| Literature DB >> 12970753 |
Young Hwa Soung1, Jong Woo Lee, Hong Sug Kim, Won Sang Park, Su Young Kim, Jong Heun Lee, Jik Young Park, Yong Gu Cho, Chang Jae Kim, Yong Gyu Park, Suk Woo Nam, Seong Whan Jeong, Sang Ho Kim, Jung Young Lee, Nam Jin Yoo, Sug Hyung Lee.
Abstract
Caspase-7 is a caspase involved in the execution phase of apoptosis. To explore the possibility that the genetic alterations of CASPASE-7 might be involved in the development of human cancers, we analysed the entire coding region and all splice sites of human CASPASE-7 gene for the detection of somatic mutations in a series of human solid cancers, including carcinomas from stomach, colon, head/neck, esophagus, urinary bladder and lung. Overall, we detected CASPASE-7 mutations in two of 98 colon carcinomas (2.0%), one of 50 esophageal carcinomas (2.0%) and one of 33 head/neck carcinomas (3.0%). We expressed the tumor-derived caspase-7 mutants in 293 T cells and found that the apoptosis was reduced compared to the wild-type caspase-7. This is the first report on the CASPASE-7 gene mutations in human malignancies, and our data suggest that the inactivating mutations of the CASPASE-7 gene might lead to the loss of its apoptotic function and contribute to the pathogenesis of some human solid cancers.Entities:
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Year: 2003 PMID: 12970753 DOI: 10.1038/sj.onc.1206727
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867