Molecular abnormalities in Syrian golden hamster pancreatic ductal adenocarcinomas
نام عام مواد
[Thesis]
نام نخستين پديدآور
K.-W. Chang
نام ساير پديدآوران
D. G. Scarpelli
وضعیت نشر و پخش و غیره
نام ناشر، پخش کننده و غيره
Northwestern University
تاریخ نشرو بخش و غیره
1995
مشخصات ظاهری
نام خاص و کميت اثر
109
یادداشتهای مربوط به پایان نامه ها
جزئيات پايان نامه و نوع درجه آن
Ph.D.
کسي که مدرک را اعطا کرده
Northwestern University
امتياز متن
1995
یادداشتهای مربوط به خلاصه یا چکیده
متن يادداشت
This study examines the involvement of the tumor suppressor genes p53, DCC and Rb-1 and the oncogene mdm2, as well as the growth factor TGF-usd\alphausd in the Syrian golden hamster pancreatic ductal adenocarcinomas induced by N-nitrosobis(2-oxopropyl)amine. Hamster p53 sequence for the genomic regions surrounding exons 5 through 8, and the partial coding sequence of mdm2, glyceraldehyde-3-phosphate dehydrogenase (G3PDH) gene and DCC were determined. Immunohistochemistry and single strand conformation polymorphism analysis showed no evidence of p53 mutation in 21 grossly evident tumors subjected to both molecular and morphological analysis, nor was it detected by immunohistochemical study of an additional 42 adenocarcinomas that were not grossly evident. A hamster mdm2 specific riboprobe was generated from the cDNA sequence for ribonuclease protection assays. After normalization to G3PDH expression, 5/19 test pairs presented overexpression of mdm2 mRNA in carcinomas when compared to adjacent grossly normal pancreas. The expression of DCC and Rb-1 in hamster pancreatic adenocarcinomas was analyzed by semi-quantitative RT-PCR under conditions optimized to insure a valid analysis. Ten of 19 neoplasms showed a complete or partial loss of DCC expression while 8 showed similar losses of Rb-1 expression when compared to matched controls. Using immunohistochemistry, 76% of the gross tumors and 60% of total tumors showed TGF-usd\alphausd overexpression. TGF-usd\alphausd overexpression was also found in 33% of preneoplastic lesions. These results support the multiple-hit hypothesis in the pathogenesis of pancreatic carcinogenesis in the Syrian golden hamster model. A 90% incidence of K-ras mutation and the absence of p53 mutations are prominent features of hamster pancreatic ductal adenocarcinomas. Our observations indicate the involvement of mdm2 deregulation in 26% of tumors that lack p53 mutation and the underexpression of DCC in 53% and Rb-1 in 42% as well as overexpression of TGF-usd\alphausd. Deregulation of TGF-usd\alphausd appears to be as crucial as the K-ras mutation as indicated by its frequent and sustained presence through the various phases of hamster pancreatic duct carcinogenesis.
موضوع (اسم عام یاعبارت اسمی عام)
موضوع مستند نشده
Biological sciences
موضوع مستند نشده
Genetics
موضوع مستند نشده
Health and environmental sciences
موضوع مستند نشده
Pathology
موضوع مستند نشده
Pathology
نام شخص به منزله سر شناسه - (مسئولیت معنوی درجه اول )