ADAPTOR PROTEIN Ruk/CIN85REGULATES REDOX BALANCE IN 4T1MOUSE BREAST CANCER CELLS EXPOSED TO PLASMIN(OGEN)

I R Horak, N V Latyshko, O O Hudkova, K O Tokarchuk, T O Kishko, O I Yusova, L B Drobot, A A Tykhomyrov
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Abstract

Cell surface plasmin is involved in tumor growth and metastatic dissemination by regulating cancer cells adhesion, migration and invasion. Plasmin-induced cell detachment is accompanied by an increased rate of reactive oxygen species (ROS) generation and cell death. However, cancer cells acquire the ability to develop adaptive mechanisms to resist ROS-mediated apoptosis.To establish the role of adaptor protein Ruk/CIN85 in the control of viability and redox balance in breast adenocarcinoma cells exposed to plasmin(ogen).Mouse 4T1 cells with the stable overexpression of adaptor protein Ruk/CIN85 (RukUp subline) and corresponding control (Mock subline) were treated with Glu-plasminogen (1-100 nM). Plasminogen to plasmin conversion was monitored spectrophotometrically by cleavage of the specific chromogenic substrate S2251. Specific uPA inhibitor BC11 was used to verify the uPA-mediated mechanism of plasminogen pericellular activation by 4T1 cells. Cell survival rate was assessed by MTT-test and cell proliferation was estimated by colony formation assay. Enzymatic activities of catalase, glutathione peroxidase, superoxide dismutase, as well as hydrogen peroxide (H2O2) levels were measured by spectrophotomertric and fluorometric assays. The intracellular ROS generation was monitored by flow cytometry using H2DCF-DA fluorescent probe.Plasminogen was shown to be converted into an active proteinase plasmin on the surface of carcinoma cells in uPA-dependent manner. Plasmin(ogen) suppressed proliferation and affected survival of both studied 4T1 sublines. However, RukUp cells displayed higher resistance to plasmin(ogen)-induced cytotoxicity than Mock cells. Plasmin(ogen) promoted significant elevation in ROS generation rate in cells with the basal level of Ruk/CIN85 expression. In contrast, RukUp cells appear to be more effective in counteracting prooxidant changes due to the activation of some enzymes of the glutathione system, in particular glutathione peroxidase, and a concomitant decrease of H2O2 accumulation.Adaptor protein Ruk/CIN85 is involved in the regulation of redox homeostasis in cancer cells to maintain levels of ROS, thus promoting redox adaptation in cancer cells exposed to plasmin(ogen). Thus, Ruk/CIN85 may represent one of the relevant targets in order to diminish the resistance of cancer cells to ROS-mediated apoptosis.
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受体蛋白Ruk/ cin85调控纤溶酶(原)作用下4t1小鼠乳腺癌细胞的氧化还原平衡
细胞表面纤溶酶通过调节癌细胞的粘附、迁移和侵袭,参与肿瘤的生长和转移传播。纤溶蛋白诱导的细胞脱离伴随着活性氧(ROS)生成速率的增加和细胞死亡。然而,癌细胞获得了发展适应机制的能力来抵抗ros介导的细胞凋亡。目的:探讨受体蛋白Ruk/CIN85在控制纤溶酶(原)作用下乳腺腺癌细胞活力和氧化还原平衡中的作用。用1-100 nM的葡萄糖-纤溶酶原处理过表达Ruk/CIN85 (RukUp亚线)和相应对照(Mock亚线)的小鼠4T1细胞。通过裂解特定显色底物S2251,分光光度法监测纤溶酶原到纤溶酶的转化。使用特异性uPA抑制剂BC11验证了uPA介导的4T1细胞纤溶酶原细胞周活化机制。mtt法测定细胞存活率,菌落形成法测定细胞增殖。用分光光度法和荧光法测定过氧化氢酶、谷胱甘肽过氧化物酶、超氧化物歧化酶以及过氧化氢(H2O2)水平的酶活性。采用H2DCF-DA荧光探针,流式细胞术检测细胞内ROS生成情况。纤溶酶原在癌细胞表面以upa依赖的方式转化为活性蛋白酶纤溶酶。纤溶蛋白(原)抑制4T1亚型的增殖并影响其存活。然而,RukUp细胞对纤溶酶(原)诱导的细胞毒性表现出比Mock细胞更高的抗性。在Ruk/CIN85基础表达水平的细胞中,纤溶蛋白(原)促进ROS生成率显著升高。相比之下,RukUp细胞似乎更有效地对抗促氧化变化,这是由于谷胱甘肽系统的一些酶的激活,特别是谷胱甘肽过氧化物酶,以及伴随的H2O2积累的减少。接合蛋白Ruk/CIN85参与调节癌细胞氧化还原稳态以维持活性氧水平,从而促进暴露于纤溶蛋白(原)的癌细胞的氧化还原适应。因此,Ruk/CIN85可能是降低癌细胞对ros介导的凋亡的抗性的相关靶点之一。
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