Investigation of the Possible Association Between Galectin and Apoptosis in Gastric Cancer Patients

F. Kosova, N. Umur, Bahadır Çetin, Özgü Kemal Beksaç
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Abstract

Cancer is a type of disease that occurs as a result of the uncontrolled growth of cells, which has been very common in recent years, and some species have a poor prognosis. Galectin-3 is a multifunctional protein and is associated with the developmental process of tumors, including cell growth, adhesion, proliferation and metastasis. Galectin-3 has a broad effect on tumor development, including cell proliferation, apoptosis, cell adhesion, invasion, angiogenesis, and metastasis. Members of the BCLF-2 family are anti-apoptotic molecules required for the proteolytic degradation of the cell by caspases, which is the ultimate drive of programmed cell death, which plays a very important role in the regulation of the apoptotic pathway, ensures the integrity of the mitochondrial membrane and prevents the release of cytochrome C from the mitochondria. NF-kB, which is one of the important factors in cancer formation, is found in the cytoplasm, and there is a correlation between the protein levels of proinflammatory cytokines such as interlukin (IL)-1b, and IL-8, and the high incidence of cancer.  There are two types of apoptotic caspases: initiator (apical) caspases and effector (executioner) caspases. Initiator caspases (e.g., caspase-2, -8, -9 and -10) cleave inactive pro-forms of effector caspases, thereby activating them. Effector caspases (e.g., caspase-3, -6, -7) in turn cleave other protein substrates within the cell resulting in the apoptotic process. At least fourteen caspases have so far been implicated in human apoptotic pathway cascade. Among these, caspase-3 is considered to be a major executioner protease in apoptosis. To examine this mechanism in more detail, we aimed to examine the difference between Galectin, BCLF-2, Kaspase3, Kaspas 8, Nfkb levels before and after treatment in operable gastric cancer patients with the Elisa test. In this study, We observed a statistical increase in Galectin, BCLF-2, Kaspase3, Kaspas 8, Nfkb levels when the control group was compared with the preoperative group. There was a statistically significant increase in Galectin, BCLF-2, Nfkb, Caspase3, Caspase 8 levels in the preoperative group compared to the control. There is a statistical increased in Galectin, BCLF-2, Kaspase3, Kaspas 8, Nfkb levels in the postoperative group compared to the control. Although there was no statistical difference in Galectin, BCLF-2, Caspase-3, Caspase-8, Nfkb levels between pre and postoperative groups, a significant decrease was observed in Galectin, BCLF-2, Nfkb levels. A very slight increase was observed in Caspase-3 and Caspase-8 levels. In conclusion, we think that Galectin-3 Bcl-2 and NF-kB may be markers for gastric cancer patients. We think that it is appropriate to conduct this study with more patient groups and a longer period.
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胃癌患者体内 Galectin 与细胞凋亡之间可能存在的关联调查
癌症是一种由于细胞不受控制地生长而发生的疾病,近年来非常常见,有些种类的癌症预后很差。Galectin-3 是一种多功能蛋白,与肿瘤的发育过程有关,包括细胞生长、粘附、增殖和转移。Galectin-3对肿瘤的发展具有广泛的影响,包括细胞增殖、凋亡、细胞粘附、侵袭、血管生成和转移。BCLF-2 家族成员是抗凋亡分子,需要通过 caspases 对细胞进行蛋白分解,这是细胞程序性死亡的最终驱动力,它在细胞凋亡途径的调控中起着非常重要的作用,能确保线粒体膜的完整性,防止细胞色素 C 从线粒体中释放出来。NF-kB是癌症形成的重要因素之一,它存在于细胞质中,促炎细胞因子(如interlukin (IL)-1b和IL-8)的蛋白质水平与癌症的高发病率之间存在相关性。 凋亡caspases有两种类型:启动器(顶端)caspases和效应器(执行器)caspases。启动器 caspases(如 caspase-2、-8、-9 和-10)会裂解效应器 caspases 的非活性原形,从而激活它们。效应 caspase(如 caspase-3、-6、-7)反过来又会裂解细胞内的其他蛋白质底物,从而导致细胞凋亡过程。迄今为止,至少有 14 种 caspase 与人类凋亡途径级联有关。其中,caspase-3 被认为是细胞凋亡的主要执行蛋白酶。为了更详细地研究这一机制,我们利用 Elisa 试验检测了可手术胃癌患者治疗前后 Galectin、BCLF-2、Kaspase3、Kaspas 8 和 Nfkb 水平的差异。在这项研究中,我们观察到对照组与术前组相比,Galectin、BCLF-2、Kaspase3、Kaspas 8、Nfkb 水平均有统计学意义的升高。与对照组相比,术前组的 Galectin、BCLF-2、Nfkb、Caspase3、Caspase 8 水平有统计学意义的增加。与对照组相比,术后组的 Galectin、BCLF-2、Kaspase3、Kaspas 8 和 Nfkb 水平在统计学上有所增加。虽然术前和术后组的 Galectin、BCLF-2、Caspase-3、Caspase-8、Nfkb 水平没有统计学差异,但观察到 Galectin、BCLF-2、Nfkb 水平显著下降。Caspase-3和Caspase-8水平略有升高。总之,我们认为 Galectin-3 Bcl-2 和 NF-kB 可能是胃癌患者的标志物。我们认为这项研究应该在更多的患者群体和更长的时间内进行。
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