首页> 外文期刊>International journal of colorectal disease. >Tumour-derived mutated K-ras codon 12 expression in regional lymph nodes of stage II colorectal cancer patients is not associated with increased risk of cancer-related death.
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Tumour-derived mutated K-ras codon 12 expression in regional lymph nodes of stage II colorectal cancer patients is not associated with increased risk of cancer-related death.

机译:II期大肠癌患者区域淋巴结中源自肿瘤的突变型K-ras密码子12表达与癌症相关死亡的风险增加无关。

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摘要

This study examined the frequency of lymph node micrometastases detected by expression of mutant K-ras oncogene present in the respective primary tumour. The study population consisted of consecutive patients with stage II colorectal cancer (CRC) undergoing curative resection and with disease-free survival of 60 months or longer or CRC-related death. Of 27 patients found to have K-ras mutations at codon 12, 17 had genomic DNA suitable for PCR recovered from corresponding regional lymph node tissue. The same K-ras mutation was identified in the lymph nodes of 13 patients (76%), four of whom (30%) died of CRC recurrence within 5 years. A single patient in the negative group (25%) also died. Lymph node micrometastases detected by this technique thus show no relationship to mortality in stage II CRC. Further study of this technique is necessary before it can be used in the selection of patients for adjuvant chemotherapy.
机译:这项研究检查了通过在各个原发肿瘤中存在的突变K-ras癌基因的表达检测到的淋巴结微转移的频率。研究人群包括接受根治性切除且无病生存时间为60个月或更长时间或CRC相关死亡的II期大肠癌(CRC)连续患者。在27位密码子12位出现K-ras突变的患者中,有17位具有适合从相应区域淋巴结组织中回收的PCR的基因组DNA。在13名患者(76%)的淋巴结中发现了相同的K-ras突变,其中4名(30%)在5年内死于CRC复发。阴性组中有一名患者(25%)也死亡。因此,通过这种技术检测到的淋巴结微转移与II期CRC的死亡率没有关系。在将该技术用于选择辅助化疗患者之前,有必要对该技术进行进一步的研究。

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