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Mild hyperthermia enhances sensitivity of gastric cancer cells to chemotherapy through reactive oxygen species–induced autophagic death

机译:轻度高温会通过活性氧引起的自噬死亡增强胃癌细胞对化疗的敏感性

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Mild hyperthermia enhances anti-cancer effects of chemotherapy, but the precise biochemical mechanisms involved are not clear. This study was carried out to investigate whether mild hyperthermia sensitizes gastric cancer cells to chemotherapy through reactive oxygen species–induced autophagic death. In total, 20 BABL/c mice of MKN-45 human gastric cancer tumor model were divided into hyperthermia?+?chemotherapy group, hyperthermia group, chemotherapy group, N-acetyl-L-cysteine group, and mock group. Reactive oxygen species production and expression of autophagy-related genes Beclin1, LC3B, and mammalian target of rapamycin were determined. The relationships between tumor growth regression, expression of autophagy-related genes, and reactive oxygen species production were evaluated. Tumor size and wet weight of hyperthermia?+?chemotherapy group was significantly decreased relative to values from hyperthermia group, chemotherapy group, N-acetyl-L-cysteine group, and mock group (F?=?6.92, p F?=?5.36, p
机译:轻度的高温会增强化学疗法的抗癌作用,但所涉及的确切生化机制尚不清楚。这项研究旨在研究轻度高热是否通过活性氧引起的自噬死亡使胃癌细胞对化疗敏感。将MKN-45人胃癌肿瘤模型的20只BABL / c小鼠分为热疗+化疗组,热疗组,化疗组,N-乙酰-L-半胱氨酸组和模拟组。确定了活性氧的产生和自噬相关基因Beclin1,LC3B和雷帕霉素的哺乳动物靶标的表达。评价了肿瘤生长消退,自噬相关基因的表达和活性氧产生之间的关系。相对于热疗组,化学疗法组,N-乙酰基-L-半胱氨酸组和模拟组的值,热疗+化学疗法组的肿瘤大小和湿重显着降低(F?=?6.92,p F?=?5.36)。 p

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