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PMID: 2579034 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Expression of ki-ras oncogene in tumor cell variants exhibiting different metastatic capabilities.

International journal of cancer ·Vol. 35 ·No. 2 ·1985-02-15 ·Pages 227-30

Kris RM, Avivi A, Bar-Eli M, Alon Y, Carmi P, Schlessinger J, Raz A

Abstract

The expression of oncogenes in well-characterized B16 melanoma and UV-2237 fibrosarcoma cell variants that exhibit distinct metastatic properties was explored. The search for the expression of 11 different oncogenes revealed that the major oncogene in those two tumor systems is the Kirsten-ras (ki-ras). The results indicate that the amounts of specific ki-ras mRNA and the p21 protein are similar in both low- and high-metastatic counterparts. These results suggest that in these systems there is no apparent direct correlation between the amount and expression of the major cellular oncogene so far identified and the metastatic potential of these tumor cells.

MeSH Terms
Animals Cell Line Fibrosarcoma/genetics Gene Expression Regulation Immunosorbent Techniques Lung Neoplasms/secondary Melanoma/genetics Nucleic Acid Hybridization Oncogenes Poly A/analysis RNA/analysis RNA, Messenger/analysis RNA, Neoplasm/analysis Viral Proteins/analysis
Chemicals
RNA, Messenger RNA, Neoplasm Viral Proteins Poly A RNA
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Kris R M
Avivi A
Bar-Eli M
Alon Y
Carmi P
Schlessinger J
Raz A
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
1985-02-15
Pages
227-30
Language
English
Region
United States
NLM ID
0042124
Subset
IM
Grants
NCI NIH HHS · CA-25820 · United States
NCI NIH HHS · CA-31330 · United States
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