Literature DB >> 1634442

Serum and insulin inhibit cell death induced by cycloheximide in the human breast cancer cell line MCF-7.

A Geier1, R Beery, M Haimshon, R Hemi, B Lunenfeld.   

Abstract

Continuous exposure of cells to cycloheximide (CHM) terminates in cell death. This may result from CHM's inhibition of protein synthesis. In the present study we investigated the effect of serum and insulin on cell death induced by CHM in the human breast cancer cell line MCF-7, and correlated this effect to the inhibition of protein synthesis. Cell death was evaluated by measuring either dead cells by the trypan blue dye exclusion test or by the release of lactic dehydrogenase into the culture medium. CHM (0.1 to 50 micrograms/ml) was shown to induce cell death in a time- and concentration-dependent manner. Including either fetal bovine serum or insulin in the culture medium inhibited this cell death in a concentration-dependent manner. Protein synthesis as measured by [3H]leucine incorporation was inhibited by the increasing concentration of CHM. However, fetal bovine serum and insulin did not alter the protein synthesis inhibition rate induced by CHM. These results indicate that inhibition of protein synthesis is not enough for cell death to proceed. Insulin or factors present in serum may stabilize some crucial cell proteins (key enzymes, cytoskeletal or membrane components) which are vital for cell life.

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Year:  1992        PMID: 1634442     DOI: 10.1007/bf02634045

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol        ISSN: 0883-8364


  27 in total

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Review 3.  The insulin receptor: molecular biology and transmembrane signaling.

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Journal:  Cancer Res       Date:  1984-05       Impact factor: 12.701

5.  Endogenous endonuclease-induced DNA fragmentation: an early event in cell-mediated cytolysis.

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Journal:  Proc Natl Acad Sci U S A       Date:  1983-10       Impact factor: 11.205

6.  Chromatin cleavage in apoptosis: association with condensed chromatin morphology and dependence on macromolecular synthesis.

Authors:  A H Wyllie; R G Morris; A L Smith; D Dunlop
Journal:  J Pathol       Date:  1984-01       Impact factor: 7.996

7.  An electron-microscope study of the mode of cell death induced by cancer-chemotherapeutic agents in populations of proliferating normal and neoplastic cells.

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Journal:  J Pathol       Date:  1975-07       Impact factor: 7.996

8.  Induction of apoptosis (programmed cell death) in human leukemic HL-60 cells by inhibition of RNA or protein synthesis.

Authors:  S J Martin; S V Lennon; A M Bonham; T G Cotter
Journal:  J Immunol       Date:  1990-09-15       Impact factor: 5.422

9.  Purification of a hepatic S6 kinase from cycloheximide-treated Rats.

Authors:  D J Price; R A Nemenoff; J Avruch
Journal:  J Biol Chem       Date:  1989-08-15       Impact factor: 5.157

10.  Phenol red in tissue culture media is a weak estrogen: implications concerning the study of estrogen-responsive cells in culture.

Authors:  Y Berthois; J A Katzenellenbogen; B S Katzenellenbogen
Journal:  Proc Natl Acad Sci U S A       Date:  1986-04       Impact factor: 11.205

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  4 in total

1.  Epidermal growth factor, phorbol esters, and aurintricarboxylic acid are survival factors for MDA-231 cells exposed to adriamycin.

Authors:  A Geier; R Beery; M Haimsohn; R Hemi; Z Malik; A Karasik
Journal:  In Vitro Cell Dev Biol Anim       Date:  1994-12       Impact factor: 2.416

2.  Insulinlike growth factor-1 inhibits cell death induced by cycloheximide in MCF-7 cells: a model system for analyzing control of cell death.

Authors:  A Geier; M Haimshon; R Beery; R Hemi; B Lunenfeld
Journal:  In Vitro Cell Dev Biol       Date:  1992 Nov-Dec

3.  Epidermal growth factor and insulin-like growth factor-1 protect MDA-231 cells from death induced by actinomycin D: the involvement of growth factors in drug resistance.

Authors:  A Geier; R Hemi; M Haimsohn; R Beery; Z Malik; A Karasik
Journal:  In Vitro Cell Dev Biol Anim       Date:  1994-05       Impact factor: 2.416

4.  ER network formation and membrane fusion by atlastin1/SPG3A disease variants.

Authors:  Idil Ulengin; John J Park; Tina H Lee
Journal:  Mol Biol Cell       Date:  2015-03-11       Impact factor: 4.138

  4 in total

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