Department of Molecular and Comparative Pathobiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Division of Cancer Genome Research, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Int J Mol Sci. 2023 Feb 24;24(5):4507. doi: 10.3390/ijms24054507.
Hypoxia, or low oxygen tension, is frequently found in highly proliferative solid tumors such as anaplastic thyroid carcinoma (ATC) and is believed to promote resistance to chemotherapy and radiation. Identifying hypoxic cells for targeted therapy may thus be an effective approach to treating aggressive cancers. Here, we explore the potential of the well-known hypoxia-responsive microRNA (miRNA) miR-210-3p as a cellular and extracellular biological marker of hypoxia. We compare miRNA expression across several ATC and papillary thyroid cancer (PTC) cell lines. In the ATC cell line SW1736, miR-210-3p expression levels indicate hypoxia during exposure to low oxygen conditions (2% O). Furthermore, when released by SW1736 cells into the extracellular space, miR-210-3p is associated with RNA carriers such as extracellular vesicles (EVs) and Argonaute-2 (AGO2), making it a potential extracellular marker for hypoxia.
缺氧,或低氧张力,常发生在高度增殖的实体肿瘤中,如间变性甲状腺癌(ATC),并被认为可促进对化疗和放疗的耐药性。因此,识别缺氧细胞进行靶向治疗可能是治疗侵袭性癌症的有效方法。在这里,我们探讨了众所周知的缺氧反应性 microRNA(miRNA)miR-210-3p 作为缺氧的细胞内和细胞外生物学标志物的潜力。我们比较了几种 ATC 和甲状腺乳头状癌(PTC)细胞系中的 miRNA 表达。在 ATC 细胞系 SW1736 中,miR-210-3p 的表达水平表明在低氧条件(2% O)下存在缺氧。此外,当 SW1736 细胞释放到细胞外空间时,miR-210-3p 与 RNA 载体(如外泌体(EVs)和 Argonaute-2(AGO2))相关,使其成为缺氧的潜在细胞外标志物。