Varying oncomodulin mRNA abundance in developing placenta and solid tumors
An antisense RNA probe complementary to rat oncomodulin mRNA has been prepared by run-off transcription. Blots of RNA isolated from tumors arising from both a chemically-induced hepatoma or virally transformed sarcomas, when probed with this antisense RNA, identified a common single hybridizable RNA...
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Published in | Cancer letters Vol. 40; no. 2; pp. 151 - 160 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Shannon
Elsevier Ireland Ltd
15.06.1988
Elsevier |
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Abstract | An antisense RNA probe complementary to rat oncomodulin mRNA has been prepared by run-off transcription. Blots of RNA isolated from tumors arising from both a chemically-induced hepatoma or virally transformed sarcomas, when probed with this antisense RNA, identified a common single hybridizable RNA of approx. 750 nucleotides, corresponding in size to that found in blots of RNA from rat placenta. Quantitative densitometry of dot blot autoradiographs allowed for relative measurements of oncomodulin mRNA in the various tumors. The increased sensitivity of detection afforded by the antisense probe permitted the measurement of oncomodulin mRNA in the developing placenta, which was not possible using DNA probes. In both tumors and placenta, a plot of mRNA versus protein revealed a direct relationship suggesting transcriptional control of oncomodulin abundance. |
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AbstractList | An antisense RNA probe complementary to rat oncomodulin mRNA has been prepared by run-off transcription. Blots of RNA isolated from tumors arising from both a chemically-induced hepatoma or virally transformed sarcomas, when probed with this antisense RNA, identified a common single hybridizable RNA of approx. 750 nucleotides, corresponding in size to that found in blots of RNA from rat placenta. Quantitative densitometry of dot blot autoradiographs allowed for relative measurements of oncomodulin mRNA in the various tumors. The increased sensitivity of detection afforded by the antisense probe permitted the measurement of oncomodulin mRNA in the developing placenta, which was not possible using DNA probes. In both tumors and placenta, a plot of mRNA versus protein revealed a direct relationship suggesting transcriptional control of oncomodulin abundance. |
Author | Gillen, M.F. Macmanus, J.P. Brewer, L.M. |
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Keywords | Placenta Solid tumors mRNA abundance Oncomodulin Molecular hybridization RNA Rat Sarcoma Rodentia Antisense RNA Northern blotting Vertebrata Mammalia Messenger RNA Liver cell carcinoma Tumor Molecular probe Nucleic acid |
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Snippet | An antisense RNA probe complementary to rat oncomodulin mRNA has been prepared by run-off transcription. Blots of RNA isolated from tumors arising from both a... |
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SubjectTerms | Animals Biological and medical sciences Calcium-Binding Proteins - genetics Cell physiology Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes Female Fundamental and applied biological sciences. Psychology Molecular and cellular biology mRNA abundance Neoplasms, Experimental - analysis Oncomodulin Placenta Placenta - analysis Pregnancy Rats RNA, Messenger - analysis Solid tumors |
Title | Varying oncomodulin mRNA abundance in developing placenta and solid tumors |
URI | https://dx.doi.org/10.1016/0304-3835(88)90005-5 https://www.ncbi.nlm.nih.gov/pubmed/3383173 https://search.proquest.com/docview/78260747 |
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