Department of Radiotherapy, Martin Luther University of Halle‑Wittenberg, D‑06112 Halle (Saale), Germany.
Julius Bernstein Institute of Physiology, Martin Luther University of Halle‑Wittenberg, D‑06112 Halle (Saale), Germany.
Oncol Rep. 2019 Apr;41(4):2585-2594. doi: 10.3892/or.2019.7001. Epub 2019 Feb 5.
Hypoxia‑induced carbonic anhydrase IX (CAIX) is involved in intracellular and extracellular pH regulation, which is critical for tumor growth and metastasis. CAIX is overexpressed in breast cancer and is associated with the poor survival of patients after radiotherapy. Therefore, we evaluated the cellular and radiobiological effects of CAIX inhibition in human breast cancer cells. We used CA9 siRNA and the CA inhibitor (CAI) U104, respectively, to inhibit CAIX expression and activity in basal triple‑negative MDA‑MB‑231 and luminal MCF‑7 cells under hypoxic conditions. We investigated the effects of CAIX inhibition on CA9 mRNA and CAIX protein level, as well as on CAIX activity, intracellular pH, proliferation, apoptosis, clonogenic survival, migration, cell cycle distribution and radiosensitivity. CA9 siRNA and CAI U104 decreased CA9 mRNA and CAIX protein level in MDA‑MB‑231 and MCF‑7 cells. Furthermore, incubation with CAI U104 significantly decreased carbonic anhydrase activity and reduced the intracellular pH. Additionally, CA9 siRNA or U104 reduced clonogenic survival, migration and the number of cells in the G0/G1 phase, induced apoptosis and demonstrated additive or synergistic effects in combination with irradiation. In conclusion, combination of CAIX inhibition and irradiation is a promising treatment strategy against breast cancer with hypoxia‑induced CAIX expression.
缺氧诱导的碳酸酐酶 IX(CAIX)参与细胞内和细胞外 pH 值的调节,这对于肿瘤的生长和转移至关重要。CAIX 在乳腺癌中过表达,并与放疗后患者的生存不良相关。因此,我们评估了 CAIX 抑制在人乳腺癌细胞中的细胞和放射生物学效应。我们分别使用 CA9 siRNA 和 CA 抑制剂(CAI)U104 抑制基础三阴性 MDA-MB-231 和腔性 MCF-7 细胞在缺氧条件下的 CAIX 表达和活性。我们研究了 CAIX 抑制对 CA9 mRNA 和 CAIX 蛋白水平以及 CAIX 活性、细胞内 pH 值、增殖、凋亡、集落形成存活、迁移、细胞周期分布和放射敏感性的影响。CA9 siRNA 和 CAI U104 降低了 MDA-MB-231 和 MCF-7 细胞中的 CA9 mRNA 和 CAIX 蛋白水平。此外,CAI U104 的孵育显著降低了碳酸酐酶活性并降低了细胞内 pH 值。此外,CA9 siRNA 或 U104 降低了集落形成存活、迁移和 G0/G1 期细胞数量,诱导了细胞凋亡,并与照射联合具有相加或协同作用。总之,CAIX 抑制与照射相结合是治疗缺氧诱导 CAIX 表达的乳腺癌的一种有前途的治疗策略。