Published December 1988 | Version v1
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Oncogene expression in primary lung tumors in dogs that inhaled 239PuO2

Description

Ten radiation-induced and three spontaneous lung tumors were analyzed for aberrant expression of known oncogenes. In 12 of 13 tumors tested, sequences hybridizing to the c-myc oncogene were expressed at levels 1.5 times higher than sequences hybridizing to β-actin. This level of oncogene expression was also observed in 9 of 13 tumors for 1 or more members of the ras family of oncogenes. Seven of thirteen tumors examined express sequences that hybridize with clones of v-ros or c-met. The ros and met clones both code for oncogenes whose normal homologues are transmembrane proteins related to the insulin receptor. (author)

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Part of:
Inhalation Toxicology Research Institute annual report 1987-1988

Additional details

Publishing Information

Imprint Title
Inhalation Toxicology Research Institute annual report 1987-1988
Imprint Pagination
659 p.
Journal Page Range
p. 333-337
Report number
LMF--121

Optional Information

Contract/Grant/Project number
Contract DE-AC04-76EV01013
Notes
9 refs, 1 fig., 3 tabs
Secondary number(s)
INIS-XA-N--170