Dominant Negative α-Subunit of FTase Inhibits Effects of Insulin and IGF-I in MCF-7 Cells

We recently designed a dominant negative (DN) farnesyltransferase (FTase)/geranyl-gerahyltransferase I (GGTase I) α-subunit that when expressed in vascular smooth muscle cells decreased insulin-stimulated phosphorylation of FTase, FTase activity, amounts of farnesylated p21Ras, DNA synthesis, and ce...

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Published inBiochemical and biophysical research communications Vol. 291; no. 3; pp. 458 - 465
Main Authors Solomon, Curtis Scott, Goalstone, Marc Lee
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.03.2002
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Abstract We recently designed a dominant negative (DN) farnesyltransferase (FTase)/geranyl-gerahyltransferase I (GGTase I) α-subunit that when expressed in vascular smooth muscle cells decreased insulin-stimulated phosphorylation of FTase, FTase activity, amounts of farnesylated p21Ras, DNA synthesis, and cell migration. Currently, we explored the inhibitory effects of DN FTase/GGTase I α-subunit in MCF-7 cells on IGF-1- and insulin-stimulated DNA synthesis and cell proliferation. Expression of the DN FTase/GGTase I α-subunit completely blocked IGF-1- and insulin-stimulated BrdU incorporation and cell count. DN FTase/GGTase I α-subunit inhibited insulin-stimulated phosphorylation of FTase/GGTase I α-subunit, FTase and GGTase I activity, and prenylation of p21Ras and RhoA. Expression of DN FTase/GGTase I α-subunit diminished IGF-1- and insulin-stimulated phosphorylation of ERK (extracellular signal-regulated kinase), but had no effect on IGF-1- and insulin-stimulated phosphorylation of Akt. Taken together, these data suggest that DN FTase/GGTase I α-subunit can assuage the mitogenic effects of IGF-1 and insulin on MCF-7 breast cancer cells.
AbstractList We recently designed a dominant negative (DN) farnesyltransferase (FTase)/geranyl-gerahyltransferase I (GGTase I) alpha-subunit that when expressed in vascular smooth muscle cells decreased insulin-stimulated phosphorylation of FTase, FTase activity, amounts of farnesylated p21Ras, DNA synthesis, and cell migration. Currently, we explored the inhibitory effects of DN FTase/GGTase I alpha-subunit in MCF-7 cells on IGF-1- and insulin-stimulated DNA synthesis and cell proliferation. Expression of the DN FTase/GGTase I alpha-subunit completely blocked IGF-1- and insulin-stimulated BrdU incorporation and cell count. DN FTase/GGTase I alpha-subunit inhibited insulin-stimulated phosphorylation of FTase/GGTase I alpha-subunit, FTase and GGTase I activity, and prenylation of p21Ras and RhoA. Expression of DN FTase/GGTase I alpha-subunit diminished IGF-1- and insulin-stimulated phosphorylation of ERK (extracellular signal-regulated kinase), but had no effect on IGF-1- and insulin-stimulated phosphorylation of Akt. Taken together, these data suggest that DN FTase/GGTase I alpha-subunit can assuage the mitogenic effects of IGF-1 and insulin on MCF-7 breast cancer cells.
We recently designed a dominant negative (DN) farnesyltransferase (FTase)/geranyl-geranyltransferase I (GGTase I) alpha -subunit that when expressed in vascular smooth muscle cells decreased insulin-stimulated phosphorylation of FTase, FTase activity, amounts of farnesylated p21Ras, DNA synthesis, and cell migration. Currently, we explored the inhibitory effects of DN FTase/GGTase I alpha -subunit in MCF-7 cells on IGF-1- and insulin-stimulated DNA synthesis and cell proliferation. Expression of the DN FTase/GGTase I alpha -subunit completely blocked IGF-1- and insulin-stimulated BrdU incorporation and cell count. DN FTase/GGTase I alpha -subunit inhibited insulin-stimulated phosphorylation of FTase/GGTase I alpha -subunit, FTase and GGTase I activity, and prenylation of p21Ras and RhoA. Expression of DN FTase/GGTase I alpha -subunit diminished IGF-1- and insulin-stimulated phosphorylation of ERK (extracellular signal-regulated kinase), but had no effect on IGF-1- and insulin-stimulated phosphorylation of Akt. Taken together, these data suggest that DN FTase/GGTase I alpha -subunit can assuage the mitogenic effects of IGF-1 and insulin on MCF-7 breast cancer cells.
We recently designed a dominant negative (DN) farnesyltransferase (FTase)/geranyl-gerahyltransferase I (GGTase I) α-subunit that when expressed in vascular smooth muscle cells decreased insulin-stimulated phosphorylation of FTase, FTase activity, amounts of farnesylated p21Ras, DNA synthesis, and cell migration. Currently, we explored the inhibitory effects of DN FTase/GGTase I α-subunit in MCF-7 cells on IGF-1- and insulin-stimulated DNA synthesis and cell proliferation. Expression of the DN FTase/GGTase I α-subunit completely blocked IGF-1- and insulin-stimulated BrdU incorporation and cell count. DN FTase/GGTase I α-subunit inhibited insulin-stimulated phosphorylation of FTase/GGTase I α-subunit, FTase and GGTase I activity, and prenylation of p21Ras and RhoA. Expression of DN FTase/GGTase I α-subunit diminished IGF-1- and insulin-stimulated phosphorylation of ERK (extracellular signal-regulated kinase), but had no effect on IGF-1- and insulin-stimulated phosphorylation of Akt. Taken together, these data suggest that DN FTase/GGTase I α-subunit can assuage the mitogenic effects of IGF-1 and insulin on MCF-7 breast cancer cells.
Author Goalstone, Marc Lee
Solomon, Curtis Scott
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Keywords geranylgeranyltransferase I
MCF-7 cells
farnesyltransferase
insulin
dominant negative α-subunit
Language English
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SSID ssj0011469
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Snippet We recently designed a dominant negative (DN) farnesyltransferase (FTase)/geranyl-gerahyltransferase I (GGTase I) α-subunit that when expressed in vascular...
We recently designed a dominant negative (DN) farnesyltransferase (FTase)/geranyl-gerahyltransferase I (GGTase I) alpha-subunit that when expressed in vascular...
We recently designed a dominant negative (DN) farnesyltransferase (FTase)/geranyl-geranyltransferase I (GGTase I) alpha -subunit that when expressed in...
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SubjectTerms Akt protein
Alkyl and Aryl Transferases - chemistry
Alkyl and Aryl Transferases - genetics
Alkyl and Aryl Transferases - metabolism
Alkyl and Aryl Transferases - physiology
Breast Neoplasms - enzymology
Breast Neoplasms - metabolism
Breast Neoplasms - pathology
Breast Neoplasms - therapy
Cell Division
DNA, Neoplasm - biosynthesis
dominant negative α-subunit
farnesyltransferase
Female
geranyl-geranyltransferase
geranylgeranyltransferase I
Humans
insulin
Insulin - pharmacology
Insulin Antagonists - pharmacology
Insulin-Like Growth Factor I - antagonists & inhibitors
MCF-7 cells
Mutation
Phosphorylation
Protein Prenylation
Protein Subunits
Proto-Oncogene Proteins p21(ras) - metabolism
rhoA GTP-Binding Protein - metabolism
Tumor Cells, Cultured
Title Dominant Negative α-Subunit of FTase Inhibits Effects of Insulin and IGF-I in MCF-7 Cells
URI https://dx.doi.org/10.1006/bbrc.2002.6471
https://www.ncbi.nlm.nih.gov/pubmed/11855811
https://search.proquest.com/docview/18290036
https://search.proquest.com/docview/71461676
Volume 291
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