Matsui Toma, Toda Yuki, Sato Haruka, Itagaki Rina, Konishi Kazuya, Moshnikova Anna, Andreev Oleg A, Hosogi Shigekuni, Reshetnyak Yana K, Ashihara Eishi
Laboratory of Clinical and Translational Physiology, Kyoto Pharmaceutical University, Kyoto, Japan.
Physics Department, University of Rhode Island, Kingston, RI, United States.
Front Oncol. 2023 Nov 15;13:1258442. doi: 10.3389/fonc.2023.1258442. eCollection 2023.
Dysregulated extracellular pH, the universal feature of tumor, works as an evolutional force to drive dissemination of tumor cells. It is well-established that tumor acidity is associated with tumor growth and metastasis. However, the pH of pre-metastatic niche remains unclear. We hypothesized that primary tumor cells remotely prime acidity in secondary organ to achieve metastatic colonization. Herein, we demonstrated that the pH responsive probe pH Low Insertion Peptide (pHLIP) was notably accumulated in pre-metastatic lungs of 4T1.2 breast tumor-bearing mice. The pHLIP-targeted lungs showed high amounts of lactate and overexpressed glycolysis-related proteins. Pharmacological inhibition of glycolysis suppressed the lung acidification induced by 4T1.2 cancer cell culture supernatant and delayed subsequent metastatic burden of disseminated tumor cells. In the acidic lungs, pHLIP was primarily localized in alveolar type 2 cells which strongly expressed glycolysis-related proteins. 4T1.2-derived extracellular vesicles expressed some of the glycolysis-related proteins, and their administration increased pHLIP accumulation and glycolytic enhancement in lungs. pHLIP-conjugated dexamethasone effectively attenuated lung metastatic burden by disrupting pro-inflammatory response in the acidic lungs. From these results, targeting the metastasis-supporting microenvironment by pHLIP technology creates possibility to identify pre-metastatic organ and prevent metastatic recurrence.
细胞外pH失调是肿瘤的普遍特征,作为一种进化驱动力促使肿瘤细胞扩散。肿瘤酸性与肿瘤生长和转移相关,这一点已得到充分证实。然而,转移前微环境的pH仍不清楚。我们假设原发性肿瘤细胞可远程调节继发性器官的酸度以实现转移定植。在此,我们证明pH响应探针pH低插入肽(pHLIP)在携带4T1.2乳腺肿瘤的小鼠转移前肺中显著积累。pHLIP靶向的肺显示出大量乳酸和糖酵解相关蛋白过表达。糖酵解的药理学抑制作用抑制了4T1.2癌细胞培养上清液诱导的肺酸化,并延迟了随后播散肿瘤细胞的转移负担。在酸性肺中,pHLIP主要定位于强烈表达糖酵解相关蛋白的2型肺泡细胞。4T1.2来源的细胞外囊泡表达一些糖酵解相关蛋白,其给药增加了肺中pHLIP的积累和糖酵解增强。pHLIP偶联地塞米松通过破坏酸性肺中的促炎反应有效减轻了肺转移负担。基于这些结果,通过pHLIP技术靶向支持转移的微环境为识别转移前器官和预防转移复发创造了可能性。