酸性培养基上调黑色素瘤细胞的体外自我更新能力•慢性酸中毒适应诱导黑色素瘤细胞的反分化能力•适应酸中毒的黑色素瘤细胞比对照细胞表现出更高的肿瘤启动潜能•细胞外酸中毒促进前列腺和结直肠癌细胞的茎样表型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信