Twomey Julianne D, Zhang Baolin
Office of Biotechnology Products, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20993, USA.
Biomedicines. 2023 Mar 17;11(3):934. doi: 10.3390/biomedicines11030934.
Circulating tumor cells (CTCs) in the peripheral blood are believed to be the source of metastasis and can be used as a liquid biopsy to monitor cancer progression and therapeutic response. However, it has been challenging to accurately detect CTCs because of their low frequency and the heterogeneity of the population. In this study, we have developed an in vitro model of CTCs by using non-adherent suspension culture. We used this model to study a group of breast cancer cell lines with distinct molecular subtypes (TNBC, HER2, and ER/PR). We found that, when these breast cancer cell lines lost their attachment to the extracellular matrix, they accumulated a subtype of cancer stem cells (CSC) that expressed the surface markers of stem cells (e.g., CD44CD24). These stem-like CTCs also showed high expressions of hypoxia-inducible gene products, particularly the hypoxia-inducible carbonic anhydrase IX (CAIX). Inhibition of CAIX activity was found to reduce CAIX expression and stem cell phenotypes in the targeted CTCs. Further studies are needed, using CTC samples from breast cancer patients, to determine the role of CAIX in CTC survival, CSC transition, and metastasis. CAIX may be a useful surface marker for the detection of CSCs in the blood, and a potential target for treating metastatic breast cancers.
外周血中的循环肿瘤细胞(CTC)被认为是转移的来源,并且可以用作液体活检来监测癌症进展和治疗反应。然而,由于CTC的低频率和群体的异质性,准确检测它们一直具有挑战性。在本研究中,我们通过使用非贴壁悬浮培养开发了一种CTC的体外模型。我们使用该模型研究了一组具有不同分子亚型(三阴性乳腺癌、人表皮生长因子受体2和雌激素受体/孕激素受体)的乳腺癌细胞系。我们发现,当这些乳腺癌细胞系失去与细胞外基质的附着时,它们积累了一种表达干细胞表面标志物(例如CD44CD24)的癌症干细胞(CSC)亚型。这些干细胞样CTC还显示缺氧诱导基因产物的高表达,特别是缺氧诱导碳酸酐酶IX(CAIX)。发现抑制CAIX活性可降低靶向CTC中CAIX的表达和干细胞表型。需要使用来自乳腺癌患者的CTC样本进行进一步研究,以确定CAIX在CTC存活、CSC转变和转移中的作用。CAIX可能是血液中CSC检测的有用表面标志物,也是治疗转移性乳腺癌的潜在靶点。