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结直肠癌中半胱天冬酶-8基因的失活突变

Inactivating mutations of caspase-8 gene in colorectal carcinomas.

作者信息

Kim Hong Sug, Lee Jong Woo, Soung Young Hwa, Park Won Sang, Kim Su Young, Lee Jong Heun, Park Jik Young, Cho Youg Gu, Kim Chang Jae, Jeong Seong Whan, Nam Suk Woo, Kim Sang Ho, Lee Jung Young, Yoo Nam Jin, Lee Sug Hyung

机构信息

Department of Pathaology, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Gastroenterology. 2003 Sep;125(3):708-15. doi: 10.1016/s0016-5085(03)01059-x.

Abstract

BACKGROUND & AIMS: There has been evidence that dysregulation of apoptosis is involved in the pathogenesis of cancer development. Caspase-8 is an initiation caspase that activates the caspase cascade during apoptosis. The aim of this study was to explore the possibility that mutation of the caspase-8 gene might be involved in the development of colorectal cancer.

METHODS

We analyzed the entire coding region of the caspase-8 gene for the detection of somatic mutations in 180 colorectal tumors (98 invasive carcinomas and 82 adenomas) by polymerase chain reaction, single-strand conformation polymorphism, and DNA sequencing.

RESULTS

Overall, we detected a total of 5 somatic mutations in 98 invasive carcinomas (5.1%), but no mutations were detected in 82 adenomas (0%). The frequency of caspase-8 mutation in the carcinomas was significantly higher than that in adenomas (P < 0.05). The 5 mutations consisted of 1 frameshift, 1 nonsense mutation, and 3 missense mutations. We expressed the 5 tumor-derived caspase-8 mutants and found that 3 of the 5 mutations markedly decreased apoptosis activity of caspase-8. Furthermore, expression of the inactivating caspase-8 mutants interfered with apoptosis by death receptor overexpression, indicating that these mutants have dominant-negative inhibition of the death receptor-induced apoptosis.

CONCLUSIONS

The presence of caspase-8 mutation in colon carcinomas suggests that caspase-8 gene mutation might lead to the loss of its apoptotic function and contribute to the pathogenesis of colorectal carcinomas, especially at the late stage of colorectal carcinogenesis.

摘要

背景与目的

有证据表明细胞凋亡失调参与癌症发生的病理过程。半胱天冬酶 - 8是一种起始半胱天冬酶,在细胞凋亡过程中激活半胱天冬酶级联反应。本研究的目的是探讨半胱天冬酶 - 8基因突变可能参与结直肠癌发生的可能性。

方法

我们通过聚合酶链反应、单链构象多态性和DNA测序分析了180例结直肠肿瘤(98例浸润性癌和82例腺瘤)中半胱天冬酶 - 8基因的整个编码区,以检测体细胞突变。

结果

总体而言,我们在98例浸润性癌中总共检测到5个体细胞突变(5.1%),但在82例腺瘤中未检测到突变(0%)。癌组织中半胱天冬酶 - 8突变的频率显著高于腺瘤(P < 0.05)。这5个突变包括1个移码突变、1个无义突变和3个错义突变。我们表达了5个肿瘤来源的半胱天冬酶 - 8突变体,发现5个突变中有3个显著降低了半胱天冬酶 - 8的凋亡活性。此外,失活的半胱天冬酶 - 8突变体的表达通过死亡受体过表达干扰细胞凋亡,表明这些突变体对死亡受体诱导的细胞凋亡具有显性负性抑制作用。

结论

结肠癌中存在半胱天冬酶 - 8突变表明,半胱天冬酶 - 8基因突变可能导致其凋亡功能丧失,并有助于结直肠癌的发病机制,尤其是在结直肠癌发生的晚期。

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