首页> 美国卫生研究院文献>British Journal of Cancer >Analysis of histological therapeutic effect apoptosis rate and p53 status after combined treatment with radiation hyperthermia and 5-fluorouracil suppositories for advanced rectal cancers.
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Analysis of histological therapeutic effect apoptosis rate and p53 status after combined treatment with radiation hyperthermia and 5-fluorouracil suppositories for advanced rectal cancers.

机译:放射高温和5-氟尿嘧啶栓剂联合治疗晚期直肠癌后的组织学治疗效果凋亡率和p53状态分析。

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摘要

The tumour-suppressor gene p53 encodes a transcription factor that plays a critical role in the induction of G1 cell cycle arrest and apoptosis after DNA damage. To clarify the role of the p53 gene and apoptosis in combined hyperthermia, chemotherapy and radiation (hyperthermochemoradiotherapy, HCR therapy) for rectal cancer, we examined the histological response, rate of apoptosis, DNA fragmentation and p53 status in tumours from 28 patients undergoing HCR therapy before surgery and from 22 patients who did not have preoperative treatment. The therapeutic effect of HCR therapy was closely correlated with the rate of apoptosis; the correlation was statistically significant, suggesting that this effect occurs through apoptosis. The incidence of p53 mutations in the treated group were as follows: in tumours resistant to HCR therapy, four of seven (57.1%); intermediately sensitive, 7 of 13 (53.9%); or sensitive, three of eight (37.5%), suggesting that the therapeutic effect and apoptosis rate were related to the p53 status of the tumours to some extent, but the relation was not statistically significant. In the 22 control tumours (non-treated group), the apoptosis rate was 2.0 +/- 1.1%, and there was no significant difference in p53 status compared with the HCR group. Our study indicates that the pathological response to HCR therapy correlates with the rate of apoptosis with statistical significance and that it induces the therapeutic effect more significantly in rectal cancer cells with wild-type p53, although HCR therapy-induced apoptosis also occurs in some rectal cancers with mutated p53. Therefore, this combination therapy can induce an additive or synergistic anti-tumour effect in rectal cancers with wild-type p53 as well as in those with mutated p53 through apoptosis, offering new therapeutic opportunities and a better prognosis.
机译:肿瘤抑制基因p53编码的转录因子在DNA损伤后诱导G1细胞周期停滞和细胞凋亡中起关键作用。为了阐明p53基因和细胞凋亡在直肠癌热疗,化学疗法和放射疗法(热化学放疗,HCR治疗)联合中的作用,我们检查了28例接受HCR治疗的患者的肿瘤的组织学应答,细胞凋亡率,DNA片段化和p53状态术前未接受术前治疗的22例患者。 HCR治疗的疗效与细胞凋亡率密切相关。相关性具有统计学意义,表明该效应是通过凋亡发生的。在治疗组中p53突变的发生率如下:在对HCR治疗有抗性的肿瘤中,七分之四(57.1%);中级敏感,在13中的7(53.9%);敏感或敏感,占八分之三(37.5%),表明治疗效果和凋亡率在一定程度上与肿瘤的p53状态有关,但无统计学意义。在22个对照肿瘤(未治疗组)中,凋亡率是2.0 +/- 1.1%,与HCR组相比,p53状态没有显着差异。我们的研究表明,对HCR治疗的病理反应与凋亡率具有统计学意义,并且它对野生型p53直肠癌细胞具有更显着的诱导治疗作用,尽管在某些直肠癌中也发生了HCR治疗诱导的凋亡。 p53突变。因此,这种联合疗法可在具有野生型p53的直肠癌以及通过细胞凋亡使p53突变的直肠癌中产生累加或协同抗肿瘤作用,从而提供新的治疗机会和更好的预后。

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