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膜联蛋白A1与结肠癌细胞对5-氟尿嘧啶的耐药性有关。

Annexin A1 is involved in resistance to 5-FU in colon cancer cells.

作者信息

Onozawa Hisashi, Saito Motonobu, Saito Katsuharu, Kanke Yasuyuki, Watanabe Yohei, Hayase Suguru, Sakamoto Wataru, Ishigame Teruhide, Momma Tomoyuki, Ohki Shinji, Takenoshita Seiichi

机构信息

Department of Organ Regulatory Surgery, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan.

出版信息

Oncol Rep. 2017 Jan;37(1):235-240. doi: 10.3892/or.2016.5234. Epub 2016 Nov 8.

DOI:10.3892/or.2016.5234
PMID:27840982
Abstract

Resistance to 5-fluorouracil (5‑FU), a key drug in the treatment of colorectal cancer, is one of the major reasons for poor patient prognosis during cancer treatment. Annexin A1 (ANXA1) is a calcium‑dependent phospholipid‑linked protein that is associated with drug resistance, anti‑inflammatory effects, regulation of cellular differentiation, proliferation and apoptosis. Although there have been several studies investigating ANXA1 expression in drug resistant cells, the role of ANXA1 is yet to be fully understood. We therefore, in this study, generated SW480 cells resistant to 5‑FU (SW480/5‑FU) to evaluate ANXA1 expression. When compared to the control cells, ANXA1 expression was significantly induced in the SW480/5‑FU cells. We then revealed the role of ANXA1 expression in 5‑FU resistance by using overexpression and knockdown methods in colon cancer cells. Overexpression of ANXA1 induced a significant increase of cell viability to 5‑FU, whereas ANXA1 knockdown induced a significant decrease of cell viability to 5‑FU. Further experiments revealed that ANXA1 expression was induced by hypoxia in colon cancer cells. These results suggest that ANXA1 expression may play a critical role in 5‑FU resistance and may be induced by hypoxia during cancer progression. Our results provide a possible strategy to overcome 5‑FU resistance by modulating ANXA1 expression.

摘要

5-氟尿嘧啶(5-FU)是治疗结直肠癌的关键药物,对其产生耐药性是癌症治疗期间患者预后不良的主要原因之一。膜联蛋白A1(ANXA1)是一种钙依赖性磷脂结合蛋白,与耐药性、抗炎作用、细胞分化、增殖及凋亡的调节相关。尽管已有多项研究探讨ANXA1在耐药细胞中的表达情况,但其作用尚未完全明确。因此,在本研究中,我们构建了对5-FU耐药的SW480细胞(SW480/5-FU)以评估ANXA1的表达。与对照细胞相比,SW480/5-FU细胞中ANXA1的表达显著上调。随后,我们通过在结肠癌细胞中运用过表达和敲低方法揭示了ANXA1表达在5-FU耐药中的作用。ANXA1过表达导致细胞对5-FU的活力显著增加,而ANXA1敲低则导致细胞对5-FU的活力显著降低。进一步实验表明,缺氧可诱导结肠癌细胞中ANXA1的表达。这些结果提示,ANXA1表达可能在5-FU耐药中起关键作用,且可能在癌症进展过程中由缺氧诱导产生。我们的研究结果为通过调节ANXA1表达来克服5-FU耐药提供了一种可能的策略。

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